Product Name:4-Aminophenyl-1-Phenethylpiperidine
Alias:4-ANPP,Fentanyl Intermediate
Chemical Name:N-Phenyl-1-(2-Phenylethyl)-4-Piperidinamine
CAS NO.:21409-26-7
Molecular Formula:C19H24N2
Molecular Weight:280.4073
Purity:99%
Appearance:Pale Yellow Powder
Grade:Pharmaceutical Grade
Usage:Fenspiride Intermediate
4-ANPP (Item No. 18810) is an analytical reference material that is structurally categorized as a piperidinamine. It is an intermediate in the synthesis of fentan(Item Nos. ISO60197 | 14719) from N-phenethyl-4-piperidone (NPP). As such, 4-ANPP may be used as a precursor for the manufacture of fentanylni and related opioids. 4-ANPP is also an impurity found in fentanylni preparations. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.
This product is a qualified Reference Material (RM) that has been manufactured and tested to meet ISO17025 and Guide 34 guidelines. These materials are tested using validated analytical methods on qualified instrumentation to ensure traceability of measurements.
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Showing posts with label Hot selling. Show all posts
Showing posts with label Hot selling. Show all posts
Monday, December 11, 2017
1-Phenethyl-4-Piperidone/steroidmisty@ycphar.com
Product Name:1-Phenethyl-4-Piperidone,NPP
Alias:NPP,N-Phenethyl-4-piperidone,1-Phenethylpiperidin-4-one
CAS NO.:39742-60-4
Molecular Formula:C13H17NO
Molecular Weight:203.28
Purity:99%
Appearance:Light Yellow Crystalline Powder
Grade:Pharmaceutical Grade
Usage:Fenspiride Intermediate
What is N-Phenethyl-4-piperidinone(NPP)
N-Phenethyl-4-piperidinone (NPP) is a derivative of 4-piperidinone with the molecular formula C13H17NO. 4-Piperidinone is used as an intermediate in the manufacture of chemicals and pharmaceutical drugs such as fentanni.
1-Phenethyl-4-piperidone was used in the preparation of phenethyl derivative of the propanamide. It was also used to synthesize l-Phenethylazacycloheptan-4-one.
Alias:NPP,N-Phenethyl-4-piperidone,1-Phenethylpiperidin-4-one
CAS NO.:39742-60-4
Molecular Formula:C13H17NO
Molecular Weight:203.28
Purity:99%
Appearance:Light Yellow Crystalline Powder
Grade:Pharmaceutical Grade
Usage:Fenspiride Intermediate
What is N-Phenethyl-4-piperidinone(NPP)
N-Phenethyl-4-piperidinone (NPP) is a derivative of 4-piperidinone with the molecular formula C13H17NO. 4-Piperidinone is used as an intermediate in the manufacture of chemicals and pharmaceutical drugs such as fentanni.
1-Phenethyl-4-piperidone was used in the preparation of phenethyl derivative of the propanamide. It was also used to synthesize l-Phenethylazacycloheptan-4-one.
Hot selling Benzhydramine Hydrochloride/steroidmisty@ycphar.com
Product Name: Diphenhydramine hydrochloride
CAS No.: 147-24-0
EINECS:205-687-2
Assay: 99%
Moleular Formula: C17H22ClNO
Molecular Weight: 291.82
Appearance: White or White crystalline powder
Grade:Pharmaceutical Grade
Diphenhydramine is a first-generation antihistamine possessing anticholinergic, antitussive, antiemetic, and sedative properties that is mainly used to treat allergies. It is used to treat a number of conditions including allergic symptoms and itchiness, the common cold, insomnia, motion sickness, and extrapyramidal symptoms.It is also used in the management of drug-induced parkinsonism and other extrapyramidal symptoms.
Diphenhydramine is an antihistamine mainly used to treat allergies.It is also used for insomnia, symptoms of the common cold, tremor in parkinsonism, and nausea.It is used by mouth, injection into a vein, and injection into a muscle.Maximal effect is typically around two hours after a dose and effects can last for up to seven hours.
Medical Uses:Diphenhydramine is a first-generation antihistamine used to treat a number of conditions including allergic symptoms and itchiness, the common cold, insomnia, motion sickness, and extrapyramidal symptoms.Diphenhydramine also has local anesthetic properties, and has been used as such in people allergic to common local anesthetics such as lidocaine.
Allergies:Diphenhydramine is effective in treatment of allergies,it is the most commonly used antihistamine for acute allergic reactions in the emergency department.Topical formulations of diphenhydramine are available, including creams, lotions, gels, and sprays. These are used to relieve itching, and have the advantage of causing fewer systemic effects than oral forms.
Movement Disorders:Diphenhydramine is used to treat Parkinson's disease-like extrapyramidal symptoms caused by antipsychotics.
Sleep:Because of its sedative properties, diphenhydramine is widely used in nonprescription sleep aids for insomnia. The drug is an ingredient in several products sold as sleep aids, either alone or in combination with other ingredients such as acetaminophen (paracetamol). An example of the latter is Tylenol PM. Diphenhydramine can cause minor psychological dependence.Diphenhydramine can cause sedation and has also been used as an anxiolytic.
Nausea:Diphenhydramine also has antiemetic properties, which make it useful in treating the nausea that occurs in vertigo and motion sickness.
CAS No.: 147-24-0
EINECS:205-687-2
Assay: 99%
Moleular Formula: C17H22ClNO
Molecular Weight: 291.82
Appearance: White or White crystalline powder
Grade:Pharmaceutical Grade
Diphenhydramine is a first-generation antihistamine possessing anticholinergic, antitussive, antiemetic, and sedative properties that is mainly used to treat allergies. It is used to treat a number of conditions including allergic symptoms and itchiness, the common cold, insomnia, motion sickness, and extrapyramidal symptoms.It is also used in the management of drug-induced parkinsonism and other extrapyramidal symptoms.
Diphenhydramine is an antihistamine mainly used to treat allergies.It is also used for insomnia, symptoms of the common cold, tremor in parkinsonism, and nausea.It is used by mouth, injection into a vein, and injection into a muscle.Maximal effect is typically around two hours after a dose and effects can last for up to seven hours.
Medical Uses:Diphenhydramine is a first-generation antihistamine used to treat a number of conditions including allergic symptoms and itchiness, the common cold, insomnia, motion sickness, and extrapyramidal symptoms.Diphenhydramine also has local anesthetic properties, and has been used as such in people allergic to common local anesthetics such as lidocaine.
Allergies:Diphenhydramine is effective in treatment of allergies,it is the most commonly used antihistamine for acute allergic reactions in the emergency department.Topical formulations of diphenhydramine are available, including creams, lotions, gels, and sprays. These are used to relieve itching, and have the advantage of causing fewer systemic effects than oral forms.
Movement Disorders:Diphenhydramine is used to treat Parkinson's disease-like extrapyramidal symptoms caused by antipsychotics.
Sleep:Because of its sedative properties, diphenhydramine is widely used in nonprescription sleep aids for insomnia. The drug is an ingredient in several products sold as sleep aids, either alone or in combination with other ingredients such as acetaminophen (paracetamol). An example of the latter is Tylenol PM. Diphenhydramine can cause minor psychological dependence.Diphenhydramine can cause sedation and has also been used as an anxiolytic.
Nausea:Diphenhydramine also has antiemetic properties, which make it useful in treating the nausea that occurs in vertigo and motion sickness.
Promethazine Hydrochlorine/steroidmisty@ycphar.com
Product Name:Promethazine HCl
Molecular Weight:319.8726
CAS Registry Number:58-33-3
EINECS:200-375-2
Molecular Formula:C17H21ClN2S
Molecular Weight:320.88
Assay:99%
Appearance:White Powder
Grade:Pharmaceutical Grade
Promethazine is a neuroleptic medication and first-generation antihistamine of the phenothiazine family. The drug has strong sedative and weak antipsychotic effects. It also reduces motion sickness and has antiemetic and anticholinergic properties (via its action on the dopamine receptor D2). In some countries it is prescribed for insomnia when benzodiazepines are contraindicated.
Promethazine is in a group of drugs called phenothiazines (FEEN-oh-THYE-a-zeens). It works by changing the actions of chemicals in your brain. Promethazine also acts as an antihistamine. It blocks the effects of the naturally occurring chemical histamine in your body.
Promethazine is used to treat allergy symptoms such as itching, runny nose, sneezing, itchy or watery eyes, hives, and itchy skin rashes. It also prevents motion sickness, and treats nausea and vomiting or pain after surgery. It is also used as a sedative or sleep aid.
Molecular Weight:319.8726
CAS Registry Number:58-33-3
EINECS:200-375-2
Molecular Formula:C17H21ClN2S
Molecular Weight:320.88
Assay:99%
Appearance:White Powder
Grade:Pharmaceutical Grade
Promethazine is a neuroleptic medication and first-generation antihistamine of the phenothiazine family. The drug has strong sedative and weak antipsychotic effects. It also reduces motion sickness and has antiemetic and anticholinergic properties (via its action on the dopamine receptor D2). In some countries it is prescribed for insomnia when benzodiazepines are contraindicated.
Promethazine is in a group of drugs called phenothiazines (FEEN-oh-THYE-a-zeens). It works by changing the actions of chemicals in your brain. Promethazine also acts as an antihistamine. It blocks the effects of the naturally occurring chemical histamine in your body.
Promethazine is used to treat allergy symptoms such as itching, runny nose, sneezing, itchy or watery eyes, hives, and itchy skin rashes. It also prevents motion sickness, and treats nausea and vomiting or pain after surgery. It is also used as a sedative or sleep aid.
CAS 56-75-7 Chloramphenicol/steroidmisty@ycphar.com
Product Name:Chloramphenicol
Alias:Chloromycetin
CAS NO.:56-75-7
EINECS:200-287-4
Molecular Formula:C11H12Cl2N2O5
Molecular Weight:323.13
Appearance:white powder
Grade:Pharmaceutical Grade,Industrial Grade
Purity:99%
Chloramphenicol is an antibiotic useful for the treatment of a number of bacterial infections.This includes meningitis, plague, cholera, and typhoid fever. Its use is only recommended when safer antibiotics cannot be used. Monitoring both blood levels of the medication and blood cell levels every two days is recommended during treatment.It is available intravenously, by mouth, and as an eye ointment.
The original indication of chloramphenicol was in the treatment of typhoid, but the now almost universal presence of multiple drug-resistant Salmonella typhi has meant it is seldom used for this indication except when the organism is known to be sensitive. Chloramphenicol may be used as a second-line agent in the treatment of tetracycline-resistant cholera.
Chloramphenicol is active against the three main bacterial causes of meningitis: Neisseria meningitidis, Streptococcus pneumoniae, and Haemophilus influenzae. In the West, chloramphenicol remains the drug of choice in the treatment of meningitis in patients with severe penicillin or cephalosporin allergy and general practitioners are recommended to carry intravenous chloramphenicol in their bag. In low-income countries, the WHO recommend oily chloramphenicol as first-line to treat meningitis.
Although its use in veterinary medicine is highly restricted, chloramphenicol still has some important veterinary uses.It is currently considered the most useful treatment of chlamydial disease in koalas.The pharmacokinetics of chloramphenicol have been investigated in koalas.
Alias:Chloromycetin
CAS NO.:56-75-7
EINECS:200-287-4
Molecular Formula:C11H12Cl2N2O5
Molecular Weight:323.13
Appearance:white powder
Grade:Pharmaceutical Grade,Industrial Grade
Purity:99%
Chloramphenicol is an antibiotic useful for the treatment of a number of bacterial infections.This includes meningitis, plague, cholera, and typhoid fever. Its use is only recommended when safer antibiotics cannot be used. Monitoring both blood levels of the medication and blood cell levels every two days is recommended during treatment.It is available intravenously, by mouth, and as an eye ointment.
The original indication of chloramphenicol was in the treatment of typhoid, but the now almost universal presence of multiple drug-resistant Salmonella typhi has meant it is seldom used for this indication except when the organism is known to be sensitive. Chloramphenicol may be used as a second-line agent in the treatment of tetracycline-resistant cholera.
Chloramphenicol is active against the three main bacterial causes of meningitis: Neisseria meningitidis, Streptococcus pneumoniae, and Haemophilus influenzae. In the West, chloramphenicol remains the drug of choice in the treatment of meningitis in patients with severe penicillin or cephalosporin allergy and general practitioners are recommended to carry intravenous chloramphenicol in their bag. In low-income countries, the WHO recommend oily chloramphenicol as first-line to treat meningitis.
Although its use in veterinary medicine is highly restricted, chloramphenicol still has some important veterinary uses.It is currently considered the most useful treatment of chlamydial disease in koalas.The pharmacokinetics of chloramphenicol have been investigated in koalas.
Hot selling CAS 86386-73-4 Fluconazole/steroidmisty@ycphar.com
CAS 86386-73-4 Fluconazole
Product Name:Fluconazole
Alias: Diflucan; fluconazole; Triflucan
CAS number: 86386-73-4
Molecular formula: C13H12F2N6O
Molecular weight: 306.27
Melting point:137~141℃
Grade:Pharmaceutical grade
Appearance:white crystal or crystalline
Fluconazole is an antifungal medication that is administered orally or intravenously. It is used to treat a variety of fungal infections, especially Candida infections of the vagina,mouth, throat, and bloodstream. It is also used to prevent infections in people with weak immune systems, including those with neutropenia due to cancer chemotherapy, transplant patients, and premature babies. Its mechanism of action involves interfering with synthesis of the fungal cell membrane.
Fluconazole is a first-generation triazole antifungal medication. It differs from earlier azole antifungals (such as ketoconazole) in that its structure contains a triazole ring instead of an imidazole ring. While the imidazole antifungals are mainly used topically, fluconazole and certain other triazole antifungals are preferred when systemic treatment is required because of their improved safety and predictable absorption when administered orally.
Fluconazole's spectrum of activity includes most Candida species (but not Candida krusei or Candida glabrata), Cryptococcus neoformans, some dimorphic fungi, and dermatophytes, among others. Common uses include:
1)The treatment of non-systemic Candida infections of the vagina,throat, and mouth.
2)Certain systemic Candida infections in people with healthy immune systems, including infections of the bloodstream, kidney, or joints. Other antifungals are usually preferred when the infection is in the heart or central nervous system, and for the treatment of active infections in people with weak immune systems.
3)The prevention of Candida infections in people with weak immune systems, such as those neutropenic due to cancer chemotherapy, those with advanced HIV infections, transplant patients, and premature infants.
4)As a second-line agent for the treatment of cryptococcal meningoencephalitis, a fungal infection of the central nervous system.
Product Name:Fluconazole
Alias: Diflucan; fluconazole; Triflucan
CAS number: 86386-73-4
Molecular formula: C13H12F2N6O
Molecular weight: 306.27
Melting point:137~141℃
Grade:Pharmaceutical grade
Appearance:white crystal or crystalline
Fluconazole is an antifungal medication that is administered orally or intravenously. It is used to treat a variety of fungal infections, especially Candida infections of the vagina,mouth, throat, and bloodstream. It is also used to prevent infections in people with weak immune systems, including those with neutropenia due to cancer chemotherapy, transplant patients, and premature babies. Its mechanism of action involves interfering with synthesis of the fungal cell membrane.
Fluconazole is a first-generation triazole antifungal medication. It differs from earlier azole antifungals (such as ketoconazole) in that its structure contains a triazole ring instead of an imidazole ring. While the imidazole antifungals are mainly used topically, fluconazole and certain other triazole antifungals are preferred when systemic treatment is required because of their improved safety and predictable absorption when administered orally.
Fluconazole's spectrum of activity includes most Candida species (but not Candida krusei or Candida glabrata), Cryptococcus neoformans, some dimorphic fungi, and dermatophytes, among others. Common uses include:
1)The treatment of non-systemic Candida infections of the vagina,throat, and mouth.
2)Certain systemic Candida infections in people with healthy immune systems, including infections of the bloodstream, kidney, or joints. Other antifungals are usually preferred when the infection is in the heart or central nervous system, and for the treatment of active infections in people with weak immune systems.
3)The prevention of Candida infections in people with weak immune systems, such as those neutropenic due to cancer chemotherapy, those with advanced HIV infections, transplant patients, and premature infants.
4)As a second-line agent for the treatment of cryptococcal meningoencephalitis, a fungal infection of the central nervous system.
CAS 25122-46-7 Clobetasol Propionate/steroidmisty@ycphar.com
Product name: Clobetasol Propionate
Alias:Clobetasolprop,lobet,lobetasol pro
CAS NO.: 25122-46-7
EINECS:246-634-3
Molecular Formula:C25H32ClFO5
Molecular Weight:466.97
Assay: 99%
Appearance: White crystalline powder
Grade:Pharmaceutical Grade
Clobetasol propionate is a corticosteroid of synthetic steroid used to treat various skin disorders including inflammation, itching, herpes labialis, eczema, psoriasis and lichen sclerosus.
Clobetasol propionate is also highly effective for contact dermatitis caused by exposure to poison ivy/oak and auto-immune diseases including alopecia areata, vitiligo, lichen planus (auto immune skin nodules), and mycosis fungoides (T-cell skin lymphoma).
Clobetasol propionate is used as first-line treatment for both acute and chronic GVHD of the skin.
Clobetasol propionate is a topical corticosteroid preparation usually found in the form of cream, ointment, gel or shampoo. It is used on the skin or scalp to treat common dermatological disorders such as eczema and psoriasis. Its main effect is to reduce the swelling, inflammation, redness and itching associated with skin conditions such as these. It is a high potency corticosteroid, so it should be used cautiously, for a limited period, and under the supervision of a medical practitioner.
The way in which clobetasol propionate works is by reducing swelling, its anti-inflammatory effect; itching, its anti-pruritic effect; and redness, its vasoconstrictive action. This treats the symptoms commonly associated with dermatological conditions such as eczema, psoriasis and some contact dermatitis. As with any medication, clobetasol propionate may also cause unwanted side effects in some people. It is because of these possible side effects that the medication should be used cautiously, under medical supervision.
Side Effects
One of the most serious possible side effects is an effect on the adrenal gland. Clobetasol propionate, especially used long-term or over large areas, may cause suppression of the hypothalamic-pituitary-adrenal (HPA) axis, a sensitive system that controls neuroendocrine regulation of the body. Other, less serious side effects may include stinging or burning of the skin. If any untoward effects are experienced when using clobetasol propionate, medical advice should be sought.
Alias:Clobetasolprop,lobet,lobetasol pro
CAS NO.: 25122-46-7
EINECS:246-634-3
Molecular Formula:C25H32ClFO5
Molecular Weight:466.97
Assay: 99%
Appearance: White crystalline powder
Grade:Pharmaceutical Grade
Clobetasol propionate is a corticosteroid of synthetic steroid used to treat various skin disorders including inflammation, itching, herpes labialis, eczema, psoriasis and lichen sclerosus.
Clobetasol propionate is also highly effective for contact dermatitis caused by exposure to poison ivy/oak and auto-immune diseases including alopecia areata, vitiligo, lichen planus (auto immune skin nodules), and mycosis fungoides (T-cell skin lymphoma).
Clobetasol propionate is used as first-line treatment for both acute and chronic GVHD of the skin.
Clobetasol propionate is a topical corticosteroid preparation usually found in the form of cream, ointment, gel or shampoo. It is used on the skin or scalp to treat common dermatological disorders such as eczema and psoriasis. Its main effect is to reduce the swelling, inflammation, redness and itching associated with skin conditions such as these. It is a high potency corticosteroid, so it should be used cautiously, for a limited period, and under the supervision of a medical practitioner.
The way in which clobetasol propionate works is by reducing swelling, its anti-inflammatory effect; itching, its anti-pruritic effect; and redness, its vasoconstrictive action. This treats the symptoms commonly associated with dermatological conditions such as eczema, psoriasis and some contact dermatitis. As with any medication, clobetasol propionate may also cause unwanted side effects in some people. It is because of these possible side effects that the medication should be used cautiously, under medical supervision.
Side Effects
One of the most serious possible side effects is an effect on the adrenal gland. Clobetasol propionate, especially used long-term or over large areas, may cause suppression of the hypothalamic-pituitary-adrenal (HPA) axis, a sensitive system that controls neuroendocrine regulation of the body. Other, less serious side effects may include stinging or burning of the skin. If any untoward effects are experienced when using clobetasol propionate, medical advice should be sought.
Hot selling CAS 57-83-0 Progesterone/steroidmisty@ycphar.com
Product name:Progesterone
Alias:Progestin, progestone,Lutren,Lutein,Flavolutan,Corporin,Luteal hormone
CAS: 57-83-0
EINECS:200-350-6
Assay: 99%
M. F.: C21H30O2
M. W.: 314.46
Appearance: White or almost white crystalline powder
Category: Progestoneis belong to Progesterone Hormone
Usage: Sterid hormone produced by the corpus luteum. Induces maturation and secretory activity of the uterine endothelium; suppresses ovulation. Progesterone is implicated in the etiology of breast cancer.
Progesterone (abbreviated as P4), also known as pregn-4-ene-3,20-dione,is an endogenous steroid and progestogen sex hormone involved in the menstrual cycle, pregnancy, and embryogenesis of humans and other species.It belongs to a group of steroid hormones called the progestogens,and is the major progestogen in the body. Progesterone is also a crucial metabolic intermediate in the production of other endogenous steroids, including the sex hormones and the corticosteroids, and plays an important role in brain function as a neurosteroid.
The use of progesterone and its analogues have many medical applications, both to address acute situations and to address the long-term decline of natural progesterone levels. Because of the poor bioavailability of progesterone when taken orally, many synthetic progestins have been designed with improved oral bioavailability and have been used long before progesterone formulations became available.
Progesterone is a female Progesterone Hormones important for the regulation of ovulation and menstruation.
Women take progesterone by mouth for inducing menstrual periods who have not yet reached menopause but are not having periods due to a lack of progesterone in the body; and treating abnormal uterine bleeding associated with hormonal imbalance, and severe symptoms of premenstrual syndrome (PMS). progesterone is also used to prevent overgrowth in the lining of the uterus in postmenopausal women who are receiving estrogen hormone replacement therapy. Progesterone is also used in combination with the hormone estrogen to “oppose estrogen” as part of hormone replacement therapy. If estrogen is given without progesterone, estrogen increases the risk of uterine cancer
Alias:Progestin, progestone,Lutren,Lutein,Flavolutan,Corporin,Luteal hormone
CAS: 57-83-0
EINECS:200-350-6
Assay: 99%
M. F.: C21H30O2
M. W.: 314.46
Appearance: White or almost white crystalline powder
Category: Progestoneis belong to Progesterone Hormone
Usage: Sterid hormone produced by the corpus luteum. Induces maturation and secretory activity of the uterine endothelium; suppresses ovulation. Progesterone is implicated in the etiology of breast cancer.
Progesterone (abbreviated as P4), also known as pregn-4-ene-3,20-dione,is an endogenous steroid and progestogen sex hormone involved in the menstrual cycle, pregnancy, and embryogenesis of humans and other species.It belongs to a group of steroid hormones called the progestogens,and is the major progestogen in the body. Progesterone is also a crucial metabolic intermediate in the production of other endogenous steroids, including the sex hormones and the corticosteroids, and plays an important role in brain function as a neurosteroid.
The use of progesterone and its analogues have many medical applications, both to address acute situations and to address the long-term decline of natural progesterone levels. Because of the poor bioavailability of progesterone when taken orally, many synthetic progestins have been designed with improved oral bioavailability and have been used long before progesterone formulations became available.
Progesterone is a female Progesterone Hormones important for the regulation of ovulation and menstruation.
Women take progesterone by mouth for inducing menstrual periods who have not yet reached menopause but are not having periods due to a lack of progesterone in the body; and treating abnormal uterine bleeding associated with hormonal imbalance, and severe symptoms of premenstrual syndrome (PMS). progesterone is also used to prevent overgrowth in the lining of the uterus in postmenopausal women who are receiving estrogen hormone replacement therapy. Progesterone is also used in combination with the hormone estrogen to “oppose estrogen” as part of hormone replacement therapy. If estrogen is given without progesterone, estrogen increases the risk of uterine cancer
Hot selling CAS 50-28-2 Estradiol/steroidmisty@ycphar.com
Product name: Estradiol,Dihydrofolliculin
CAS No.: 50-28-2
EINECS:200-023-8
Molecular Formula: C18H24O2
Molecular Weight: 272.38
Assay: 98.66%
Reference Standard: USP28
Appearance: White or creamy white crystalline powder
Estradiol, or more precisely, 17β-estradiol, is a steroid and estrogen sex hormone, and the primary female sex hormone. It is named for and is important in the regulation of the estrous and menstrual female reproductive cycles. Estradiol is essential for the development and maintenance of female reproductive tissues but it also has important effects in many other tissues including bone. While estrogen levels in men are lower compared to women, estrogens have essential functions in men as well. Estradiol is found in most vertebrates as well as many crustaceans, insects, fish, and other animal species.
Function and use: It is a kind of estrogen, can promote and regulate the normal development of women's genitals and secondary. Can cause hyperplasia of mammary gland carcinoma development, but in larger doses, can inhibit pituitary prolactin release, and reduce the secretion of milk. Potent mammalian estrogenic hormone produced by the ovary.
This medication is a female hormone (estrogen). It is used by women to help reduce symptoms of menopause (such as hot flashes, vaginal dryness). These symptoms are caused by the body making less estrogen. If you are using this medication to treat symptoms only in and around the vagina, products applied directly inside the vagina should be considered before medications that are taken by mouth, absorbed through the skin, or injected. This medication may also be used by women who are not able to produce enough estrogen (for example, due to hypogonadism, primary ovarian failure).
CAS No.: 50-28-2
EINECS:200-023-8
Molecular Formula: C18H24O2
Molecular Weight: 272.38
Assay: 98.66%
Reference Standard: USP28
Appearance: White or creamy white crystalline powder
Estradiol, or more precisely, 17β-estradiol, is a steroid and estrogen sex hormone, and the primary female sex hormone. It is named for and is important in the regulation of the estrous and menstrual female reproductive cycles. Estradiol is essential for the development and maintenance of female reproductive tissues but it also has important effects in many other tissues including bone. While estrogen levels in men are lower compared to women, estrogens have essential functions in men as well. Estradiol is found in most vertebrates as well as many crustaceans, insects, fish, and other animal species.
Function and use: It is a kind of estrogen, can promote and regulate the normal development of women's genitals and secondary. Can cause hyperplasia of mammary gland carcinoma development, but in larger doses, can inhibit pituitary prolactin release, and reduce the secretion of milk. Potent mammalian estrogenic hormone produced by the ovary.
This medication is a female hormone (estrogen). It is used by women to help reduce symptoms of menopause (such as hot flashes, vaginal dryness). These symptoms are caused by the body making less estrogen. If you are using this medication to treat symptoms only in and around the vagina, products applied directly inside the vagina should be considered before medications that are taken by mouth, absorbed through the skin, or injected. This medication may also be used by women who are not able to produce enough estrogen (for example, due to hypogonadism, primary ovarian failure).
Hot selling Tranexamic Acid/steroidmisty@ycphar.com
Product Name: Tranexamic Acid
Alias:Amstat,tranexa,transamic acid
CAS No.: 1197-18-8
EINECS No.: 214-818-2
Molecular Formula: C8H15NO2
Molecular Weight: 157.21
Purity:99%
Melting point: >300 °C(lit.)
Appearance: white powder
Grade:Pharmaceutical Grade
Application: Mainly used for Whitening freckle,Hemostasis
Tranexamic acid (TXA) is used to treat or prevent excessive blood loss from trauma, surgery, and in various medical conditions including hemophilia and heavy menstrual bleeding.It comes in oral and intravenous forms.
Tranexamic acid is frequently used following major trauma.Tranexamic acid is used to prevent and treat blood loss in a variety of situations, such as dental procedures for hemophiliacs, heavy menstrual bleeding, and surgeries with high risk of blood loss.
Trauma:Tranexamic acid has been found to decrease the risk of death in people who have significant bleeding due to trauma.[7] However, its benefit only appears to be within the first three hours.
Heavy menstrual bleeding:Tranexamic acid is used treat heavy menstrual bleeding.When taken by mouth it is both safely and effectively treated regularly occurring heavy menstrual bleeding.Another study demonstrated that the dose does not need to be adjusted in people who are between ages 12 and 16.
Surgery:Tranexamic acid is used in orthopedic surgery to reduce blood loss, to the extent of reducing or altogether abolishing the need for perioperative blood collection. It is of proven value in clearing the field of surgery and reducing blood loss when given before or after surgery. Drain and number of transfusions are reduced. However, the hidden blood loss is not reduced. Still, it is becoming an important tool in the anaesthetist's arsenal. It is commonly used in joint replacement surgery.
Use of tranexamic acid in surgical corrections of craniosynostosis in children reduces the need for blood transfusions.
Tranexamic acid is commonly used in cardiac surgery, both with and without cardiopulmonary bypass. It replaces aprotinin
Alias:Amstat,tranexa,transamic acid
CAS No.: 1197-18-8
EINECS No.: 214-818-2
Molecular Formula: C8H15NO2
Molecular Weight: 157.21
Purity:99%
Melting point: >300 °C(lit.)
Appearance: white powder
Grade:Pharmaceutical Grade
Application: Mainly used for Whitening freckle,Hemostasis
Tranexamic acid (TXA) is used to treat or prevent excessive blood loss from trauma, surgery, and in various medical conditions including hemophilia and heavy menstrual bleeding.It comes in oral and intravenous forms.
Tranexamic acid is frequently used following major trauma.Tranexamic acid is used to prevent and treat blood loss in a variety of situations, such as dental procedures for hemophiliacs, heavy menstrual bleeding, and surgeries with high risk of blood loss.
Trauma:Tranexamic acid has been found to decrease the risk of death in people who have significant bleeding due to trauma.[7] However, its benefit only appears to be within the first three hours.
Heavy menstrual bleeding:Tranexamic acid is used treat heavy menstrual bleeding.When taken by mouth it is both safely and effectively treated regularly occurring heavy menstrual bleeding.Another study demonstrated that the dose does not need to be adjusted in people who are between ages 12 and 16.
Surgery:Tranexamic acid is used in orthopedic surgery to reduce blood loss, to the extent of reducing or altogether abolishing the need for perioperative blood collection. It is of proven value in clearing the field of surgery and reducing blood loss when given before or after surgery. Drain and number of transfusions are reduced. However, the hidden blood loss is not reduced. Still, it is becoming an important tool in the anaesthetist's arsenal. It is commonly used in joint replacement surgery.
Use of tranexamic acid in surgical corrections of craniosynostosis in children reduces the need for blood transfusions.
Tranexamic acid is commonly used in cardiac surgery, both with and without cardiopulmonary bypass. It replaces aprotinin
CAS 550-99-2 Naphazoline HCl/steroidmisty@ycphar.com
Product Name: Naphazoline Hydrochloride
Synonyms:niazol;coldan;naphcon;rhinoperd;rhinantin;stricylon;strictylon;naphconforte;sanorin-spofa
CAS No.: 550-99-2
EINECS:208-989-2
Molecular Formula: C14H15ClN2
Molecular Weight: 246.74
Melting point: 254-260 °C
Appearance: white crystalline powder
Purity:99%
Grade:Pharmaceutical Grade
Application: applied to treatment of rhinallergosis,Inflammatory nasal congestion,Acute and chronic rhinitis
Naphazoline HCl is α-receptor agonist, a contraction of nasal blood vessels, reducing blood vessel exudate, reduce nasal congestion swelling. Clinically used to treat colds and allergic rhinitis, inflammatory nasal congestion, acute and chronic rhinitis.
Naphazoline is the common name for 2-(1-naphthylmethyl)-2-imidazoline hydrochloride. It is a sympathomimetic agent with marked alpha adrenergic activity. It is a vasoconstrictor with a rapid action in reducing swelling when applied to mucous membrane. It acts on alpha-receptors in the arterioles of the conjunctiva to produce constriction, resulting in decreased congestion. It is an active ingredient in several over-the-counter formulations including Clear Eyes and Naphcon eye drops.
Synonyms:niazol;coldan;naphcon;rhinoperd;rhinantin;stricylon;strictylon;naphconforte;sanorin-spofa
CAS No.: 550-99-2
EINECS:208-989-2
Molecular Formula: C14H15ClN2
Molecular Weight: 246.74
Melting point: 254-260 °C
Appearance: white crystalline powder
Purity:99%
Grade:Pharmaceutical Grade
Application: applied to treatment of rhinallergosis,Inflammatory nasal congestion,Acute and chronic rhinitis
Naphazoline HCl is α-receptor agonist, a contraction of nasal blood vessels, reducing blood vessel exudate, reduce nasal congestion swelling. Clinically used to treat colds and allergic rhinitis, inflammatory nasal congestion, acute and chronic rhinitis.
Naphazoline is the common name for 2-(1-naphthylmethyl)-2-imidazoline hydrochloride. It is a sympathomimetic agent with marked alpha adrenergic activity. It is a vasoconstrictor with a rapid action in reducing swelling when applied to mucous membrane. It acts on alpha-receptors in the arterioles of the conjunctiva to produce constriction, resulting in decreased congestion. It is an active ingredient in several over-the-counter formulations including Clear Eyes and Naphcon eye drops.
Clotrimazole/steroidmisty@ycphar.com
Product Name:Clotrimazole
CAS:23593-75-1
Einecs:245-764-8
Mf:C22H17ClN2
MW:344.84
Purity:99%
Grade:Pharmaceutical Grade
Appearance:White or Pale Yellow Crystalline Powder
Clotrimazole (brand name Canesten or Lotrimin) is an antifungal medication commonly used in the treatment of fungal infections (of both humans and other animals) such as vaginal yeast infections, oral thrush, and ringworm. It is also used to treat athlete's foot and jock itch.It is on the World Health Organization's List of Essential Medicines, the most important medication needed in a basic health system.
It is commonly available as an over-the-counter substance in various dosage forms, such as a cream, vaginal tablet, or as a prescription troche or throat lozenge (prescription only). Topically, clotrimazole is used for vulvovaginal candidiasis (yeast infection) or yeast infections of the skin. For vulvovaginal candidiasis (yeast infection), clotrimazole tablets and creams are inserted into the vagina. Troche or throat lozenge preparations are used for oropharyngeal candidiasis (oral thrush) or prophylaxis against oral thrush in neutropenic patients.
Clotrimazole is usually used 5 times daily for 14 days for oral thrush, twice daily for 2 to 8 weeks for skin infections, and once daily for 3 or 7 days for vaginal infections.
Clotrimazole is also commonly used in conjunction with betamethasone as a topical cream for tinea corporis (ringworm), tinea cruris (jock itch), or tinea pedis (athlete's foot).
Topical and oral clotrimazole can be used in both adult and pediatric populations.
Additionally, clotrimazole may be used to treat the sickling of cells (related to sickle cell anemia).
CAS:23593-75-1
Einecs:245-764-8
Mf:C22H17ClN2
MW:344.84
Purity:99%
Grade:Pharmaceutical Grade
Appearance:White or Pale Yellow Crystalline Powder
Clotrimazole (brand name Canesten or Lotrimin) is an antifungal medication commonly used in the treatment of fungal infections (of both humans and other animals) such as vaginal yeast infections, oral thrush, and ringworm. It is also used to treat athlete's foot and jock itch.It is on the World Health Organization's List of Essential Medicines, the most important medication needed in a basic health system.
It is commonly available as an over-the-counter substance in various dosage forms, such as a cream, vaginal tablet, or as a prescription troche or throat lozenge (prescription only). Topically, clotrimazole is used for vulvovaginal candidiasis (yeast infection) or yeast infections of the skin. For vulvovaginal candidiasis (yeast infection), clotrimazole tablets and creams are inserted into the vagina. Troche or throat lozenge preparations are used for oropharyngeal candidiasis (oral thrush) or prophylaxis against oral thrush in neutropenic patients.
Clotrimazole is usually used 5 times daily for 14 days for oral thrush, twice daily for 2 to 8 weeks for skin infections, and once daily for 3 or 7 days for vaginal infections.
Clotrimazole is also commonly used in conjunction with betamethasone as a topical cream for tinea corporis (ringworm), tinea cruris (jock itch), or tinea pedis (athlete's foot).
Topical and oral clotrimazole can be used in both adult and pediatric populations.
Additionally, clotrimazole may be used to treat the sickling of cells (related to sickle cell anemia).
CAS 110-63-4 1,4-Butanediol/steroidmisty@ycphar.com
Product Name: 1,4-Butanediol
Alias:1,4-Dihydroxybutane;1,4-Butylene glycol;Tetramethylene glycol
CAS NO.: 110-63-4
EINECS NO.: 203-786-5
MF: C4H10O2
MW:90.12
PURITY: 99%
APPEARANCE: colorless viscous liquid
MELTING POINT: 20°C
BOILING POINT: 230°C
Flash Point: 135°C
Solubility: Miscible
Density: 1.017g/mL
1,4-Butanediol (1,4-B, butylene glycol, or BD) is a thick, colourless liquid which is nearly odorless with a distinct bitter taste. 1,4-Butanediol is used industrially as a solvent and in the manufacture of some types of plastics, elastic fibers and polyurethanes. In organic chemistry, 1,4-butanediol is used for the synthesis of γ-butyrolactone (GBL).
In humans, it acts as a depressant and a prodrug for GHB where 1ml is equivalent to 1g of GHB. It is used as a recreational intoxicant with effects similar to alcohol.
1,4-Butanediol, as well as GBL, will dissolve most types of plastic over time.For this reason, it is recommended to only transport and store the drug using a glass container, standard gelatin capsules (not vegetarian), or high-density polyethylene plastic (also known as #2 recycled plastic). To check the type of plastic used on a bottle, one can look at the bottom for a number in the triangle shaped recycling label.
Physical effects
Stimulation and Sedation - At lower doses, 1,4-butanediol is physically stimulating, encouraging movement and wakefulness. At higher doses, however, it becomes physically sedating, encouraging sleep and lethargy.
Euphoria
Nausea
Motor control loss
Dizziness
Dehydration
Respiratory depression - Many reportedly experience an abnormal pattern of breathing characterized by progressively deeper and sometimes faster breathing followed by a gradual decrease that results in a temporary stop in breathing called an apnea.
Cognitive effects
Empathy, love and sociability enhancement - Unlike alcohol which merely increases sociability through disinhibition, 1,4-butanediol presents strong entactogenic effects which, although weaker than that of MDMA, are still prominent and well-defined.
Disinhibition
Information processing suppression
Thought deceleration
Amnesia
Euphoria
Anxiety suppression
Increased libido - - This effect is manifested differently in comparison to dopaminergic stimulants such as cocaine or amphetamine in a way that is more emotionally driven and cerebral in its perception as opposed to being primarily physically driven by dopaminergic stimulation. It is most felt when dosage remains low to moderate and intensifies proportionally to the duration of consumption
Toxicity and harm potential
1,4-Butanediol is not active in its own right; its mechanism of action stems from its identity as a prodrug of GHB, meaning that it is rapidly converted into GHB in the body.
GHB is considered to be a safe and non-toxic substance when used responsibly or medically. The LD50 is above the active dosage, and there is no danger of acute toxicity when this compound is taken at appropriate dosages. However, it can be dangerous when used as a recreational drug or abused. There have been many negative reports from recreational users who have overdosed, combined GHB with alcohol or other drugs, or accidentally dosed themselves unexpectedly.
One publication has investigated 226 deaths attributed to GHB.Seventy-one deaths (34%) were caused by GHB alone while the other deaths were from respiratory depression caused by interaction with alcohol or other drugs.To avoid a possible overdose of GHB/1,4-Butanediol, it is important to start with a low dose and work your way up slowly by increasing the dosage in small increments as the exact toxic dosage is unknown.
Accidental ingestions of 1,4-Butanediol have also occurred due to inadequate storage methods. If 1,4-Butanediol is put into a clear liquid, glass, or bottle, it can be easily mistaken for water. It is recommended to clearly label your 1,4-Butanediol in writing and dye the liquid with blue food coloring so it no longer resembles a drinkable beverage. It is also recommended to store your 1,4-Butanediol in a container that no one would drink out of.
It is strongly recommended that one use harm reduction practices when using this drug.
Alias:1,4-Dihydroxybutane;1,4-Butylene glycol;Tetramethylene glycol
CAS NO.: 110-63-4
EINECS NO.: 203-786-5
MF: C4H10O2
MW:90.12
PURITY: 99%
APPEARANCE: colorless viscous liquid
MELTING POINT: 20°C
BOILING POINT: 230°C
Flash Point: 135°C
Solubility: Miscible
Density: 1.017g/mL
1,4-Butanediol (1,4-B, butylene glycol, or BD) is a thick, colourless liquid which is nearly odorless with a distinct bitter taste. 1,4-Butanediol is used industrially as a solvent and in the manufacture of some types of plastics, elastic fibers and polyurethanes. In organic chemistry, 1,4-butanediol is used for the synthesis of γ-butyrolactone (GBL).
In humans, it acts as a depressant and a prodrug for GHB where 1ml is equivalent to 1g of GHB. It is used as a recreational intoxicant with effects similar to alcohol.
1,4-Butanediol, as well as GBL, will dissolve most types of plastic over time.For this reason, it is recommended to only transport and store the drug using a glass container, standard gelatin capsules (not vegetarian), or high-density polyethylene plastic (also known as #2 recycled plastic). To check the type of plastic used on a bottle, one can look at the bottom for a number in the triangle shaped recycling label.
Physical effects
Stimulation and Sedation - At lower doses, 1,4-butanediol is physically stimulating, encouraging movement and wakefulness. At higher doses, however, it becomes physically sedating, encouraging sleep and lethargy.
Euphoria
Nausea
Motor control loss
Dizziness
Dehydration
Respiratory depression - Many reportedly experience an abnormal pattern of breathing characterized by progressively deeper and sometimes faster breathing followed by a gradual decrease that results in a temporary stop in breathing called an apnea.
Cognitive effects
Empathy, love and sociability enhancement - Unlike alcohol which merely increases sociability through disinhibition, 1,4-butanediol presents strong entactogenic effects which, although weaker than that of MDMA, are still prominent and well-defined.
Disinhibition
Information processing suppression
Thought deceleration
Amnesia
Euphoria
Anxiety suppression
Increased libido - - This effect is manifested differently in comparison to dopaminergic stimulants such as cocaine or amphetamine in a way that is more emotionally driven and cerebral in its perception as opposed to being primarily physically driven by dopaminergic stimulation. It is most felt when dosage remains low to moderate and intensifies proportionally to the duration of consumption
Toxicity and harm potential
1,4-Butanediol is not active in its own right; its mechanism of action stems from its identity as a prodrug of GHB, meaning that it is rapidly converted into GHB in the body.
GHB is considered to be a safe and non-toxic substance when used responsibly or medically. The LD50 is above the active dosage, and there is no danger of acute toxicity when this compound is taken at appropriate dosages. However, it can be dangerous when used as a recreational drug or abused. There have been many negative reports from recreational users who have overdosed, combined GHB with alcohol or other drugs, or accidentally dosed themselves unexpectedly.
One publication has investigated 226 deaths attributed to GHB.Seventy-one deaths (34%) were caused by GHB alone while the other deaths were from respiratory depression caused by interaction with alcohol or other drugs.To avoid a possible overdose of GHB/1,4-Butanediol, it is important to start with a low dose and work your way up slowly by increasing the dosage in small increments as the exact toxic dosage is unknown.
Accidental ingestions of 1,4-Butanediol have also occurred due to inadequate storage methods. If 1,4-Butanediol is put into a clear liquid, glass, or bottle, it can be easily mistaken for water. It is recommended to clearly label your 1,4-Butanediol in writing and dye the liquid with blue food coloring so it no longer resembles a drinkable beverage. It is also recommended to store your 1,4-Butanediol in a container that no one would drink out of.
It is strongly recommended that one use harm reduction practices when using this drug.
CAS 121-57-3 Sulfanilic acid/steroidmisty@ycphar.com
Product Name:Sulfanilic acid
Alias:4-Aminobenzenesulfonic acid,4-Anilinesulfonic acid
CAS NO.:121-57-3
EINECS:204-482-5
Molecular Formula:C6H7NO3S
Molecular Weight:173.19
Purity:99%
Grade:Industrial Grade
Appearance:White Powder
Sulfanilic acid (4-aminobenzenesulfonic acid ) is an off-white crystalline solid which finds application in quantitative analysis of nitrate and nitrite ions. The solid acid exists as a zwitterion, and has an unusually high melting point.
As the compound readily form diazo compounds, it is used to make dyes and sulpha drugs. This property is also used for the quantitative analysis of nitrate and nitrite ions by diazonium coupling reaction with N-(1-Naphthyl)ethylenediamine, resulting in an azo dye, and the concentration of nitrate or nitrite ions were deduced from the color intensity of the resulting red solution by colorimetry.
It is also used as a standard in combustion analysis and in the Pauly reaction.
Alias:4-Aminobenzenesulfonic acid,4-Anilinesulfonic acid
CAS NO.:121-57-3
EINECS:204-482-5
Molecular Formula:C6H7NO3S
Molecular Weight:173.19
Purity:99%
Grade:Industrial Grade
Appearance:White Powder
Sulfanilic acid (4-aminobenzenesulfonic acid ) is an off-white crystalline solid which finds application in quantitative analysis of nitrate and nitrite ions. The solid acid exists as a zwitterion, and has an unusually high melting point.
As the compound readily form diazo compounds, it is used to make dyes and sulpha drugs. This property is also used for the quantitative analysis of nitrate and nitrite ions by diazonium coupling reaction with N-(1-Naphthyl)ethylenediamine, resulting in an azo dye, and the concentration of nitrate or nitrite ions were deduced from the color intensity of the resulting red solution by colorimetry.
It is also used as a standard in combustion analysis and in the Pauly reaction.
Hot selling L-Carnitine/steroidmisty@ycphar.com
Product Name:L-carnitine,Vitamin BT,L-ca greatrnitine,L-ctheirrnitine
CAS NO.:541-15-1
EINECS:208-768-0
Molecular Formula:C7H15NO3
Molecular Weight:161.20
Melting Point:200℃
Appearance:white crystal or transparent powder
Application: used in drugs, Nutrition and health care products,Energy drinks and feed additives
Usage: L-Carnitine is a natural, vitamin-like nutrient wich plays an important role inhuman metabolism. It is essential in the utilization of fatty acids and in transporting metabolic energy
Carnitine (carnitine) is an essential, non-toxic, natural nutrient that helps burn fat for fuel. Because deficiencies have been linked to a profound impairment of muscle function, there has been great interest in studying carnitine supplementation. Over the past decade, my research, as well as countless others, has shed light on carnitine’s role in metabolism, performance and overall health.
Carnitine burns body fat
Carnitine has an essential role in transporting fat into mitochondria (the furnace of the cell). Therefore, carnitine has been marketed as a fat burning supplement.Carnitine is a substance that helps the body turn fat into energy. Your body makes it in the liver and kidneys and stores it in the skeletal muscles, heart, brain, and sperm.
Usually, your body can make all the carnitine it needs. Some people, however, may not have enough carnitine because their bodies cannot make enough or can’t transport it into tissues so it can be used. Some other conditions, such as angina or intermittent claudication, can also cause low levels of carnitine in the body, as can some medications.
Carnitine has been proposed as a treatment for many conditions because it acts as an antioxidant. Antioxidants fight harmful particles in the body known as free radicals, which damage cells and tamper with DNA. Antioxidants can neutralize free radicals and may reduce or help prevent some of the damage they cause.
CAS NO.:541-15-1
EINECS:208-768-0
Molecular Formula:C7H15NO3
Molecular Weight:161.20
Melting Point:200℃
Appearance:white crystal or transparent powder
Application: used in drugs, Nutrition and health care products,Energy drinks and feed additives
Usage: L-Carnitine is a natural, vitamin-like nutrient wich plays an important role inhuman metabolism. It is essential in the utilization of fatty acids and in transporting metabolic energy
Carnitine (carnitine) is an essential, non-toxic, natural nutrient that helps burn fat for fuel. Because deficiencies have been linked to a profound impairment of muscle function, there has been great interest in studying carnitine supplementation. Over the past decade, my research, as well as countless others, has shed light on carnitine’s role in metabolism, performance and overall health.
Carnitine burns body fat
Carnitine has an essential role in transporting fat into mitochondria (the furnace of the cell). Therefore, carnitine has been marketed as a fat burning supplement.Carnitine is a substance that helps the body turn fat into energy. Your body makes it in the liver and kidneys and stores it in the skeletal muscles, heart, brain, and sperm.
Usually, your body can make all the carnitine it needs. Some people, however, may not have enough carnitine because their bodies cannot make enough or can’t transport it into tissues so it can be used. Some other conditions, such as angina or intermittent claudication, can also cause low levels of carnitine in the body, as can some medications.
Carnitine has been proposed as a treatment for many conditions because it acts as an antioxidant. Antioxidants fight harmful particles in the body known as free radicals, which damage cells and tamper with DNA. Antioxidants can neutralize free radicals and may reduce or help prevent some of the damage they cause.
Antipyretic Analgesics Paracetamol /steroidmisty@ycphar.com
CAS 103-90-2 Paracetamol
Product Name: Paracetamol
Assay: 99%
CAS No.: 103-90-2
EINECS No.: 203-157-5
Molecular Formula: C8H9NO2
Molecular Weight: 151.16
Melting point: 168-172 ° C(lit. )
Appearance: White crystalline powder
Packing: 25KG/Drum
Application: Antipyretic Analgesics
Usage:used as analgesic-antipyretic pharmaceutical material
Paracetamol, also known as acetaminophen or APAP, chemically named N-acetyl-p-aminophenol, is a widely used over-the-counter analgesic (pain reliever) and antipyretic (fever reducer). Acetaminophen is the name adopted for this pharmacologic agent in the U. S. (USAN) and Japan; Paracetamol is approved in a variety of international venues (INN, AAN, BAN, etc. ). Common trade names in English-speaking markets are Tylenol and Panadol.
Paracetamol is classified as a mild analgesic. It is commonly used for the relief of headaches and other minor aches and pains and is a major ingredient in numerous cold and flu remedies. In combination with opioid analgesics, paracetamol can also be used in the management of more severe pain such as post-surgical pain and providing palliative care in advanced cancer patients. Though paracetamol is used to treat inflammatory pain, it is not generally classified as an NSAID because it exhibits only weak anti-inflammatory activity.
Fever
Paracetamol is approved for reducing fever in people of all ages. The World Health Organization (WHO) recommends that paracetamol be used to treat fever in children only if their temperature is greater than 38.5 ° C (101.3 ° F). The efficacy of paracetamol by itself in children with fevers has been questioned and a meta-analysis showed that it is less effective than ibuprofen.
Pain
Paracetamol is used for the relief of pains associated with many parts of the body. It has analgesic properties comparable to those of aspirin, while its anti-inflammatory effects are weaker. It is better tolerated than aspirin in patients in whom excessive gastric acid secretion or prolongation of bleeding time may be a concern. Available without a prescription since 1959, it has since become a common household drug.
Paracetamol has relatively little anti-inflammatory activity, unlike other common analgesics such as the NSAIDs aspirin and ibuprofen, but ibuprofen and paracetamol have similar effects in the treatment of headache. Paracetamol can relieve pain in mild arthritis, but has no effect on the underlying inflammation, redness, and swelling of the joint
Product Name: Paracetamol
Assay: 99%
CAS No.: 103-90-2
EINECS No.: 203-157-5
Molecular Formula: C8H9NO2
Molecular Weight: 151.16
Melting point: 168-172 ° C(lit. )
Appearance: White crystalline powder
Packing: 25KG/Drum
Application: Antipyretic Analgesics
Usage:used as analgesic-antipyretic pharmaceutical material
Paracetamol, also known as acetaminophen or APAP, chemically named N-acetyl-p-aminophenol, is a widely used over-the-counter analgesic (pain reliever) and antipyretic (fever reducer). Acetaminophen is the name adopted for this pharmacologic agent in the U. S. (USAN) and Japan; Paracetamol is approved in a variety of international venues (INN, AAN, BAN, etc. ). Common trade names in English-speaking markets are Tylenol and Panadol.
Paracetamol is classified as a mild analgesic. It is commonly used for the relief of headaches and other minor aches and pains and is a major ingredient in numerous cold and flu remedies. In combination with opioid analgesics, paracetamol can also be used in the management of more severe pain such as post-surgical pain and providing palliative care in advanced cancer patients. Though paracetamol is used to treat inflammatory pain, it is not generally classified as an NSAID because it exhibits only weak anti-inflammatory activity.
Fever
Paracetamol is approved for reducing fever in people of all ages. The World Health Organization (WHO) recommends that paracetamol be used to treat fever in children only if their temperature is greater than 38.5 ° C (101.3 ° F). The efficacy of paracetamol by itself in children with fevers has been questioned and a meta-analysis showed that it is less effective than ibuprofen.
Pain
Paracetamol is used for the relief of pains associated with many parts of the body. It has analgesic properties comparable to those of aspirin, while its anti-inflammatory effects are weaker. It is better tolerated than aspirin in patients in whom excessive gastric acid secretion or prolongation of bleeding time may be a concern. Available without a prescription since 1959, it has since become a common household drug.
Paracetamol has relatively little anti-inflammatory activity, unlike other common analgesics such as the NSAIDs aspirin and ibuprofen, but ibuprofen and paracetamol have similar effects in the treatment of headache. Paracetamol can relieve pain in mild arthritis, but has no effect on the underlying inflammation, redness, and swelling of the joint
Methylamine Hydrochloride/steroidmisty@ycphar.com
Product Name:Methylammonium chloride
CAS Registry Number: 593-51-1
Molecular Formula:CH5N.HCl
Molecular Weight:67.52
EINECS:209-795-0
Purity:99%
Grade:Industrial Grade
Appearance: white to light tan solid
Melting Point: 230 C
Water Solubility: moderate
Stability: Stable, but may be moisture sensitive. Incompatible with strong oxidizing agents.
Methylamine is an organic compound with a formula of CH3NH2. This colorless gas is a derivative of ammonia, but with one H atom replaced by a methyl group. It is the simplest primary amine. It is sold as a solution in methanol, ethanol, THF, and water, or as the anhydrous gas in pressurized metal containers. Industrially, methylamine is transported in its anhydrous form in pressurized railcars and tank trailers. It has a strong odor similar to fish. Methylamine is used as a building block for the synthesis of many other commercially available compounds.
In the laboratory methylamine hydrochloride is readily prepared by various other methods. One method entails treating formaldehyde with ammonium chloride.
Methylamine hydrochloride is Used as basic raw materials, such as fuel, pesticides, oil pharmaceuticals, and other organic synthesis.Representative commercially significant chemicals produced from methylamine include the pharmaceuticals and theophylline, the pesticides carbofuran, carbaryl, and metham sodium, and the solvents N-methylformamide and N-methylpyrrolidone. The preparation of some surfactants and photographic developers require methylamine as a building block.
Methylamine is a good nucleophile as it is highly basic and unhindered, although, as an amine it is considered a weak base. Its use in organic chemistry is pervasive. Some reactions involving simple reagents include: with phosgene to methyl isocyanate, with carbon disulfide and sodium hydroxide to the sodium methyldithiocarbamate, with chloroform and base to methyl isocyanide and with ethylene oxide to methylethanolamines. Liquid methylamine has solvent properties analogous to those for liquid ammonia.
Representative commercially significant chemicals produced from methylamine include the pharmaceuticals ephedrine and theophylline, the pesticides carbofuran, carbaryl, and metham sodium, and the solvents N-methylformamide and N-methylpyrrolidone. The preparation of some surfactants and photographic developers require methylamine as a building block.
Methylamine arises as a result of putrefaction and is a substrate for methanogenesis.
Additionally, methylamine is produced during PADI4-dependent arginine demethylation.
Methylamines are used to make intermediates for a wide range of agricultural chemicals, including herbicides, fungicides, insecticides, biocides, and miticides. Agricultural chemicals are one of the widest uses for methylamines.
CAS Registry Number: 593-51-1
Molecular Formula:CH5N.HCl
Molecular Weight:67.52
EINECS:209-795-0
Purity:99%
Grade:Industrial Grade
Appearance: white to light tan solid
Melting Point: 230 C
Water Solubility: moderate
Stability: Stable, but may be moisture sensitive. Incompatible with strong oxidizing agents.
Methylamine is an organic compound with a formula of CH3NH2. This colorless gas is a derivative of ammonia, but with one H atom replaced by a methyl group. It is the simplest primary amine. It is sold as a solution in methanol, ethanol, THF, and water, or as the anhydrous gas in pressurized metal containers. Industrially, methylamine is transported in its anhydrous form in pressurized railcars and tank trailers. It has a strong odor similar to fish. Methylamine is used as a building block for the synthesis of many other commercially available compounds.
In the laboratory methylamine hydrochloride is readily prepared by various other methods. One method entails treating formaldehyde with ammonium chloride.
Methylamine hydrochloride is Used as basic raw materials, such as fuel, pesticides, oil pharmaceuticals, and other organic synthesis.Representative commercially significant chemicals produced from methylamine include the pharmaceuticals and theophylline, the pesticides carbofuran, carbaryl, and metham sodium, and the solvents N-methylformamide and N-methylpyrrolidone. The preparation of some surfactants and photographic developers require methylamine as a building block.
Methylamine is a good nucleophile as it is highly basic and unhindered, although, as an amine it is considered a weak base. Its use in organic chemistry is pervasive. Some reactions involving simple reagents include: with phosgene to methyl isocyanate, with carbon disulfide and sodium hydroxide to the sodium methyldithiocarbamate, with chloroform and base to methyl isocyanide and with ethylene oxide to methylethanolamines. Liquid methylamine has solvent properties analogous to those for liquid ammonia.
Representative commercially significant chemicals produced from methylamine include the pharmaceuticals ephedrine and theophylline, the pesticides carbofuran, carbaryl, and metham sodium, and the solvents N-methylformamide and N-methylpyrrolidone. The preparation of some surfactants and photographic developers require methylamine as a building block.
Methylamine arises as a result of putrefaction and is a substrate for methanogenesis.
Additionally, methylamine is produced during PADI4-dependent arginine demethylation.
Methylamines are used to make intermediates for a wide range of agricultural chemicals, including herbicides, fungicides, insecticides, biocides, and miticides. Agricultural chemicals are one of the widest uses for methylamines.
Dextromethorphan hydrobromide monohydrate/steroidmisty@ycphar.com
Product Name: Dextromethorphan Hydrobromide,Methoratehydrobromide,Medicon,Dextromethorphan bromide
Synonyms: Delsym;Sisaal;Dextro;tusilan;Tussade;antussan;metrorat;Dormetan;Romilar
CAS No.: 125-69-9
Molecular Formula: C18H26BrNO
Molecular Weight: 352.31
Appearance: white crystalline powder
Purity:99%
Grade:Pharmaceutical Grade
Dextromethorphan (DXM or DM) is an antitussive (cough suppressant) drug of the morphinan class with sedative and dissociative properties. It is one of the active ingredients in many over-the-counter cold and cough medicines, including generic labels and store brands, Benylin DM, Mucinex DM, Robitussin, NyQuil, Dimetapp, Vicks, Coricidin, Delsym, TheraFlu, and others. Dextromethorphan has also found numerous other uses in medicine, ranging from pain relief (as either the primary analgesic, or an opioid potentiater) over psychological applications to the treatment of addiction. It is sold in syrup, tablet, spray, and lozenge forms. In its pure form, dextromethorphan occurs as a white powder.
DXM is also used recreationally. When exceeding label-specified maximum dosages, dextromethorphan acts as a dissociative hallucinogen. Its mechanism of action is via multiple effects, including actions as a nonselective serotonin reuptake inhibitor and a sigma-1 receptor agonist.DXM and its major metabolite, dextrorphan, also act as an NMDA receptor antagonist at high doses, which produces effects similar to, yet distinct from, the dissociative states created by other dissociative anaesthetics such as ketamine and phencyclidine. As well, the metabolite 3-methoxymorphinan of dextrorphan (thus a second-level metabolite of DXM) produces local anesthetic effects in rats with potency above dextrorphan, but below that of DXM.
The primary use of dextromethorphan is as a cough suppressant, for the temporary relief of cough caused by minor throat and bronchial irritation (such as commonly accompanies the flu and common cold), as well as those resulting from inhaled particle irritants.
Over-the-counter preparations containing dextromethorphan have been used in manners inconsistent with their labeling, often as a recreational drug.At doses much higher than medically recommended, DXM and its major metabolite, dextrorphan, acts as an NMDA receptor antagonist, which produces effects similar to, yet distinct from, the dissociative hallucinogenic states created by other dissociative anaesthetics such as ketamine and phencyclidine.It may produce distortions of the visual field - feelings of dissociation, distorted bodily perception, and excitement, as well as a loss of sense of time. Some users report stimulant-like euphoria, particularly in response to music. Dextromethorphan usually provides its recreational effects in a non-linear fashion, so that they are experienced in significantly varied stages. These stages are commonly referred to as "plateaus.
Synonyms: Delsym;Sisaal;Dextro;tusilan;Tussade;antussan;metrorat;Dormetan;Romilar
CAS No.: 125-69-9
Molecular Formula: C18H26BrNO
Molecular Weight: 352.31
Appearance: white crystalline powder
Purity:99%
Grade:Pharmaceutical Grade
Dextromethorphan (DXM or DM) is an antitussive (cough suppressant) drug of the morphinan class with sedative and dissociative properties. It is one of the active ingredients in many over-the-counter cold and cough medicines, including generic labels and store brands, Benylin DM, Mucinex DM, Robitussin, NyQuil, Dimetapp, Vicks, Coricidin, Delsym, TheraFlu, and others. Dextromethorphan has also found numerous other uses in medicine, ranging from pain relief (as either the primary analgesic, or an opioid potentiater) over psychological applications to the treatment of addiction. It is sold in syrup, tablet, spray, and lozenge forms. In its pure form, dextromethorphan occurs as a white powder.
DXM is also used recreationally. When exceeding label-specified maximum dosages, dextromethorphan acts as a dissociative hallucinogen. Its mechanism of action is via multiple effects, including actions as a nonselective serotonin reuptake inhibitor and a sigma-1 receptor agonist.DXM and its major metabolite, dextrorphan, also act as an NMDA receptor antagonist at high doses, which produces effects similar to, yet distinct from, the dissociative states created by other dissociative anaesthetics such as ketamine and phencyclidine. As well, the metabolite 3-methoxymorphinan of dextrorphan (thus a second-level metabolite of DXM) produces local anesthetic effects in rats with potency above dextrorphan, but below that of DXM.
The primary use of dextromethorphan is as a cough suppressant, for the temporary relief of cough caused by minor throat and bronchial irritation (such as commonly accompanies the flu and common cold), as well as those resulting from inhaled particle irritants.
Over-the-counter preparations containing dextromethorphan have been used in manners inconsistent with their labeling, often as a recreational drug.At doses much higher than medically recommended, DXM and its major metabolite, dextrorphan, acts as an NMDA receptor antagonist, which produces effects similar to, yet distinct from, the dissociative hallucinogenic states created by other dissociative anaesthetics such as ketamine and phencyclidine.It may produce distortions of the visual field - feelings of dissociation, distorted bodily perception, and excitement, as well as a loss of sense of time. Some users report stimulant-like euphoria, particularly in response to music. Dextromethorphan usually provides its recreational effects in a non-linear fashion, so that they are experienced in significantly varied stages. These stages are commonly referred to as "plateaus.
Pharmaceutical grade Isotretinoin/steroidmisty@ycphar.com
Product Name: Isotretinoin (Roaccutane),Accutane
Synonyms:Isoretinoin;isotrex;neovitaminaacid;roaccutane;teriosal;Lsotretinoin
CAS No.: 4759-48-2
EINECS No.: 225-296-0
Molecular Formula: C20H28O2
Molecular Weight: 300.44
Purity:99%
Appearance: orange red crystal
Grade:Pharmaceutical grade
Isotretinoin (Accutane) is primarily used to treat bad cases of cystic acne, and to help the skin more rapidly renew itself. In addition, it is used in rare cases for certain skin cancers and skin diseases. It is a type of retinoid, which is naturally found in the body in small amounts.
How it Works
Accutane works as an isomer of Vitamin A, which reduces the amount of oil released by the oil glands in the skin; this will make it difficult for acne to form and reduce it significantly. Nearly all patients achieve clearing of acne during a course, with 90% reporting‘excellent’ results with higher dosages.
Bodybuilding
Bodybuilders who use anabolic steroids have utilized accutane to counteract the negative effects of steroids on their skin; especially, the acne related side effects.
Since chances of acne are increased with anabolic steroid use, and bodybuilding requires looking good (especially physique competitors), many athletes who have failed to conquer their acne with natural remedies will turn to accutane.
It is the androgenic increases associated with steroids that will trigger increased acne. This is especially true for those genetically prone to the condition. Also, the hormonal changes can trigger acne as well, such as increased testosterone levels.
Accutane Dosage
Among bodybuilders, the dosage should be conservative. Once a day dose of 10-20mgs for 6-8 weeks maximum should work fine. Among the general public fighting acne, a dosage of 50-150mg per day may be prescribed by their physician. It is a good idea to take the drug with a large meal. In addition, it may be necessary to use multiple courses of treatment
Synonyms:Isoretinoin;isotrex;neovitaminaacid;roaccutane;teriosal;Lsotretinoin
CAS No.: 4759-48-2
EINECS No.: 225-296-0
Molecular Formula: C20H28O2
Molecular Weight: 300.44
Purity:99%
Appearance: orange red crystal
Grade:Pharmaceutical grade
Isotretinoin (Accutane) is primarily used to treat bad cases of cystic acne, and to help the skin more rapidly renew itself. In addition, it is used in rare cases for certain skin cancers and skin diseases. It is a type of retinoid, which is naturally found in the body in small amounts.
How it Works
Accutane works as an isomer of Vitamin A, which reduces the amount of oil released by the oil glands in the skin; this will make it difficult for acne to form and reduce it significantly. Nearly all patients achieve clearing of acne during a course, with 90% reporting‘excellent’ results with higher dosages.
Bodybuilding
Bodybuilders who use anabolic steroids have utilized accutane to counteract the negative effects of steroids on their skin; especially, the acne related side effects.
Since chances of acne are increased with anabolic steroid use, and bodybuilding requires looking good (especially physique competitors), many athletes who have failed to conquer their acne with natural remedies will turn to accutane.
It is the androgenic increases associated with steroids that will trigger increased acne. This is especially true for those genetically prone to the condition. Also, the hormonal changes can trigger acne as well, such as increased testosterone levels.
Accutane Dosage
Among bodybuilders, the dosage should be conservative. Once a day dose of 10-20mgs for 6-8 weeks maximum should work fine. Among the general public fighting acne, a dosage of 50-150mg per day may be prescribed by their physician. It is a good idea to take the drug with a large meal. In addition, it may be necessary to use multiple courses of treatment
Hot selling Gamma-Butyrolactone /steroidmisty@ycphar.com
Product Name: Gamma Butyrolactone,γ -Butyroladone
Alias:1, 4- Butyrolactone,GBL, BLO
Purity : 99.0%
CAS Registry Number: 96-48-0
Einecs No: 202-509-5
Molecular Formula: C4H6O2
Molecular Weight: 86.09
Appearance: Colourless oily liquid
GBL Application and Function
γ-Butyrolactone (GBL) is a hygroscopic colorless liquid with a weak characteristic odor. Soluble in water, GBL is a common solvent and reagent in chemistry
as well as being used as a flavouring, as a cleaning solvent, as a super glue remover, and as asolvent in some wet aluminium electrolytic capacitors.
In humans it acts as a prodrug for γ-hydroxybutyric acid (GHB), and it is used as a recreational intoxicant with effects similar to alcohol.
Despite serious safety concerns and illegality, people take gamma butyrolactone for improving athletic performance, sleep, and sexual performance and pleasure. They also take it for relieving depression and stress, prolonging life, promoting clear thinking, causing relaxation, and releasing growth hormone. GBL is also used to trim fat and as a body- or muscle-builder. Some people take it as a recreational drug.
GHB for Bodybuilding
GBL is converted to GHB shortly after entering the body. Both produce a feeling of euphoria and can reduce inhibitions and cause sleepiness. Gamma butyrolactone is a chemical. People use it as medicine. Be careful not to confuse gamma butyrolactone (GBL) with gamma hydroxybutyrate (GHB). Gamma-Butyrolactone + NaOH => Sodium Gamma-Hydroxy Butyrate (Na-GHB).
GHB has many potential therapeutic uses and is considered to have a very low toxicity profile. In some European countries, it's used as a general anesthetic, for sleep disorders, an aid to childbirth and a treatment for alcoholism. It also is reported to be a great aphrodisiac.
Bodybuilders and other athletes have used GHB because of its ability to stimulate the pituitary to release growth hormone (GH).GHB should lower the secretion of the stress hormone cortisol, especially at night. This is perceived as a major benefit because cortisol release keeps increasing as the night goes on. t certainly makes sense that a relaxing agent should depress cortisol level.If you are in a state of acidosis because of your diet, this particular action of GHB will spare some of your muscle mass while permitting fat loss. The extra GH release due to GHB will also help you to get rid of the extra acid and therefore spare your muscle mass and glutamine. If you are not in a state of acidosis, this anti-catabolic action of GHB will not appear.
Relaxation, calming, increased mental clarity, fat loss, use as a body or muscle “builder,” recreational drug use, releasing growth hormone, improving athletic performance, trouble sleeping (insomnia), relieving depression and stress, prolonging life, improving sexual performance and pleasure, and other conditions.
Alias:1, 4- Butyrolactone,GBL, BLO
Purity : 99.0%
CAS Registry Number: 96-48-0
Einecs No: 202-509-5
Molecular Formula: C4H6O2
Molecular Weight: 86.09
Appearance: Colourless oily liquid
GBL Application and Function
γ-Butyrolactone (GBL) is a hygroscopic colorless liquid with a weak characteristic odor. Soluble in water, GBL is a common solvent and reagent in chemistry
as well as being used as a flavouring, as a cleaning solvent, as a super glue remover, and as asolvent in some wet aluminium electrolytic capacitors.
In humans it acts as a prodrug for γ-hydroxybutyric acid (GHB), and it is used as a recreational intoxicant with effects similar to alcohol.
Despite serious safety concerns and illegality, people take gamma butyrolactone for improving athletic performance, sleep, and sexual performance and pleasure. They also take it for relieving depression and stress, prolonging life, promoting clear thinking, causing relaxation, and releasing growth hormone. GBL is also used to trim fat and as a body- or muscle-builder. Some people take it as a recreational drug.
GHB for Bodybuilding
GBL is converted to GHB shortly after entering the body. Both produce a feeling of euphoria and can reduce inhibitions and cause sleepiness. Gamma butyrolactone is a chemical. People use it as medicine. Be careful not to confuse gamma butyrolactone (GBL) with gamma hydroxybutyrate (GHB). Gamma-Butyrolactone + NaOH => Sodium Gamma-Hydroxy Butyrate (Na-GHB).
GHB has many potential therapeutic uses and is considered to have a very low toxicity profile. In some European countries, it's used as a general anesthetic, for sleep disorders, an aid to childbirth and a treatment for alcoholism. It also is reported to be a great aphrodisiac.
Bodybuilders and other athletes have used GHB because of its ability to stimulate the pituitary to release growth hormone (GH).GHB should lower the secretion of the stress hormone cortisol, especially at night. This is perceived as a major benefit because cortisol release keeps increasing as the night goes on. t certainly makes sense that a relaxing agent should depress cortisol level.If you are in a state of acidosis because of your diet, this particular action of GHB will spare some of your muscle mass while permitting fat loss. The extra GH release due to GHB will also help you to get rid of the extra acid and therefore spare your muscle mass and glutamine. If you are not in a state of acidosis, this anti-catabolic action of GHB will not appear.
Relaxation, calming, increased mental clarity, fat loss, use as a body or muscle “builder,” recreational drug use, releasing growth hormone, improving athletic performance, trouble sleeping (insomnia), relieving depression and stress, prolonging life, improving sexual performance and pleasure, and other conditions.
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