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5,6,7,7a-tetrahydrothieno[3,2-c]PYRIDINE-2(4H)-one Hydrochloride 98.5%

Product Name: 5,6,7,7a-tetrahydrothieno[3,2-c]pyridine-2(4H)-one hydrochloride
CAS Number: 115473-15-9
Purity:≥98.5%
Formula: C7H10ClNOS
Molecular weight: 191.68
DeliveryTime: 3-5 days after received your deposit
Port: Tianjin
Production Capacity: 500 Kilogram/Week
Storage: Keep away from fire and heat source

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Anti Disease Immune System Enhancement Tripeptide Glutathione 70-18-8

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Anti Disease Immune System Enhancement Tripeptide Glutathione 70-18-8

Glutathione Basic Info.:

Product Name: L-Glutathione Reduced

CAS NO.: 70-18-8

Molecular Formula: C10H17N3O6S

Molecular Weight: 307.32

Appearance:  white crystalline powder

Specification: . 98.0%~101.0% L-Glutathione Reduced

Appearance: white crystalline powder

Assay: 98.0%~101.0%

Optical Rotation: -15.5°~ -17.5°

Loss on drying: ≤0.50%

Residue on ignition: ≤0.10%

Heavy Metals: ≤10ppm

Arsenic: ≤2ppm

Sulphates: ≤300ppm

Ammonium: ≤200ppm

Iron: ≤10ppm

Glutathione Descriptions:

1. Glutathione is a non-protein sulfhydryl tripeptide compound formed by glutamic acid, cysteine and glycine through peptide bond condensation. It is an active short peptide with wide usage.

2. Glutathione is soluble in water, dilute alcohol, liquid ammonia and dimethyl formamide, but insoluble in ethanol, ether and acetone. The solid of glutathione is relative stable and its aqueous solution can easily be oxidized in the air.

Glutathione Applications:

Widely used in medicine, health products, food, beverage, cosmetics, biological and chemical reagents and other industries.

GSH Clinical Application

There are a large number of documents about GSH clinical application, which indicates the curative effects in following fields:

1) GSH's effect on hepatic diseases: it can treat virus hepatitis, alcoholic liver disease, NAFLD, hepatocirrhosis, and DILI, etc.

2) Renal diseases;

3) Protective action to drug-included renal and hepatitis

4) Acute pancreatitis systemic inflammatory response syndrome;

5) Cure diabetes mellitus and DPN;

6) Adjuvant drug in antineoplaston;

7) GSH cures age-related eye diseases;

8) GSH's protection to intestinal trace;

9) GSH cures anaphylactoid purpura;

10) Treatment to neonatal HIE;

11) Sharing with anticancer drugs: recently, it arouses increasing concern from clinical experts to restrain the side effects of anticancer drugs and strengthen curative effect and host resistance in combination of anticancer drugs;

12) Detoxication: GSH has detoxication to intoxication of medicine, food, heavy metal and carbon monoxide;

13) Anti-aging;

 

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Cosmetic Peptide Argireline Anti-Aging Argreline Acetate 616204-22-9

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Cosmetic Peptide Argireline Anti-Aging Argreline Acetate 616204-22-9 
 
Argireline Basic Info.:
 
Product Name: Argreline Acetate (Argireline)
Specification: 5mg/vial
Synonyms: Argireline;Argireline Acetate;Argirelin Acetate(Acetyl Hexapeptide-3);Acetyl Hexapeptide;Acetyl Hexapeptide-8
CAS: 616204-22-9
MF: C{46}H{56}N{12}O{6}
MW: 888.99
Density: 1.54
Storage temp.: -20°C
Product Categories: Peptide;Cosmetic Peptide
 

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Pharmaceutical Raw Material Metformin HCl Hydrochloride CAS 1115-70-4

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Pharmaceutical Raw Material Metformin HCl Hydrochloride CAS 1115-70-4
 
Metformin HCL Basic Info.:
 
Product Name: Metformin HCL
Metformin Hydrochloride; 3-(diaminomethylidene)-1,1-dimethylguanidine hydrochloride
CAS No.: 1115-70-4
EINECS: 214-230-6
Molecular Formula: C4H12ClN5
Molecular Weight: 165.6246
Melting Point: 220~225 °C.
Appearance: white crystalline powder; odorless.  soluble in water, dissolved in methanol, slightly soluble in ethanol, insoluble in chloroform or ether. 
Absorption coefficient of this product, accurately weighed, dissolved in water and diluted quantitatively per 1ml solution containing 5μg. According to the spectrophotometric determination of absorbance at 233nm wavelength, the absorption coefficient of 778 ~ 818.
 

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High Purity Male Sex Hormones Sildenafil Mesylate For Male 131543-23-2

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High Purity Male Sex Hormones Sildenafil Mesylate For Male 131543-23-2
 
Sildenafil Mesylate Basic Info.:
 
Product Name: Sildenafil Mesylate
English name: Win 55,212-2 Mesylate
English Synonyms: Sildenafil Mesylate
CAS: 131543-23-2
MF: C28H30N2O6S
MW: 522.6126
Boiling point: 627.7 °C at 760 mmHg
Flash Point: 333.4 °C
Vapor Pressure: 1.14E-15mmHg at 25 °C
Properties:Solubility: 0.1 M HCl: 0.25 mg / mL
Appearance: White or white crystalline powder, odorless, bitter astringent taste, soluble in water and ethanol
Usage: Pharmaceutical raw materials, aphrodisiac It is medicine treatment raw material, indicated for the treatment of erectile dysfunction.
 
Sildenafil Mesylate Description:
 
Sildenafil Mesylate, same as Sildenafil is an inhibitor of type 5 -cGMP phosphodiesterase relaxing and smoothing muscle cells of the corpus cavernosum which leads to penile erection. This relaxation may be
mediated by nitric oxide via cyclic guanosine monophosphate.
 
pharmaceutical material, hormone. As a cyclic guanosine monophosphate (cGMP) specific phosphodiesterase type 5 (PDE5) selective inhibitor, penile smooth muscle relaxation allows rapid erection. Sildenafil is cheap, is the development and production of low-cost classes available kidney yang-like the perfect material for medicine and health products.
 
Sildenafil Mesylate Applications:
 
In 16 separate 4-24 week trials of men (over 18 years old) who suffered from impotence for longer than 6 months, dosages between 10-200 mgs were administered. Significant improvements in erectile function, including frequency of penetration as well as erection duration post penetration, were reported with Sildenfi* treatment compared to the placebo group.
Erections were improved in 72% of group verses 18% of the placebo group. In all cases effects were dependant upon dosage and improvement was the greatest when dosage exceeded 100 mgs. Responses were decreased by 40-60% in patients suffering from diabetes and prostatectomy, respectively. Withdrawal rates were less than 5% related to negative side effects and limited response rates
 

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Peptides Alarelin Acetate For Ovulation And Endmometriosis 79561-22-1

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Peptides Alarelin Acetate For Ovulation And Endmometriosis 79561-22-1 
 
Alarelin Acetate Basic Info.:
 
Product Name: Alarelin Acetate
Synonyms: Des-Gly10,[D-Ala6]-Lh-Rh Ethylamide Acetate Salt.
CAS: 79561-22-1
MF: C56H78N16O12
MW: 1167.32
Storage temp.: −20°C
Form: Powder
Product Categories: Amino Acid Derivatives;Peptide;LH-RH;LH-RHPeptides for Cell Biology;Neuropeptides;Releasing Factors;API.
 
Alarelin Acetate (79561-22-1) Description:
 
Alarelin acetate is a gondatrophin releasing hormone. Natural forms of alarelin found in animals are used to induce ovulation. Synthetic versions of this product are created using an LH-RH antagonist which is commonly set in larger doses than the natural LH-RH that is typically found in the rat hypophyseal stimulation or the gondatoropin secretions in induced ovulation or in vitro.
 
This chemical is the acetate form of the natural hypothalamic peptide which is used by an animal’s body to release LH and FSH from the pituitary gland. The peptide alarelin acetate has a single non-glycosylated polypeptide structure that is made up of nine amino acids. This has a molecular mass of 1167.3.
 
Alarelin is commonly used in research settings both to better understand this peptide’s effects on an animal’s body and to induce conditions that may assist with reproductive research. Samples of this chemical intended for research settings are typically stable for around three weeks at room temperature, and will need to be stored at temperatures below -18 degrees Celsius for long term use.
 
Most versions of this chemical are shipped as a lyophilized powder that can be reconstituted at a sterile temperature. This chemical may remain stable for up to three weeks at room temperature if it is kept sealed when it is not in use. If this product will be used for long periods of time is should be kept in a freezer with a waterproof sea.
 
If the mixture has already been reconstituted it can be kept at 40 degrees Celsius for 2-7 days but should be kept at -180 degrees Celsius for longer periods of time. Do not continually refreeze and thaw the product.
 

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Polypeptide Human Growth Powder Hormone Peptide Selank CAS 129954-34-3

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Polypeptide Human Growth Powder Hormone Peptide Selank CAS 129954-34-3
 
Selank Basic Info.
 
Product Name: Selank
Alias: Selanc;Selank
Sequence: Thr-Lys-PRO-Arg-PRO-Gly-PRO
CAS: 129954-34-3
MF: C33H57N11O9
MW: 751.9
Purity: 99%
Specification: 5mg/vial
Appearance: White Lyophilized Powder
Place of Origin: China
Standard: USP
Certification: SGS
Method of Analysis: HPLC
Use: Reduce stress, relieve depression, insomnia quit. Of course, with Selank a puzzle-anxiolytic
 
Descriptions Of Selank:
 
Selank was developed by the Russian Academy of Sciences. anxiolytic peptide based drugs. Selank is a heptapeptide with the sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro. It is a synthetic analogue of a human tetrapeptide tuftsin.
 
it uses relief of anxiety and improved cognitive functioning alone. Selank used for : Stress reduction, the alleviation of depression, reversal of anhedonia, improvement in mood in emotionally stable individuals, and cessation of insomnia.
 
In fact,Selank more suitable for long-term use. for the large majority of researchers claiming that it is a "side effect free" compound. Some believe an overdose might cause fatigue.
 
Application Of Selank:
 
(1)Selank as a nootropic:
Recreationally Selank is used to improve one's ability to focus and concentrate, reduce mental fatigue, increase mental sharpness and increase memory and learning capacity. The first noticeable effect is usually stabilization of mood and general feeling of well-being.
 
(2)Selank as an antiviral agent:
Selank neuropeptide also expresses immunomodulatory effects. In 2009 a study by F. Ershov et all. has evaluated antiviral properties of Selank both in vitro and in vivo against the influenza virus strain A/Aichi 2/68 (H3N2). The pronounced antiviral effect of Selank was detected in both systems. The highest efficiency - completely supressed viral reproduction was shown when Selank was added to the cell culture 24 hours before inoculation.
 

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Steroid Hormone Powder Eplerenone For Lowering Blood Press 107724-20-9

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Steroid Hormone Powder Eplerenone For Lowering Blood Press 107724-20-9
 
Eplerenone Basic Info.:
 
Product Name: Eplerenone
Chemical Name: Pregn-4-ene-7,21-dicarboxylic acid 9,11-epoxy-17-hydroxy-3-oxo gamma-
lactone methyl ester
CAS No.: 107724-20-9
Molecular Formula: C24H30O6
Molecular weight: 414.49
Appearance: white crystalline powder; slightly soluble in water.
Standard: Enterprise Standard
 
Eplerenone Description:
 
Eplerenone (INN) /plrnon/ is an aldosterone antagonist used as an adjunct in the management of chronic heart failure. It is similar to the diuretic spironolactone, though it is much more selective for the mineralocorticoid receptor in comparison (i.e., does not possess any antiandrogen, progestogen, or estrogenic effects), and is specifically marketed for reducing cardiovascular risk in patients following myocardial infarction. It was marketed byPfizer under the trade name Inspra but is now only available as a generic in every country except the United Kingdom. Eplerenone is a potassium-sparing diuretic, meaning that it helps the body get rid of water but still keep potassium.
 
Eplerenone Application:
 
Eplerenone is specifically indicated for the reduction of risk of cardiovascular death in people with heart failure andleft ventricular dysfunction within 3-14 days of an acute myocardial infarction, in combination with standard therapies and as treatment against hypertension. It appears equivalent to spironolactone but is much more expensive.
 

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99% Pharmaceutical Sarms Powder Ostarine Enobosarm Mk-2866 1202044-20-9

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99% Pharmaceutical Sarms Powder Ostarine Enobosarm Mk-2866 1202044-20-9
 
MK-2866 (Ostarine) Basic Info.:
 
Product Name: MK-2866
Synonyms: Ostarine
CAS: 1202044-20-9
MF: C19H10D4F3N3O3
Product Categories: Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Hormone Drugs
Recommended maximum dose OSTARINE about 25 mg once a day for men, females and 12.5 mg. It has a half-life of 24 hours a day.Improve the minimum recommended dose aesthetic constitution (means) male is 12.5 mg. Low dose may produce little results notification clause or muscle growth, but it will help to health. Women's minimum recommended dose, and for those who seek to improve health, 5 mg per day, it should be noted that therapeutic doses as low as 3 mg a day have been reported in the gender is good.
 
MK-2866 (Ostarine) Description:
 
Ostarine (MK-2866) is a SARM developed by GTx for the prevention and treatment of muscle wasting. It may eventually be a medical prescription for the prevention of cachexia, atrophy and sarcopenia as well as for Hormone or Testosterone Replacement Therapy.
As a research chemical, Ostarine belongs to a class of chemicals know as SARMS or selective androgen receptor modulators. SARMS create selective anabolic activity at certain androgen receptors. In comparison to testosterone and other anabolic steroids, the advantage of SARMS, is they do not have androgenic activity in non-skeletal muscle tissues. Ostarine is effective in maintaining and increasing lean body mass.
Ostarine is a potent and tissue-selective androgen receptor modulator (SARM) for treatment of conditions such as muscle wasting and osteoporosis. These patent products for research purposes only use. Ostarine (GTx-024, MK-2866, Enobosarm, S-22) is an orally bioavailable nonsteroidal selective androgen receptor modulator. Therefore, ostarine can be used for treatment of conditions such as muscle wasting and osteoporosis.
 
MK-2866 (Ostarine) Application:
 
Selective androgen receptor modulators may be used by athletes to assist in training and increase physical stamina and fitness, potentially producing effects similar to anabolic steroids.
Ostarine is a potent and tissue-selective androgen receptor modulator (SARM) for treatment of conditions such as muscle wasting and osteoporosis. These patent products for research purposes only use. Ostarine (GTx-024, MK-2866, Enobosarm, S-22) is an orally bioavailable nonsteroidal selective androgen receptor modulator. Therefore, ostarine can be used for treatment of conditions such as muscle wasting and osteoporosis.
 
MK-2866 (Ostarine) Function:
 
1.Enobosarm (Ostarine, MK-2866, GTx-024) - affects both muscle and bone, intended mainly for osteoporosis but also general treatment for andropause and reversing muscle sarcopenia in the elderly and for cachexia in cancer patients
2.Nonsteroidal selective androgen receptor modulator (SARM) used in the treatment of osteoporosis and muscle wasting in animal models. A potential compound for the treatment of hypoactive sexual desire disorder.
 

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99% Purity Cancer Treatment Steroids Formestane For Breast CAS 566-48-3

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99% Purity Cancer Treatment Steroids Formestane For Breast CAS 566-48-3
 
Formestane Basic Info.:
 
Product name: Formestane
Other name: Formestane; Lentaron; Formestqne; Hydroxyandrostenedione
CAS Registry Number: 566-48-3
Assay: 98%Packing: 1kg/aluminum foil bag
Molecular Formula: C19H26O3
Molecular Weight: 302.41
Appearance: White crystalline powder
 
Product Description Of Formestane:
 
Formestane was the first selective, type I, steroidal aromatase inhibitor used in the treatment of estrogen-receptor positive breast cancer in post-menopausal women. Formestane suppresses estrogen production from anabolic steroids or prohormones. It also acts as a prohormone to 4-hydroxytestosterone, an active steroid which displays weak androgenic activity in addition to acting as a mild aromatase inhibitor. It is listed as a prohibited substance by the World Anti-Doping Agency for use in athletes. 
 
Formestane has poor oral bioavailability, and thus must be administered forthnightly (bi-weekly) by intramuscular injection. Some clinical data has suggested that the clinically recommended dose of 250mg was too low. With the discovery of newer, non-steroidal and steroidal, aromatase inhibitors which were orally active and less expensive than formestane, formestane lost popularity. 
 
Currently, formestane (categorized as an anti-estrogenic agent) is prohibited from use in sports in accordance to the regulations of the World Anti-Doping Agency. It is not US FDA approved, and the intramuscular injection form of formestane (Lentaron) which was approved in Europe has been withdrawn. 
 
Formestane (Lentaron) is a type I, steroidal aromatase inhibitor. It is used in the treatment of estrogen-receptor positive breast cancer in post-menopausal women. It is available as an intramuscular depot injection.
 
Formestane is often used to suppress estrogen production from anabolic steroids or prohormones. It also acts as a prohormone to 4-hydroxytestosteron, an active steroid which displays weak androgenic activity in addition to acting as a mild aromatase inhibitor.
 
Formestane has poor oral bioavailability and as such is no longer popular as many orally active aromatase inhibitors have been identified.
 
Formestane Applications:
 
Formestane is a second generation, irreversible, steroidal aromatase inhibitor. It inhibits the aromatase enzyme responsible for converting androgens to estrogens, thereby preventing estrogen production. Breast cancer may be estrogen sensitive or insensitive. A majority of breast cancers are estrogen sensitive. Estrogen sensitive breast cancer cells depend on estrogen for viability. Thus removal of estrogen from the body can be an effective treatment for hormone sensitive breast cancers. Formestane has been targeted specifically for the treatment of postmenopausal women. Unlike premenopausal women who produce most estrogen in the ovaries, postmenopausal women produce most estrogen in peripheral tissues with the help of the aromatase enzyme. Formestane, an aromatase inhibitor, can thus help to decrease the local production of estrogen by blocking the aromatase enzyme in peripheral tissues (ie. Adispose tissue of the breast) to treat hormone sensitive breast cancer.
 

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