Pharmaceutical raw materials used in synthesizing new medications

chemical-categories

Hormone Raw Powders Anabolic Pharmaceutical Intermediates Epiandrosterone For Bodybuilding 481-29-8

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Hormone Raw Powders Anabolic Pharmaceutical Intermediates Epiandrosterone For Bodybuilding 481-29-8
 
Epiandrosterone Basic Info.:
 
Product Name: Epiandrosterone
Synonyms: Trans-Androsterone;3beta-Androsterone;3-Epiandrosterone;3-Hydroxyandrostan-17-one;
CAS No.: 481-29-8
MF: C19H30O2
MW: 290.44
EINECS: 207-563-3
Purity: ≥ 99%
Melting point: 172-174 °C
Loss on drying: 0.23%
Alpha: 91°(c=1, CH3OH)
Storage temp.: Refrigerator
Water Solubility: practically insoluble
Appearance: White to off-white crystalline powder
Packaged by: 25kg/drum
Product Categories: Pharmaceutical Intermediates;Steroids;17-Ketosteroids;Biochemistry;Hydroxyketosteroids;Intermediates & Fine Chemicals;Pharmaceuticals;API;Inhibitors
Usage: For the steroid hormone drugs.
 
Epiandrosterone Description:
 
Epiandrosterone, or 3β-androsterone, also known as 3β-hydroxy-5α-androstan-17-one or 5α-androstan-3β-ol-17-one, is a steroid hormone with weak androgenic activity. It is a natural metabolite of dehydroepiandrosterone (DHEA) via the 5α-reductase enzyme. It was first isolated in 1931, by Adolf Friedrich Johann Butenandt and Kurt Tscherning.
 
They distilled over 17,000 litres of male urine, from which they got 50 milligrams of crystalline androsterone (most likely mixed isomers), which was sufficient to find that the chemical formula was very similar to estrone.
 
Epiandrosterone Applications:
 
Typical dosage is in the range of 300-400 mg/day, though some users may dose higher than this. This is best used in 4-6 week cycles. Although Epiandrosterone does not cause severe shut down of testosterone production like many other prohormones, it is still a good idea too use a mild over the counter post-cycle therapy. An over the counter anti-estrogen/test booster will do just fine for recovery from an epiandrosterone cycle.
 
As mentioned earlier, epiandrosterone and its 3-alpha isomer androsterone are completely legal and available over the counter. LG Sciences MMv3 uses the 3-alpha isomer of this compound because it is better for the special sublingual delivery system that this product utilizes. By placing a tablet under the tongue, the compound is absorbed directly through the tissues in that area and into the blood stream.
 

Properties Suppliers
Hot Selling 99% Purity Steroid Raw Powder Clomiphene Citrate 50-41-9

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Hot Selling 99% Purity Steroid Raw Powder Clomiphene Citrate 50-41-9
 
Clomiphene Citrate Basic Info.:
 
Product Name: Clomiphene Citrate
Alias: Clomid;Clomifen;Clomiphene;Clomiphene Citrate;Serophene;Pergotime;Clomphid;Clomiphene Citrate Salt.
CAS No: 50-41-9
MF: C32H36ClNO8
MW: 598.09
Einecs No: 200-035-3
Purity: 99%
Melting point: 116.5-118°C
Storage temp.: 2-8°C
Appearance: Crystalline Solid; Odourless.
Product Categories: API;Intermediates & Fine Chemicals;Pharmaceuticals;Amines;Aromatics;Peptides;CLOMID
Usage:
(1)An unducer of ovulation. A gonad-stimulating principle
(2)Synthetic estrogen agonist-antagonist. Gonad-stimulating principle.
(3)A selective estrogen receptor modulator
Male Anti Estrogenic Clomid for Steroid Cycle Clomiphene.
 
Clomiphene Citrate Description:
 
Clomiphene Citrateis a mixed estrogen agonist/antagonist (activator/blocker) which, when bound to the estrogen receptor, putsClomiphene Citratein a somewhat different conformation (shape) than does estradiol. The estrogen receptor requires binding of an estrogen or drug at its binding site and also the binding of any of several cofactors at different sites. As for women, the only real use for Clomiphene Citrate is the possible management of endogenous estrogen levels near contest time. This can increase fat loss and muscularity, particularly in female trouble areas such as this HIPS and thighs. Clomiphene Citrate however often produces troubling side effects in women (discussed below), and is likewise not in very high demand among this group of athletes. Clomid are also occasionally used periodically during a steroid cycle, in an effort to prevent natural testosterone levels from diminishing. In many instances this practice can prove difficult however, especially when using strong androgens for longer periods of time.
 
Clomiphene Citrate Application:
 
As for toxicity and side effects, Clomiphene Citrateis considered a very safe drug. Bodybuilders seldom report any problems, but listed possible side effects do include hot flashes, nausea, dizziness, headaches and temporarily blurred vision. Clomifene citrate is a drug treatment that stimulates your ovaries to release eggs. Ovulation stimulation using clomifene citrate is a well-established, effective treatment. Clomifene citrate is the most widely used of all fertility drugs. Other drugs that may be used to treat ovulation disorders include metformin and bromocriptin.
 

Properties Suppliers
Human Growth Hormone Active Pharmaceutical Ingredient Gonadorelin 33515-09-2

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Human Growth Hormone Active Pharmaceutical Ingredient Gonadorelin 33515-09-2
 
Gonadorelin Basic Info.:
 
Product Name: Gonadorelin
Other Name: LH-RH, human, Gonadoreline
CAS: 33515-09-2
Purity (HPLC): 98.0%min.
Appearance: White powder
Molecular Formula: C59H83N17O17
Molecular Weight: 1302.39
Single Impurity (HPLC): 0.5%max
Amino Acid Composition: ±10% of theoretical
Peptide Content (N%): ≥80.0% 
Water Content(Karl Fischer): ≤8.0%
Acetate Content(HPIC): ≤10.0%
Specific Rotation (20/D): -55.0~-65.0°(c=1 1%HAc)
MS (ESI): Consistent
Mass Balance: 95.0~105.0%
 
Gonadorelin Description:
 
Gonadorelin is another name for gonadotropin-releasing hormone (GnRH). It is a synthetic decapeptide prepared using solid phase peptide synthesis. GnRH is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary.
GnRH is available as gonadorelin hydrochloride(Factrel®)and gonadorelin diacetate tetrahydrate(Cystorelin®)for injectable use. Studies have described it being used via an infusion pump system to induce ovulation in patients with hypothalamic hypogonadism. It is also used in veterinary medicine as a treatment for cattle with cystic ovarian disease.
 
Gonadorelin Application:
 
Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens. The pulsatility of GnRH secretion has been seen in all vertebrates, and it is necessary to ensure a correct reproductive function. Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male. Its short half life requires infusion pumps for its clinical use.
 

Properties Suppliers
Human Growth Hormone Active Pharmaceutical Ingredient Gonadorelin Acetate 71447-49-9

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 

Properties Suppliers
Human Growth Peptides IGF-1 IGF1 Human Des1-3

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Human Growth Peptides IGF-1 IGF1 Human Des1-3
 
IGF-1 Basic Info.
 
Product Name: IGF1 Human Des1-3 (IGF-1)
Molar Mass: 7,372 Da
Synonyms: IGF-1Des(1-3); Des1-3; Des 1-3; Des (1-3)
Compound: Thr-Leu-Cys-Gly-Ala.
Purity: 99.21%
 
IGF-1 IGF-1DES Dose:
 
DES IGF-1 can be dosed at 50-150mcg multiple times a day (prior to training) into specific target areas. since DES has such a short half life (20-30 minutes), desensitization was not noticed at all . Injection sites should be localized; preferably, at the muscle group you want to grow. In simple terms, if you want to grow your biceps, inject IGF-1DES right into your bicep.
 
IGF-1 IGF-1DES Half-life:
 
DES IGF-1 is the shorter version of the IGF-1 chain. It is five (5) times more powerful than IGF-1LR3 and ten (10) times more powerful than regular base IGF-1. The half-life for DES is about 20-30 minutes, which means this is a very delicate chain. Therefore, administration should only be done at the site where you want to see muscle growth. DES has the ability to stimulate muscle hyperplasia better than LR3. In simple terms, it's best used for site injections, rather than overall growth.
In addition, DES is known to bind to receptors that have been deformed by lactic acid, which is often present during workouts. This allows the DES to attach itself to a mutated receptor and signal tissue growth during training. DES can be used longer and more frequently than LR3.
 

Properties Suppliers
Human Growth SR9009 Powder SR-9009 1379686-30-2

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Human Growth SR9009 Powder SR-9009 1379686-30-2
 
SR 9009 Basic Info.
 
Product Name: SR 9009
SR9009 Prohormone Steroids SARMS
CAS: 1379686-30-2
MF: C20H24ClN3O4S
MW: 437.94
Purity: 99%
Appearance: White powder
Solubility: DMSO
Application: SR9009 increase exercise endurance and loss weight.
 
SR 9009 Description:
 
SR9009 also known as Stenabolic,is a synthetic Rev-Erb ligand and PPAR alpha modifier drug,which is taken orally.This is a very unique compound. By stimulating the Rev-Erb protein, SR9009 has the ability to greatly influence a lot of regulatory mechanisms in the human body.it can affect the circadian rhythms, lipid and glucose metabolism, fat-storing cells, as well as macrophages. SR9009 will allow the user to lose fat and drastically increase endurance, both of which are very desirable effects for an athlete.
 
How SR 9009 Works?
 
By binding and activating the Rev-Erb protein, Stenabolic triggers a very wide range of processes in the body. The most prominent being the increase of mitochondria count in the muscles and an enhanced metabolism.That causes a drastic improvement in endurance and muscle strength.And thanks to the increase in number of macrophages, defective mitochondria are removed from the muscles and replaced with new ones.
 
Furthermore, the change in metabolic rates increases energy expenditure by 5% even when the user is resting.It burns excess calories and doesn’t allow them to convert into fat.Coupled with enhanced metabolism of glucose, helps effectively burn fat, which makes the body act is if it were in a constant state of exercise.
 
This means that less fat is stored, less cholesterol is developed by the liver, and more fat and glucose is burned in the muscles.
 

Properties Suppliers
Human type 3 inositol 1,4,5-trisphosphate receptor (2354-2362) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply Human type 3 inositol 1,4,5-trisphosphate receptor (2354-2362).http://www.creative-peptides.com/product/human-type-inositol-trisphosphate-receptor-item-ta-085-3168.html

Properties Suppliers
Hyaluronan mediated motility receptor (165-173) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply Hyaluronan mediated motility receptor (165-173).http://www.creative-peptides.com/product/hyaluronan-mediated-motility-receptor-item-ta-541-31360.html

Properties Suppliers
Hydroxyurea 99%

Name

Hydroxyurea

Synonyms

Hydroxycarbamide

Molecular Formula

CH4N2O2

Molecular Weight

76.05

CAS Registry Number

127-07-1

EINECS

204-821-7

Melting point

142-146

Water solubility

soluble

Off-White Crystalline Solid

An anti-neoplastic - inhibits ribonucleoside reductase and DNA replication. A potential therapy for sickle cell anemia which involves the nitrosylation of sickle cell hemoglobin. Horseradish peroxidase catalyzes nitric oxide formation from hydroxyurea in the presence of hydrogen peroxide.

Properties Suppliers
Idrocilamide Purified 99.4%

Product Name: Idrocilamide

Synonyms: 230-155-1; N-(2-hydroxyethyl)-3-phenylprop-2-enamide; (3R,4S)-4-(2,3-dimethylphenoxy) piperidin-3-ol; (2E)-N-(2-hydroxyethyl)-3-phenylprop-2-enamide

Molecular Formula: C11H13NO2

Molecular Weight: 191.2264

InChI: InChI=1/C11H13NO2/c13-9-8-12-11(14)7-6-10-4-2-1-3-5-10/h1-7,13H,8-9H2,(H,12,14)/b7-6+

CAS Registry Number: 66208-11-5;6961-46-2

EINECS: 230-155-1

Density: 1.146g/cm3

Boiling point: 439.4 deg C at 760 mmHg

Refractive index: 1.593

Flash point: 219.5 deg C

Vapour Pressure: 1.7E-08mmHg at 25 deg C

Properties Suppliers