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Dehydroepiandrosterone Suppliers list
Company Name: Kono Chem Co., Ltd
Tel: +86-132 8924 6953(Whatsapp/Wechat)
Products Intro: Product Name:Dehydroepiandrosterone
Purity:0.99 Package:1g;25g;1kg;25kg;119kg Remarks:Pharmaceutical grade
Company Name: Shaanxi Pioneer Biotech Co., Ltd .
Tel: 86-13259417953(Whatsapp)
Products Intro: Product Name:Dehydroepiandrosterone
Purity:0.99 Package:1g;25g;1kg;25kg;100kg
Company Name: Hubei XinRunde Chemical Co., Ltd.
Tel: +8615102730682; +8618874586545
Products Intro: Product Name:Dehydroepiandrosterone
Purity:98% Package:1KG;800USD
Company Name: Shaanxi Yikanglong Biotechnology Co., Ltd.
Tel: 17791478691
Products Intro: Product Name:Dehydroepiandrosterone
Purity:99%(Customizable specifications) Package:1KG;1USD Remarks:Factory stock, quality assurance, price concessions
Company Name: Hebei Jimi Trading Co., Ltd.
Tel: +86 319 5273535
Products Intro: Product Name:Dehydroepiandrosterone
Purity:99.9% Package:10kg;1USD

Lastest Price from Dehydroepiandrosterone manufacturers

  • Dehydroepiandrosterone
  • US $0.00 / mg
  • 2019-12-31
  • CAS:53-43-0
  • Min. Order: 5mg
  • Purity: ≥98%(HPLC)
  • Supply Ability: 10 g
  • Dehydroepiandrosterone
  • US $1.00 / Kg/Bag
  • 2019-11-29
  • CAS:53-43-0
  • Min. Order: 1Kg/Bag
  • Purity: 99.95%
  • Supply Ability: 30tons

Related articles

Dehydroepiandrosterone Basic information
Indications and Usage Mechanisms of Action
Product Name:Dehydroepiandrosterone
Synonyms:DHEA - CAS 53-43-0 - Calbiochem;5,6-Dehydroisoandrosterone;5,6-Dehydroisoandrostorone;5,6-Didehydroisoandrosterone;5-Androsten-3B-ol-17-one;5-Dehydroepiandrosterone;Androst-5-en-17-one, 3beta-hydroxy-;Androst-5-en-17-one, 3-hydroxy-, (3beta)-
Product Categories:API;Pharmaceutical Intermediates;Steroids;17-Ketosteroids;Biochemistry;Hydroxyketosteroids;Nutritional Supplements;Intermediates & Fine Chemicals;Pharmaceuticals;Steroid and Hormone;Inhibitors
Mol File:53-43-0.mol
Dehydroepiandrosterone Structure
Dehydroepiandrosterone Chemical Properties
Melting point 149-151 °C(lit.)
alpha 12 º (c=2, ethanol 96% 25 ºC)
Boiling point 370.65°C (rough estimate)
density 1.0484 (rough estimate)
refractive index 1.4709 (estimate)
Fp 9℃
storage temp. Hormones
form Fine Crystalline Powder
color White
Water Solubility 21.8mg/L(23.5 ºC)
Merck 2871
BRN 2058110
CAS DataBase Reference53-43-0
NIST Chemistry Reference5-Androstene-3«beta»-ol-17-one(53-43-0)
EPA Substance Registry SystemPrasterone (53-43-0)
Safety Information
Hazard Codes Xi,T,F
Risk Statements 36/37/38-39/23/24/25-23/24/25-11
Safety Statements 26-36-24/25-45-36/37-16-7
RIDADR UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany 2
RTECS BV8396000
HS Code 29372900
MSDS Information
Prasterone English
ACROS English
SigmaAldrich English
Dehydroepiandrosterone Usage And Synthesis
Indications and UsageDehydroepiandrosterone (DHEA,) chemical name 3β-hydroxy-5alpha-androstane-17-ketone, is an esterifying 3–β–hydroxy steroid retaining 5,6 cholesterol. A white crystalline powder, soluable in ethanol, ether, and benzene, and slightly soluable in chroloform and petroleum ether. Precipitates in digitalis.
DHEA is an estrogen precursor secreted by the reticular layer of the human adrenal cortex. Prevents obesity, resists diabetes, fights cancer, fights cortical disease, and delays senility treats immune deficiencies, promotes the growth and differentiation of bone cells, and promotes the synthesis of protein. It also resists viral infections, improves memory, and relieves nervous tension. DHEA is the main ingredient in steroid hormone intermediates (such as norethindrone and bisacetylene, etc.) and in birth control, and is involved in the secretion of many adrenal hormones. It has undergone extensive clinical research on treating menopausal syndrom, chorionitis, coronary heart disease, gout, psoriasis, AIDS and so on.
Mechanisms of ActionDHEA has a thyroid stimulating effect inhibiting food and fat intake and reducing fat accumulation, etc. It improves glucose tolerance, increases insulin level and fights diabetes. It can enhance endocrine system actiity, reduce cortisol levels, and resist a variety of pathological processes. It can help the body obtain cortical antibodies. DHEA has a strong protective and synergistic effect when used to treat tumors, becuase it inhibits ribose 5-phosphate. Inhibits cancer by inhibiting excessive mitochondria (NADPH) and ribose 5-phosphate esters. Regulates the growth of pancreatic cancer cells by regulating the concentration of estrogen in blood plasma. A decline in GnRH gene expression leads to aging, and DHEA can restore GnRH neuronal activity, stopping or improving certain diseases associated with declines in DHEA by stimulating GnRH biosynthesis. Restores impaired immune response, improves T- and B-cell function, and plays an important role in enhancing the physiological activity of insulin-like growth factor (IGF-1,) and is a potentially useful drug for immunodeficiency. DHEA alone cannot directly affect the growth and differential of osteoblasts, but it can do so by influencing 1,25-dihydroxyvitamin D3. The effects of DHEA on bone mass depend on the presence and form of sex hormones in bone cells and their endrocine effects on osteoblasts. DHEA is an anabolic protein hormone which promotes protein synthesis. According to the findings of Marrero and others, feeding DHEA (0.45%) to mice increased liver weight, increasing liver mitochondria by guiding liver protein restoring RNA and protein synthesis.
Chemical Propertieswhite fine crystalline powder
OccurrenceDHEA is naturally occurring in yam (see Wild Yam, p. 596-597).
UsesMajor secretory steroidal product of the adrenal gland; secretion progresively declines with aging. May have estrogen-or androgen-like effects depending on the hormonal milieu. Intracellularly converted to androstenedione. It is used in treatment of menopausal syndrome.
Usesadrenocortical hormone, antidepressant
Brand name17-chetovis 17-hormoforin;Cetavister;Climatost;Dastonil;Dha-s (prasterone);Gynodian;Longevital 5000;Maxepa;Mentalormon;Mylis;Neurocotex;Psicosterone;Ro 66827;Sh 833;Ultrapla.
World Health Organization (WHO)The World Health Organization has no information further to the above regarding preparations containing prasterone or to indicate that such preparations remain available.
Safety ProfileAn experimental teratogen.Experimental reproductive effects. Questionablecarcinogen with experimental neoplastigenic data. Whenheated to decomposition it emits acrid smoke andirritating fumes.
Dehydroepiandrosterone Preparation Products And Raw materials
Preparation ProductsEthisterone
Raw materialsCholesterol-->Stigmasterol-->Dioscin
Tag:Dehydroepiandrosterone(53-43-0) Related Product Information
5-ANDROSTEN-3BETA-OL-17-ONE 3-(O->1BETA)-D-GLUCOPYRANOSIDURONIC SODIUM 5-ANDROSTEN-3-BETA-OL-17-ONE BENZOATE (3b,16a)-3,16-dihydroxy-Androst-5-en-17-one 19-IODO-5-ANDROSTENE-3BETA-OL-17-ONE 3-ACETATE ALDOSTERONE Ecdysone Metandienone BANISTERINE MONOHYDRATE 7-Oxo-Dehydroepiandrosterone(7-OXO-DHEA) Epiandrosterone Dehydroepiandrosterone 3-sulfate Androsterone 4-CHLORODEHYDROMETHYLTESTOSTERONE 7-KETO-DEHYDROEPIANDROSTERONE,7-KETO DHEA/7-KETO-DEHYDROEPIANDROSTERONE Testosterone trans,trans-2,4-Undecadienal Dehydroepiandrosterone Dydrogesterone