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Dehydroepiandrosterone is white fine crystalline powder, while it's Molecular Formula is C19H28O2. Dehydroepiandrosterone (DHEA) is a major C19 steroid produced by the adrenal cortex. It is a major 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. People living with HIV may be interested in taking DHEA for a variety of reasons, including treatment of depression, increasing bone density, decreasing arterial plaques, improvement of immune function with HIV, increased memory, and increased muscle strength.
The CAS number of Dehydroepiandrosterone is 53-43-0.
More information of Dehydroepiandrosterone 53-43-0 are:
Synonyms |
(3-beta)-3-Hydroxyandrost-5-en-17-one;17-Hormoforin;5, 6-Dehydroisoandrostorone;EPA Pesticide Chemical Code 126510;Andrestenol;Prasterone [INN];Deandros;Prasteronum [INN-Latin]; |
CAS Number |
53-43-0 |
Molecular Formula |
C19H28O2 |
Molecular Weight |
288.43 |
Density |
1.12 g/cm3 |
Melting Point |
149-151 °C(lit.) |
Boiling Point |
426.7 °C at 760 mmHg |
Flash Point |
182.1 °C |
HS CODE |
29372900 |
PSA |
37.30000 |
LogP |
3.87920 |
Pka |
15.02±0.60(Predicted) |
Dehydroepiandrosterone(DHEA) is an endogenous steroid hormone that is secreted primarily by the adrenal gland and is the most abundant sex steroid. It is a neurohormone; small quantities of DHEA are produced in the brain and declines in serum and CSF with age. (Knopman and Henderson, 2003). Metabolites of DHEA include androstenedione , which subsequently may be metabolized to testosterone or estrone which is an estradiol precursor. In addition to serving as an intermediate in the biosynthesis of sex steroids, DHEA directly modulates a number of cellular and nuclear receptors.
InChI:InChI=1/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3,13-16,20H,4-11H2,1-2H3/t13-,14-,15?,16?,18-,19-/m0/s1
Articles related to Dehydroepiandrosterone:
Article |
Source |
Synthesis and structure determination of 3β-hydroxyandrost-5-en-17-one (C19H28O2·CH3OH) |
Verma, Rajnikant,Jasrotia, Dinesh,Sawhney, Anshu,Bhat, Mousmi,Gupta , p. 523 - 528 (2004) |
Isolation of new androstenol-3()-on-17 from the urine of a patient with |
DINGEMANSE,HUIS IN T VELD,HARTOGH-KATZ , p. 848 - 848 (1948) |
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