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E3375

Sigma-Aldrich

trans-Androsterone

Sinónimos:

3β-Hydroxy-5α-androstan-17-one, 3β-Hydroxyetioallocholan-17-one, 5α-Androstan-3β-ol-17-one, Epi-androsterone, Isoandrosterone

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About This Item

Fórmula empírica (notación de Hill):
C19H30O2
Número de CAS:
481-29-8
Peso molecular:
290.44
Beilstein/REAXYS Number:
1884007
EC Number:
207-563-3
MDL number:
MFCD00064134
UNSPSC Code:
51111800
PubChem Substance ID:
24894509
NACRES:
NA.77

biological source

synthetic (organic)

Quality Level

200

sterility

non-sterile

assay

≥98% (HPLC)

form

powder

drug control

regulated under CDSA - not available from Sigma-Aldrich Canada

solubility

chloroform: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow

shipped in

ambient

storage temp.

room temp

SMILES string

[H][C@@]12CC[C@@]3([H])[C@]4([H])CCC(=O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@H](O)C2

InChI

1S/C19H30O2/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/h12-16,20H,3-11H2,1-2H3/t12-,13-,14-,15-,16-,18-,19-/m0/s1

InChI key

QGXBDMJGAMFCBF-LUJOEAJASA-N

Gene Information

human ... HSD17B3(3293)

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pictograms

Health hazard
GHS08

signalword

Warning

hcodes

H361fd

Hazard Classifications

Repr. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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17α-Hydroxypregnenolone

Sigma-Aldrich

H5002

17α-Hydroxypregnenolone

5α-Androstan-17β-ol-3-one ≥97.5%

Sigma-Aldrich

A8380

5α-Androstan-17β-ol-3-one

5α-Androstane

Sigma-Aldrich

A0887

5α-Androstane

Christopher C Waller et al.
Drug testing and analysis, 12(6), 752-762 (2020-01-18)
Hemapolin (2α,3α-epithio-17α-methyl-5α-androstan-17β-ol) is a designer steroid that is an ingredient in several "dietary" and "nutritional" supplements available online. As an unusual chemical modification to the steroid A-ring could allow this compound to pass through antidoping screens undetected, the metabolism of
Anna Panek et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-19)
The biotransformation of steroid compounds is a promising, environmentally friendly route to new pharmaceuticals and hormones. One of the reaction types common in the metabolic fate of steroids is Baeyer-Villiger oxidation, which in the case of cyclic ketones, such as
Argitxu Esquivel et al.
Drug testing and analysis, 11(3), 392-402 (2018-10-27)
The detection of testosterone (T) misuse is performed using the steroid profile that includes concentrations of T and related metabolites excreted free and glucuronoconjugated, and the ratios between them. In this work, the usefulness of 14 endogenous steroid sulfates to
Laurie De Wilde et al.
Drug testing and analysis, 12(8), 1006-1018 (2020-04-09)
In doping control, to confirm the exogenous origin of exogenously administered anabolic androgenic steroids (AAS), a gas chromatography combustion isotope ratio mass spectrometry (GC-C-IRMS) analysis is performed. Recently published work suggests that epiandrosterone sulfate (EpiAS) is a promising IRMS target
Christopher D Chouinard et al.
Journal of the American Society for Mass Spectrometry, 28(2), 323-331 (2016-12-04)
Ion mobility-mass spectrometry (IM-MS) has recently seen increased use in the analysis of small molecules, especially in the field of metabolomics, for increased breadth of information and improved separation of isomers. In this study, steroid epimers androsterone and trans-androsterone were
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