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709549

Sigma-Aldrich

Dehydroepiandrosterone-2,2,3,4,4,6-d6

97 atom % D, 98% (CP)

Synonym(s):

3ß-Hydroxy-5-androsten-17-one-d6, 5-Androsten-3ß-ol-17-one-d6, DHEA-d6, Dehydroisoandrosterone-d6, Prasterone-d6

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About This Item

Empirical Formula (Hill Notation):
C19D6H22O2
CAS Number:
1261254-39-0
Molecular Weight:
294.46
MDL number:
MFCD15146313
UNSPSC Code:
12352211
PubChem Substance ID:
329762879
NACRES:
NA.24

isotopic purity

97 atom % D

Quality Level

200

Assay

98% (CP)

form

powder

drug control

Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada

technique(s)

mass spectrometry (MS): suitable

mp

149-151 °C

mass shift

M+6

storage temp.

−20°C

SMILES string

[2H]C1=C2C([2H])([2H])[C@@]([2H])(O)C([2H])([2H])C[C@]2(C)[C@H]3CC[C@@]4(C)[C@@H](CCC4=O)[C@@H]3C1

InChI

1S/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/i3D,7D2,11D2,13D

InChI key

FMGSKLZLMKYGDP-BQXVJGQMSA-N

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Pictograms

Health hazard
GHS08

Signal Word

Warning

Hazard Statements

H361fd

Hazard Classifications

Repr. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Journal of pharmaceutical and biomedical analysis, 138, 344-350 (2017-03-02)
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As a crucial factor in male reproduction, androgens may represent an intermediate biological mechanism linking metal exposure with effects on semen quality. This study aimed to investigate the association between metal exposure and semen quality, and to assess the mediating
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Sulfated steroids can act as a latent form of active free steroids, coexisting with them in biological specimens. To evaluate the metabolic significance of free and sulfated steroid species, a simultaneous analysis of eight free steroids [cholesterol, pregnenolone, 17α-hydroxypregnenolone, progesterone
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