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5-Androstenediol (exempt preparation)

Item No. 46244

Exempt Product (US)
Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 5-Adiol
  • Androstenediol
  • 5-Androsten-17β,3β-diol
  • NSC 12163
Technical Information
Formal Name
androst-5-ene-3β,17β-diol
CAS Number
521-17-5
Molecular Formula
C19H30O2
Formula Weight
290.4
Purity
≥98%
Formulation (Request formulation change)
A 1 mg/ml solution in methanol
SMILES
C[C@@]12[C@]3([H])[C@](CC=C1C[C@H](CC2)O)([H])[C@@]4([H])[C@](CC3)([C@H](CC4)O)C
InChi Code
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/h3,13-17,20-21H,4-11H2,1-2H3/t13-,14-,15-,16-,17-,18-,19-/m0/s1
InChi Key
QADHLRWLCPCEKT-LOVVWNRFSA-N
Regulatory Information
DEA Exempt Notification
This product is a DEA exempt preparation of a scheduled compound - does not require DEA Controlled Substance registration or DEA 222 form. For alternate sizes please contact sales.
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    1 mg

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    Product Description

    5-Androstenediol (exempt preparation) (Item No. 46244) is an analytical reference standard categorized as an anabolic androgenic steroid.1 5-Androstenediol is a precursor in the biosynthesis of testosterone (Item Nos. ISO60154 | ISO00154 | 15645).2 5-Androstenediol is regulated as a Schedule III compound in the United States. 5-Androstenediol (exempt preparation) (Item No. 46244) is provided as a DEA exempt preparation. This product is intended for research and forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Poucke, C.V., Detavernier, C., Van Cauwenberghe, R., et al. Determination of anabolic steroids in dietary supplements by liquid chromatography-tandem mass spectrometry. Anal. Chim. Acta 586(1-2), 35-42 (2007).

    2. Inaba, M., and Nakao, T. Conversion of 4-androstenediol and 5-androstenediol to testosterone, and conversion of dehydroepiandrosterone to 4-androstenediol by rat testis in vitro. Endocrinol. Jpn. 13(2), 160-172 (1966).