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Sigma-Aldrich

17α-Methyltestosteron

≥97.0% (HPLC)

Synonym(e):

17α-Methyl-4-androsten-17β-ol-3-on, 17β-Hydroxy-17a-methyl-4-androsten-3-on, Mesteron, Methyl-testosteron

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About This Item

Empirische Formel (Hill-System):
C20H30O2
CAS-Nummer:
58-18-4
Molekulargewicht:
302.45
Beilstein:
2057425
EG-Nummer:
200-366-3
MDL-Nummer:
MFCD00003655
UNSPSC-Code:
51111800
PubChem Substanz-ID:
57652183
NACRES:
NA.22

Assay

≥97.0% (HPLC)

Form

powder

Optische Aktivität

[α]20/D +82±3°, c = 1% in ethanol

Arzneimittelkontrolle

USDEA Schedule IIIN; regulated under CDSA - not available from Sigma-Aldrich Canada

Verlust

≤2% loss on drying

mp (Schmelzpunkt)

162-168 °C (lit.)

SMILES String

C[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

InChI

1S/C20H30O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h12,15-17,22H,4-11H2,1-3H3/t15-,16+,17+,18+,19+,20+/m1/s1

InChIKey

GCKMFJBGXUYNAG-HLXURNFRSA-N

Angaben zum Gen

human ... AR(367)
rat ... Ar(24208)

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Verwandte Kategorien

Sonstige Hinweise

Kann Verkaufsbeschränkungen unterliegen.

Piktogramme

Health hazard
GHS08

Signalwort

Danger

H-Sätze

H350,H361fd

Gefahreneinstufungen

Carc. 1B - Repr. 2

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Persönliche Schutzausrüstung

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Analysenzertifikate (COA)

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Daniela Stange et al.
Ecotoxicology and environmental safety, 75(1), 94-101 (2011-09-29)
Molluscs are raising attention as ecotoxicological test organisms due to their high diversity and ecological importance. The ovoviviparous prosobranch gastropod Potamopyrgus antipodarum (freshwater mudsnail) responds very sensitively to xenobiotics and has therefore been proposed as OECD standard test organism. Endocrine
C Gómez et al.
Steroids, 78(1), 44-52 (2012-11-07)
Methyltestosterone (MT) is one of the most frequently detected anabolic androgenic steroids in doping control analysis. MT misuse is commonly detected by the identification of its two main metabolites excreted as glucuronide conjugates, 17α-methyl-5α-androstan-3α,17β-diol and 17α-methyl-5β-androstan-3α,17β-diol. The detection of these
Yuqian Han et al.
Food chemistry, 135(4), 2988-2993 (2012-09-18)
A simple, rapid and sensitive method was developed for determination of 17α-methyltestosterone in aquatic products by extraction with subcritical 1,1,1,2-tetrafluoroethane (R134a) extraction and high performance liquid chromatography (HPLC). Response surface methodology (RSM) was adopted to optimise extraction pressure, temperature and
Carlos A A Penatti et al.
Neuropharmacology, 61(4), 653-664 (2011-06-08)
Disruption of reproductive function is a hallmark of abuse of anabolic androgenic steroids (AAS) in female subjects. To understand the central actions of AAS, patch clamp recordings were made in estrous, diestrous and AAS-treated mice from gonadotropin releasing hormone (GnRH)
Wenbo Jiang et al.
Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology, 160(4), 187-193 (2011-09-06)
Gobiocypris rarus is an emerging fish model for aquatic toxicology in China as it is sensitive to environmental hormone disruptors. Exogenous sex steroids can affect sex differentiation and the expression of sex-related genes. Foxl2, a member of forkhead-box transcription factor
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