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E3375

Sigma-Aldrich

trans-Androsteron

Synonym(e):

3β-Hydroxy-5α-androstan-17-on, 3β-Hydroxyetioallocholan-17-on, 5α-Androstan-3β-ol-17-on, Epi-androsteron, Iso-androsteron

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About This Item

Empirische Formel (Hill-System):
C19H30O2
CAS-Nummer:
481-29-8
Molekulargewicht:
290.44
Beilstein:
1884007
EG-Nummer:
207-563-3
MDL-Nummer:
MFCD00064134
UNSPSC-Code:
12352200
PubChem Substanz-ID:
24894509
NACRES:
NA.77

Biologische Quelle

synthetic (organic)

Qualitätsniveau

200

Sterilität

non-sterile

Assay

≥98% (HPLC)

Form

powder

Arzneimittelkontrolle

regulated under CDSA - not available from Sigma-Aldrich Canada

Löslichkeit

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

Versandbedingung

ambient

Lagertemp.

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

InChIKey

QGXBDMJGAMFCBF-LUJOEAJASA-N

Angaben zum Gen

human ... HSD17B3(3293)

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Piktogramme

Health hazard
GHS08

Signalwort

Warning

H-Sätze

H361fd

Gefahreneinstufungen

Repr. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Slide 1 of 4

1 of 4

5α-Androst-16-en-3α-ol

Sigma-Aldrich

A7883

5α-Androst-16-en-3α-ol

17α-Hydroxypregnenolone

Sigma-Aldrich

H5002

17α-Hydroxypregnenolone

5α-Androstan-17β-ol-3-on ≥97.5%

Sigma-Aldrich

A8380

5α-Androstan-17β-ol-3-on

5α-Androstane

Sigma-Aldrich

A0887

5α-Androstane

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
Adriana M Cirigliano et al.
Phytochemical analysis : PCA, 31(5), 606-615 (2020-02-12)
An efficient characterisation of metabolites is a crucial task in many aspects of basic research, such as the de-replication of crude extracts in natural products chemistry or the tentative identification of compounds in untargeted metabolomics. The goal of this work
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
Argitxu Esquivel et al.
Drug testing and analysis, 11(8), 1218-1230 (2019-04-02)
The introduction of alternative markers to the steroid profile can be an effective approach to improving the screening capabilities for the detection of testosterone (T) misuse. In this work, endogenous steroid sulfates were evaluated as potential markers to detect intramuscular
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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