Pular para o conteúdo
Merck
Todas as fotos(3)

Key Documents

E3375

Sigma-Aldrich

trans-Androsterone

Sinônimo(s):

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

Faça loginpara ver os preços organizacionais e de contrato


About This Item

Fórmula empírica (Notação de Hill):
C19H30O2
Número CAS:
Peso molecular:
290.44
Beilstein:
1884007
Número CE:
Número MDL:
Código UNSPSC:
12352200
ID de substância PubChem:
NACRES:
NA.77

fonte biológica

synthetic (organic)

Nível de qualidade

esterilidade

non-sterile

Ensaio

≥98% (HPLC)

forma

powder

controle de medicamentos

regulated under CDSA - not available from Sigma-Aldrich Canada

solubilidade

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

Condições de expedição

ambient

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

[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

chave InChI

QGXBDMJGAMFCBF-LUJOEAJASA-N

Informações sobre genes

human ... HSD17B3(3293)

Procurando produtos similares? Visita Guia de comparação de produtos

Pictogramas

Health hazard

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Repr. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

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

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica