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Merck

O0380

Supelco

Oxymetholone

analytical standard

Sinónimos:

17β-Hydroxy-2-(hydroxymethylene)-17-methyl-5α-androstan-3-one, Anasterone

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About This Item

Fórmula empírica (notación de Hill):
C21H32O3
Número de CAS:
Peso molecular:
332.48
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

Análisis

≥95%

formulario

solid

control farmacológico

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

técnicas

HPLC: suitable
gas chromatography (GC): suitable

color

white to light yellow

solubilidad

H2O: ≤0.5 mg/mL
ethanol: 6.7 mg/mL

aplicaciones

forensics and toxicology
pharmaceutical (small molecule)
veterinary

formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

[H][C@@]12CC[C@]3([H])C(CC[C@@]4(C)[C@@]3([H])CC[C@]4(C)O)[C@@]1(C)C\C(=C\O)C(=O)C2

InChI

1S/C21H32O3/c1-19-11-13(12-22)18(23)10-14(19)4-5-15-16(19)6-8-20(2)17(15)7-9-21(20,3)24/h12,14-17,22,24H,4-11H2,1-3H3/b13-12-/t14-,15+,16?,17-,19-,20-,21-/m0/s1

Clave InChI

ICMWWNHDUZJFDW-ZDBQEZQZSA-N

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Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Acciones bioquímicas o fisiológicas

Androgen

Productos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogramas

Health hazard

Palabra de señalización

Warning

Frases de peligro

Consejos de prudencia

Clasificaciones de peligro

Carc. 2 - Repr. 2

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

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


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Certificados de análisis (COA)

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Visite la Librería de documentos

Erkan Ilhan et al.
Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir, 38(4), 275-278 (2010-10-12)
A 41-year-old male bodybuilder was admitted with acute inferior myocardial infarction. The patient had been using oxymetholone and methenolone to increase his performance for 15 years and quitted smoking three years before. He underwent successful primary percutaneous coronary intervention (PCI)
Seyed Jalal Hosseinimehr et al.
Molecular and cellular biochemistry, 287(1-2), 193-199 (2006-03-15)
Oxymetholone is a 17alpha -alkylated anabolic-androgenic steroid. This drug can stimulate bone marrow cells and increase the blood cells in the peripheral blood vessels. It has been used for the treatment of anemia caused by low red cell production. Since
Hajeong Lee et al.
Journal of Korean medical science, 25(11), 1676-1679 (2010-11-10)
Anti-erythropoietin antibodies usually cross-react with all kinds of recombinant erythropoietins; therefore, erythropoiesis-stimulating agent (ESA)-induced pure red-cell aplasia (PRCA) is not rescued by different ESAs. Here, we present a case of ESA-induced PRCA in a 36-yr-old woman with chronic kidney disease
P Aramwit et al.
Clinical nephrology, 71(4), 413-422 (2009-04-10)
To investigate the beneficial effects of oral oxymetholone on IR in hemodialysis (HD) patients by increasing skeletal muscle function and stimulating myocyte glucose uptake and metabolism. In a randomized, controlled double-blind study, 44 patients were randomly assigned to one of
Tim Sobolevsky et al.
Drug testing and analysis, 4(9), 682-691 (2012-09-05)
The metabolism of two anabolic steroids - oxymetholone and desoxymethyltestosterone - was reinvestigated to identify new targets potentially valuable for the antidoping analysis. Excretion urine samples from the laboratory reference collection were used in this study. Following fractionation of the

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