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Merck
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Principaux documents

O0380

Supelco

Oxymetholone

analytical standard

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C21H32O3
Numéro CAS:
Poids moléculaire :
332.48
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Essai

≥95%

Forme

solid

Contrôle du médicament

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

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Couleur

white to light yellow

Solubilité

H2O: ≤0.5 mg/mL
ethanol: 6.7 mg/mL

Application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Format

neat

Température de stockage

2-8°C

Chaîne 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

Clé InChI

ICMWWNHDUZJFDW-ZDBQEZQZSA-N

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Application

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

Actions biochimiques/physiologiques

Androgen

Produits recommandés

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.

Pictogrammes

Health hazard

Mention d'avertissement

Warning

Mentions de danger

Conseils de prudence

Classification des risques

Carc. 2 - Repr. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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


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Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Aleena Banerji et al.
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 100(1 Suppl 2), S19-S22 (2008-01-29)
To provide a summary of the literature regarding the use of attenuated androgens during the past 40 to 50 years for the treatment of hereditary angioedema (HAE). MEDLINE and PubMed were searched to identify studies involving the treatment of HAE
Micheal P Jokinen et al.
Cardiovascular toxicology, 5(2), 227-244 (2005-07-28)
Induction of heart disease can be related to exposure to a number of agents, including environmental chemicals. Studies with laboratory rodents are commonly used to identify cardiotoxic agents and to investigate mechanisms of toxicity. This study was conducted to characterize
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
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
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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