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O0380

Supelco

Oxymetholone

analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C21H32O3
Numero CAS:
434-07-1
Peso molecolare:
332.48
Numero CE:
207-098-6
Numero MDL:
MFCD00133083
Codice UNSPSC:
41116107
ID PubChem:
329818839
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

200

Saggio

≥95%

Forma fisica

solid

Controllo stupefacenti

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

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Colore

white to light yellow

Solubilità

H2O: ≤0.5 mg/mL
ethanol: 6.7 mg/mL

applicazioni

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

[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
ICMWWNHDUZJFDW-ZDBQEZQZSA-N

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Categorie correlate

Applicazioni

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

Azioni biochim/fisiol

Androgen

Prodotti consigliati

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.

Pittogrammi

Health hazard
GHS08

Avvertenze

Warning

Indicazioni di pericolo

H351,H361

Consigli di prudenza

P201 - P308 + P313

Classi di pericolo

Carc. 2 - Repr. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
SLCD9612
SLCD9610
SLBV3427
SLBT1571
SLBT1569

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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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