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Testosterone acetate solution

VETRANAL®, 100 μg/mL in acetonitrile, analytical standard

Synonym(s):

17β-Acetoxy-4-androsten-3-one solution, 17β-Hydroxy-4-androsten-3-one 17-acetate solution, 4-Androsten-17β-ol-3-one 17-acetate solution, Deposteron solution

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About This Item

Empirical Formula (Hill Notation):
C21H30O3
CAS Number:
Molecular Weight:
330.46
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

drug control

USDEA Schedule IIIN; regulated under CDSA - not available from Sigma-Aldrich Canada

concentration

100 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

single component solution

storage temp.

2-8°C

SMILES string

CC(=O)O[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

InChI

1S/C21H30O3/c1-13(22)24-19-7-6-17-16-5-4-14-12-15(23)8-10-20(14,2)18(16)9-11-21(17,19)3/h12,16-19H,4-11H2,1-3H3/t16-,17-,18-,19-,20-,21-/m0/s1

InChI key

DJPZSBANTAQNFN-PXQJOHHUSA-N

General description

Testosterone acetate belongs to the class of androgenic steroid esters that can be utilized to enhance muscle strength and physical performance.[1]

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Testosterone acetate solution may be used as an analytical reference standard for the determination of the analyte in:
  • Horse hair samples using ultra-high performance liquid chromatography-high resolution mass spectrometry (UHPLC-HRMS) in multiplexed targeted MS2 mode and gas chromatography-tandem mass spectrometry (GC-MS/MS).[2]
  • Aquatic matrices by UHPLC combined with high resolution Q-Orbitrap-MS method.[3]

Legal Information

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2.0 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Guro Forsdahl et al.
Drug testing and analysis, 7(11-12), 983-989 (2015-12-24)
Injections of synthetic esters of testosterone are among the most common forms of testosterone application. In doping control, the detection of an intact ester of testosterone in blood gives unequivocal proof of the administration of exogenous testosterone. The aim of
Development and validation of an ultra-high performance liquid chromatographic high resolution Q-Orbitrap mass spectrometric method for the simultaneous determination of steroidal endocrine disrupting compounds in aquatic matrices.
Huysman S, et al.
Analytica Chimica Acta, 984, 140-150 (2017)
Detection of seventy-two anabolic and androgenic steroids and/or their esters in horse hair using ultra-high performance liquid chromatography-high resolution mass spectrometry in multiplexed targeted MS2 mode and gas chromatography-tandem mass spectrometry.
Choi TLS, et al.
Journal of Chromatography A, 1493, 76-86 (2018)
Yogan Khatri et al.
Chembiochem : a European journal of chemical biology, 17(1), 90-101 (2015-10-21)
Cytochromes P450 catalyze a variety of synthetically useful reactions. However, it is difficult to determine their physiological or artificial functions when a plethora of orphan P450 systems are present in a genome. CYP260A1 from Sorangium cellulosum So ce56 is a new
B A Foster et al.
Endocrinology, 140(1), 318-328 (1999-01-14)
The studies presented herein quantitated ductal branching morphogenesis in the anterior prostate (AP) of the newborn rat. Four parameters were measured: epithelial area, epithelial perimeter, node number, and form factor. Nine natural and synthetic androgens were tested for their effectiveness

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