Skip to Content
Merck
CN

46924

Supelco

Testosterone acetate

VETRANAL®, analytical standard

Synonym(s):

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

Sign Into View Organizational & Contract Pricing

Select a Size

About This Item

Empirical Formula (Hill Notation):
C21H30O3
CAS Number:
1045-69-8
Molecular Weight:
330.46
Beilstein:
2062555
EC Number:
213-876-6
MDL number:
MFCD00021154
UNSPSC Code:
41116107
PubChem Substance ID:
24870575

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

grade

analytical standard

product line

VETRANAL®

drug control

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

SMILES string

[H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)[C@H](CC[C@@]24[H])OC(C)=O

Looking for similar products? Visit Product Comparison Guide

Legal Information

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

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Yoanna María Alvarez-Ginarte et al.
Bioorganic & medicinal chemistry, 16(12), 6448-6459 (2008-06-03)
Predictive quantitative structure-activity relationship (QSAR) models of anabolic and androgenic activities for the testosterone and dihydrotestosterone steroid analogues were obtained by means of multiple linear regression using quantum and physicochemical molecular descriptors (MD) as well as a genetic algorithm for

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service