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T3925

Supelco

Trenbolone

analytical standard, for drug analysis

Synonym(s):

17β-Hydroxyestra-4,9,11-trien-3-one

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About This Item

Empirical Formula (Hill Notation):
C18H22O2
CAS Number:
Molecular Weight:
270.37
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard, for drug analysis

Quality Level

Assay

≥93%

drug control

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

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

storage temp.

2-8°C

SMILES string

[H][C@@]12CCC3=CC(=O)CCC3=C1C=C[C@]4(C)[C@@H](O)CC[C@@]24[H]

InChI

1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h8-10,15-17,20H,2-7H2,1H3/t15-,16+,17+,18+/m1/s1

InChI key

MEHHPFQKXOUFFV-OWSLCNJRSA-N

Gene Information

rat ... Ar(24208)

Application

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

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Carc. 2 - Repr. 2 - STOT RE 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Erica K Brockmeier et al.
Aquatic toxicology (Amsterdam, Netherlands), 128-129, 163-170 (2013-01-15)
The Eastern and Western mosquitofish (Gambusia holbrooki and G. affinis) are potential bioindicator organisms for endocrine disruptors. Male mosquitofish have an elongated anal fin (gonopodium) used for internal fertilization whose formation is driven by androgens. Normal female mosquitofish have a
D R Ekman et al.
Environmental science & technology, 46(17), 9673-9680 (2012-08-01)
Widespread environmental contamination by bisphenol A (BPA) has created the need to fully define its potential toxic mechanisms of action (MOA) to properly assess human health and ecological risks from exposure. Although long recognized as an estrogen receptor (ER) agonist
Bushra Khan et al.
Chemosphere, 89(11), 1443-1449 (2012-07-17)
The increasing size of concentrated animal feeding operations has led to a concomitant increase in the land-application of manure, which has spawned research on the concentrations and environmental risk assessment of natural and synthetic hormones in animal manures. 17β-Trenbolone acetate
Toine F H Bovee et al.
Analytical and bioanalytical chemistry, 389(5), 1549-1558 (2007-09-13)
Public concern about the presence of natural and anthropogenic compounds which affect human health by modulating normal endocrine functions is continuously growing. Fast and simple high-throughput screening methods for the detection of hormone activities are thus indispensable. During the last
Sean C McCoy et al.
Bone, 51(4), 667-673 (2012-07-31)
Testosterone enanthate (TE) administration attenuates bone loss in orchiectomized (ORX) rats. However, testosterone administration may increase risk for prostate/lower urinary tract related adverse events and polycythemia in humans. Trenbolone enanthate (TREN) is a synthetic testosterone analogue that preserves bone mineral

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