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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:
10161-33-8
Molecular Weight:
270.37
MDL number:
MFCD00214395
UNSPSC Code:
41116107
PubChem Substance ID:
329826780
NACRES:
NA.24
Pricing and availability is not currently available.

grade

analytical standard, for drug analysis

Quality Level

200

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

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Trenbolone analytical standard, for drug analysis

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17α-Methylandrostan-17β-ol-3-one analytical standard

M5626

17α-Methylandrostan-17β-ol-3-one

Mesterolone analytical standard

M7655

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technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

format

neat

format

neat

format

neat

Quality Level

200

Quality Level

100

Quality Level

200

Quality Level

200

grade

analytical standard, for drug analysis

grade

analytical standard

grade

analytical standard

grade

analytical standard

assay

≥93%

assay

-

assay

-

assay

-

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
GHS08

signalword

Danger

Hazard Classifications

Carc. 2 - Repr. 2 - STOT RE 1

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    SLCM1844
    SLCL5392
    SLCG3627
    SLCC7819
    SLCB6132

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    Testosterone enanthate United States Pharmacopeia (USP) Reference Standard

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    1648004

    Testosterone enanthate

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    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
    Shan Liu et al.
    Environmental pollution (Barking, Essex : 1987), 170, 190-201 (2012-07-28)
    Fate and occurrence of fourteen androgens, four estrogens, five glucocorticoids and five progestagens were investigated in three swine farms and three dairy cattle farms with different farming scales and wastes disposal systems in China. Twenty-one, 22, and 12 of total
    R D Munson et al.
    Journal of animal science, 90(11), 4037-4041 (2012-11-14)
    Auction-derived feeder calves (n = 1,601; initial BW = 273.5 ± 4.7 kg) were used to examine effects of delayed administration of the initial steroid implant on health, performance, and carcass characteristics of feedlot cattle. Steers were procured from multiple
    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
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