CAS 4642-95-9
:Trendione
Description:
Trendione, with the CAS number 4642-95-9, is a synthetic anabolic steroid that is derived from the hormone testosterone. It is known for its potential to enhance muscle growth and improve athletic performance, making it popular among bodybuilders and athletes. Chemically, Trendione is characterized by its unique structure, which includes a ketone group that contributes to its anabolic properties. It is typically administered in a form that allows for oral consumption, and its effects can include increased protein synthesis, improved nitrogen retention, and enhanced recovery from exercise. However, like many anabolic steroids, Trendione may also carry a risk of side effects, including hormonal imbalances, liver toxicity, and cardiovascular issues. Its use is often regulated or banned in competitive sports due to these potential health risks and its performance-enhancing effects. As with any anabolic agent, individuals considering its use should be aware of the legal and health implications associated with its consumption.
Formula:C18H20O2
InChI:InChI=1S/C18H20O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h8-10,15-16H,2-7H2,1H3/t15-,16+,18+/m1/s1
InChI key:InChIKey=KBSXJBBFQODDTQ-RYRKJORJSA-N
SMILES:C[C@@]12[C@]([C@]3(C(=C4C(CC3)=CC(=O)CC4)C=C1)[H])(CCC2=O)[H]
Synonyms:- 10758-25A
- Ru 2065
- Trendione
- Estra-4,9,11-triene-3,17-dione
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Found 2 products.
Trendione
CAS:Controlled Product<p>Applications Trendione is a secondary metabolite of Trenbolone acetate, a principal metabolite found in cattle excreta and endocrine-active contaminants discharged into the aquatic environment from agricultural fields.<br>References Robinson, J. A., et al.: Environ. Toxicol. Chem., (2016); Cole, E. A., et al.: Environ. Toxicol. Chem., 34, 1472-1484 (2015)<br></p>Formula:C18H20O2Color and Shape:Light YellowMolecular weight:268.40Trendione
CAS:Controlled Product<p>Trendione is an analytical chemistry technique that can be used to detect 17β-estradiol and trenbolone in test samples. It is a sensitive immunoassay with good precision, specificity, and reproducibility. The technique uses monoclonal antibodies to detect the concentrations of estradiol benzoate and estrone 3-sulfate in rat liver microsomes. Trendione has been used in vitro to assess the effects of chronic exposure to 17β-estradiol on gene expression levels in fish cells. The redox potentials of the cells were measured as a response element for estrogenic activity.</p>Formula:C18H20O2Purity:Min. 95%Color and Shape:PowderMolecular weight:268.35 g/mol

