361432-76-0

Basic information

• Product Name: d3-17β-Boldenone
• Synonyms: d3-17β-Boldenone;d3-17β-Boldenone Solution, 10ppm
• CAS NO: 361432-76-0
• Molecular Formula: C19H26O2
• Molecular Weight: 286.42
• Mol File: 361432-76-0.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: d3-17β-Boldenone(CAS DataBase Reference)
• NIST Chemistry Reference: d3-17β-Boldenone(361432-76-0)
• EPA Substance Registry System: d3-17β-Boldenone(361432-76-0)

Safety Data

• Hazardous Substances Data: 361432-76-0(Hazardous Substances Data)

Usage

Description

d3-17β-Boldenone, also known as Equipoise, is a synthetic anabolic steroid derived from testosterone. It is commonly used in veterinary medicine to promote growth and weight gain in animals, particularly livestock. Known for its ability to increase muscle mass and strength, it is typically administered as an injection. However, its use in humans is prohibited by several sporting organizations and is classified as a controlled substance due to its potential for misuse and abuse. The chemical has also been linked to various adverse health effects, including liver damage, cardiovascular issues, and hormonal imbalances.

Uses

Used in Veterinary Medicine:
d3-17β-Boldenone is used as a growth promoter for livestock, particularly to increase muscle mass and strength. It is administered as an injection to promote growth and weight gain in animals.
Used in Bodybuilding and Athletic Competitions (Illegally):
In humans, d3-17β-Boldenone has been used illegally to enhance performance in bodybuilding and athletic competitions. However, its use is prohibited by several sporting organizations and is classified as a controlled substance due to its potential for misuse and abuse.

Upstream product

• 58-22-0 testosterone 
• 897-06-3 Androsta-1,4-diene-3,17-dione 
• 100428-85-1 17α-hydroxyandrost-5-en-3β-yl 3-acetate 
• 40768-04-5 3β-hydroxyandrost-5-en-17α-yl benzoate 
• 40768-03-4 androst-5-ene-3β,17α-diyl 3-acetate 17-benzoate 
• 1639-43-6 androstenediol-3-acetate 
• 853-23-6 prasterone acetate 
• 36025-82-8 3-oxoandrost-4-en-17α-yl benzoate 
• 1259-22-9 5-androstene-3β,17β-diol 3-acetate 17-p-toluene-δ-sulfonate 
• 846-48-0 1-dehydrotestosterone 
• 150054-81-2 3-oxoandrosta-1,4-dien-17α-yl benzoate 
• 481-29-8 Epiandrosterone 
• 63-05-8 Androstenedione 
• 83-46-5 β-sitosterol 

Downstream Products

• 27833-18-7 17β-hydroxy-1,4-androstadien-3-one. 

Relevant articles and documents

Microbiological synthesis of 17β-hydroxyandrosta-1,4-dien-3-one

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Old yellow enzyme-catalyzed dehydrogenation of saturated ketones

Enzymes from extremophiles have always been of great interest for biotechnology because of their ruggedness against various stress factors. We have isolated, cloned, heterologously expressed and characterized a thermostable old yellow enzyme (OYE) from Geobacillus kaustophilus. In addition to the expected 'enone' reduction, GkOYE also catalyzes the reverse reaction, i.e., the desaturation of C-C bonds adjacent to a carbonyl to give the corresponding α,β-unsaturated ketone. The reaction proceeds at the expense of molecular oxygen without the need for a nicotinamide cofactor and represents an environmentally benign alternative to known chemical dehydrogenation methods.

Reduction of steroidal ketones with amine - Boranes

Complexes of secondary amines with borane, R2NH·BH 3, surpass sodium borohydride as reducing agents for saturated and unsaturated steroidal 3-, 12-, 17-, and 20-ketones as regards chemo- and regioselectivity and mildness of the reaction conditions. In the case of 12-ketones, stereoselectivity is also improved.