27833-18-7

Usage

Uses

Used in Pharmaceutical Industry:
17α-Boldenone (Epiboldenone) is used as an anabolic agent for its ability to promote muscle growth and strength, as well as to increase red blood cell production. It is particularly useful in the treatment of conditions that involve muscle wasting, such as osteoporosis, anemia, and muscle dystrophy.
Used in Sports Performance Enhancement:
In the sports industry, 17α-Boldenone (Epiboldenone) is used as a performance-enhancing drug to improve athletic performance. It is favored for its ability to increase muscle mass, strength, and endurance, making it a popular choice among athletes seeking a competitive edge.
Used in Veterinary Medicine:
17α-Boldenone (Epiboldenone) is also used in veterinary medicine as an anabolic agent for promoting muscle growth and improving the overall health of animals, particularly in the context of racehorses and other high-performance animals.

Upstream product

• 36025-82-8 3-oxoandrost-4-en-17α-yl benzoate 
• 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 
• 1259-22-9 5-androstene-3β,17β-diol 3-acetate 17-p-toluene-δ-sulfonate 
• 846-48-0 1-dehydrotestosterone 
• 897-06-3 Androsta-1,4-diene-3,17-dione 
• 150054-81-2 3-oxoandrosta-1,4-dien-17α-yl benzoate 

Relevant academic research and scientific papers

Complete 1H and 13C NMR spectral assignment of 17-hydroxy epimeric sterols with planar A or A and B rings.

Complete 1H and 13C spectral assignments of 17beta- and 17alpha-hydroxy epimers of three biologically active sterols (boldenone, 3-methoxyestradiol and 3-methoxydihydroequilenin) were achieved making use of one- and two-dimensional NMR techniques (1D-HOHAHA, DEPT, COSY, NOESY, TOCSY, HSQC and COLOC). Copyright 2004 John Wiley & Sons, Ltd.

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.

PREPARATION OF UNLABELLED AND 3H>-LABELLED EPITESTOSTERONE AND ITS METABOLITES

Cold as well as 3H>-labelled substrates and metabolites IX-XI, XV, XVI, XX-XXII, XXIV, XXV and XXVIII were prepared by catalytic hydrogenation of epitestosterone (VIII) and Λ1-dehydroepitestosterone (XIII).The key step in the preparation of compound XXVIII was reaction of 3β-tosylates XXVI and XXX with potassium nitrite in dimethyl sulfoxide.