27833-18-7 Usage
Description
17α-Boldenone (Epiboldenone) is a synthetic anabolic steroid derived from the parent compound Boldenone. It is the 17α-epimer and metabolite of Boldenone, which means it is a stereoisomer with a specific orientation of the 17α-hydroxyl group. As a white solid, it possesses chemical properties that make it a potential candidate for various applications in the pharmaceutical and sports industries.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 27833-18-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,3 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27833-18:
(7*2)+(6*7)+(5*8)+(4*3)+(3*3)+(2*1)+(1*8)=127
127 % 10 = 7
So 27833-18-7 is a valid CAS Registry Number.
27833-18-7Relevant articles and documents
Complete 1H and 13C NMR spectral assignment of 17-hydroxy epimeric sterols with planar A or A and B rings.
Ciuffreda,Casati,Manzocchi
, p. 360 - 363 (2007/10/03)
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.
PREPARATION OF UNLABELLED AND 3H>-LABELLED EPITESTOSTERONE AND ITS METABOLITES
Kasal, Alexander,Fuksova, Kveta,Pouzar, Vladimir
, p. 600 - 611 (2007/10/02)
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.