Basic information Description Sources Safety Supplier Related
ChemicalBook >  Product Catalog >  API >  Hormones and the Endocrine System >  Androgen and anabolic hormones >  Boldenone

Boldenone

Basic information Description Sources Safety Supplier Related

Boldenone Basic information

Product Name:
Boldenone
Synonyms:
  • 17-beta-hydroxy-17-alpha-1,4-androstadien-3-one
  • 17-beta-hydroxy-androsta-4-dien-3-one
  • dehydrotestosterone
  • 17-hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
  • Boldenone(846-48-0)
  • Boldenone (eq)
  • High purity 99% Boldenone powder
  • Testosterone Impurity 8(Testosterone EP Impurity H)
CAS:
846-48-0
MF:
C19H26O2
MW:
286.41
EINECS:
212-686-0
Product Categories:
  • boldenone
  • API
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Steroids
  • Steroid and Hormone
Mol File:
846-48-0.mol
More
Less

Boldenone Chemical Properties

Melting point:
164-166°C
alpha 
D25 +25° (in chloroform)
Boiling point:
368.77°C (rough estimate)
Density 
1.0655 (rough estimate)
refractive index 
1.4709 (estimate)
storage temp. 
Controlled Substance, -20°C Freezer
solubility 
DMF: 25 mg/ml; DMSO: 15 mg/ml; DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml; Ethanol: 10 mg/ml
form 
A crystalline solid
pka
15.05±0.60(Predicted)
Water Solubility 
57.1mg/L at 20℃
InChI
InChI=1/C19H26O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h7,9,11,14-17,21H,3-6,8,10H2,1-2H3/t14-,15-,16-,17-,18-,19-/s3
InChIKey
RSIHSRDYCUFFLA-KRHBYBJCNA-N
SMILES
[C@@]12([H])CCC3=CC(=O)C=C[C@]3(C)[C@@]1([H])CC[C@]1(C)[C@H](CC[C@@]21[H])O |&1:0,10,12,16,18,21,r|
CAS DataBase Reference
846-48-0(CAS DataBase Reference)
NIST Chemistry Reference
Boldenone(846-48-0)
More
Less

Safety Information

Hazard Codes 
F,Xn
Risk Statements 
11-20/21/22-36
Safety Statements 
16-36/37
RTECS 
BV7994400
HS Code 
29372900

MSDS

More
Less

Boldenone Usage And Synthesis

Description

Boldenone is the chemical precursor of its endecylenate ester prodrug boldenone undecylenate – which is used extensively as a steroid for animals, mainly horses and cattle, under the brand name Equipoise, among others. For this application, it is injected to improve the weight, hair coat, appetite, and general physical condition of horses affected by disease, anorexia, or overwork. It is also used as an illegal doping agent for human athletes. As a derivative of testosterone, it retains its anabolic strength, but exhibits reduced androgenic effects.

Sources

https://en.wikipedia.org/wiki/Boldenone_undecylenate
https://en.wikipedia.org/wiki/Boldenone
https://www.drugs.com/vet/equipoise.html
https://www.steroidal.com/steroid-profiles/equipoise/
https://www.evolutionary.org/equipoise-boldenone-undecylenate

Description

Boldenone (Item No. 15432) is an analytical reference standard categorized as an anabolic androgenic steroid. Anabolic steroids, including boldenone, have been used to enhance physical performance in athletes. Boldenone is regulated as a Schedule III compound in the United States. This product is intended for research and forensic applications.

Chemical Properties

Crystalline Solid

Uses

Controlled substance. Anabolic steroid

Uses

Boldenone is an anabolic steroid. Controlled substance.

Definition

ChEBI: An 3-oxo-Delta1,Delta4-steroid substituted by an oxo group at position 3 and a beta-hydroxy group at position 17. It is an anabolic androgenic steroid that has been eveloped for veterinary use.

brand name

Equipoise [Veterinary] (Fort Dodge Animal Health).

Synthesis

Boldenone is obtained by reacting Testosterone with tert-butyldimethylsilyl chloride in the presence of DDQ.
Experimental Procedure: 29.0 g Testosterone was dissolved in 220 ml dioxan/THF 8:2 and cooled to 0°C on ice. After cooling down a solution of tert-butyldimethylsilyl chloride (46.0 g in 100 ml dioxan/THF 8:2) was added dropwise and stirred for 90 min at 0°C. Then a suspension of 32.0 g of DDQ in 200 ml dioxan/THF 8:2 was added in 4 equal portions over a period of 4 h. The reaction mixture was stirred for additional 12 h within coming from 0°C to room temperature. The resulting suspension was then filtered over Celite and rinsed with 300 ml THF. The filtrate was evaporated and brown oil was obtained. The oil was diluted in 1500 ml DCM and washed with 500 ml of 5% aqueous sodium hydroxide. The yellow organic phase was washed with 400 ml water and 400 ml saturated sodium chloride solution, before drying over magnesium sulfate. After evaporation, the crude product was chromatographed on silica gel by using hexane-ethyl acetate (3:7), followed by a recrystallization in ethyl acetate. 16.50 g of Boldenone was obtained as an amber solid (58%).

BoldenoneSupplier

Shanghai Boyle Chemical Co., Ltd.
Tel
021-50182298 021-50180596
Email
sales@boylechem.com
LGM Pharma
Tel
1-(800)-881-8210
Email
inquiries@lgmpharma.com
China Langchem Inc.
Tel
0086-21-58956006
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
BioBioPha Co., Ltd.
Tel
0871-65217109 13211707573;
Email
y.liu@mail.biobiopha.com