Bolddenone

Base Information

• Chemical Name: Bolddenone
• CAS No.: 846-48-0
• Molecular Formula: C19H26O2
• Molecular Weight: 286.414
• Hs Code.: 29372900
• European Community (EC) Number: 212-686-0
• Wikipedia: Boldenone
• Mol file: 846-48-0.mol

Synonyms:Bolddenone;846-48-0;(8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one

Chemical Property of Bolddenone

Chemical Property:

• Appearance/Colour: crystalline solid
• Vapor Pressure: 2.04E-09mmHg at 25°C
• Melting Point: 164-166 °C
• Refractive Index: 1.577
• Boiling Point: 435.6 °C at 760 mmHg
• PKA: 15.05±0.60(Predicted)
• Flash Point: 185.8 °C
• PSA: 37.30000
• Density: 1.14 g/cm³
• LogP: 3.65520
• Storage Temp.: Controlled Substance, -20°C Freezer
• Water Solubility.: 57.1mg/L at 20℃
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 286.193280068
• Heavy Atom Count: 21
• Complexity: 546

Purity/Quality:

99% ^*data from raw suppliers

Boldenone ^*data from reagent suppliers

Safty Information:

• Pictogram(s): F,Xn
• Hazard Codes: F,Xn
• Statements: 11-20/21/22-36
• Safety Statements: 16-36/37

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC12CCC3C(C1CCC2O)CCC4=CC(=O)C=CC34C
• Isomeric SMILES: C[C@@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)CCC4=CC(=O)C=C[C@]34C
• 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. 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.
• Uses: Boldenone is an anabolic steroid. Controlled substance. Controlled substance. Anabolic steroid

Technology Process of Bolddenone

There total 20 articles about Bolddenone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 74.0%

testosterone (58-22-0) → 1-dehydrotestosterone (846-48-0,361432-76-0)

Guidance literature:

With tert-butyldimethylsilyl chloride; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In 1,4-dioxane; at 0 - 20 ℃; for 40h;

DOI:10.1016/j.steroids.2010.03.002

Reference yield: 64.0%

Androsta-1,4-diene-3,17-dione (897-06-3) → 1-dehydrotestosterone (846-48-0,361432-76-0)

Guidance literature:

for 336h; Rhodotorula mucilaginosa;

Reference yield: 51.0%

cholesterol (57-88-5) → testosterone (58-22-0) + Androstenedione (63-05-8) + Androsta-1,4-diene-3,17-dione (897-06-3) + 1-dehydrotestosterone (846-48-0,361432-76-0) + 2-[(8S,9S,10R,13S,14S)-10,13-Dimethyl-3-oxo-3,6,7,8,9,10,11,12,13,14,15,16-dodecahydro-cyclopenta[a]phenanthren-(17Z)-ylidene]-propionic acid methyl ester (79694-52-3) + 22-hydroxy-23,24-bisnor-1,4-choladien-3-one (71658-22-5)

Guidance literature:

With Mycobacterium sp. CCM 3529; Product distribution;

upstream raw materials:

2,4,6-trimethyl-pyridine

2α,4α-dibromo-17β-hydroxy-5α-androstan-3-one

testosterone

progesterone

Downstream raw materials:

estradiol

4-methyl-estratriene-(1.3.5(10))-diol-(1.17β)

boldenone benzoate

Quinbolone

Refernces

• 1、 Schittmayer, Matthias,Glieder, Anton,Uhl, Michael K.,Winkler, Andreas,Zach, Simone,Schrittwieser, Joerg H.,Kroutil, Wolfgang,MacHeroux, Peter,Gruber, Karl,Kambourakis, Spiros,Rozzell, J. David,Winkler, Margit. "Old yellow enzyme-catalyzed dehydrogenation of saturated ketones". experimental part. p. 268 - 274. Retrieved 2011/04/22.
• 2、 Verheyden,Noppe,Zorn,Van Immerseel,Bussche, J. Vanden,Wille,Bekaert,Janssen,De Brabander,Vanhaecke. "Endogenous boldenone-formation in cattle: Alternative invertebrate organisms to elucidate the enzymatic pathway and the potential role of edible fungi on cattle's feed". experimental part. p. 161 - 170. Retrieved 2011/03/19.