Boldenone Acetate

Base Information

• Chemical Name: Boldenone Acetate
• CAS No.: 2363-59-9
• Molecular Formula: C21H28O3
• Molecular Weight: 328.452
• Hs Code.: 29372900
• European Community (EC) Number: 219-112-8
• UNII: 3T5IZ3HS3X
• DSSTox Substance ID: DTXSID60946450
• Nikkaji Number: J213.218D
• Wikidata: Q27258009
• Mol file: 2363-59-9.mol

Synonyms:17 beta-acetoxy-delta-(1,5)-androstadien-3-one

Chemical Property of Boldenone Acetate

Chemical Property:

• Vapor Pressure: 4.58E-08mmHg at 25°C
• Melting Point: 149-151 °C
• Refractive Index: 1.555
• Boiling Point: 443.6 °C at 760 mmHg
• Flash Point: 192.7 °C
• PSA: 43.37000
• Density: 1.13 g/cm³
• LogP: 4.22600
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 328.20384475
• Heavy Atom Count: 24
• Complexity: 646

Purity/Quality:

99%, ^*data from raw suppliers

17beta-Acetoxyandrosta-1,4-dien-3-one 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 40-48-48/22
• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OC1CCC2C1(CCC3C2CCC4=CC(=O)C=CC34C)C
• Isomeric SMILES: CC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)C=C[C@]34C)C
• Description: Boldenone 17-acetate is a white or white solid powder, belongs to the hormone class.
• Uses: The parent of 17-acetate bodanone is a derivative of testosterone and thus inherits most of its properties, such as androgenic ability and protein synthesis.

Technology Process of Boldenone Acetate

There total 18 articles about Boldenone Acetate 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:

testosterone acetate (1045-69-8) → 17β-acetoxy-androsta-1,4-dien-3-one (2363-59-9)

Guidance literature:

With thallium(III) acetate; In acetic acid;

Reference yield:

Acetic acid (8R,9S,10R,13S,14S,17S)-6-bromo-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl ester → 17β-acetoxy-androsta-1,4-dien-3-one (2363-59-9)

Guidance literature:

Multi-step reaction with 2 steps

1: Zn / aq. ethanol

2: (i) (UV-irradiation), EtOH, (ii) KOH, MeOH, (iii) /BRN= 385737/, Py

With zinc; In ethanol;

DOI:10.1002/hlca.19650480729

Reference yield:

→ 17β-acetoxy-androsta-1,4-dien-3-one (2363-59-9)

Guidance literature:

With 2,3,5-trimethyl-pyridine;

upstream raw materials:

2,4,6-trimethyl-pyridine

17β-acetoxy-2β,4β-dibromo-5β-androstan-3-one

17β-Acetoxy-3-oxo-Δ^1,5-androstadien

acetic anhydride

Downstream raw materials:

1-Methyl-17-o-acetyl-oestradiol

(1Ξ,6Ξ,3'aS)-6't-acetoxy-4,5'a-dimethyl-(3'ar,5'at,8'ac,8'bt)-decahydro-spiro[bicyclo[3.1.0]hex-3-ene-6,3'-As-indacen]-2-one

17β-acetoxy-1β,5β-cyclo-10α-androst-3-en-2-one

2-Oxo-17β-acetoxy-1α.5β-cyclo-Δ³-10α-androsten

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