Boldenone 17-acetate supplier

Name
Boldenone 17-acetate
EINECS 219-112-8
CAS No. 2363-59-9
Article Data19
CAS DataBase
Density 1.13 g/cm³
Solubility
Melting Point 149-151 °C
Formula C₂₁H₂₈O₃
Boiling Point 443.6 °C at 760 mmHg
Molecular Weight 328.452
Flash Point 192.7 °C
Transport Information
Appearance
Safety 22-24/25
Risk Codes 40-48
Molecular Structure
Hazard Symbols Xn
Synonyms Androsta-1,4-dien-3-one,17b-hydroxy-, acetate (6CI,7CI,8CI);1,2-Didehydrotestosterone 17-O-acetate;1-Dehydrotestosterone acetate;17beta-Acetoxyandrosta-1,4-dien-3-one;
PSA 43.37000
LogP 4.22600

Synthetic route

: 108-75-8
2,4,6-trimethyl-pyridine

: 82926-51-0
17β-acetoxy-2β,4β-dibromo-5β-androstan-3-one

A: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

B: 111687-29-7
17β-acetoxy-2-bromo-5β-androst-1-en-3-one

...Expand

: 82926-51-0
17β-acetoxy-2β,4β-dibromo-5β-androstan-3-one

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
With lithium carbonate; lithium bromide

: 82926-51-0
17β-acetoxy-2β,4β-dibromo-5β-androstan-3-one

A: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

B: 111687-29-7
17β-acetoxy-2-bromo-5β-androst-1-en-3-one

Conditions

Conditions	Yield
With 2,4,6-trimethyl-pyridine

: 15359-18-9
17β-Acetoxy-3-oxo-Δ1,5-androstadien

: 108-24-7
acetic anhydride

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
(i) (UV-irradiation), EtOH, (ii) KOH, MeOH, (iii) /BRN= 385737/, Py; Multistep reaction;

: 1045-69-8
testosterone acetate

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
With thallium(III) acetate In acetic acid
With 2,6-dichloro-3,5-dicyano-1,4-benzoquinone

2α.4α-dibromo-17β-acetoxy-androstanone-(3): 2α.4α-dibromo-17β-acetoxy-androstanone-(3)

A: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

B 17β-acetoxy-androstadien-(4.6)-one-(3): 17β-acetoxy-androstadien-(4.6)-one-(3)

Conditions

Conditions	Yield
With 2,3,5-trimethyl-pyridine

: 82926-51-0
17β-acetoxy-2β,4β-dibromo-5β-androstan-3-one

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

LiBr: LiBr

Li2CO3: Li2CO3

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
60 min;

...Expand

: 58-22-0
testosterone

<2,4,6-triiodo-phenoxy>-acetyl chloride: <2,4,6-triiodo-phenoxy>-acetyl chloride

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 2,6-dichloro-3,5-dicyano-1,4-benzoquinone View Scheme

: 1164-92-7
17β-acetoxy-5β-androstan-3-one

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: acetic acid; bromine 2: 2,4,6-trimethyl-pyridine View Scheme

: 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

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: Zn / aq. ethanol 2: (i) (UV-irradiation), EtOH, (ii) KOH, MeOH, (iii) /BRN= 385737/, Py View Scheme

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 75-24-1
trimethylaluminum

: 5824-29-3
17β-acetyloxy-1α-methylandrost-4-en-3-one

Conditions

Conditions	Yield
copper(I) bromide In 1,4-dioxane; water; toluene	75.58%

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 84871-43-2
17β-acetoxyandrosta-1,4-diene-3-thione

Conditions

Conditions	Yield
With Lawessons reagent In tetrahydrofuran for 1h; Ambient temperature;	60%

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 1045-69-8
testosterone acetate

Conditions

Conditions	Yield
With thallium(III) nitrate trihydrate In diethylene glycol dimethyl ether for 24h; Ambient temperature;	34%

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 97455-04-4
androsta-1,4-diene-11α,17β-diol-3-one, 17-acetate

Conditions

Conditions	Yield
for 72h; Rhizopus arrhizus ATCC 11145;	15%

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 6223-90-1
17β-acetoxy-2-methyl-estra-1,3,5(10)-trien-4-ol

Conditions

Conditions	Yield
With 1,4-dioxane Irradiation.UV-Licht;
In 1,4-dioxane for 9h; Irradiation;
In methanol Heating; Irradiation;
Multi-step reaction with 2 steps 1: dioxane / Irradiation 2: dioxane / Irradiation View Scheme

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 1855-85-2
17β-acetoxy-2-hydroxy-4-methyl-19-norpregna-1,3,5(10)-triene

Conditions

Conditions	Yield
With 1,4-dioxane Irradiation.UV-Licht;
In 1,4-dioxane for 9h; Irradiation;
With acetic acid Heating; Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 2242-09-3
17β-acetoxy-1-hydroxy-4-methylestra-1,3,5(10)-triene

Conditions

Conditions	Yield
With 1,4-dioxane Irradiation.UV-Licht;
In 1,4-dioxane for 9h; Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 2456-11-3
17β-acetoxy-1-methyl-estra-1,3,5(10)-trien-3-ol

Conditions

Conditions	Yield
With 1,4-dioxane Irradiation.UV-Licht;
In 1,4-dioxane for 9h; Irradiation;
In methanol Heating; Irradiation;
Multi-step reaction with 2 steps 1: dioxane / Irradiation 2: dioxane / Irradiation View Scheme

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

A: 2383-80-4, 2587-20-4
(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

B: 2363-60-2, 2506-73-2, 114029-64-0
17β-acetoxy-1β,5β-cyclo-10α-androst-3-en-2-one

Conditions

Conditions	Yield
With 1,4-dioxane Irradiation.UV-Licht;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

A: 14407-07-9, 14532-16-2
(1Ξ,3'aS)-6't-acetoxy-4,5'a-dimethyl-(3'ar,5'at,8'ac,8'bt)-decahydro-spiro[cyclohexa-3,5-diene-1,3'-As-indacen]-2-one

B: 2456-09-9, 6173-73-5
(1Ξ,3'aS)-6't-acetoxy-2,5'a-dimethyl-(3'ar,5'at,8'ac,8'bt)-decahydro-spiro[cyclohexa-2,5-diene-1,3'-As-indacen]-4-one

Conditions

Conditions	Yield
With 1,4-dioxane Irradiation.UV-Licht;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 41982-55-2, 95118-63-1
17β-acetoxy-6β-bromo-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
With N-Bromosuccinimide; dibenzoyl peroxide

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 2383-80-4, 2587-20-4
(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

Conditions

Conditions	Yield
In 1,4-dioxane for 1.5h; Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 2363-60-2
2-Oxo-17β-acetoxy-1α.5β-cyclo-Δ3-10α-androsten

Conditions

Conditions	Yield
In 1,4-dioxane for 1.5h; Irradiation;
With acetic acid Heating; Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 14407-07-9, 14532-16-2
(1Ξ,3'aS)-6't-acetoxy-4,5'a-dimethyl-(3'ar,5'at,8'ac,8'bt)-decahydro-spiro[cyclohexa-3,5-diene-1,3'-As-indacen]-2-one

Conditions

Conditions	Yield
In 1,4-dioxane for 1.5h; Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 2456-09-9, 6173-73-5
(1Ξ,3'aS)-6't-acetoxy-2,5'a-dimethyl-(3'ar,5'at,8'ac,8'bt)-decahydro-spiro[cyclohexa-2,5-diene-1,3'-As-indacen]-4-one

Conditions

Conditions	Yield
In 1,4-dioxane for 1.5h; Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 108-24-7
acetic anhydride

: 798-35-6
17β-acetoxy-4-methylestra-1,3,5(10)-triene

Conditions

Conditions	Yield
(i) LiAlH4, Et2O, (ii) /BRN= 385737/, Py; Multistep reaction;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 122-52-1
triethyl phosphite

: 14413-08-2
1-Diaethoxyphosphinyl-testosteron-acetat

Conditions

Conditions	Yield
With phenol

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

A: 977-83-3
17β-acetoxy-2-chloroandrosta-1,4-diene-3-one

B: 62799-78-4
17β-acetoxy-4-chloroandrosta-1,4-diene-3-one

Conditions

Conditions	Yield
With pyridine; sulfuryl dichloride for 1h; Ambient temperature;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 17β-acetoxy-4ξ,5ξ-dihydroxy-1-androsten-3-one

: 17β-acetoxy-1ξ,2ξ-dihydroxy-4-androsten-3-one

Conditions

Conditions	Yield
With osmium(VIII) oxide; potassium chlorate In water; tert-butyl alcohol for 600h; Ambient temperature; Yield given. Yields of byproduct given;

: 593-77-1
N-Methylhydroxylamine

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

A: 84871-34-1, 84871-35-2
(Z)-17β-acetoxy-3-methylimino-1,4-androstadiene N-oxide

B: 84871-34-1, 84871-35-2
(E)-17β-acetoxy-3-methylimino-1,4-androstadiene N-oxide

Conditions

Conditions	Yield
With pyridine at 40℃; Yield given. Yields of byproduct given;

...Expand

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 3-Oxo-17β-acetoxy-Δ1:10.19-1(10->5)-abeo-5α-androstadien

Conditions

Conditions	Yield
With acetic acid Heating; Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 73398-07-9
3-Oxo-10β-hydroxy-17β-acetoxy-Δ1-1(10->5)-abeo-5α-androsten

Conditions

Conditions	Yield
With acetic acid Heating; Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 15267-01-3
3β,5aβ-Dimethyl-6β-acetoxy-(3aα,8aα,8bβ)-perhydro-cyclopent-inden-3α-carbonsaeure

Conditions

Conditions	Yield
(i) O3, AcOEt, (ii) aq. H2O2; Multistep reaction;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 3-Oxo-17β-acetoxy-Δ1.9-1(10->5)-abeo-5α-androstadien

Conditions

Conditions	Yield
With acetic acid Heating; Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 2242-10-6
1-Oxo-4α-methyl-17β-acetoxy-4β.10β-cyclo-(9(10-5β)-abeo-Δ2-10αH-oestren

Conditions

Conditions	Yield
In 1,4-dioxane Irradiation;

: 2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one

: 1-Oxo-3-methyl-17β-acetoxy-4α.10α-cyclo-(9(10-5β)-abeo-Δ2-10βH-oestren

Conditions

Conditions	Yield
In 1,4-dioxane Irradiation;

Boldenone 17-acetate Specification

The Boldenone 17-acetate, with the CAS registry number 2363-59-9, is also known as (17beta)-Hydroxyandrosta-1,4-dien-3-one acetate. It belongs to the product category of Steroids. Its EINECS registry number is 219-112-8. This chemical's molecular formula is C₂₁H₂₈O₃ and molecular weight is 328.45. Its IUPAC name is called [(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] acetate.

Physical properties of Boldenone 17-acetate: (1)ACD/LogP: 4.39; (2)ACD/LogD (pH 5.5): 4.39; (3)ACD/LogD (pH 7.4): 4.39; (4)ACD/BCF (pH 5.5): 1286.17; (5)ACD/BCF (pH 7.4): 1286.17; (6)ACD/KOC (pH 5.5): 5851.06; (7)ACD/KOC (pH 7.4): 5851.06; (8)#H bond acceptors: 3; (9)#Freely Rotating Bonds: 2; (10)Index of Refraction: 1.555; (11)Molar Refractivity: 92.6 cm³; (12)Molar Volume: 288.3 cm³; (13)Surface Tension: 43.3 dyne/cm; (14)Density: 1.13 g/cm³; (15)Flash Point: 192.7 °C; (16)Enthalpy of Vaporization: 70.13 kJ/mol; (17)Boiling Point: 443.6 °C at 760 mmHg; (18)Vapour Pressure: 4.58E-08 mmHg at 25°C.

When you are using this chemical, please be cautious about it. This chemical may cause damage to health. There will be a danger of serious damage to health by prolonged exposure. In addition, you should not breathe its dust. Finally, you must avoid contact with skin and eyes.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C\1\C=C/C4(/C(=C/1)CCC3C4CCC2(C3CCC2OC(=O)C)C)C
(2)InChI: InChI=1/C21H28O3/c1-13(22)24-19-7-6-17-16-5-4-14-12-15(23)8-10-20(14,2)18(16)9-11-21(17,19)3/h8,10,12,16-19H,4-7,9,11H2,1-3H3
(3)InChIKey: KPCDGGNHYODURF-UHFFFAOYAO

Product Name

Boldenone 17-acetate

Synthetic route

Boldenone 17-acetate Specification

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