Boldenone supplier | CasNO.846-48-0

Name
Boldenone
EINECS 212-686-0
CAS No. 846-48-0
Article Data44
CAS DataBase
Density 1.14 g/cm³
Solubility 57.1mg/L at 20℃
Melting Point 164-166 °C
Formula C₁₉H₂₆O₂
Boiling Point 435.6 °C at 760 mmHg
Molecular Weight 286.414
Flash Point 185.8 °C
Transport Information
Appearance crystalline solid
Safety 16-36/37
Risk Codes 11-20/21/22-36
Molecular Structure
Hazard Symbols F,Xn
Synonyms Androsta-1,4-dien-3-one,17b-hydroxy- (6CI,8CI);1,2-Dehydrotestosterone;1,2-Didehydrotestosterone;1,4-Androstadien-17b-ol-3-one;1-Dehydrotestosterone;17b-Boldenone;17b-Hydroxy-1,4-androstadiene-3-one;17b-Hydroxyandrost-1,4-dien-3-one;17b-Hydroxyandrost-1,4-diene-3-one;17b-Hydroxyandrosta-1,4-dien-3-one;Androsta-1,4-diene-17b-ol-3-one;Boldane;Dehydrotestosterone;NSC 79102;RU 18761;D1-Testosterone;b-Boldenone;Androsta-1,4-dien-3-one,17-hydroxy-, (17b)-;
PSA 37.30000
LogP 3.65520

Synthetic route

: 58-22-0
testosterone

: 846-48-0
1-dehydrotestosterone

Conditions

Conditions	Yield
With tert-butyldimethylsilyl chloride; 2,3-dicyano-5,6-dichloro-p-benzoquinone In 1,4-dioxane at 0 - 20℃; for 40h;	74%
With selenium(IV) oxide
With selenious acid
With old yellow enzyme from Geobacillus kaustophilus at 70℃; for 48h; pH=7; aq. phosphate buffer; Enzymatic reaction; regioselective reaction;
mit Hilfe von Corynebacterium simplex;

: 897-06-3
Androsta-1,4-diene-3,17-dione

: 846-48-0
1-dehydrotestosterone

Conditions

Conditions	Yield
for 336h; Rhodotorula mucilaginosa;	64%
With potato dextrose broth medium In ethanol at 24 - 26℃; for 96h; Penicillium decumbens ATCC 10436;	3%

: 57-88-5
cholesterol

A: 58-22-0
testosterone

B: 63-05-8
Androstenedione

C: 897-06-3
Androsta-1,4-diene-3,17-dione

D: 846-48-0
1-dehydrotestosterone

E: 79694-52-3
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

F: 71658-22-5
22-hydroxy-23,24-bisnor-1,4-choladien-3-one

Conditions

Conditions	Yield
With Mycobacterium sp. CCM 3529 Product distribution;	A 0.01 g B 0.03 g C 51% D 0.06 g E n/a F 0.38 g

...Expand

: 897-06-3
Androsta-1,4-diene-3,17-dione

A: 846-48-0
1-dehydrotestosterone

B: 30915-20-9
11α,17β-dihydroxyandrosta-1,4-dien-3-one

Conditions

Conditions	Yield
With phosphate buffer; Beauveria sp. culture at 28℃; for 24h;	A 38% B 46%
With phosphate buffer; Beauveria sp. culture at 28℃; for 24h; Yield given. Yields of byproduct given;

: 481-29-8
Epiandrosterone

A: 58-22-0
testosterone

B: 25848-75-3
3β,11α-dihydroxy-5α-androstan-17-one

C: 25848-68-4
3beta-7alpha-Dihydroxy-5alpha-androstane-17-one

D: 25848-69-5
3beta-7beta-Dihydroxy-5alpha-androstane-17-one

E: 2260-01-7
1α,3β-dihydroxy-5α-androstan-17-one

F: 897-06-3
Androsta-1,4-diene-3,17-dione

G: 846-48-0
1-dehydrotestosterone

H: 62-99-7, 2944-87-8, 34096-63-4, 34442-08-5, 145772-79-8
6β-hydroxytestosterone

I: 571-40-4
5α-androst-1-ene-3,17-dione

J: 63-00-3
6β-hydroxy-4-androstene-3,17-dione

Conditions

Conditions	Yield
With malt extract; disodium hydrogenphosphate; calcium(II) chloride dihydrate; magnesium(II) chloride hexahydrate; strontium (III) chloride hexahydrate; potassium chloride; boric acid; sodium hydrogencarbonate; sodium sulfate; sodium chloride; potassium bromide; potassium hydroxide In water; N,N-dimethyl-formamide at 32℃; for 168h; pH=8; Enzymatic reaction;	A 2% B 2% C 2% D 3% E 5% F 5% G 3% H 2% I 2% J 32%

...Expand

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

: 119369-73-2
2α,4α-dibromo-17β-hydroxy-5α-androstan-3-one

: 846-48-0
1-dehydrotestosterone

: 57-83-0, 851-22-9, 2000-66-0, 2755-10-4, 3562-13-8, 3795-19-5, 5750-05-0, 14546-13-5, 36027-73-3, 36027-74-4, 55122-80-0, 56271-98-8, 59952-90-8, 73889-98-2, 137940-28-4
progesterone

: 846-48-0
1-dehydrotestosterone

Conditions

Conditions	Yield
mit Hilfe von Streptomyces lavendulae;

: 897-06-3
Androsta-1,4-diene-3,17-dione

A: 58-22-0
testosterone

B: 63-05-8
Androstenedione

C: 846-48-0
1-dehydrotestosterone

Conditions

Conditions	Yield
at 25℃; for 72h; stereoselective reduction in the biotransformation by cell suspension cultures of Marchantia Polymorpha, other androsterone derivative;
With Mycobacterium sp. No. 22 for 24h; Microbiological reaction;	A n/a B n/a C 0.5 g
With unidentified fungal species isolated from grinded corn In water at 37℃; for 1h; pH=7; aq. phosphate buffer; Microbiological reaction; Enzymatic reaction;

...Expand

: 57-83-0
Progesterone

A: 58-22-0
testosterone

B: 1162-54-5
pregna-1,4-diene-3,20-dione

C: 63-05-8
Androstenedione

D: 1045-69-8
testosterone acetate

E: 80-75-1
11-alpha-hydroxyprogesterone

F: 846-48-0
1-dehydrotestosterone

Conditions

Conditions	Yield
With immobilized spores of Aspergillus ochraceus; Tris-maleate buffer at 30℃; for 48h; Product distribution; Mechanism; various water activity of the biocatalysts;

...Expand

17β-acetoxy-androstadien-(1.4)-one-(3): 17β-acetoxy-androstadien-(1.4)-one-(3)

: 846-48-0
1-dehydrotestosterone

Conditions

Conditions	Yield
With potassium hydroxide

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

: 846-48-0
1-dehydrotestosterone

Conditions

Conditions	Yield
With 2,3,5-trimethyl-pyridine
With Potassium benzoate; toluene; butan-1-ol Erhitzen des Reaktionsprodukts unter 6 Torr auf 220-230grad;

: 63-05-8
Androstenedione

A: 58-22-0
testosterone

B: 846-48-0
1-dehydrotestosterone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: unidentified fungal species isolated from grinded corn / water / 1 h / 37 °C / pH 7 / aq. phosphate buffer; Microbiological reaction; Enzymatic reaction 2: unidentified fungal species isolated from grinded corn / water / 1 h / 37 °C / pH 7 / aq. phosphate buffer; Microbiological reaction; Enzymatic reaction View Scheme

: 846-48-0
1-dehydrotestosterone

: 143613-56-3, 143679-03-2
C38H52O2

Conditions

Conditions	Yield
With zinc In tetrahydrofuran Heating;	96%

: 846-48-0
1-dehydrotestosterone

: 968-93-4
testolactone

Conditions

Conditions	Yield
With Penicillium notatum KCH 904 In water; acetone at 27℃; for 96h; Enzymatic reaction;	90%

: 846-48-0
1-dehydrotestosterone

: 18162-48-6
tert-butyldimethylsilyl chloride

: 102054-23-9
17β-O-tert-butyldimethylsilylandrosta-1,4-dien-3-one

Conditions

Conditions	Yield
With 1H-imidazole In N,N-dimethyl-formamide Ambient temperature;	89%
With 1H-imidazole In N,N-dimethyl-formamide for 4.5h; Ambient temperature;	83%

: 846-48-0
1-dehydrotestosterone

: 64-19-7
acetic acid

: 17a-acetoxy-androst-1,4-dien-3-one

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene at 40℃; for 0.5h;	83%

: 64-18-6
formic acid

: 846-48-0
1-dehydrotestosterone

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene at 40℃; for 0.5h;	82%

: 846-48-0
1-dehydrotestosterone

: 21085-72-3
1-bromo-2,3,4-tri-O-acetyl-α-D-glucuronic acid methyl ester

: 1177368-54-5
methyl (androsta-1,4-dien-17β-ol-3-one)-17-O-2,3,4-tri-O-acetyl-β-D-glucuronate

Conditions

Conditions	Yield
With cadmium(II) carbonate In toluene for 6h; Koenigs-Knorr synthesis; Heating;	80%

: 846-48-0
1-dehydrotestosterone

: 65-85-0
benzoic acid

: 150054-81-2
3-oxoandrosta-1,4-dien-17α-yl benzoate

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene at 40℃; for 0.5h;	80%

: 846-48-0
1-dehydrotestosterone

: 13551-83-2
bis-(2-methyl-1H-imidazol-1-yl)methanone

: 1138159-98-4
3-oxoandrosta-1,4-dien-17β-yl-2'-methyl-1H-imidazole-1-carboxylate

Conditions

Conditions	Yield
In dichloromethane for 28h; Heating;	73%

: 846-48-0
1-dehydrotestosterone

: 98406-40-7
2-(1,1-Dimethyl-prop-2-ynylperoxy)-2-methyl-pentane

: 920-46-7
Methacryloyl chloride

: 3,17β-dimethacryloyloxy-3-(3-methyl-3-tert-pentylperoxybut-1-ynyl)-androsta-1,4-diene

Conditions

Conditions	Yield
Stage #1: 2-(1,1-Dimethyl-prop-2-ynylperoxy)-2-methyl-pentane With n-butyllithium In hexane at -40 - -20℃; for 1h; Stage #2: 1-dehydrotestosterone In diethyl ether; hexane at 15 - 20℃; for 18h; Stage #3: Methacryloyl chloride In diethyl ether; hexane at 0 - 20℃; for 19h;	66%

...Expand

: 846-48-0
1-dehydrotestosterone

: 897-06-3
Androsta-1,4-diene-3,17-dione

Conditions

Conditions	Yield
for 336h; Rhodotorula mucilaginosa;	54%

: 846-48-0
1-dehydrotestosterone

A: 58105-34-3
14α,17β-dihydroxyandrosta-1,4-dien-3-one

B: 6β,17β-dihydroxyandrosta-1,4-dien-3-one

Conditions

Conditions	Yield
With fungus Cephalosporium aphidicola In ethanol for 120h; hydroxylation;	A 2% B 48%

: 846-48-0
1-dehydrotestosterone

: 507-09-5
thioacetic acid

A: 99371-90-1
1α-acetylthio-17β-hydroxy-4-androsten-3-one

B: 116104-58-6
1α-acetylthio-17β-hydroxy-4-androsten-3-one 17-acetat

Conditions

Conditions	Yield
In chloroform at 40℃; for 24h;	A 47% B 16%

...Expand

: 846-48-0
1-dehydrotestosterone

A: [1-2H]4-methylestra-1,3,5(10)-trien-17β-ol

B: [1α-2H]testosterone

C: 898529-69-6
[1α,3ξ-2H2]androst-4-ene-3ξ,17β-diol

Conditions

Conditions	Yield
With lithium aluminium deuteride In tetrahydrofuran for 0.25h; Heating;	A 31% B 18% C 28%

...Expand

: 846-48-0
1-dehydrotestosterone

A: [1α-2H]testosterone

B: 898529-69-6
[1α,3ξ-2H2]androst-4-ene-3ξ,17β-diol

Conditions

Conditions	Yield
With sodium borodeuteride In tetrahydrofuran for 0.25h; Heating;	A 15% B 30%

: 846-48-0
1-dehydrotestosterone

: 108-98-5
thiophenol

: 1α-phenylthio-17β-hydroxyandrost-4-ene-3-one

Conditions

Conditions	Yield
With sodium ethanolate In ethanol for 3h; Heating;	20%

: 846-48-0
1-dehydrotestosterone

: 30915-20-9
11α,17β-dihydroxyandrosta-1,4-dien-3-one

Conditions

Conditions	Yield
for 72h; Rhizopus arrhizus ATCC 11145;	13%

: 91-22-5
quinoline

: 846-48-0
1-dehydrotestosterone

: 50-28-2
estradiol

Conditions

Conditions	Yield
at 370 - 390℃;
at 370 - 390℃;

: 106-31-0
butanoic acid anhydride

: 846-48-0
1-dehydrotestosterone

: 17β-butyryloxy-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
With pyridine

: 119-64-2
tetralin

: 846-48-0
1-dehydrotestosterone

: 50-28-2
estradiol

Conditions

Conditions	Yield
at 370 - 390℃;
at 370 - 390℃;

: 507-09-5
thioacetic acid

: 846-48-0
1-dehydrotestosterone

: 99371-90-1
1α-acetylthio-17β-hydroxy-4-androsten-3-one

: 2082-59-9
pentanoic anhydride

: 846-48-0
1-dehydrotestosterone

: 17β-valeryloxy-androsta-1,4-dien-3-one

Conditions

Conditions	Yield
at 130℃;

: 447-53-0
1,2-Dihydronaphthalene

: 846-48-0
1-dehydrotestosterone

: 50-28-2
estradiol

Conditions

Conditions	Yield
at 370 - 390℃;
at 370 - 390℃;

: 776-35-2
9,10-dihydrophenanthrene

: 846-48-0
1-dehydrotestosterone

A: 50-28-2
estradiol

B: 3597-39-5
4-methyl-estratriene-(1.3.5(10))-diol-(1.17β)

Conditions

Conditions	Yield
at 390℃;

...Expand

Boldenone Specification

1. Introduction of Boldenone
Boldenone is one kind of white or kind of white crystal powder or crystalline solid. The IUPAC Name of this chemical is (8R,9S,10R,13S,14S,17S)-17-Hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one. Its Classification Code isAnabolic Agents ; Hormone ; Hormones ; Hormones, Hormone Substitutes, and Hormone Antagonists ; Reproductive Effect. It belongs to Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Steroid and Hormone.

2. Properties of Boldenone
Physical properties about Boldenone are:
(1)Melting point: 164-166°C; (2)Polar Surface Area: 26.3 Å²; (3)Index of Refraction: 1.577; (4)Molar Refractivity: 83.02 cm³; (5)Molar Volume: 250.2 cm³; (6)Surface Tension: 45.8 dyne/cm; (7)Density of Boldenone (CAS NO.846-48-0): 1.14 g/cm³; (8)Flash Point: 185.8 °C; (9)Enthalpy of Vaporization: 79.87 kJ/mol; (10)Boiling Point: 435.6 °C at 760 mmHg; (11)Vapour Pressure: 2.04E-09 mmHg at 25°C.

3. Structure Descriptors of Boldenone
(1)InChI: InChI=1S/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-/m0/s1
(2)InChIKey: InChIKey=RSIHSRDYCUFFLA-DYKIIFRCSA-N
(3)Smiles: C1[C@@H]2[C@@H]([C@@]3(C(=CC(=O)C=C3)C1)C)CC[C@@]1([C@H]2CC[C@@H]1O)C

4. Safety information of Boldenone
RTECS of Boldenone (CAS NO.846-48-0): BV7994400

5. Uses of Boldenone
Boldenone is used as controlled substance and anabolic steroid. It is a controlled substance. It belongs to anabolic steroid developed for veterinary use, mostly for treatment of horses. In the US it is not indicated for use in humans and is only available through veterinary clinics.

Product Name

Boldenone

Synthetic route

Boldenone Specification

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