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Oxymesterone

Product Name
Oxymesterone
CAS No.
145-12-0
Chemical Name
Oxymesterone
Synonyms
Aranabol;Anamidol;ORANABOL;Theranabol;Oxymestrone;OXYMESTERONE;4-HYDROXY-METHYLTESTOSTERONE;4-Hydroxy-17-methyltestosterone;Testosterone, 4-hydroxy-17-methyl-;4-HYDROXY-17ALPHA-METHYLTESTOSTERONE
CBNumber
CB6364959
Molecular Formula
C20H30O3
Formula Weight
318.45
MOL File
145-12-0.mol
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Oxymesterone Property

Melting point:
166-169°C
alpha 
D20 +69° (ethanol)
Boiling point:
475.6±45.0 °C(Predicted)
Density 
1.17±0.1 g/cm3(Predicted)
storage temp. 
Controlled Substance, -20°C Freezer, Under Inert Atmosphere
solubility 
Acetonitrile (Very Slightly), Chloroform (Slightly), Ethanol (Slightly), Methano
form 
Solid
pka
9.32±0.70(Predicted)
color 
White to Off-White
CAS DataBase Reference
145-12-0(CAS DataBase Reference)
NIST Chemistry Reference
Oxymesterone(145-12-0)
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Safety

DEA Controlled Substances
CSCN: 4000
CSA SCH: Schedule III
NARC: No
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H361Suspected of damaging fertility or the unborn child

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P281Use personal protective equipment as required.

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0003721
Product name
OXYMESTERONE
Purity
95.00%
Packaging
10MG
Price
$866.25
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0003721
Product name
OXYMESTERONE
Purity
95.00%
Packaging
100MG
Price
$2887.5
Updated
2021/12/16
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Oxymesterone Chemical Properties,Usage,Production

Chemical Properties

White Solid

Originator

Anamidol,Iwaki

Uses

An anabolic steroid.

Definition

ChEBI: Oranabol is a 3-hydroxy steroid. It has a role as an androgen.

Manufacturing Process

2 Methods of producing of 4-hydroxy-17α-methyltestosterone: 1. A solution of 1.0 g of crude 4,5-oxido-17α-methyltestosterone in 50 ml of methanol is allowed to stand at room temperature overnight with 10 ml of water and 1 ml of concentrated sulfuric acid. It is then poured into water containing sodium chloride and extracted three times with ethyl acetate. The solvent is washed with water, then with 10% sodium bicarbonate solution and again with water to neutrality. The residue remaining after evaporation of the solvent is crystallized from methanol, giving 17α-methyl-androstane4β,5α,17β-triol-3-one with a melting point of 203°-205°C.
A solution of 0.22 g of 17α-methyl-androstane-4β,5α,17β-triol-3-one in 100 ml of methanol is allowed to stand at room temperature for 22 h, under nitrogen, with 0.30 g of potassium hydroxide in 4 ml of water and 20 ml of methanol. The solution is then neutralized with acetic acid, concentrated in vacuo, diluted with water and extracted three times with ethyl acetate. The extract is washed with water and the solvent removed by distillation. The remaining residue is chromatographed over Florisil 30-60 mesh. The fractions eluted with benzene and benzene-ether (10:1) are combined and by crystallization from ether-petroleum ether give 4-hydroxy-17α-methyltestosterone (0.120 g) melting at 168°-170°C.
2. A solution of 20.0 g of 17α-testosterone in 500 ml of trimethylcarbinol is treated by addition of 56 ml of 30% hydrogen peroxide and 1.0 g of osmium tetroxide in 80 ml of trimethylcarbinol. After the mixture has stood at room temperature for 22 h, 12 ml of hydrogen peroxide are added. The reaction mixture is allowed to stand at room temperature for an additional 20 h, then concentrated in vacuo to 1/3 of its original volume, diluted with water, and the reaction product extracted with ethyl acetate. The extract is washed with water, several times with 10% sodium bisulfite solution, then with 4% sodium bicarbonate solution and finally with water to neutrality. The residue remaining after evaporation of the solvent does not show ultraviolet absorption. 1.0 g of this crude substance, by crystallization from methanol, gives l7αmethylandrostane-4,5,17β-triol-3-one (0.400 g) melting at 192°-194°C.
A solution of 20.0 g of crude 17β-methylandrostane-4,5,17β-triol-3-one in 1 L of methanol is heated under reflux in a stream of nitrogen for 20 min; then 20.0 g of potassium hydroxide in 40 ml of water and 200 ml of methanol are added. 5 min after the addition, the solution is treated by addition of 20 ml of acetic acid and concentrated in vacuo. The residue is diluted with water containing sodium chloride and extracted three times with ethyl acetate. The extract is washed with 10% sodium bicarbonate solution and then with water to neutrality. The residue remaining after evaporation of the solvent is dissolved in acetone; addition of petroleum ether gives 4-hydroxy-17αmethyl-testosterone (8.0 g) melting at 168°-170°C. The mother liquors chromatographed over Florisil 30-60 mesh yield an additional 5.0 g of the same substance melting at 168°-170°C.

Therapeutic Function

Anabolic, Androgen

Oxymesterone Preparation Products And Raw materials

Raw materials

Preparation Products

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Oxymesterone Suppliers

LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
Aishilun biotechnology (Shanghai) co., LTD
Tel
021-50676523 18019098996
Email
info@acelybio.com
Country
China
ProdList
3960
Advantage
58
CONIER CHEM AND PHARMA LIMITED
Tel
+8618523575427
Email
sales@conier.com
Country
China
ProdList
49374
Advantage
58
Apeloa production Co.,Limited
Tel
+8619933239880
Email
admin@apcl.com.cn
Country
China
ProdList
852
Advantage
58
GIHI CHEMICALS CO.,LIMITED
Tel
+8618058761490
Email
info@gihichemicals.com
Country
China
ProdList
49979
Advantage
58

145-12-0, OxymesteroneRelated Search:


  • 4,17beta-Dihydroxy-17alpha-methylandrost-4-en-3-one
  • 4,17beta-Dihydroxy-17-methylandrost-4-en-3-one
  • 4,17beta-Dihydroxy-17-methylandrosta-4-en-3-one
  • 4,17-Dihydroxy-17-methylandrost-4-en-3-one
  • 4-Hydroxy-17-methyltestosterone
  • Anamidol
  • Androst-4-en-3-one, 4,17beta-dihydroxy-17-methyl-
  • Androst-4-en-3-one, 4,17-dihydroxy-17-methyl-, (17beta)-
  • Aranabol
  • Oxymestrone
  • Testosterone, 4-hydroxy-17-methyl-
  • Theranabol
  • 4-ANDROSTEN-17ALPHA-METHYL-4,17BETA-DIOL-3-ONE
  • 4-HYDROXY-METHYLTESTOSTERONE
  • 4-HYDROXY-17ALPHA-METHYLTESTOSTERONE
  • 4,17b-dihydroxy-17-methylandrosta-4-en-3-one
  • ORANABOL
  • OXYMESTERONE
  • OXYMESTERONE ENTERPRISE STANDARD =98%
  • (8R,9S,10R,13S,14S,17S)-4,17-dihydroxy-10,13,17-trimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one
  • 4,17b-Dihydroxy-17-methylandrost-4-en-3-one
  • Androst-4-en-3-one, 4,17-dihydroxy-17-methyl-, (17b)-
  • (17S)-4,17-Dihydroxy-17-methylandrost-4-en-3-one
  • 145-12-0
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Steroids