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oxymetholone--dea schedule iii

oxymetholone--dea schedule iii

CAS: 434-07-1

Molecular Formula: C21H32O3

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oxymetholone--dea schedule iii - Names and Identifiers

Name oxymetholone--dea schedule iii
Synonyms ANASTERONE
Oxymetholone
Oxymethenolone
Stanozolol impurity B
OxyMetholone (Anadrol)
oxymetholone--dea schedule iii
4,5-dihydro-2-hydroxymethylene-17-a-methyltestosterone
(5α,17β)-17-Hydroxy-2-(hydroxyMethylene)-17-Methylandrostan-3-one
5ALPHA-ANDROSTAN-17ALPHA-METHYL-17BETA-OL-2-HYDROXYMETHYLENE-3-ONE
5-ALPHA-ANDROSTAN-2-HYDROXYMETHYLENE-17-ALPHA-METHYL-17-BETA-OL-3-ONE
(5alpha,17beta)-17-hydroxy-2-(hydroxymethylidene)-17-methylandrostan-3-one
17-beta-hydroxy-2-hydroxymethylene-17-alpha-methyl-5-alpha-androstan-3-one
(2E,5alpha,17beta)-17-hydroxy-2-(hydroxymethylidene)-17-methylandrostan-3-one
(2Z,5alpha,17beta)-17-hydroxy-2-(hydroxymethylidene)-17-methylandrostan-3-one
17beta-Hydroxy-2-(hydroxymethylene)-17-methyl-5alpha-androstan-3-oneAnasterone
CAS 434-07-1
EINECS 207-098-6
InChI InChI=1/C21H32O3/c1-19-11-13(12-22)18(23)10-14(19)4-5-15-16(19)6-8-20(2)17(15)7-9-21(20,3)24/h12,14-17,22,24H,4-11H2,1-3H3/b13-12-/t14-,15+,16-,17-,19-,20-,21-/m0/s1
InChIKey ICMWWNHDUZJFDW-CCTJMHFWSA-N

oxymetholone--dea schedule iii - Physico-chemical Properties

Molecular FormulaC21H32O3
Molar Mass332.48
Density1.0834 (rough estimate)
Melting Point172-180°C
Boling Point409.59°C (rough estimate)
Specific Rotation(α)34 º
Flash Point249.7°C
Solubility H2O: ≤0.5mg/mL
Vapor Presure1.23E-10mmHg at 25°C
Appearancesolid
Colorwhite to light yellow
Merck6967
pKa5.28±0.70(Predicted)
Storage Condition2-8°C
StabilityStability May be light sensitive. Combustible. Incompatible with strong oxidizing agents.
Refractive Index38 ° (C=1, CHCl3)
Physical and Chemical PropertiesWhite crystalline powder, odorless. Melting point 173-176 °c (178-180 °c). [Α] D 38 ° (chloroform), insoluble in water, soluble in chloroform, soluble in dioxane, vegetable oil, slightly soluble in ethanol, ether.
UseCan promote protein synthesis and inhibit protein alienation, and can reduce blood cholesterol, reduce calcium and phosphorus excretion and reduce bone marrow suppression, promote development and so on

oxymetholone--dea schedule iii - Risk and Safety

Risk CodesR40 - Limited evidence of a carcinogenic effect
R63 - Possible risk of harm to the unborn child
Safety DescriptionS53 - Avoid exposure - obtain special instructions before use.
S22 - Do not breathe dust.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S36 - Wear suitable protective clothing.
WGK Germany3
RTECSBV8060000
HS Code29372900
ToxicityTDLo orl-hmn: 46 mg/kg/14W-I:LIV JAMAAP 240,243,78

oxymetholone--dea schedule iii - Reference Information

NIST chemical information Information provided by: webbook.nist.gov (external link)
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
Use Intermediate of Canilone. It is a protein anabolic hormone drug, which can promote protein synthesis and inhibit protein heterogenesis, and can reduce blood cholesterol, reduce calcium and phosphorus excretion and reduce bone marrow suppression, promote development, and promote tissue regeneration and granulation formation. It has preventive and antagonistic effects on adrenal hypofunction caused by long-term use of adrenal cortex hormones.
It can promote protein synthesis and inhibit protein alienation, and can reduce blood cholesterol, reduce calcium and phosphorus excretion, reduce bone marrow suppression, and promote development.
production method the product can be prepared by acetylation, reduction, ring opening, oxidation, hydrolysis, elimination, oxime, rearrangement, hydrolysis, addition, oxidation, hydrolysis, condensation and other multi-step reactions of sisaponin or sisaponin.
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 21:04:16
oxymetholone--dea schedule iii
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View History
oxymetholone--dea schedule iii
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