oxymetholone

oxymetholone structural formula

structural formula

business number 04tf
molecular formula c21h32o3
molecular weight 332.48
label

17β-hydroxy-2-hydroxymethylene-17α-methyl-5α-androstan-3-one,

2-hydroxymethylene-17α-methyl-5α-androst(alkane)-17β-ol-3-one,

hydroxytestosterone,

anadrol,

oxymetholone,

oxymetholone,

hydroxymethonolone,

17-alpha-methyl-2-hydroxymethylene-17-hydroxy-5-alpha-androstan-3-one,

17-beta-androstan-3-one,17-hydroxy-2-(hydroxymethylene)-17-methyl-5-alph,

17-beta-hydroxy-2-(hydroxymethylene)-17-alpha-methyl-5-alpha-androstan-3-one,

17-beta-hydroxy-2-(hydroxymethylene

numbering system

cas number:434-07-1

mdl number:mfcd00133083

einecs number:207-098-6

rtecs number:bv8060000

brn number:none

pubchem number:24897930

physical property data

一 , physical property data

traits :white crystalline powder, odorless

density (g/ml,25/4): not available

relative vapor density (g/ml, air=1)not available

melting point (ºc): 173-176

boiling point (ºc, normal pressure): not available

boiling point (ºc, 5.2kpa): not available

refraction rate: not available

flash point (ºc): not available

optical rotation (º): not available

spontaneous combustion point or ignition temperature (ºc): not available

steam pressure (kpa, 25ºc): not available

saturated vapor pressure (kpa, 60ºc): not available

burn heat (kj/mol):not available

critical temperature (ºc): not available

critical pressure (kpa): not available

oil and water log value of the (octanol/water) partition coefficient:not available

explosion upper limit (%, v/v): not available

lower explosion limit (%, v/v): not available

dissolve properties:insoluble in water, soluble in chloroform, soluble in dioxane, vegetable oil, slightly soluble in ethanol and ether

toxicological data

two , toxicological data:

acute toxicity:not available .

ecological data

three , ecological data:

1 ,other harmful effects: this substance may be harmful to the environment, and special treatment should be given to water bodies. notice.

molecular structure data

1 molar refractive index:95.89

2 molar volumem3/mol)284.2

3 isotonic specific volume (90.2k):757.0

4 surface tensiondyne/cm)50.3

5 polarizability(10-24cm3)38.01

compute chemical data

none yet

properties and stability

none yet

storage method

none yet

synthesis method

it can be used with saponin or sisal saponin through acetylation, reduction, ring opening, oxidation, hydrolysis, elimination, oximation, rearrangement, hydrolysis, this product is prepared through multi-step reactions such as addition, oxidation, hydrolysis, and condensation.

purpose

an intermediate of stanozolol. it is an anabolic hormone drug that can promote protein synthesis and inhibit proteogenesis, lower blood cholesterol, reduce calcium and phosphorus excretion, alleviate bone marrow suppression, promote development, and promote tissue regeneration and granulation formation. it has preventive and counteracting effects on adrenocortical hypofunction caused by long-term use of adrenocortical hormones.

resource:allhdi.com

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/30870

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