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Desoxycorticosterone

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Desoxycorticosterone manufacturers

Desoxycorticosterone Basic information
Product Name:Desoxycorticosterone
Synonyms:Corthormon;Corticosterone, 11-deoxy-;Deoxycortone;Pregn-4-en-21-ol-3,20-dione;Pregn-4-ene-3,20-dione, 21-hydroxy-;Progesterone, 21-hydroxy-;deoxycorticosterone crystalline;Desoxycorton
CAS:64-85-7
MF:C21H30O3
MW:330.46
EINECS:200-596-4
Product Categories:Intermediates & Fine Chemicals;Pharmaceuticals;Steroids
Mol File:64-85-7.mol
Desoxycorticosterone Structure
Desoxycorticosterone Chemical Properties
Melting point 138-144 °C
alpha 184 º (c=1, C2H5OH)
Boiling point 407.89°C (rough estimate)
density 1.0998 (rough estimate)
refractive index 1.5192 (estimate)
Fp 9℃
storage temp. -20°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka12.98±0.10(Predicted)
color White to Pale Yellow
Optical Rotation+17822 (c 1.5, ethanol)
Water Solubility slightly soluble
Merck 13,2917
BRN 2062123
InChI1S/C21H30O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h11,15-18,22H,3-10,12H2,1-2H3/t15-,16-,17-,18+,20-,21-/m0/s1
InChIKeyZESRJSPZRDMNHY-YFWFAHHUSA-N
SMILES[H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)[C@H](CC[C@@]24[H])C(=O)CO
LogP2.880
CAS DataBase Reference64-85-7(CAS DataBase Reference)
NIST Chemistry ReferenceDeoxycorticosterone(64-85-7)
EPA Substance Registry SystemDeoxycorticosterone (64-85-7)
Safety Information
Hazard Codes Xn,T,F
Risk Statements 40-48-39/23/24/25-23/24/25-11
Safety Statements 22-24/25-45-36/37-16-7
RIDADR UN 2811 6.1/PG 2
WGK Germany 3
RTECS HG0350000
Storage Class11 - Combustible Solids
Hazard ClassificationsCarc. 2
STOT RE 2
MSDS Information
ProviderLanguage
21-Hydroxypregn-4-ene-3,20-dione English
SigmaAldrich English
ACROS English
Desoxycorticosterone Usage And Synthesis
Chemical Propertieswhite to creamy-white crystalline powder
UsesA mineralocorticoid that occurs in adrenal cortex. It acts as a precursor to Aldosterone (A514700).
UsesAntiinflammatory;Corticoide
DefinitionChEBI: A mineralocorticoid that is progesterone substituted at position 21 by a hydroxy group.
General Description11-Deoxycorticosterone is a steroid hormone produced in the adrenal glands that acts as a precursor for the hormone aldosterone. Levels of 11-deoxycorticosterone are measured by LC-MS/MS to aid in diagnosing disorders of steroid synthesis, such as 11-hydroxylase deficiency and glucocorticoid responsive hyperaldosteronism. This Certified Spiking Solution is suitable for use as starting material inlinearity standards, calibrators, and controls for numerous LC-MS/MS applications in endocrinology, clinical chemistry, and neonatal screening.
HazardToxic.
Mechanism of actionDesoxycorticosterone causes an increase in reabsorption of sodium ions and excretion of potassium ions from the renal tubules, which leads to increased tissue hydrophilicity. This facilitates an elevated volume of plasma and increased arterial pressure. Muscle tonicity and work capability are increased. It is used for an insufficiency of function of the adrenal cortex, myasthenia, asthenia, adynamia, and overall muscle weakness.
SynthesisDesoxycorticosterone, 21-hydroxypregn-4-en-3,20-dione acetate (27.2.6), is synthesized in a number of ways, the easiest of which being iodination of progesterone at C21 in the methyl group, and subsequent reaction of the resulting iodo-derivative 27.2.5 with potassium acetate, which leads to formation of the desired desoxycorticosterone in the form of the acetate (27.2.6) .

Synthesis_64-85-7

Purification MethodsCrystallise 11-deoxycorticosterone from diethyl ether. [Schindler et al. Helv Chim Acta 24 360 1941, Steiger & Reichstein Helv Chim Acta 20 1164 1937.]
Tag:Desoxycorticosterone(64-85-7) Related Product Information
Doxifluridine Chenodeoxycholic acid CORTICOSTERONE Ursodeoxycholic acid 4-Pregnen-21-ol-3,20-dione-2,2,4,6,6,17alpha,21,21-d8 Cortisone acetate Flurandrenolide CORTISONE Hydrocortisone 21-hemisuccinate Hydrocortisone sodium succinate Hydrocortisone Hydrocortisone acetate (-)-2-[Methylamino]-1-phenylpropane D-Methamphetamine Reichstein's substance S 21-acetate 4-Pregnen-6-beta, 17,21-triol-3,11,20-trione 11-Dehydrocorticosterone Deoxycorticosterone acetate