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Desoxycorticosterone

Desoxycorticosterone Structure
CAS No.
64-85-7
Chemical Name:
Desoxycorticosterone
Synonyms
DOC;CORTEXONE;Corthormon;Deoxycortone;Desoxycorton;DOC【steroid】;DESOXYCORTONE;'REICHSTEIN Q';DEOXYCORTICOSTERONE;DESOXYCORTICOSTERONE
CBNumber:
CB4314147
Molecular Formula:
C21H30O3
Molecular Weight:
330.46
MOL File:
64-85-7.mol
Modify Date:
2023/5/25 18:01:09

Desoxycorticosterone 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)
Flash point 9℃
storage temp. -20°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka 12.98±0.10(Predicted)
color White to Pale Yellow
Water Solubility slightly soluble
Merck 13,2917
BRN 2062123
LogP 2.880
CAS DataBase Reference 64-85-7(CAS DataBase Reference)
NIST Chemistry Reference Deoxycorticosterone(64-85-7)
EPA Substance Registry System Deoxycorticosterone (64-85-7)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08
Signal word  Warning
Hazard statements  H351-H373
Precautionary statements  P201-P308+P313
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

Desoxycorticosterone price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) D6875 21-Hydroxyprogesterone ≥97% (HPLC) 64-85-7 500MG ₹21595.88 2022-06-14 Buy
Sigma-Aldrich(India) D6875 21-Hydroxyprogesterone ≥97% (HPLC) 64-85-7 1G ₹35841.58 2022-06-14 Buy
Sigma-Aldrich(India) D6875 21-Hydroxyprogesterone ≥97% (HPLC) 64-85-7 5G ₹126804.05 2022-06-14 Buy
Sigma-Aldrich(India) D-105 11-Deoxycorticosterone solution 100?μg/mL in methanol, ampule of 1?mL, certified reference material, Cerilliant? 64-85-7 1ML ₹15374.8 2022-06-14 Buy
Product number Packaging Price Buy
D6875 500MG ₹21595.88 Buy
D6875 1G ₹35841.58 Buy
D6875 5G ₹126804.05 Buy
D-105 1ML ₹15374.8 Buy

Desoxycorticosterone Chemical Properties,Uses,Production

Chemical Properties

white to creamy-white crystalline powder

Uses

A mineralocorticoid that occurs in adrenal cortex. It acts as a precursor to Aldosterone (A514700).

Definition

ChEBI: A mineralocorticoid that is progesterone substituted at position 21 by a hydroxy group.

General Description

11-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.

Hazard

Toxic.

Mechanism of action

Desoxycorticosterone 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.

Purification Methods

Crystallise 11-deoxycorticosterone from diethyl ether. [Schindler et al. Helv Chim Acta 24 360 1941, Steiger & Reichstein Helv Chim Acta 20 1164 1937.]

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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 21-HYDROXYPROGESTERON VETRANAL, 250 MG 17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one HYDROXYPROGESTERONE, 21-(RG) Reichstein Q, 11-Deoxycorticosterone, 11-Desoxycorticosterone, 21-Hydroxy-4-pregnene-3,20-dione, 4-Pregnen-21-ol-3,20-dione, Cortexone, Desoxycortone, DOC, Kendalls desoxy compound B Deoxycorticosterone Propionate DOC【steroid】 DesoxycorticosteroneDeoxycorticosterone 21-Hydroxy-3,20-dioxopregn -4-ene 21-Hydroxy-4-pregnane-3,20-dione CORTEXONE DELTA4-PREGNEN-21-OL-3,20-DIONE DEOXYCORTICOSTERONE DESOXYCORTICOSTERONE DESOXYCORTONE DOC HYDROXYPROGESTERONE, 21- KENDALL'S DESOXY COMPOUND B 4-PREGNENE-21-OL-3,20-DIONE 4-PREGNEN-21-OL-3,20-DIONE 11-DESOXYCORTICOSTERONE 11-DEOXYCORTICOSTERONE 21-HYDROXY-4-PREGNENE-3,20-DIONE 21-hydroxypregn-4-ene-3,20-dione 21-HYDROXYPROGESTERONE 'REICHSTEIN Q' REICHSTEIN'S COMPOUND ''Q'' REICHSTEIN'S SUBSTANCE Q (8S,10R,13S,17S)-17-(2-Hydroxy-acetyl)-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-3-one 11-Dehydroxycorticosterone 21-Hydroxypregn-4-en-3,20-dione 21-hydroxy-progesteron Desoxycorticosterone Solution, 100ppm 11-Deoxycorticosterone solution Corticosterone Impurity 5 11-Deoxycorticosterone-2,3,4-13C3 solution 100 mug/mL in methanol, >=99 atom % 13C, >=98% (CP) Desoxycorticosterone USP/EP/BP 21-hydroxyprogesteroneQ: What is 21-hydroxyprogesterone Q: What is the CAS Number of 21-hydroxyprogesterone Q: What is the storage condition of 21-hydroxyprogesterone 13C2,2H2]-Deoxycorticosterone 2H6]-Deoxycorticosterone 2H4]-11-Deoxycorticosterone 64-85-7 Intermediates & Fine Chemicals Pharmaceuticals Steroids