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CORTISONE

CORTISONE Structure
CAS No.
53-06-5
Chemical Name:
CORTISONE
Synonyms
KE;Corlin;CORTONE;Cortison;17A 21-DIHYDROXY-4-PREGNEN-3 17 20-TRIONE;Corton;Adreson;Andreson;Cortisal;Cortogen
CBNumber:
CB6413305
Molecular Formula:
C21H28O5
Molecular Weight:
360.44
MOL File:
53-06-5.mol
MSDS File:
SDS
Modify Date:
2023/9/25 13:50:22

CORTISONE Properties

Melting point 223-228 °C (dec.)(lit.)
alpha D25 +209° (c = 1.2 in 95% alcohol); 25546 +269° (c = 0.125 in benzene); 25546 +248° (c = 0.1 to 0.2 in alcohol)
Boiling point 412.46°C (rough estimate)
Density 1.28±0.1 g/cm3 (20 ºC 760 Torr)
refractive index 210 ° (C=1, EtOH)
Flash point 9℃
storage temp. -20°C Freezer
solubility Chloroform (Slightly, Heated, Sonicated), DMSO (Slightly), Ethanol (Slightly, Heated)
form Solid
pka 12.37±0.60(Predicted)
color White to Pale Beige
Water Solubility 229.9mg/L(25 ºC)
Merck 2539
LogP 1.470
CAS DataBase Reference 53-06-5(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS06,GHS08
Signal word  Danger
Hazard statements  H225-H301+H311+H331-H370
Precautionary statements  P210-P260-P280-P301+P310-P311
Hazard Codes  F,T,Xn
Risk Statements  11-23/24/25-39/23/24/25-63
Safety Statements  22-24/25-45-36/37-16-7
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  3
RTECS  GM9020000
18
HS Code  2937210000

CORTISONE price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) C-130 Cortisone solution 100?μg/mL in methanol, ampule of 1?mL, certified reference material, Cerilliant? 53-06-5 1ML ₹8498.7 2022-06-14 Buy
TCI Chemicals (India) C1317 Cortisone 53-06-5 1G ₹3100 2022-05-26 Buy
ottokemi C 2520 Cortisone 98% 53-06-5 250mg ₹3069 2022-05-26 Buy
ottokemi C 2520 Cortisone 98% 53-06-5 1gm ₹8208 2022-05-26 Buy
Product number Packaging Price Buy
C-130 1ML ₹8498.7 Buy
C1317 1G ₹3100 Buy
C 2520 250mg ₹3069 Buy
C 2520 1gm ₹8208 Buy

CORTISONE Chemical Properties,Uses,Production

Chemical Properties

Off-White Crystalline Powder

Uses

Cortisone is used for inflammatory processes, allergies, and adrenal insufficiency.

Definition

ChEBI: A C21-steroid that is pregn-4-ene substituted by hydroxy groups at positions 17 and 21 and oxo group at positions 3, 11 and 20.

General Description

Cortisone is a corticosteroid produced in the adrenal glands. Cortisone is administered for short term pain relief and to reduce swelling from inflammation. This Certified Spiking Solution? is applicable in LC-MS/MS applications for endocrinology, clinical chemistry and neonatal screening.

Hazard

Damaging side effects, e.g., sodium retention from ingestion.

Pharmacokinetics

Following oral administration, cortisone acetate and hydrocortisone acetate are completely and rapidly deacetylated by first-pass metabolism. Much of the oral cortisone, however, is inactivated by oxidative metabolism before it can be converted to hydrocortisone in the liver. The pharmacokinetics for hydrocortisone acetate is indistinguishable from that of orally administered hydrocortisone. Oral hydrocortisone is completely absorbed, with a bioavailability of greater than 95% and a half-life of 1 to 2 hours (23).

Clinical Use

Cortisone is administered orally or by intramuscular (IM) injection as its 21-acetate (cortisone acetate).Cortisone acetate or hydrocortisone usually is the corticosteroid of choice for replacement therapy in patients with adrenocortical insufficiency, because these drugs have both glucocorticoid and mineralocorticoid properties.

Metabolism

The metabolism of hydrocortisone has been previously described. Cortisone acetate is slowly absorbed from IM injection sites over a period of 24 to 48 hours and is reserved for patients who are unable to take the drug orally. The acetate ester derivative demonstrates increased stability and has a longer duration of action when administered by IM injection. Thus, smaller doses can be used. Similarly, hydrocortisone may be dispensed as its 21-acetate (hydrocortisone acetate), which is superior to cortisone acetate when injected intra-articularly.

Purification Methods

Crystallise cortisone from 95% EtOH or acetone. The UV has 14,000 M-1cm -1 at 237nm (EtOH). [Beilstein 8 IV 3480, Hems J Pharm Pharmacol 5 409 1953, Beilstein 8 IV 3480.]

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17ALPHA,21-DIHYDROXYPREGN-4-ENE-3,11,20-TRIONE 17ALPHA,21-DIHYDROXY-4-PREGNENE-3,11,20-TRIONE 17ALPHA-HYDROXY-11-DEHYDROCORTICOSTERONE 17-HYDROXY-11-DEHYDROCORTICOSTERONE 4-PREGNENE-17ALPHA,21-DIOL-3,11,20-TRIONE 4-PREGNEN-17ALPHA,21-DIOL-3,11,20-TRIONE 4-PREGNEN-17,21-DIOL-3,11,20-TRIONE 4-PREGEN-17A,21-DIOL-3,11,20-TRIONE KENDALL'S CMPD ''E'' KENDALL'S ''E'' 4-Pregnene-17α,21-diol-3,11,20-trione (8S,9S,10R,13S,14S,17R)-17-glycoloyl-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,11-quinone (8S,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxyethanoyl)-10,13-dimethyl-1,2,6,7,8,9,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,11-dione (8S,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxy-1-oxoethyl)-10,13-dimethyl-1,2,6,7,8,9,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,11-dione (8S,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxyethanoyl)-10,13-dimethyl-1,2,6,7,8,9,12 Cortisone solution,100ppm KENDALL'S COMPOUND E KENDALL'S COMPOUND 'E' CORTISONE DELTA4-PREGNENE-17, 21-DIOL-3, 11, 20-TRIONE DELTA4-PREGNENE-17ALPHA,21-DIOL-3,11,20-TRIONE DELTA-PREGNENE-17ALPHA,21-DIOL-3,11,20-TRIONE REICHSTEIN'S SUBSTANCE FA REICHSTEIN'S SUBSTANCE 'FA' REICHSTEIN'S COMPOUND ''FA'' WINTERSTEINER'S COMPOUND 'F' WINTERSTEINER'S CMPD ''F'' Corton (8S,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,11-dione 17α,21-Dihydroxy-4-pregnene-3,11,20-trione, 17α-Hydroxy-11-dehydrocorticosterone, 4-Pregnene-17α,21-diol-3,11,20-trione, Kendalls Compound E, Reichsteins Substance Fa 17α,21-Dihydroxypregn-4-en-3,11,20-trione 17,21-Dihydroxy-4-pregnene-3,11,20-trione 17,21-Dihydroxypregn-4-ene-3,11,20-trione 20-trione,17,21-dihydroxy-pregn-4-ene-11 Adrenalex Adreson Andreson Cortadren Cortandren Cortisal Cortisate Cortistal Cortivite Cortogen delta(sup4)-pregnene-17alpha,21-diol-3,11,20-trione Incortin Kendall's compound Pregn-4-en-17alpha,21-diol-3,11,20-trione Pregn-4-ene-3,11,20-trione, 17,21-dihydroxy- Reichstein Fa Scheroson (8S,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-diMethyl-7,8,9,10,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,11(2H,6H)-dione Cortisone solution Cortisone-[2H7] NSC 9703 4-Pregnen-17a,21-diol-3,11,20-trione-d2 11-DEHYDRO-17-HYDROXYCORTICOSTERONE 4-Pregnen-17α?21-diol-3?11?20-trione-1?2-d2