Prednisolone-21-acetate

Prednisolone-21-acetate
  • CAS No.:52-21-1
Other grades of this product :
Prednisolone-21-acetate Basic information
Product Name:Prednisolone-21-acetate
Synonyms:PREDNISOLONE ACETATE;PREDNISOLONE 21-ACETATE;PRICORTIN;1,4-PREGNADIENE-11BETA,17ALPHA,21-TRIOL 3,20-DIONE 21-ACETATE;1,4-PREGNADIENE-3,20-DIONE-11BETA,17ALPHA,21-TRIOL 21-ACETATE;1,4-PREGNADIEN-11BETA,17ALPHA,21-TRIOL-3,20-DIONE 21-ACETATE;1,4-PREGNADIEN-11-BETA, 17,21-TRIOL-3,20-DIONE 21-ACETATE;1-DEHYDROCORTISOL 21-ACETATE
CAS:52-21-1
MF:C23H30O6
MW:402.49
EINECS:200-134-1
Product Categories:Applicable to rheumatoid arthritis, rheumatic fever, lupus erythematosus (sle), scleroderma, dermatomyositis, acute lymphocytic leukemia, etc;METICOTOLONE;Biochemistry;Hydroxyketosteroids;Steroids;API;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:52-21-1.mol
Prednisolone-21-acetate Chemical Properties
Melting point 240-244 °C
alpha D25 +116° (dioxane)
Boiling point 579.8±50.0 °C(Predicted)
density 1.28±0.1 g/cm3(Predicted)
refractive index 112 ° (C=1, Dioxane)
storage temp. 2-8°C
solubility Practically insoluble in water, slightly soluble in ethanol (96 per cent) and in methylene chloride.
form neat
pka12.41±0.70(Predicted)
color White to Off-White
Water Solubility 11.6mg/L(25 ºC)
Merck 7721
BRN 3111798
Stability:Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference52-21-1(CAS DataBase Reference)
NIST Chemistry Reference1,4-Pregnadiene-3,20-dione, 11beta,17alpha,21-trihydroxy-, acetate(52-21-1)
Safety Information
Hazard Codes N
Risk Statements 25-34-11
Safety Statements 45-36/37/39-26-16
WGK Germany 3
RTECS TU4152500
HS Code 29372900
MSDS Information
ProviderLanguage
SigmaAldrich English
Prednisolone-21-acetate Usage And Synthesis
Chemical PropertiesWhite or almost white, crystalline powder.
OriginatorSterane, Phipharmex ,US ,1955
UsesSynthetic corticosteroid; metabolically interconvertible with prednisone.
Usesglucocorticoid
Manufacturing ProcessTo a solution of 0.85 gram of 1,4-pregnadiene-11β,17α,21-triol-3,20-dione (prednisolone) in 5 ml of pyridine are added 3 ml of acetic anhydride. The reaction mixture is allowed to stand at room temperature overnight and is then diluted with ice water. The resulting precipitate is filtered from the mixture and recrystallized from acetone-hexane. There is recovered 0.45 gram of 1,4-pregnadiene-11β,17α,21-triol-3,20-dione 21-acetate, MP 235°239°C. On recrystallization, the MP rose to 237°-239°C.
Brand nameEconopred (Alcon); Meticortelone (Schering); Omnipred (Alcon); Sterane (Pfizer).
Therapeutic FunctionGlucocorticoid
Biological ActivityPrednisolone Acetate (Omnipred) is a synthetic corticosteroid that is a particularly potent immunosuppressant.
Clinical UseFor rheumatoid arthritis, rheumatic fever, lupus erythematosus, scleroderma, dermatomyositis, acute lymphoblastic leukemia, etc.
Purification MethodsRecrystallise prednisolone acetate from EtOH, Me2CO, Me2CO/hexane, and it has UV with max at 243nm in EtOH. [Joly et al. Bull Soc Chim Fr 366 1958; Herzog et al. J Am Chem Soc 77 4781 1955, Beilstein 8 IV 3468.]
Prednisolone-21-acetate Preparation Products And Raw materials
Preparation ProductsIsoflupredone Acetate

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