Hormone and Endocri...

Hormone and Endocrine-Regulating Drugs CAS 50-23-7 Hydrocortisone

Hormone and Endocrine-Regulating Drugs CAS 50-23-7 Hydrocortisone

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1 Kilogram

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  • Min.Order :1 Kilogram
  • Purity: >99%
  • Payment Terms : L/C,T/T,

Keywords

50-23-7 Hydrocortisone C21H30O5

Quick Details

  • Appearance:white powder
  • Application:For adrenal insufficiency caused by disease, rheumatoid arthritis, rheumatic fever, gout, bronchial asthma. For atopic dermatitis, seborrheic dermatitis, pruritus. Large doses cause Cushing's syndrom
  • PackAge:1kg/2kg/5kg aluminum foil/tin, 25kg/drum
  • ProductionCapacity:1000 |Metric Ton|Year
  • Storage:Cool Dry Place
  • Transportation:by sea or by air

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Details:

Description

Hydrocortisone is the pharmaceutical term for cortisol used in oral administration, intravenous injection, or topical application. It is used as an immunosuppressive drug, given by injection in the treatment of severe allergic reactions such as anaphylaxis and angioedema, in place of prednisolone in patients needing steroid treatment but unable to take oral medication, and perioperatively in patients on long-term steroid treatment to prevent Addisonian crisis. It may also be injected into inflamed joints resulting from diseases such as gout.
It may be used topically for allergic rashes, eczema, psoriasis, itching and other inflammatory skin conditions.

Function & Application:

1. For adrenal insufficiency caused by disease, rheumatoid arthritis, rheumatic fever, gout, bronchial asthma. For atopic
dermatitis, seborrheic dermatitis, pruritus. Large doses cause Cushing's syndrome, sodium retention, psychiatric symptoms, digestive ulcers, osteoporosis, growth inhibition.
2. For iridocyclitis, keratitis, scleritis, conjunctivitis. For neurodermatitis, for tuberculous meningitis, pleurisy, arthritis,
tenosynovitis, acute and chronic sprain, strain, etc. sheath.

Product HYDROCORTISONE BASE
Shelf Life 3 years
ITEM SPECIFICATION RESULT
CHARACTER  WHITE TO ALMOST WHITE CRYSTALLINE POWDER ALMOST WHITE CRYSTALLINE POWDER
IDENTIFICATION （A）COMPLIES BY IR  CONFORMS
（B）UV:△E/EES≤2.5% 0.2%
TEST
SPECIFIC ROTATION  +150° TO +156°  +153.0°
LOSS ON DRYING ≤1.0% 0.3%
RESIDUE ON IGNITION ≤0.5% 0.1%
RELATED SUBSTANCES INDIVIDUAL IMPURITY ≤0.5% 0.28%
TOTAL IMPURITIES ≤2.0% 0.09%
RESIDUAL SOLVENT CYCLOHEXANE ≤3880ppm 2PPM
METHANOL≤3000PPM 82PPM
ASSAY 
 		 CONTAINS 97.0% TO 102.0% OF C21H30O5 CALCULATED ON DRIED BASIS 100.1%
CONCLUSION: THE PRODUCT CONFORMS TO USP38 AND CUSTOMER STANDARD.

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