FINASTERIDE

PRODUCT IDENTIFICATION

CAS NO. 98319-26-7

FINASTERIDE

EINECS NO.  
FORMULA C23H36N2O2
MOL WT. 372.55

H.S. CODE

 

TOXICITY

 

SYNONYMS MK-906; Proscar;
(5alpha,17beta)-N-(1,1-dimethylethyl)-3-oxo-4-azaandrost-1-ene-17-carboxamide;
SMILES

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE white to off-white crystalline powder
MELTING POINT 251 - 255 C
BOILING POINT

 

SPECIFIC GRAVITY

 

SOLUBILITY IN WATER  
pH  
VAPOR DENSITY

 

AUTOIGNITION

 

NFPA RATINGS

 

REFRACTIVE INDEX

 

FLASH POINT

 

STABILITY

Stable under ordinary conditions.

APPLICATIONS

Finasteride is an inhibitor of 5alpha-reductase and is used to treat benign prostatic hypertrophy (BPH) which causes urinary problems by prostate gland enlargement. It is an androgen hormone inhibitor. 5Alpha-reductase is an intracellular enzyme which converts androgen testosterone to 5alpha-dihydrotestosterone (DHT). Finasteride has also an act to treat androgenetic alopecia as a hair growth stimulant. It is a 4-azasteroid compound. Chemically it is described as (5alpha,17beta)-N-(1,1- dimethylethyl)-3-oxo-4-azaandrost-1-ene-17-carboxamide; white crystalline powder; melting point 251 C; insoluble in water, soluble in chloroform and alcohol; administered orally.
SALES SPECIFICATION

BIBLIOGRAPHY

USP23 / BP93

APPEARANCE

white to off-white crystalline powder

IDENTIFICATION

complies

ASSAY

98.0% min
RESIDUE ON IGNITION

0.2% max

WATER

0.5% max

HEAVY METALS

10ppm max

OPTICAL ROTATION

+6° ~ 13°

TRANSPORTATION
PACKING
 
HAZARD CLASS Not regulated
UN NO.  

GENERAL DESCRIPTION OF CORTICOSTEROID

Corticosteroid is a synthetic or naturally occurring 21-carbon steroid structure substances with four fused rings and vary functional branches attached to the ring system. Cholesterol and steroid hormones have this carbon skeleton. The term steroid refers to these three groups that contain a hydrogenated cyclopentano perhydro phenanthrene ring system. In restricted context for medical usage by non-endocrinologists, it refers to corticosteroids. Natural corticosteroids are elaborated by the adrenal cortex in response to physiological carbohydrate metabolism. According to their predominant biologic activity, they are divided into two major groups: glucocorticoid and mineralocorticoid. Glucocorticoid's chief function is to regulate carbohydrate, lipid, and protein metabolism and inhibit the release of ACTH (adrenocorticotropic hormone). Glucocorticoids also affect muscle tone and the microcirculation, participate in the maintenance of arterial blood pressure, increase gastric secretion, alter connective tissue response to injury, impede cartilage production, inhibit inflammatory, allergic, and immunologic responses, invoke shrinkage of lymphatic tissue, reduce the number of circulating lymphocytes, and affect the functions of the central nervous system. In humans, the most important ones are cortisol, cortisone, and corticosterone. Mineralocorticoids, uniuqely aldosterone in human, regulate the balance of water and promote retention of sodium, loss of potassium. Aldosterone plays a role also in promoting tissue repair. Spironolactone is the aldosterone antagonist called potassium-sparing diuretic used in the treatment of hypertension. Corticosteroids are used in clinically for hormonal replacement therapy, for suppression of ACTH, as antineoplastic, antiallergic, and anti-inflammatory agents, and to suppress immune responses.
  • Glucocorticoid Receptor Agonists
    • Dexamethasone
    • Triamcinolone
    • Hydrocortisone
    • Prednisone
  • Glucocorticoid Receptor Antagonists
    • Mifepristone
    • Onapristone
  • Mineralocorticoid Receptor Agonists
    • Aldosterone
  • Mineralocorticoid Receptor Antagonists
    • Spironolactone
    • Eplerenone
PRICE INFORMATION

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