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Prednisolone CAS 50-24-8

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 50-24-8

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Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Bag,Drum

Delivery Time: 7-15 days

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Supply Ability: TON

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Highlight:
CAS NO::
50-24-8
Appearance::
White To White Powder
Molecular Formula::
C21H28O5
Molecular Weight::
360.45
EINECS NO::
200-021-7
MDL NO::
MFCD00003649
CAS NO::
50-24-8
Appearance::
White To White Powder
Molecular Formula::
C21H28O5
Molecular Weight::
360.45
EINECS NO::
200-021-7
MDL NO::
MFCD00003649
Prednisolone CAS 50-24-8

Product Description:

Product Name: Prednisolone CAS NO: 50-24-8

 

 

Synonyms:

DEHYDROHYDROCORTISONE;

HYDRODELTALONE;

METACORT AND RALONE;

 

 

Chemical & Physical Properties:

Appearance:White to white powder

Assay :≥99.0%

Density: 1.3±0.1 g/cm3

Boiling Point: 570.6±50.0℃ at 760 mmHg

Melting Point: 240℃ (dec.)(lit.)

Flash Point: 313.0±26.6℃

Vapour Pressure: 0.0±3.6 mmHg at 25℃

Index of Refraction: 1.612

Storage Condition: -20℃ Freezer

 

 

Safety Information:

HS Code: 2937229000

 

 

Prednisolone is a glucocorticoid with the general properties of the corticosteroids.Target: Glucocorticoid ReceptorPrednisolone is a glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states. Prednisolone, 5 or 50 mg/kg, was administered intravenously to adrenalectomized rats. Total plasma, free plasma, CBG-free plasma, and liver prednisolone concentrations were measured simultaneously with free hepatic cytosolic glucocorticoid receptor concentrations and tyrosine aminotransferase (TAT) activity of the liver as a function of time. prednisolone pharmacokinetics were dose-dependent, parameters describing receptor kinetics and TAT activity were constant at each prednisolone dose. The major determinants of receptor-mediated glucocorticoid activity are confirmed to be the availability of the receptor, drug-receptor dissociation rate, and corticosteroid persistence in the biophase.

 

 

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