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Benorilate Powder Raw Anti-inflammatory and Antipyretic Medication

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  • Specifications

Buy Benorilate Powder Raw Anti-inflammatory and Antipyretic Medication Online CAS 5003-48-5

 

Benorilate Specification

Product Name: Benoyyl Ester
CAS: 5003-48-5
Level: Medical grade
Content: 99%
Appearance: white powder
Packing: 25kg/plastic drum detachable
Ingredients: Benoyyl Ester
Physical and chemical properties: white crystalline powder
Category: Pharmaceutical raw materials
Area: Anti-inflammatory, antipyretic, analgesic
Down product: Benoy ester tablets
Use: Mainly used for rheumatoid arthritis, acute and chronic rheumatoid arthritis, rheumatic pain, cold fever, headache, neuralgia and postoperative pain
Dosage: Rheumatoid arthritis, rheumatoid arthritis: oral 4g each time, 1 time each morning and evening; or 2g each time, 3-4 times a day. General antipyretic, analgesic: 0.5-1.5g each time, 3-4 times a day. Children: 3 months to 1 year old, 25mg per kilogram body weight, 4 times a day; 250mg every 1~2 years old, 4 times a day; 3-5 years old, 500mg each time, 3 times a day; 6-12 years old , 500mg each time, 4 times a day. Juvenile rheumatoid arthritis, 1g each time, 3~4 times a day.

 

What is Benorilate?

Benorilate or benorylate, is an ester-linked codrug of aspirin with paracetamol. It is used as an anti-inflammatory and antipyretic medication. In the treatment of childhood fever, it has been shown to be inferior to paracetamol and aspirin taken separately.

 

Benorilate Certificate of Analysis

Product name Benorilate
CAS No. 5003-48-5 Outer Packing 25kg/drum
Production date 2017.4.28 Shelf life 2020.4.27
Standard adopted CP2015
Items of analysis Specification Results
Appearance white crystal or crystalline powder White crystalline powder
Melting point 177-181℃ 177-179℃
Absorption coefficient 730-760 745
Identification positively reacted Conforms
Identification The infrared spectrum should be consistent with the control map Conforms
Identification positively reacted Conforms
Chloride ≤0.01% 〈0.01%
Sulfate ≤0.02% 〈0.02%
P-aminophenol meets the requirments Conforms
Free salicylic acid ≤0.1% 〈0.1%
Acetaminophen ≤0.1% 0
Single impurity ≤0.5% 0.16%
Total impurities ≤1.0% 0.23%
Loss on drying ≤0.5% 0.07%
Residue on ignition ≤0.1% 0.04%
Heavy metal ≤0.001% 〈0.001%
Assay 99.0~102.0% 99.9%
Conclusion Qualified

 

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