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Ketoprofen Powder Raw Nonsteroidal Anti-inflammatory Drugs

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Buy Ketoprofen Powder Raw Nonsteroidal Anti-inflammatory Drugs Online CAS 22071-15-4

 

Ketoprofen Specification

Product Name: Ketoprofen
CAS: 22071-15-4
Standard: USP
Level: Medical grade
Content: 99%
Appearance: white powder
Packing: 25KG/ cardboard drum detachable
Ingredients: α-methyl-3-benzoyl-phenylacetic acid. Calculated as dry product, containing C16H14O3 not less than 98.5% agent
Physical and chemical properties: White crystalline powder; odorless or almost odorless. This product is very soluble in methanol, soluble in ethanol, acetone or ether, almost insoluble in water.
Category: Pharmaceutical raw materials
Area: Anti-inflammatory analgesia
Deferred product: Ketoprofen enteric-coated capsules
Application: For various arthritis: joint pain, swelling and various pains such as dysmenorrhea, toothache, postoperative pain, cancerous Pain, etc.
Dosage: Oral Adult dosage: 1 anti-rheumatic, 50mg once, 3 to 4 times a day. The maximum dosage is 200mg a day; 2 treatment of dysmenorrhea, once 50mg, once every 6 to 8 hours, if necessary, can be increased to 75mg each time. To avoid gastrointestinal irritation, take it after meals and swallow the whole capsule.

 

What is Ketoprofen?

Ketoprofen, (RS)-2-(3-benzoylphenyl)-propionic acid (chemical formula C16H14O3) is one of the propionic acid class of nonsteroidal anti-inflammatory drugs (NSAID) with analgesic and antipyretic effects. It acts by inhibiting the body’s production of prostaglandin.

 

Ketoprofen Certificate of Analysis

Product name Ketoprofen
CAS No. 22071-15-4 Outer Packing 25KG/drum
Production date 2018.6.20 Shelf life 2020.6.19
Standard adopted USP37
Items of analysis Specification Results
Appearance White crystalline powder White crystalline powder
Identification Infrared Absorption/Ultraviolet Absorption Compares with Authentic Spectrum (KBr)/Compares with Authentic Spectrum
Melting range -1°~ +1° 0.000°
Loss on drying ≤0.5% 0.14%
Residue on Ignition ≤0.2% 0.04%
Heavy metals ≤0.002% Conform
Individual Impurity ≤0.2% 0.05%
Total Impurities ≤1.0% 0.33%
Assay(By Titrimetry) on Dried Basis 98.5%~101.0% 99.26%
Conclusion Qualified

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