Ketoprofen
| Parameter | Technische Daten |
|---|---|
| Produktname | Ketoprofen |
| CAS-Nummer | 22071-15-4 |
| Molekülformel | C16H14O3 |
| Molekulargewicht | 254.28 g/mol |
| Aussehen | Weißes bis cremefarbenes kristallines Pulver |
| Analyse (HPLC) | ≥99.0% |
| Löslichkeit | Slightly soluble in water; freely soluble in ethanol, acetone, and chloroform |
| Verpackung | 25 kg fiber drum with double polyethylene liner |
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Synonyme: 2-(3-Benzoylphenyl)propionic acid, (±)-Ketoprofen, Orudis, Oruvail, Actron, 22071-15-4
Ketoprofen belongs to the propionic acid class of nonsteroidal anti-inflammatory drugs (NSAIDs), distinguished by a 3-benzoylphenyl substituent on the propionic acid backbone. This structural motif enhances lipophilicity and facilitates rapid penetration into synovial fluid, where the drug reaches concentrations approaching those in plasma. The molecule exists as a racemic mixture, but pharmacological activity resides almost entirely in the S-enantiomer, which reversibly inhibits cyclooxygenase (COX) enzymes and thereby reduces prostaglandin synthesis.
First introduced in the 1970s, ketoprofen remains a mainstay in both human and veterinary medicine for its potent analgesic, antipyretic, and anti-inflammatory effects. It is supplied as a high-purity active pharmaceutical ingredient (API) that meets current pharmacopeial monographs, including USP, EP, and BP. Our ketoprofen is manufactured under cGMP conditions and is available in both racemic and enantiopure forms to support formulation development.
Formulators value ketoprofen for its favorable balance of efficacy and tolerability, as well as its compatibility with a range of dosage forms—from immediate-release tablets and capsules to topical gels and transdermal patches. In the research setting, it serves as a reference compound for COX inhibition studies and as a precursor for prodrug design. The following sections provide technical details on its properties, mechanism, quality control, and supply.
Ketoprofen is a chiral 2-arylpropionic acid derivative with the molecular formula C16H14O3 and a molecular weight of 254.28 g/mol. The molecule contains a benzophenone moiety, which contributes to its UV absorbance and photolability. It is a white to off-white crystalline powder, practically insoluble in water but freely soluble in common organic solvents such as ethanol, acetone, and chloroform. The pKa is approximately 4.5, and the octanol-water partition coefficient (log P) is around 3.1, reflecting its moderate lipophilicity. Ketoprofen exhibits polymorphism, and the crystalline form can influence dissolution rate and stability; therefore, our API is routinely characterized by X-ray powder diffraction (XRPD) and differential scanning calorimetry (DSC) to ensure consistent solid-state properties.
| Test Item | Technische Daten |
|---|---|
| Identification | IR and UV spectra conform to reference standard |
| Trocknungsverlust | ≤0,5% |
| Verbrennungsrückstand | ≤0,1% |
| Schwermetalle | ≤20 ppm |
| Related Substances | Any individual impurity ≤0.1%; total impurities ≤0.5% |
| Microbial Limits | Total aerobic microbial count ≤1000 CFU/g; yeast and mold ≤100 CFU/g; absence of E. coli and Salmonella |
We offer flexible MOQs starting from 1 kg for research and development purposes. For commercial orders, we can accommodate quantities up to 500 kg per batch. Please contact our sales team to discuss your specific requirements.
For stock items, the lead time is 3-5 business days from order confirmation. We maintain sufficient inventory to ensure prompt shipment and can provide expedited shipping options if needed.
Yes, a COA is available for each batch upon request. We also provide free samples (typically 10-50 g) for evaluation, with the recipient covering shipping costs. Samples are dispatched within 1-2 days after request.
send us your specification for a quotation.
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