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Zaltoprofen CAS NO 89482-03-1
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CAS No.:89482-03-1
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Zaltoprofen is a potent non-steroidal anti-inflammatory drug (NSAID) belonging to the propionic acid derivative class. It is valued for its targeted anti-inflammatory and analgesic properties, offering a specific therapeutic profile for pharmaceutical development. This compound is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the formulation of advanced analgesic and anti-inflammatory medications.
Application
- Active Pharmaceutical Ingredient (API) in the formulation of prescription analgesic drugs.
- Key intermediate in advanced pharmaceutical research for novel NSAID development.
- Reference standard in analytical laboratories for quality control and method validation.
- Preclinical research compound for studying mechanisms of inflammation and pain.
- Component in the development of targeted drug delivery systems.
Basic Information
| Product Name | Zaltoprofen |
| CAS No. | 89482-03-1 |
| Molecular Formula | C₁₇H₁₄O₃S |
| Molecular Weight | 298.36 g/mol |
| Synonyms | 2-(10,11-Dihydro-10-oxodibenzo[b,f]thiepin-2-yl)propionic acid; Zaltoprofenum; Zaltoprofen [USAN]; Soleton; Peon; ZLT; UNII-6KZ5J5J3QJ |
| EINECS | Contact for details |
Quality Control
Our Zaltoprofen is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC, to ensure it meets high-grade pharmaceutical standards. A detailed Certificate of Analysis (COA) is provided with every shipment to guarantee traceability and compliance.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption and degradation.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.5% |
| Related Substances (HPLC) | Total impurities ≤ 1.0% Any single impurity ≤ 0.5% |
| Loss on Drying | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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