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Chloramphenicol Palmitate CAS NO 106322-62-7
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CAS No.:106322-62-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Chloramphenicol Palmitate is a lipid-soluble ester prodrug of the broad-spectrum antibiotic chloramphenicol. This formulation is critical for enhancing the drug's palatability and bioavailability, particularly in oral pediatric suspensions. It is primarily utilized by pharmaceutical manufacturers in the production of finished dosage forms, serving as a key active pharmaceutical ingredient (API) or intermediate for global antibiotic supply chains.
Application
- Pharmaceutical API: Primary use as the active ingredient in oral antibiotic formulations, especially pediatric suspensions and syrups.
- Veterinary Medicine: Manufacture of antibiotic treatments for bacterial infections in livestock and companion animals.
- Research & Development: Used as a reference standard and biochemical tool in microbiological and pharmacological research.
- Generic Drug Production: Sourcing for manufacturers producing cost-effective generic antibiotic medications.
- Intermediate Synthesis: Serves as a precursor in the synthesis of other specialized chloramphenicol derivatives.
Basic Information
| Product Name | Chloramphenicol Palmitate |
| CAS No. | 106322-62-7 |
| Molecular Formula | C27H42Cl2N2O6 |
| Molecular Weight | 561.54 g/mol |
| Synonyms | Chloramphenicol Palmitate Ester; Chloramphenicol Palmitic Acid Ester; D-(-)-Three-2,2-Dichloro-N-[β-hydroxy-α-(hydroxymethyl)-p-nitrophenethyl]acetamide α-Palmitate; Chloramphenicol Palmitate (USP); Chloromycetin Palmitate; Levomicetina Palmitato; Cloranfenicol Palmitato |
| EINECS | Contact for details |
Quality Control
Our Chloramphenicol Palmitate is manufactured and tested to meet stringent pharmacopeial standards, including USP and EP monographs. Each batch undergoes comprehensive analytical testing for identity, purity, and impurity profiles. A Certificate of Analysis (COA) documenting results for assay, related substances, residual solvents, and microbiological quality is provided to ensure full traceability and compliance with cGMP guidelines for pharmaceutical ingredients.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. The container should be kept tightly sealed after each use.
Specification
| Item | Specification |
|---|---|
| Appearance | White to yellowish-white, fine crystalline powder |
| Identification (IR) | Conforms |
| Identification (HPLC) | Conforms |
| Assay (HPLC) | 98.0% - 102.0% (on dried basis) |
| Loss on Drying | ≤ 1.0% |
| Related Substances (HPLC) | Individual impurity: ≤ 0.5% Total impurities: ≤ 2.0% |
| Residual Solvents (GC) | Complies with ICH Q3C |
| Heavy Metals | ≤ 20 ppm |
| Microbial Limits | Complies with USP <61> and <62> |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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