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L-(+)-Chloramphenicol Palmitate CAS NO 39909-95-0
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CAS No.:39909-95-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
L-(+)-Chloramphenicol Palmitate is a high-purity ester derivative of the broad-spectrum antibiotic chloramphenicol. This compound is specifically valued for its enhanced stability and modified solubility profile compared to the base antibiotic, making it a critical intermediate in advanced pharmaceutical synthesis. It is primarily required by manufacturers in the pharmaceutical and fine chemical industries for the development of specialized antibiotic formulations and as a key reference standard in quality control laboratories.
Application
- Pharmaceutical Intermediate: Key starting material for the synthesis of specialized chloramphenicol prodrugs and formulations.
- Reference Standard: Used in analytical laboratories for method development, validation, and quality control testing of antibiotic products.
- Antibiotic Research: Serves as a crucial compound in microbiological and pharmacological research for studying antibiotic efficacy and resistance.
- Veterinary Medicine: Employed in the development of long-acting antibiotic treatments for veterinary applications.
- Fine Chemical Synthesis: Acts as a building block for creating more complex molecules with targeted therapeutic properties.
Basic Information
| Product Name | L-(+)-Chloramphenicol Palmitate |
| CAS No. | 39909-95-0 |
| Molecular Formula | C27H42Cl2N2O6 |
| Molecular Weight | 561.54 g/mol |
| Synonyms | Chloramphenicol Palmitate; Chloramphenicol Palmitate Ester; D-(-)-Three-2,2-Dichloro-N-[β-hydroxy-α-(hydroxymethyl)-p-nitrophenethyl]acetamide Palmitate; L-Chloramphenicol Palmitate; (+)-Chloramphenicol Palmitate; Chloramphenicol Palmitic Acid Ester; Antibiotic Palmitate Ester; CP Palmitate |
| EINECS | Contact for details |
Quality Control
Our L-(+)-Chloramphenicol Palmitate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling, to ensure it meets stringent specifications suitable for pharmaceutical R&D and manufacturing. Certificates of Analysis (COA) documenting purity, physical characteristics, and test results are provided with every shipment and are available upon request.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and light-sensitive; containers must be kept tightly sealed and away from direct light to maintain stability and purity.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Assay (HPLC) | ≥ 98.0% |
| Specific Rotation | +18.5° to +21.5° (c=5 in ethanol) |
| Loss on Drying | ≤ 1.0% |
| 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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Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






