share

Chloramphenicol Palmitate CAS NO 106322-62-7


Unit Price:

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.

Complete Your RFQ

0/ 2000

Why choose US

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.