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Pirlimycin CAS NO 79548-73-5


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CAS No.:79548-73-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Pirlimycin is a lincosamide antibiotic specifically developed for veterinary use, with the CAS registry number 79548-73-5. This compound is valued for its targeted efficacy against Gram-positive bacteria, including strains resistant to other antibiotic classes. It is a critical active pharmaceutical ingredient (API) for manufacturers developing intramammary infusions and other therapeutic formulations for the global animal health industry, addressing mastitis and other bacterial infections in livestock.

Application

Pirlimycin is primarily utilized in veterinary pharmaceuticals. Its key applications include:

  • Veterinary Antibiotic API: As the active ingredient in intramammary infusions for the treatment of bovine mastitis, particularly during the dry period.
  • Livestock Health Management: Formulated into products for treating infections caused by susceptible Gram-positive pathogens in dairy cattle.
  • Pharmaceutical R&D: Used in research and development of new antibiotic formulations and combination therapies for veterinary medicine.
  • Generic Drug Manufacturing: Sourced by manufacturers producing generic versions of approved pirlimycin-based veterinary drugs.

Basic Information

Product Name Pirlimycin
CAS No. 79548-73-5
Molecular Formula C17H31ClN2O5S
Molecular Weight 410.96 g/mol
Synonyms Pirlimycin Hydrochloride; U-57930E; Pirlimycin HCl; (2S,4R)-N-[(1S,2S)-2-Chloro-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methylsulfanyloxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide; Pirlimycin (base); Lincosamide antibiotic U-57930E
EINECS Contact for details

Quality Control

Our Pirlimycin is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical use. We provide full traceability and Certificates of Analysis (COA) are available for all shipments, detailing purity, identity, and impurity profiles. Our quality commitment aligns with cGMP principles for active 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. For long-term storage, consider desiccated conditions.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) ≤ 5.0%
Residue on Ignition ≤ 0.5%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Individual impurity ≤ 1.0%; Total impurities ≤ 3.0%
Microbial Limits Meets standard requirements for non-sterile API

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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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.