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Mepartricin Sodium Lauryl Sulfate CAS NO 59392-70-0


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CAS No.:59392-70-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Mepartricin Sodium Lauryl Sulfate is a specialized pharmaceutical-grade salt complex of the polyene macrolide antibiotic mepartricin. This compound is valued for its enhanced solubility and bioavailability compared to the base molecule, making it a critical intermediate in advanced therapeutic formulations. It is primarily required by manufacturers in the pharmaceutical and biotechnology sectors for the development of antifungal and antiprotozoal medications.

Application

  • Primary active pharmaceutical ingredient (API) in antifungal drug formulations.
  • Key intermediate in the synthesis of topical and systemic polyene antibiotic treatments.
  • Research and development of novel antiprotozoal therapeutic agents.
  • Component in veterinary pharmaceutical products for fungal infections.
  • Reference standard in analytical laboratories for quality control and method development.
  • Starting material for the preparation of other mepartricin derivatives and prodrugs.

Basic Information

Product Name Mepartricin Sodium Lauryl Sulfate
CAS No. 59392-70-0
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Mepartricin SLS; Mepartricin Sodium Dodecyl Sulfate; Mepartricin Laurylsulfate Sodium Salt; Sodium Mepartricin Lauryl Sulfate; Mepartricin Sodium Salt with Lauryl Sulfate; Antibiotic A-28695A SLS Complex; (8E,10E,12E,14E,16E,18E,20E,22E,24E,26E,28E,30E,32E,34E,36E,38E)-36-[(3-Amino-3,6-dideoxy-β-D-mannopyranosyl)oxy]-1,3,5,7,9,11,13,15,17,19,21,23,25,27,29,31,33,35,37-nonadecahydroxy-38-methyl-2-oxo-4,39-dioxabicyclo[33.3.1]nonatriaconta-8,10,12,14,16,18,20,22,24,26,28,30,32,34,36-pentaene-40-carboxylic Acid Compound with Sodium Dodecyl Sulfate
EINECS Contact for details

Quality Control

Our Mepartricin Sodium Lauryl Sulfate is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets stringent pharmaceutical-grade specifications. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance with your quality requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material 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 Yellow to brownish-yellow powder
Identification (IR) Conforms to reference standard
Assay (HPLC) ≥ 95.0% (on anhydrous basis)
Water Content (KF) ≤ 5.0%
Residue on Ignition ≤ 1.0%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Total impurities ≤ 3.0%
Microbial Limits Meets Ph. Eur. requirements

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

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