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4'-Deoxymycaminosyltylonolide CAS NO 80240-61-5


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CAS No.:80240-61-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

4'-Deoxymycaminosyltylonolide is a key chemical intermediate in the synthesis of advanced macrolide antibiotics. This compound matters for its critical role in the research and development of novel antimicrobial agents, particularly in addressing antibiotic resistance. Pharmaceutical R&D laboratories and fine chemical manufacturers specializing in active pharmaceutical ingredients (APIs) are the primary users of this high-value intermediate.

Application

  • Pharmaceutical Intermediate: A crucial building block in the synthesis of Tylosin and related 16-membered macrolide antibiotics.
  • Antimicrobial Research: Used in the development and study of new antibiotic compounds to combat resistant bacterial strains.
  • Veterinary Medicine Development: Serves as a precursor in the manufacture of antibiotics for animal health applications.
  • Biochemical Research: Employed in studies investigating the structure-activity relationships (SAR) of macrolide compounds.
  • Process Chemistry: Utilized in scaling up and optimizing synthetic routes for complex antibiotic molecules in pilot and commercial production.
  • Reference Standard: Acts as a high-purity analytical standard for quality control and regulatory testing in pharmaceutical manufacturing.

Basic Information

Product Name 4'-Deoxymycaminosyltylonolide
CAS No. 80240-61-5
Molecular Formula C41H71NO14
Molecular Weight 801.99 g/mol
Synonyms 4'-Deoxy-5-O-mycaminosyltylonolide; 4'-Deoxymycaminosyltylonolide; Tylosin intermediate; 16-Membered macrolide intermediate; Antibiotic synthesis intermediate; 4'-Deoxy-5-O-(3,6-dideoxy-3-dimethylamino-β-D-glucopyranosyl)tylonolide; 4'-Deoxy-5-O-(3,6-dideoxy-3-dimethylamino-β-D-glucopyranosyl)tylonolide (Tylosin precursor)
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Quality Control

Our 4'-Deoxymycaminosyltylonolide is produced under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for pharmaceutical R&D. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to cGMP (current Good Manufacturing Practice) standards where applicable to support our clients' regulatory requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive) and should be handled under an inert atmosphere or in a dry environment to maintain stability.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to structure
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 95.0%
Water Content (KF) ≤ 2.0%
Residue on Ignition ≤ 0.5%
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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