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Shurimycin B CAS NO 143906-45-0


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CAS No.:143906-45-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Shurimycin B is a specialized macrolide antibiotic compound with significant research and pharmaceutical development potential. This high-purity chemical is critical for advancing studies in antibacterial mechanisms and serves as a key intermediate in the synthesis of novel therapeutic agents. It is primarily utilized by research institutions, pharmaceutical R&D departments, and fine chemical manufacturers focused on developing next-generation antibiotic treatments.

Application

  • Pharmaceutical Research & Development: Serves as a crucial reference standard and active pharmaceutical ingredient (API) intermediate in the development of new macrolide antibiotics.
  • Antibacterial Mechanism Studies: Used in microbiological and biochemical research to investigate bacterial protein synthesis inhibition and resistance pathways.
  • Veterinary Medicine: Employed in the formulation of advanced antibacterial treatments for livestock and companion animals.
  • Fine Chemical Synthesis: Acts as a sophisticated building block for the custom synthesis of complex, structurally related antibiotic analogs.
  • Academic Research: Utilized in university and institutional labs for pharmacological and microbiological educational and discovery projects.

Basic Information

Product Name Shurimycin B
CAS No. 143906-45-0
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Shurimycin B; 143906-45-0; Antibiotic Shurimycin B; Macrolide Shurimycin B; (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-11-[(2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-3,4,10-trihydroxy-13-{[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy}-3,5,8,10,12,14-hexamethyl-1-oxa-6-azacyclopentadecan-15-one
EINECS Contact for details

Quality Control

Shurimycin B is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Our products undergo rigorous quality testing, including advanced chromatographic analysis, to ensure compliance with research and pharmaceutical intermediate standards. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with each batch to support your quality assurance protocols.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). The product is hygroscopic (moisture-sensitive) and should be handled under anhydrous conditions to maintain stability.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 95.0%
Water Content (KF) ≤ 5.0%
Residue on Ignition ≤ 1.0%

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

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.