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Rubidomycin CAS NO 72060-18-5


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CAS No.:72060-18-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Rubidomycin CAS NO 72060-18-5 is an anthracycline glycoside antibiotic compound of significant interest in pharmaceutical research and development. Its primary value lies in its potent biological activity, which makes it a crucial intermediate and reference standard for the synthesis and study of novel chemotherapeutic agents. This product is essential for research institutions, pharmaceutical manufacturers, and biotechnology companies engaged in oncology drug discovery, mechanism of action studies, and analytical method development.

Application

  • Pharmaceutical Intermediate: Serves as a key starting material or precursor in the synthesis of more complex anthracycline-based anticancer drugs.
  • Biochemical Research: Used as a reference standard in studies investigating the mechanism of action of DNA-intercalating agents and topoisomerase II inhibitors.
  • Analytical Standard: Employed in High-Performance Liquid Chromatography (HPLC) and other analytical methods for quality control, method validation, and impurity profiling of related pharmaceutical compounds.
  • Antibiotic Research: Provides a foundational structure for developing new antibiotic agents with modified efficacy and reduced toxicity profiles.
  • Academic & Institutional Research: Utilized in university and institutional labs for fundamental research in medicinal chemistry, pharmacology, and cell biology.

Basic Information

Product Name Rubidomycin
CAS No. 72060-18-5
Molecular Formula C₂₇H₂₉NO₁₀
Molecular Weight 527.52 g/mol
Synonyms Daunorubicin; Daunomycin; Cerubidine; Rubomycin; (8S,10S)-8-Acetyl-10-[(2S,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy-6,8,11-trihydroxy-1-methoxy-9,10-dihydro-7H-tetracene-5,12-dione; 1-Hydroxydaunorubicin; NSC-82151; RP-13057
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Quality Control

Our Rubidomycin is produced and tested under a strict quality management system to ensure batch-to-batch consistency and high purity for research and development purposes. We adhere to relevant industry guidelines for pharmaceutical intermediates. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles via advanced analytical techniques is provided with each batch to support your regulatory and research requirements.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at a controlled room temperature (15-25°C) or as specified on the label or COA. Due to its sensitivity to oxidation and light, the container should only be opened in a controlled environment and material should be used promptly.

Specification

Item Specification
Appearance Orange-red to red crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) ≥ 95.0%
Water Content (KF) ≤ 5.0%
Residue on Ignition ≤ 0.5%
Related Substances (HPLC) Individual impurity ≤ 2.0%; Total impurities ≤ 5.0%

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.

Advanced R&D Expertise

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