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5-Imino-n-(1-Carboethoxypropen-1-Yl)Daunorubicin CAS NO 123618-02-0


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CAS No.:123618-02-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

5-Imino-n-(1-Carboethoxypropen-1-Yl)Daunorubicin is a key synthetic derivative and intermediate in the development of advanced anthracycline-based pharmaceuticals. This compound is of significant value for researchers and manufacturers focused on creating novel chemotherapeutic agents with potentially improved efficacy and reduced side-effect profiles. It is primarily utilized in the pharmaceutical and biotechnology sectors for the research, development, and synthesis of next-generation anticancer drugs.

Application

  • Pharmaceutical Intermediate: Critical building block for the synthesis of novel daunorubicin and doxorubicin analogs.
  • Anticancer Drug Research: Used in R&D to study structure-activity relationships and develop new chemotherapeutic agents targeting various cancers.
  • Biochemical Research: Serves as a tool compound in molecular biology and pharmacology studies to investigate DNA intercalation and topoisomerase II inhibition mechanisms.
  • Preclinical Development: Employed in the formulation and testing stages of new drug candidates prior to clinical trials.
  • Reference Standard: Used as a high-purity analytical standard for quality control and method validation in pharmaceutical manufacturing.

Basic Information

Product Name 5-Imino-n-(1-Carboethoxypropen-1-Yl)Daunorubicin
CAS No. 123618-02-0
Molecular Formula C₃₄H₃₈N₂O₁₂
Molecular Weight 666.67 g/mol
Synonyms 5-Imino-N-(1-carboethoxy-1-propenyl)daunorubicin; Daunorubicin, 5-imino-N-(1-carboethoxy-1-propenyl)-; 5-Imino-daunorubicin derivative; 5-ID; Carboethoxypropenyl Daunorubicin Imine; (1-Carboethoxypropen-1-yl)-5-iminodaunorubicin; 123618-02-0; N-(1-Ethoxycarbonyl-1-propenyl)-5-iminodaunorubicin
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Quality Control

Our 5-Imino-n-(1-Carboethoxypropen-1-Yl)Daunorubicin is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the high standards required for pharmaceutical research and development. Certificates of Analysis (COA) with detailed chromatographic data are provided to guarantee traceability, consistency, and compliance with your specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a desiccated environment to prevent degradation. For long-term storage, consider inert atmosphere conditions.

Specification

Item Specification
Appearance Red to orange-red powder
Identification (HPLC) Conforms
Identification (IR) Conforms
Purity (HPLC) ≥ 95.0%
Water Content (KF) ≤ 5.0%
Residual Solvents (GC) Meets ICH guidelines
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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