Description

n-(1-Carboethoxylpropen-1-Y-2)Daunorubicin is a key synthetic intermediate in the production of advanced anthracycline-based pharmaceuticals. This compound is critical for researchers and manufacturers developing targeted chemotherapeutic agents, offering a pathway to more potent and selective drug derivatives. It is primarily utilized by the pharmaceutical industry for the synthesis and research of novel anti-cancer drugs, particularly in the development of next-generation daunorubicin analogs.

Application

• Pharmaceutical Intermediate: A crucial building block in the synthesis of novel daunorubicin derivatives and other anthracycline chemotherapeutic agents.
• Oncology Research: Used in academic and industrial R&D to study structure-activity relationships (SAR) and develop new anti-cancer compounds with improved efficacy and reduced side effects.
• API Development: Serves as a precursor in the process development and scale-up manufacturing of Active Pharmaceutical Ingredients (APIs) for cancer treatment.
• Bioconjugation Studies: Employed in research focused on creating antibody-drug conjugates (ADCs) or other targeted drug delivery systems.
• Process Chemistry: Utilized by process chemists to optimize synthetic routes for complex anthracycline molecules, aiming for higher yields and purity.

Basic Information

Product Name	n-(1-Carboethoxylpropen-1-Y-2)Daunorubicin
CAS No.	95897-98-6
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Daunorubicin, 13-deoxy-13-[(1-ethoxycarbonyl-1-propen-2-yl)amino]-; 13-[(1-Ethoxycarbonyl-1-propen-2-yl)amino]-13-deoxydaunorubicin; Daunorubicin N-(1-carboethoxylpropen-1-yl-2) derivative; 95897-98-6; N-(1-Carboethoxy-1-propen-2-yl)daunorubicin; Daunorubicin carboethoxypropenyl derivative
EINECS	Contact for details

Quality Control

Our n-(1-Carboethoxylpropen-1-Y-2)Daunorubicin is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity, suitable for pharmaceutical research and development. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to relevant industry standards and can support development projects requiring material for pre-clinical and clinical studies.

Storage

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

Specification

Item	Specification
Appearance	Red to orange-red powder
Identification (HPLC)	Conforms
Identification (IR)	Conforms
Assay (HPLC)	≥ 95.0%
Related Substances (HPLC)	Total impurities ≤ 5.0%
Water Content (KF)	≤ 5.0%
Residual Solvents (GC)	Complies with ICH guidelines

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