share

Tak-041 CAS NO 1929519-13-0


Unit Price:

CAS No.:1929519-13-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Tak-041 CAS NO 1929519-13-0 is a high-purity, advanced pharmaceutical intermediate designed for the synthesis of novel active pharmaceutical ingredients (APIs). This compound is critical for research and development in medicinal chemistry, offering a reliable building block for complex molecular architectures. It is primarily utilized by pharmaceutical companies, biotechnology firms, and contract research organizations (CROs) engaged in the development of new therapeutic agents.

Application

  • Pharmaceutical Intermediate: A key precursor in the multi-step synthesis of investigational new drugs and active pharmaceutical ingredients (APIs).
  • Medicinal Chemistry Research: Serves as a versatile scaffold for structure-activity relationship (SAR) studies and lead optimization in drug discovery programs.
  • Process Development: Used in the scale-up and optimization of synthetic routes for new chemical entities (NCEs) in pilot and commercial manufacturing.
  • Bioconjugation: Potential utility in the development of antibody-drug conjugates (ADCs) and other targeted therapeutic modalities.
  • Academic Research: Employed in university and institutional labs for fundamental research in organic synthesis and chemical biology.

Basic Information

Product Name Tak-041
CAS No. 1929519-13-0
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Tak041; TAK 041; 1929519-13-0; UNII-0C7Y1F2Q3N; 0C7Y1F2Q3N; CHEMBL3186660; BDBM50157857; AKOS009158950; (S)-2-((S)-2-(4-(4-(2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)piperazin-1-yl)phenyl)chroman-7-yl)acetic acid (non-preferred IUPAC); Potential proprietary research code names.
EINECS Contact for details

Quality Control

Our Tak-041 is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all critical quality attributes. Production adheres to cGMP guidelines where applicable, ensuring suitability for use in regulated pharmaceutical development.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated place at a controlled room temperature (typically 15-25°C). This material is hygroscopic (moisture-sensitive). For long-term storage, consider desiccant or inert atmosphere conditions to maintain stability.

Specification

Item Specification
Appearance White to off-white solid
Identification (HPLC/MS) Conforms
Purity (HPLC) ≥ 98.0%
Related Substances (HPLC) Individual impurity ≤ 0.5% Total impurities ≤ 2.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

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.