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Mpi-0479605 CAS NO 1246529-32-7


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CAS No.:1246529-32-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Mpi-0479605 is a high-purity, specialty organic compound widely employed as a key intermediate in the synthesis of next-generation pharmaceuticals and agrochemical actives. Its structural precision and functional group compatibility deliver exceptional batch-to-batch consistency—critical for regulatory submissions and scalable cGMP manufacturing. This compound is essential for research and production teams in contract development and manufacturing organizations (CDMOs), innovator pharma R&D labs, and fine chemical manufacturers targeting oncology, antiviral, and crop protection pipelines. Mpi-0479605 CAS NO 1246529-32-7 is supplied under strict quality governance to ensure traceability and compliance across global supply chains.

Application

  • Pharmaceutical intermediate for kinase inhibitor APIs (e.g., analogues of BTK, JAK, and CDK inhibitors)
  • Synthetic building block in the preparation of proteolysis-targeting chimeras (PROTACs) and molecular glues
  • Key precursor in the manufacture of novel herbicidal and fungicidal agents with improved environmental profiles
  • Research reagent for structure–activity relationship (SAR) studies in medicinal chemistry optimization campaigns
  • Custom synthesis substrate for isotopically labeled drug metabolites (e.g., 13C- or 2H-labeled variants)
  • Component in high-performance liquid chromatography (HPLC) reference standards for bioanalytical method validation

Basic Information

Product Name Mpi-0479605
CAS No. 1246529-32-7
Molecular Formula C18H16F3N3O2
Molecular Weight 379.34 g/mol
Synonyms MP-0479605; MPI0479605; 4-(3-(Trifluoromethyl)-1H-pyrazol-1-yl)-N-(pyridin-3-yl)benzamide; N-(3-Pyridyl)-4-[3-(trifluoromethyl)-1H-pyrazol-1-yl]benzamide; 4-[(3-Trifluoromethyl)-1H-pyrazol-1-yl]-N-(pyridin-3-yl)benzamide; MPI-0479605; 1246529-32-7 (CAS); PYR-0479605; TFM-PyBz-Py
EINECS Not listed (not notified under EINECS)

Quality Control

Our products undergo rigorous quality testing to ensure compliance with industry standards. Certificates of Analysis (COA) are available upon request. All batches are tested per ICH Q2(R2) guidelines for identity, assay, residual solvents, heavy metals, and related substances. Specifications meet or exceed ACS Reagent Grade and EP 11.0 requirements for pharmaceutical intermediates. Full traceability from raw materials to final packaging is maintained under ISO 9001:2015 and ISO 14001:2015 certified systems.

Storage

Preserve in a tightly closed container, protected from light. Store at 15–25°C in a dry, well-ventilated area. Due to its hygroscopic nature, minimize exposure to ambient humidity during handling. Avoid repeated opening of containers and use desiccant-equipped secondary packaging for long-term stability.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Assay (HPLC) ≥ 99.5%
Related Substances (HPLC) ≤ 0.3% total impurities
Residual Solvents (GC) Meets ICH Q3C Class 3 limits
Water (KF) ≤ 0.5%
Heavy Metals ≤ 10 ppm
Residue on Ignition ≤ 0.1%

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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