Description

Unii-P9Vxv1408Y is a high-purity organic compound identified by CAS NO 866021-48-9, widely utilized as a critical intermediate in pharmaceutical synthesis and advanced materials development. Its structural precision and batch-to-batch consistency make it essential for applications demanding strict regulatory compliance and reproducible performance. This compound serves key roles in the manufacture of oncology therapeutics, kinase inhibitors, and functionalized heterocyclic scaffolds — particularly for R&D laboratories and API manufacturers operating under cGMP conditions.

Application

• Pharmaceutical active ingredient (API) synthesis, especially for targeted cancer therapies
• Building block in medicinal chemistry for structure–activity relationship (SAR) studies
• Intermediate in the production of protease and tyrosine kinase inhibitors
• Research reagent for developing novel fluorinated or nitrogen-containing heterocycles
• Custom synthesis partner for contract development and manufacturing organizations (CDMOs)
• Material science applications including organic semiconductors and emissive layer components
• Reference standard in analytical method development and validation (HPLC, LC-MS)
• Process optimization studies requiring high-chemical-integrity intermediates

Basic Information

Product Name	Unii-P9Vxv1408Y
CAS No.	866021-48-9
Molecular Formula	C15H12F3N3O2
Molecular Weight	339.27 g/mol
Synonyms	UNII-P9VXV1408Y; P9VXV1408Y; 3-(Trifluoromethyl)-N-(4-(4-methylpiperazin-1-yl)phenyl)benzamide; TFMP-MPP; N-(4-(4-Methylpiperazin-1-yl)phenyl)-3-(trifluoromethyl)benzamide; CAS-866021-48-9; MFCD17157923; Benzamide, 3-(trifluoromethyl)-N-[4-(4-methyl-1-piperazinyl)phenyl]-
EINECS	Not listed (not subject to EINECS notification)

Quality Control

Our products undergo rigorous quality testing to ensure compliance with industry standards. Certificates of Analysis (COA) are available upon request. All batches conform to cGMP-aligned quality systems, with full traceability from raw material sourcing through crystallization, drying, and packaging. Testing includes identity confirmation (IR, NMR, MS), assay (HPLC), residual solvent analysis (GC), and heavy metals screening (ICP-MS). We support compliance with USP, EP, and ICH Q3 guidelines.

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 the container and use desiccant-equipped secondary packaging for long-term storage.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 99.0%
Related Substances (HPLC)	Each impurity ≤ 0.3%; Total impurities ≤ 1.0%
Residual Solvents (GC)	Meets ICH Q3C Class 3 limits
Water (Karl Fischer)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm

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