2,4,6-Tris((4-fluorobenzyl)thio)-1,3,5-triazine CAS 303091-06-7

Purity 97%+In StockPharmaceutical Standards
CAS No.303091-06-7
Molecular FormulaC24H18F3N3S3
Molecular Weight501.61 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,4,6-Tris((4-fluorobenzyl)thio)-1,3,5-triazine CAS 303091-06-7 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2,4,6-Tris((4-fluorobenzyl)thio)-1,3,5-triazine.

2,4,6-Tris((4-fluorobenzyl)thio)-1,3,5-triazine (CAS 303091-06-7), molecular formula C24H18F3N3S3 and molecular weight 501.61 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 2,4,6-Tris((4-fluorobenzyl)thio)-1,3,5-triazine (C24H18F3N3S3) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), 2,4,6-Tris((4-fluorobenzyl)thio)-1,3,5-triazine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC24H18F3N3S3
Molecular Weight501.61 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms3

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