N-(tert-Butyl)-4-(methylthio)-1,3,5-triazin-2-amine CAS 109202-19-9

Purity 97%+In StockPharmaceutical Standards
CAS No.109202-19-9
Molecular FormulaC8H14N4S
Molecular Weight198.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(tert-Butyl)-4-(methylthio)-1,3,5-triazin-2-amine CAS 109202-19-9 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 N-(tert-Butyl)-4-(methylthio)-1,3,5-triazin-2-amine.

CATO supplies N-(tert-Butyl)-4-(methylthio)-1,3,5-triazin-2-amine (CAS 109202-19-9), a certified reference material (molecular formula C8H14N4S, MW 198.29 g/mol) for analytical method development and quality control.

N-(tert-Butyl)-4-(methylthio)-1,3,5-triazin-2-amine (C8H14N4S) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality. Its physicochemical properties are representative of its class; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), N-(tert-Butyl)-4-(methylthio)-1,3,5-triazin-2-amine 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 FormulaC8H14N4S
Molecular Weight198.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms4
Sulfur Atoms1

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