N4-(o-Tolyl)pyrimidine-2,4,6-triamine CAS 6303-45-3

Purity 97%+In StockPharmaceutical Standards
CAS No.6303-45-3
Molecular FormulaC12H12N2O3S
Molecular Weight264.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N4-(o-Tolyl)pyrimidine-2,4,6-triamine CAS 6303-45-3 chemical structure

Description

The occurrence of N4-(o-Tolyl)pyrimidine-2,4,6-triamine is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

N4-(o-Tolyl)pyrimidine-2,4,6-triamine (CAS 6303-45-3), molecular formula C12H12N2O3S and molecular weight 264.30 g/mol, is a CATO reference standard with documented purity and traceability.

N4-(o-Tolyl)pyrimidine-2,4,6-triamine (C12H12N2O3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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), N4-(o-Tolyl)pyrimidine-2,4,6-triamine 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 FormulaC12H12N2O3S
Molecular Weight264.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms2
Sulfur Atoms1

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