6-((4-Chlorobenzyl)amino)pyrimidine-2,4(1H,3H)-dione CAS 21333-15-3

Purity 97%+In StockPharmaceutical Standards
CAS No.21333-15-3
Molecular FormulaC11H10ClN3O2
Molecular Weight251.67 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-((4-Chlorobenzyl)amino)pyrimidine-2,4(1H,3H)-dione CAS 21333-15-3 chemical structure

Description

The molecular framework of 6-((4-Chlorobenzyl)amino)pyrimidine-2,4(1H,3H)-dione (C11H10ClN3O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies 6-((4-Chlorobenzyl)amino)pyrimidine-2,4(1H,3H)-dione (CAS 21333-15-3), a certified reference material (molecular formula C11H10ClN3O2, MW 251.67 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 6-((4-Chlorobenzyl)amino)pyrimidine-2,4(1H,3H)-dione under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC11H10ClN3O2
Molecular Weight251.67 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963
Halogen ContentCl-containing
Nitrogen Atoms3

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