3-(tert-Butyl)-6-methylpyrimidine-2,4(1H,3H)-dione CAS 6589-37-3

Purity 97%+In StockPharmaceutical Standards
CAS No.6589-37-3
Molecular FormulaC16H25NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(tert-Butyl)-6-methylpyrimidine-2,4(1H,3H)-dione CAS 6589-37-3 chemical structure

Description

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.

CATO supplies 3-(tert-Butyl)-6-methylpyrimidine-2,4(1H,3H)-dione (CAS 6589-37-3), a certified reference material (molecular formula C16H25NOC6H8O7, MW 439.50 g/mol) for analytical method development and quality control.

3-(tert-Butyl)-6-methylpyrimidine-2,4(1H,3H)-dione (C16H25NOC6H8O7) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; 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.

CATO manufactures 3-(tert-Butyl)-6-methylpyrimidine-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 FormulaC16H25NO C6H8O7
Molecular Weight439.50 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms1

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