6-Amino-1-butyl-5-morpholinopyrimidine-2,4(1H,3H)-dione CAS 790232-09-6

Purity 97%+In StockPharmaceutical Standards
CAS No.790232-09-6
Molecular FormulaC12H20N4O3
Molecular Weight268.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Amino-1-butyl-5-morpholinopyrimidine-2,4(1H,3H)-dione CAS 790232-09-6 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 6-Amino-1-butyl-5-morpholinopyrimidine-2,4(1H,3H)-dione (CAS 790232-09-6), a certified reference material (molecular formula C12H20N4O3, MW 268.31 g/mol) for analytical method development and quality control.

The molecular framework of 6-Amino-1-butyl-5-morpholinopyrimidine-2,4(1H,3H)-dione (C12H20N4O3) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures 6-Amino-1-butyl-5-morpholinopyrimidine-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 FormulaC12H20N4O3
Molecular Weight268.31 g/mol
AppearanceOff-white to pale yellow crystalline powder
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Nitrogen Atoms4

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