4-(3-Amino-2-oxopyridin-1(2h)-yl)-N-methylbutanamide CAS 1343966-14-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1343966-14-2
Molecular FormulaC10H15N3O2
Molecular Weight209.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-Amino-2-oxopyridin-1(2h)-yl)-N-methylbutanamide CAS 1343966-14-2 chemical structure

Description

4-(3-Amino-2-oxopyridin-1(2h)-yl)-N-methylbutanamide (C10H15N3O2) contains an amino-acid-derived structure, an amide 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 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).

4-(3-Amino-2-oxopyridin-1(2h)-yl)-N-methylbutanamide (CAS 1343966-14-2) is a high-purity analytical reference standard with the molecular formula C10H15N3O2 and a molecular weight of 209.25 g/mol.

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), 4-(3-Amino-2-oxopyridin-1(2h)-yl)-N-methylbutanamide 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 FormulaC10H15N3O2
Molecular Weight209.25 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
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.)1991
Nitrogen Atoms3

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