N-((5,6,7,8-Tetrahydroimidazo[1,2-a]pyrazin-2-yl)methyl)cyclobutanecarboxamide CAS 1422136-10-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1422136-10-4
Molecular FormulaC12H18N4O
Molecular Weight234.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-((5,6,7,8-Tetrahydroimidazo[1,2-a]pyrazin-2-yl)methyl)cyclobutanecarboxamide CAS 1422136-10-4 chemical structure

Description

The molecular framework of N-((5,6,7,8-Tetrahydroimidazo[1,2-a]pyrazin-2-yl)methyl)cyclobutanecarboxamide (C12H18N4O) is characterized by a nitrogen-containing heterocyclic scaffold, 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

N-((5,6,7,8-Tetrahydroimidazo[1,2-a]pyrazin-2-yl)methyl)cyclobutanecarboxamide (CAS 1422136-10-4), molecular formula C12H18N4O and molecular weight 234.30 g/mol, is a CATO reference standard with documented purity and traceability.

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), N-((5,6,7,8-Tetrahydroimidazo[1,2-a]pyrazin-2-yl)methyl)cyclobutanecarboxamide 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 FormulaC12H18N4O
Molecular Weight234.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms4

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