N-methyl-1-(1-phenyl-1H-imidazol-2-yl)methanamine CAS 1034566-07-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1034566-07-8
Molecular FormulaC11H13N3
Molecular Weight187.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-methyl-1-(1-phenyl-1H-imidazol-2-yl)methanamine CAS 1034566-07-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 187.24 g/mol gives N-methyl-1-(1-phenyl-1H-imidazol-2-yl)methanamine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

N-methyl-1-(1-phenyl-1H-imidazol-2-yl)methanamine (CAS 1034566-07-8) is a high-purity analytical reference standard with the molecular formula C11H13N3 and a molecular weight of 187.24 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, N-methyl-1-(1-phenyl-1H-imidazol-2-yl)methanamine is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 187.24 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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-methyl-1-(1-phenyl-1H-imidazol-2-yl)methanamine 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 FormulaC11H13N3
Molecular Weight187.24 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms3

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