[4-(1h-1,3-benzodiazol-1-ylmethyl)phenyl]methanamine CAS 953727-38-3

Purity 97%+In StockPharmaceutical Standards
CAS No.953727-38-3
Molecular FormulaC15H15N3
Molecular Weight237.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[4-(1h-1,3-benzodiazol-1-ylmethyl)phenyl]methanamine CAS 953727-38-3 chemical structure

Description

The occurrence of [4-(1h-1,3-benzodiazol-1-ylmethyl)phenyl]methanamine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

[4-(1h-1,3-benzodiazol-1-ylmethyl)phenyl]methanamine (CAS 953727-38-3) is a high-purity analytical reference standard with the molecular formula C15H15N3 and a molecular weight of 237.30 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, [4-(1h-1,3-benzodiazol-1-ylmethyl)phenyl]methanamine is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 237.30 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC15H15N3
Molecular Weight237.30 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms3

Related h Standards

Recommended Standards

Why CATO?