1-(3-Phenylpropyl)-2,3-dihydro-1H-1,3-benzodiazol-2-imine CAS 1178833-41-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1178833-41-4
Molecular FormulaC16H17N3
Molecular Weight251.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3-Phenylpropyl)-2,3-dihydro-1H-1,3-benzodiazol-2-imine CAS 1178833-41-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 251.33 g/mol gives 1-(3-Phenylpropyl)-2,3-dihydro-1H-1,3-benzodiazol-2-imine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 1-(3-Phenylpropyl)-2,3-dihydro-1H-1,3-benzodiazol-2-imine (CAS 1178833-41-4), a certified reference material (molecular formula C16H17N3, MW 251.33 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, 1-(3-Phenylpropyl)-2,3-dihydro-1H-1,3-benzodiazol-2-imine is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 251.33 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.

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 FormulaC16H17N3
Molecular Weight251.33 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.)1989
Nitrogen Atoms3

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