3-((1-(O-tolyl)ethyl)amino)propan-1-ol CAS 1038255-85-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1038255-85-4
Molecular FormulaC12H19NO
Molecular Weight193.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((1-(O-tolyl)ethyl)amino)propan-1-ol CAS 1038255-85-4 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3-((1-(O-tolyl)ethyl)amino)propan-1-ol.

CATO supplies 3-((1-(O-tolyl)ethyl)amino)propan-1-ol (CAS 1038255-85-4), a certified reference material (molecular formula C12H19NO, MW 193.29 g/mol) for analytical method development and quality control.

The molecular framework of 3-((1-(O-tolyl)ethyl)amino)propan-1-ol (C12H19NO) 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 its high hydrophobicity (logP), 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.

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 FormulaC12H19NO
Molecular Weight193.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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