N-(5-Carboxypentyl)-3-hydroxy-N-methylaniline CAS 887353-92-6

Purity 97%+In StockPharmaceutical Standards
CAS No.887353-92-6
Molecular FormulaC13H19NO3
Molecular Weight237.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(5-Carboxypentyl)-3-hydroxy-N-methylaniline CAS 887353-92-6 chemical structure

Description

N-(5-Carboxypentyl)-3-hydroxy-N-methylaniline (CAS 887353-92-6) is a high-purity analytical reference standard with the molecular formula C13H19NO3 and a molecular weight of 237.29 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, N-(5-Carboxypentyl)-3-hydroxy-N-methylaniline is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 237.29 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.

CATO manufactures N-(5-Carboxypentyl)-3-hydroxy-N-methylaniline under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC13H19NO3
Molecular Weight237.29 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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