2-((1-(m-Tolyl)pyrrolidin-3-yl)oxy)ethanamine CAS 1707571-01-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1707571-01-4
Molecular FormulaC13H20N2O
Molecular Weight220.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((1-(m-Tolyl)pyrrolidin-3-yl)oxy)ethanamine CAS 1707571-01-4 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 2-((1-(m-Tolyl)pyrrolidin-3-yl)oxy)ethanamine.

2-((1-(m-Tolyl)pyrrolidin-3-yl)oxy)ethanamine (CAS 1707571-01-4) is a high-purity analytical reference standard with the molecular formula C13H20N2O and a molecular weight of 220.31 g/mol.

The molecular framework of 2-((1-(m-Tolyl)pyrrolidin-3-yl)oxy)ethanamine (C13H20N2O) 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.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 2-((1-(m-Tolyl)pyrrolidin-3-yl)oxy)ethanamine 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 FormulaC13H20N2O
Molecular Weight220.31 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Nitrogen Atoms2

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