(S)-1-(4-ethoxyphenyl)-2-methylpropan-1-amine CAS 1213476-03-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1213476-03-9
Molecular FormulaC12H19NO
Molecular Weight193.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-1-(4-ethoxyphenyl)-2-methylpropan-1-amine CAS 1213476-03-9 chemical structure

Description

The occurrence of (S)-1-(4-ethoxyphenyl)-2-methylpropan-1-amine is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

(S)-1-(4-ethoxyphenyl)-2-methylpropan-1-amine (CAS 1213476-03-9) is a high-purity analytical reference standard with the molecular formula C12H19NO and a molecular weight of 193.29 g/mol.

The molecular framework of (S)-1-(4-ethoxyphenyl)-2-methylpropan-1-amine (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. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 (S)-1-(4-ethoxyphenyl)-2-methylpropan-1-amine 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 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.)1990
Nitrogen Atoms1

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