Ethyl 3-(4-(aminomethyl)phenyl)propanoate hydrochloride CAS 61630-10-2

Purity 97%+In StockPharmaceutical Standards
CAS No.61630-10-2
Molecular FormulaC12H17NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 3-(4-(aminomethyl)phenyl)propanoate hydrochloride CAS 61630-10-2 chemical structure

Description

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

Ethyl 3-(4-(aminomethyl)phenyl)propanoate hydrochloride (CAS 61630-10-2) is a high-purity analytical reference standard with the molecular formula C12H17NO2HCl and a molecular weight of 243.73 g/mol.

Structurally, Ethyl 3-(4-(aminomethyl)phenyl)propanoate hydrochloride (C12H17NO2HCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 243.73 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures Ethyl 3-(4-(aminomethyl)phenyl)propanoate hydrochloride 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 FormulaC12H17NO2 HCl
Molecular Weight243.73 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Halogen ContentCl-containing
Nitrogen Atoms1

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