N-(tert-Butyl)-3-phenyl-1-propanamine CAS 71193-45-8

Purity 97%+In StockPharmaceutical Standards
CAS No.71193-45-8
Molecular FormulaC13H21N
Molecular Weight191.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(tert-Butyl)-3-phenyl-1-propanamine CAS 71193-45-8 chemical structure

Description

The occurrence of N-(tert-Butyl)-3-phenyl-1-propanamine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

N-(tert-Butyl)-3-phenyl-1-propanamine (CAS 71193-45-8) is a high-purity analytical reference standard with the molecular formula C13H21N and a molecular weight of 191.31 g/mol.

Structurally, N-(tert-Butyl)-3-phenyl-1-propanamine (C13H21N) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. 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 191.31 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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-(tert-Butyl)-3-phenyl-1-propanamine 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 FormulaC13H21N
Molecular Weight191.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1977
Nitrogen Atoms1

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