1-(3-Fluorophenyl)ethylamine CAS 74788-45-7

Purity 97%+In StockPharmaceutical Standards
CAS No.74788-45-7
Molecular FormulaC8H10FN
Molecular Weight139.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3-Fluorophenyl)ethylamine CAS 74788-45-7 chemical structure

Description

The occurrence of 1-(3-Fluorophenyl)ethylamine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

1-(3-Fluorophenyl)ethylamine (CAS 74788-45-7) is a high-purity analytical reference standard with the molecular formula C8H10FN and a molecular weight of 139.17 g/mol.

Structurally, 1-(3-Fluorophenyl)ethylamine (C8H10FN) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine 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 139.17 g/mol, it falls into the low-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 1-(3-Fluorophenyl)ethylamine 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 FormulaC8H10FN
Molecular Weight139.17 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1978
Halogen ContentF-containing
Nitrogen Atoms1

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