(S)-2-Fluoro-2-phenylethan-1-amine CAS 127708-39-8

Purity 97%+In StockPharmaceutical Standards
CAS No.127708-39-8
Molecular FormulaC8H10FN
Molecular Weight139.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-Fluoro-2-phenylethan-1-amine CAS 127708-39-8 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 (S)-2-Fluoro-2-phenylethan-1-amine.

CATO supplies (S)-2-Fluoro-2-phenylethan-1-amine (CAS 127708-39-8), a certified reference material (molecular formula C8H10FN, MW 139.17 g/mol) for analytical method development and quality control.

(S)-2-Fluoro-2-phenylethan-1-amine (C8H10FN) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 (S)-2-Fluoro-2-phenylethan-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 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.)1993
Halogen ContentF-containing
Nitrogen Atoms1

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