Benzenesulfonic acid (1S,2R)-2-fluorocyclopropanamine CAS 2387566-71-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2387566-71-2
Molecular FormulaC6H5O3S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Benzenesulfonic acid (1S,2R)-2-fluorocyclopropanamine CAS 2387566-71-2 chemical structure

Description

CATO manufactures Benzenesulfonic acid (1S,2R)-2-fluorocyclopropanamine 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.

CATO supplies Benzenesulfonic acid (1S,2R)-2-fluorocyclopropanamine (CAS 2387566-71-2), a certified reference material (molecular formula C6H5O3SC3H6FN, MW 232.25 g/mol) for analytical method development and quality control.

Based on its molecular formula C6H5O3SC3H6FN, Benzenesulfonic acid (1S,2R)-2-fluorocyclopropanamine contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 232.25 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC6H5O3S C3H6FN
Molecular Weight232.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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