(1R,4R)-4-(2-fluoro-benzylamino)-cyclohexanol CAS 1261232-01-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1261232-01-2
Molecular FormulaC13H18FNO
Molecular Weight223.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1R,4R)-4-(2-fluoro-benzylamino)-cyclohexanol CAS 1261232-01-2 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution, (1R,4R)-4-(2-fluoro-benzylamino)-cyclohexanol is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 223.29 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies (1R,4R)-4-(2-fluoro-benzylamino)-cyclohexanol (CAS 1261232-01-2), a certified reference material (molecular formula C13H18FNO, MW 223.29 g/mol) for analytical method development and quality control.

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 (1R,4R)-4-(2-fluoro-benzylamino)-cyclohexanol 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 FormulaC13H18FNO
Molecular Weight223.29 g/mol
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
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1

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