[2,2'-Binaphthalen]-6-yl trifluoromethanesulfonate CAS 935472-81-4

Purity 97%+In StockPharmaceutical Standards
CAS No.935472-81-4
Molecular FormulaC21H13F3O3S
Molecular Weight402.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[2,2'-Binaphthalen]-6-yl trifluoromethanesulfonate CAS 935472-81-4 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 [2,2'-Binaphthalen]-6-yl trifluoromethanesulfonate.

[2,2'-Binaphthalen]-6-yl trifluoromethanesulfonate (CAS 935472-81-4) is a high-purity analytical reference standard with the molecular formula C21H13F3O3S and a molecular weight of 402.39 g/mol.

The molecular framework of [2,2'-Binaphthalen]-6-yl trifluoromethanesulfonate (C21H13F3O3S) is characterized by a steroid core, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 [2,2'-Binaphthalen]-6-yl trifluoromethanesulfonate 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 FormulaC21H13F3O3S
Molecular Weight402.39 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Sulfur Atoms1

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