2-Chloro-3-Methylbenzothiazolium Trifluoromethanesulphonate CAS 61765-15-9

Purity 97%+In StockPharmaceutical Standards
CAS No.61765-15-9
Molecular FormulaC8H7ClNS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Chloro-3-Methylbenzothiazolium Trifluoromethanesulphonate CAS 61765-15-9 chemical structure

Description

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.

2-Chloro-3-Methylbenzothiazolium Trifluoromethanesulphonate (CAS 61765-15-9) is a high-purity analytical reference standard with the molecular formula C8H7ClNSCF3O3S and a molecular weight of 333.72 g/mol.

The molecular framework of 2-Chloro-3-Methylbenzothiazolium Trifluoromethanesulphonate (C8H7ClNSCF3O3S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, 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).

CATO manufactures 2-Chloro-3-Methylbenzothiazolium Trifluoromethanesulphonate 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 FormulaC8H7ClNS CF3O3S
Molecular Weight333.72 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Halogen ContentF/Cl-containing
Nitrogen Atoms1
Sulfur Atoms2

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