2-(2-(Trifluoromethyl)-10H-phenothiazin-10-yl)acetic acid CAS 1179362-81-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1179362-81-2
Molecular FormulaC15H10F3NO2S
Molecular Weight325.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(2-(Trifluoromethyl)-10H-phenothiazin-10-yl)acetic acid CAS 1179362-81-2 chemical structure

Description

2-(2-(Trifluoromethyl)-10H-phenothiazin-10-yl)acetic acid (C15H10F3NO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies 2-(2-(Trifluoromethyl)-10H-phenothiazin-10-yl)acetic acid (CAS 1179362-81-2), a certified reference material (molecular formula C15H10F3NO2S, MW 325.31 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 2-(2-(Trifluoromethyl)-10H-phenothiazin-10-yl)acetic acid 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 FormulaC15H10F3NO2S
Molecular Weight325.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

Related Trifluoromethyl Standards

Recommended Standards

Why CATO?