Acridine-9(10H)-thione 2,2,2-trifluoroacetate CAS 88147-34-6

Purity 97%+In StockPharmaceutical Standards
CAS No.88147-34-6
Molecular FormulaC13H9NS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Acridine-9(10H)-thione 2,2,2-trifluoroacetate CAS 88147-34-6 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 Acridine-9(10H)-thione 2,2,2-trifluoroacetate.

Acridine-9(10H)-thione 2,2,2-trifluoroacetate (CAS 88147-34-6) is a high-purity analytical reference standard with the molecular formula C13H9NSC2HF3O2 and a molecular weight of 325.30 g/mol.

The molecular framework of Acridine-9(10H)-thione 2,2,2-trifluoroacetate (C13H9NSC2HF3O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures Acridine-9(10H)-thione 2,2,2-trifluoroacetate 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 FormulaC13H9NS C2HF3O2
Molecular Weight325.30 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.)1982
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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