(4-(Trifluoromethoxy)phenyl)methanethiol CAS 175278-03-2

Purity 97%+In StockPharmaceutical Standards
CAS No.175278-03-2
Molecular FormulaC8H7F3OS
Molecular Weight208.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-(Trifluoromethoxy)phenyl)methanethiol CAS 175278-03-2 chemical structure

Description

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

CATO supplies (4-(Trifluoromethoxy)phenyl)methanethiol (CAS 175278-03-2), a certified reference material (molecular formula C8H7F3OS, MW 208.20 g/mol) for analytical method development and quality control.

The molecular framework of (4-(Trifluoromethoxy)phenyl)methanethiol (C8H7F3OS) is characterized by sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC8H7F3OS
Molecular Weight208.20 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2007
Halogen ContentF-containing
Sulfur Atoms1

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