(2,4,5-Trifluorophenyl)methanethiol CAS 886498-39-1

Purity 97%+In StockPharmaceutical Standards
CAS No.886498-39-1
Molecular FormulaC7H5F3S
Molecular Weight178.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2,4,5-Trifluorophenyl)methanethiol CAS 886498-39-1 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 178.17 g/mol gives (2,4,5-Trifluorophenyl)methanethiol distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

(2,4,5-Trifluorophenyl)methanethiol (CAS 886498-39-1) is a high-purity analytical reference standard with the molecular formula C7H5F3S and a molecular weight of 178.17 g/mol.

Owing to sulfur-containing functionality, fluorine substitution, an aromatic ring system, (2,4,5-Trifluorophenyl)methanethiol is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 178.17 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 (2,4,5-Trifluorophenyl)methanethiol 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 FormulaC7H5F3S
Molecular Weight178.17 g/mol
Purity97%+
StorageStore at 2-8°C, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Sulfur Atoms1

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