2,2,2-Trifluoroethyl n-(1,3,4-thiadiazol-2-yl)carbamate CAS 1211199-35-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1211199-35-7
Molecular FormulaC5H4F3N3O2S
Molecular Weight227.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,2,2-Trifluoroethyl n-(1,3,4-thiadiazol-2-yl)carbamate CAS 1211199-35-7 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.

2,2,2-Trifluoroethyl n-(1,3,4-thiadiazol-2-yl)carbamate (CAS 1211199-35-7), molecular formula C5H4F3N3O2S and molecular weight 227.16 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C5H4F3N3O2S, 2,2,2-Trifluoroethyl n-(1,3,4-thiadiazol-2-yl)carbamate contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 227.16 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

As a certified reference material (CRM), 2,2,2-Trifluoroethyl n-(1,3,4-thiadiazol-2-yl)carbamate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC5H4F3N3O2S
Molecular Weight227.16 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
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)4.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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Why CATO?