2-((1-Methyl-1H-tetrazol-5-yl)thio)-N-(4-(trifluoromethoxy)phenyl)acetamide CAS 212074-56-1

Purity 97%+In StockPharmaceutical Standards
CAS No.212074-56-1
Molecular FormulaC11H10F3N5O2S
Molecular Weight333.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((1-Methyl-1H-tetrazol-5-yl)thio)-N-(4-(trifluoromethoxy)phenyl)acetamide CAS 212074-56-1 chemical structure

Description

As a certified reference material (CRM), 2-((1-Methyl-1H-tetrazol-5-yl)thio)-N-(4-(trifluoromethoxy)phenyl)acetamide 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.

2-((1-Methyl-1H-tetrazol-5-yl)thio)-N-(4-(trifluoromethoxy)phenyl)acetamide (CAS 212074-56-1), molecular formula C11H10F3N5O2S and molecular weight 333.29 g/mol, is a CATO reference standard with documented purity and traceability.

2-((1-Methyl-1H-tetrazol-5-yl)thio)-N-(4-(trifluoromethoxy)phenyl)acetamide (C11H10F3N5O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

Physical & Chemical Properties

Molecular FormulaC11H10F3N5O2S
Molecular Weight333.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2017
Halogen ContentF-containing
Nitrogen Atoms5
Sulfur Atoms1

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