5-Nitro-2-[(1-phenyl-1h-1,2,3,4-tetrazol-5-yl)sulfanyl]benzoic acid CAS 309726-59-8

Purity 97%+In StockPharmaceutical Standards
CAS No.309726-59-8
Molecular FormulaC14H9N5O4S
Molecular Weight343.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Nitro-2-[(1-phenyl-1h-1,2,3,4-tetrazol-5-yl)sulfanyl]benzoic acid CAS 309726-59-8 chemical structure

Description

5-Nitro-2-[(1-phenyl-1h-1,2,3,4-tetrazol-5-yl)sulfanyl]benzoic acid (C14H9N5O4S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

5-Nitro-2-[(1-phenyl-1h-1,2,3,4-tetrazol-5-yl)sulfanyl]benzoic acid (CAS 309726-59-8), molecular formula C14H9N5O4S and molecular weight 343.32 g/mol, is a CATO reference standard with documented purity and traceability.

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.

As a certified reference material (CRM), 5-Nitro-2-[(1-phenyl-1h-1,2,3,4-tetrazol-5-yl)sulfanyl]benzoic acid 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 FormulaC14H9N5O4S
Molecular Weight343.32 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
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms5
Sulfur Atoms1

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