Sodium 2-(2-amino-3-methoxybenzamido)-5-methylthiophene-3-carboxylate CAS 116120-36-6

Purity 97%+In StockPharmaceutical Standards
CAS No.116120-36-6
Molecular FormulaC14H13N2O4S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Sodium 2-(2-amino-3-methoxybenzamido)-5-methylthiophene-3-carboxylate CAS 116120-36-6 chemical structure

Description

CATO supplies Sodium 2-(2-amino-3-methoxybenzamido)-5-methylthiophene-3-carboxylate (CAS 116120-36-6), a certified reference material (molecular formula C14H13N2O4SNa, MW 328.32 g/mol) for analytical method development and quality control.

Structurally, Sodium 2-(2-amino-3-methoxybenzamido)-5-methylthiophene-3-carboxylate (C14H13N2O4SNa) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 9.5, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 328.32 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), Sodium 2-(2-amino-3-methoxybenzamido)-5-methylthiophene-3-carboxylate 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 FormulaC14H13N2O4S Na
Molecular Weight328.32 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)9.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms2
Sulfur Atoms1

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