N-(4-(Dimethylamino)phenyl)-1,2,5-thiadiazole-3-carboxamide CAS 700850-84-6

Purity 97%+In StockPharmaceutical Standards
CAS No.700850-84-6
Molecular FormulaC11H12N4OS
Molecular Weight248.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-(Dimethylamino)phenyl)-1,2,5-thiadiazole-3-carboxamide CAS 700850-84-6 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including N-(4-(Dimethylamino)phenyl)-1,2,5-thiadiazole-3-carboxamide.

N-(4-(Dimethylamino)phenyl)-1,2,5-thiadiazole-3-carboxamide (CAS 700850-84-6) is a high-purity analytical reference standard with the molecular formula C11H12N4OS and a molecular weight of 248.30 g/mol.

N-(4-(Dimethylamino)phenyl)-1,2,5-thiadiazole-3-carboxamide (C11H12N4OS) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage. Its physicochemical properties are representative of its class; 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.

As a certified reference material (CRM), N-(4-(Dimethylamino)phenyl)-1,2,5-thiadiazole-3-carboxamide 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 FormulaC11H12N4OS
Molecular Weight248.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Nitrogen Atoms4
Sulfur Atoms1

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