Thiamethoxam-13C4-15N1 CAS CATO-CCPD102479

Purity 1.100μg/mL in MethanolIn StockPharmaceutical Standards
CAS No.CATO-CCPD102479
Molecular FormulaC8H10ClN5O3S
Molecular Weight296.68 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Thiamethoxam-13C4-15N1 CAS CATO-CCPD102479 chemical structure

Description

The molecular framework of Thiamethoxam-13C4-15N1 (C8H10ClN5O3S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

Thiamethoxam-13C4-15N1 (CAS CATO-CCPD102479), molecular formula C8H10ClN5O3S and molecular weight 296.68 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), Thiamethoxam-13C4-15N1 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 FormulaC8H10ClN5O3S
Molecular Weight296.68 g/mol
Purity1.100μg/mL in Methanol
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Halogen ContentCl-containing
Nitrogen Atoms5
Sulfur Atoms1

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