2-((3,4-Dichlorobenzyl)thio)-3-((2,4,6-trichlorophenyl)diazenyl)-1H-indole CAS 478042-13-6

Purity 97%+In StockPharmaceutical Standards
CAS No.478042-13-6
Molecular FormulaC21H12Cl5N3S
Molecular Weight515.67 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((3,4-Dichlorobenzyl)thio)-3-((2,4,6-trichlorophenyl)diazenyl)-1H-indole CAS 478042-13-6 chemical structure

Description

As a certified reference material (CRM), 2-((3,4-Dichlorobenzyl)thio)-3-((2,4,6-trichlorophenyl)diazenyl)-1H-indole 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.

CATO supplies 2-((3,4-Dichlorobenzyl)thio)-3-((2,4,6-trichlorophenyl)diazenyl)-1H-indole (CAS 478042-13-6), a certified reference material (molecular formula C21H12Cl5N3S, MW 515.67 g/mol) for analytical method development and quality control.

2-((3,4-Dichlorobenzyl)thio)-3-((2,4,6-trichlorophenyl)diazenyl)-1H-indole (C21H12Cl5N3S) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; 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).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC21H12Cl5N3S
Molecular Weight515.67 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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