2-(3,4-Dichlorophenyl)hydrazine-1-carbothioamide CAS 13124-09-9

Purity 97%+In StockPharmaceutical Standards
CAS No.13124-09-9
Molecular FormulaC7H7Cl2N3S
Molecular Weight236.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3,4-Dichlorophenyl)hydrazine-1-carbothioamide CAS 13124-09-9 chemical structure

Description

2-(3,4-Dichlorophenyl)hydrazine-1-carbothioamide (C7H7Cl2N3S) contains a nitrile group, sulfur-containing functionality, chlorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; 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).

CATO supplies 2-(3,4-Dichlorophenyl)hydrazine-1-carbothioamide (CAS 13124-09-9), a certified reference material (molecular formula C7H7Cl2N3S, MW 236.12 g/mol) for analytical method development and quality control.

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

As a certified reference material (CRM), 2-(3,4-Dichlorophenyl)hydrazine-1-carbothioamide 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 FormulaC7H7Cl2N3S
Molecular Weight236.12 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1960
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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