38185-06-7

Basic information

• Product Name: potassium 4-chloro-3,5-dinitrobenzenesulphonate
• Synonyms: potassium 4-chloro-3,5-dinitrobenzenesulphonate;4-chloro-3,5-dinitrobenzenesulphonate;4-Chloro-3,5-DinitroBenzeneSulfonate;4-Chloro-3,5-dinitrobenzene sulfonic acid pottasium salt;4-Chloro-3,5-dinitrobenzenesulfonic acid, potassium salt;POTASSIUM4-CHLORO-3,5-DINITROBENZENESULFONATE
• CAS NO: 38185-06-7
• Molecular Formula: C₆H₂ClN₂O₇S*K
• Molecular Weight: 281.60728
• EINECS: 253-816-6
• Mol File: 38185-06-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.911g/cm³
• CAS DataBase Reference: potassium 4-chloro-3,5-dinitrobenzenesulphonate(CAS DataBase Reference)
• NIST Chemistry Reference: potassium 4-chloro-3,5-dinitrobenzenesulphonate(38185-06-7)
• EPA Substance Registry System: potassium 4-chloro-3,5-dinitrobenzenesulphonate(38185-06-7)

Safety Data

• Hazardous Substances Data: 38185-06-7(Hazardous Substances Data)

Usage

General Description

Potassium 4-chloro-3,5-dinitrobenzenesulphonate is a chemical compound with the molecular formula C6H3ClKNO7S. It is a water-soluble salt that is commonly used as a herbicide and pesticide due to its ability to inhibit plant growth and kill unwanted vegetation. It is also used in analytical chemistry as a reagent for the determination of amines and amino acids. potassium 4-chloro-3,5-dinitrobenzenesulphonate is highly toxic and should be handled with caution. Its use is regulated in many countries due to its potential environmental and health hazards.

InChI:InChI=1/C6H3ClN2O7S.K/c7-6-4(8(10)11)1-3(17(14,15)16)2-5(6)9(12)13;/h1-2H,(H,14,15,16);/q;+1/p-1

Upstream product

• 108-90-7 chlorobenzene 

Downstream Products

• 132630-03-6 Potassium; 4-decyloxycarbonylsulfanyl-3,5-dinitro-benzenesulfonate 
• 132630-06-9 Potassium; 4-decyloxythiocarbonylsulfanyl-3,5-dinitro-benzenesulfonate 
• 1246378-95-9 C₁₆H₁₆N₃O₈S^(1-)*K⁽¹⁺⁾ 
• 1246378-98-2 C₂₂H₂₀N₃O₇S^(1-)*K⁽¹⁺⁾ 
• 1246378-97-1 C₂₀H₂₈N₃O₇S^(1-)*K⁽¹⁺⁾ 
• 1246378-96-0 C₂₂H₂₀N₃O₇S^(1-)*K⁽¹⁺⁾ 
• 1428264-09-8 C₁₉H₁₃N₃O₃S 
• 1428264-10-1 C₂₀H₁₅N₃O₅S 
• 1428264-11-2 C₁₉H₁₃N₃O₄S 
• 1428264-12-3 C₂₀H₁₅N₃O₄S 
• 1428264-13-4 C₁₉H₁₃N₃O₄S 
• 1428264-14-5 C₁₉H₁₃N₃O₄S 
• 1428264-15-6 C₂₃H₂₂N₄O₄S 
• 1428264-16-7 C₁₉H₁₂N₄O₅S 

Relevant articles and documents

Synthesis of SMZ derivatives and investigation of effects on germination, root, and plant growth of Arabidopsis thaliana L.

A series of sulfonamide derivatives were synthesized by reactions with various functional groups containing benzenesulfonyl chlorides and aniline derivatives under different substitution reaction conditions. The structures of SMZ derivatives were confirmed with melting point, FT-IR, 1 H NMR, 13 C NMR, and LC-MS/MS techniques. In order to investigate the cytotoxic effects of these derivatives, we used a model plant species. The synthesized compounds (S1–S5) and sulfamethazine (SMZ) as a positive control were applied to Arabidopsis thaliana seeds. Our results indicated that S3 and S4 induced shorter roots and lower wet weight in plants. Plants treated with S2 and S5 showed no growth effects, similar to the untreated control group, while S1 slightly reduced root length and wet weight. These results suggest that S3 and the newly synthesized S4 derivatives have potential for use as herbicides since they possess cytotoxic effects on A. thaliana plants.