Interesting facts
Interesting Facts about (2,4-dichlorophenyl) benzenesulfonate
(2,4-dichlorophenyl) benzenesulfonate is an intriguing chemical compound with several noteworthy characteristics and applications. This compound is a derivative of both dichlorophenol and benzenesulfonic acid, which grants it unique properties useful in various fields.
Key Highlights
- Applications in Agriculture: One of the prominent applications of (2,4-dichlorophenyl) benzenesulfonate is as a pesticide. Its efficacy in controlling pests makes it valuable in agricultural practices.
- Role as a Surfactant: This compound also functions as a surfactant in different formulations, aiding in the emulsification process and enhancing the penetration of active ingredients.
- Environmental Impact: As with many chemical compounds, the environmental implications of (2,4-dichlorophenyl) benzenesulfonate are a point of study. Research into its persistence and breakdown in ecological systems is critical for ensuring sustainability.
- Synthetic Pathways: The synthesis of (2,4-dichlorophenyl) benzenesulfonate can involve various routes, showcasing the versatility of organic chemistry techniques. This allows chemists to customize properties for specific applications.
- Research Applications: The compound serves as a model substance in research for studying reaction mechanisms and properties of sulfonates, making it a favored choice in organic chemistry education and experimentation.
As a compound that bridges multiple disciplines, from agriculture to environmental science, (2,4-dichlorophenyl) benzenesulfonate exemplifies the complex interrelationships found within chemical substances. Its ability to impact both industrial applications and scientific research makes it a fascinating subject for further exploration.
Synonyms
Genite
97-16-5
2,4-DICHLOROPHENYL BENZENESULFONATE
Genitol
DPBS
Genitol 923
Genite 923
Compound 923
Genite-R99
2,4-Dichlorophenyl benzenesulphonate
Genite EM-923
Genite (insecticide)
Caswell No. 322
EM 923
(2,4-dichlorophenyl) benzenesulfonate
Phenol, 2,4-dichloro-, benzenesulfonate
2,4-Dichlorophenylbenzene sulfonate
Latka 923
Genit
HSDB 1577
2,4-Dichlorophenol benzenesulfonate
EINECS 202-562-4
2,4-Dichlorophenol, benzenesulfonate
NSC 27323
Benzenesulfonic acid, 2,4-dichlorophenyl ester
EPA Pesticide Chemical Code 031001
UNII-2VO951CU06
2,4-Dichlorophenyl ester of benzenesulfonic acid
BRN 2944672
DTXSID5020447
AI3-19106
2VO951CU06
GENITE [MI]
Benzenesulphonic acid, 2,4-dichlorophenyl ester
NSC-27323
NSC-38761
2,4-Benzenesulfonic acid 2,4-dichlorophenyl ester
DTXCID30447
2,4-Dichlorfenylester kyseliny benzensulfonove
PHENOL, 2,4-DICHLORO-, 1-BENZENESULFONATE
WLN: WSR & OR BG DG
Latka 923 [Czech]
Phenol,4-dichloro-, benzenesulfonate
CAS-97-16-5
Benzenesulfonic acid,4-dichlorophenyl ester
2,4-Dichlorophenylbenzenesulfonate
GeniteR99
2,4-Dichlorfenylester kyseliny benzensulfonove [Czech]
Genite EM923
SCHEMBL435809
CHEMBL3184811
2,4Dichlorophenyl benzenesulphonate
2,4Dichlorophenol, benzenesulfonate
NSC27323
NSC38761
Tox21_201552
Tox21_302810
AKOS008677995
Phenol, 2,4dichloro, benzenesulfonate
NCGC00249066-01
NCGC00256584-01
NCGC00259101-01
Phenol,2,4-dichloro-,1-benzenesulfonate
Genite, PESTANAL(R), analytical standard
2,4Dichlorfenylester kyseliny benzensulfonove
CS-0573373
NS00001453
Benzenesulfonic acid, 2,4dichlorophenyl ester
2,4Dichlorophenyl ester of benzenesulfonic acid
Benzenesulphonic acid, 2,4dichlorophenyl ester
Q27255660
Solubility of (2,4-dichlorophenyl) benzenesulfonate
The solubility of (2,4-dichlorophenyl) benzenesulfonate is characterized by several key factors that influence its behavior in various solvents. This compound exhibits a degree of solubility in polar solvents, which is primarily attributed to the presence of the sulfonate group. Here are some important points to consider:
In essence, while (2,4-dichlorophenyl) benzenesulfonate is relatively soluble in water, the extent of solubility can vary, making it essential to consider solvent choice and environmental conditions when working with this compound. As a rule of thumb, "like dissolves like," indicating that polar solutes generally dissolve better in polar solvents compared to apolar ones.