| Identification | Back Directory | [Name]
OVEX | [CAS]
80-33-1 | [Synonyms]
CCS
OVEX
d854
Onex
CPCB
CPCBS
C-854
D 854
k-101
k6451
K-6451
K 6451
Mitran
Erysit
c1,006
Ovotox
PCPCBS
Ovitox
Ovotran
Otracid
Ovatron
C 1,006
OVATRAN
danicut
Difenson
Corotran
Miticide
Ovochlor
Orochlor
Sappilan
Sappiran
SAVEY PM
Orthotran
genite883
Estonmite
ent16,358
MITRAN(R)
OVOTOX(R)
OVOTRAN(R)
dowk-6,451
ENT 16,358
Genite 883
TANGER 500
VENDEX 50WP
CHLORFENSON
Niagaratran
Chlorfensin
chlorofenson
ORTHOTRAN(R)
Chloorfenson
ESTONMITE(R)
LETHALAIRE(R)
CHLOROFENIZON
Chlorefenizon
acaricydole20
Chlorofensone
miticidek-101
lethalaireg-58
Miticide K-101
estersulfonate
Ethersulfonate
benzolsulfonat
CHLORFENSON(R)
roztoczolfluid
Trichlorfenson
ovatran (arg.)
K-6451 emulsion
Roztoczol Fluid
Benzolsulfonate
Acaricydol E 20
Lethalaire G-58
Ephirsulphonate
Ester sulfonate
Difeson emulsion
Ovex 1g [80-33-1]
chlorbenzolsulfonat
chlorbenzolsulfonate
trichlorfenson(obs.)
Chlorfenson emulsion
chlorfenson (bsi,iso)
chlorefenizon(french)
Chlorobenzolsulfonate
Chlorfensonchlorofensone
CHLORFENSON PESTANAL
4-chlorophenyl-4-chlorobenzenesulfon
4-chlorphenyl-4’-chlorbenzolsulfonat
4-Chlorphenyl-4'-chlorbenzolsulfonat
4-CHLOROPHENYL4-CHLOROBENZENSULFONATE
Dicofol (sum of p.p' and o.p' isomers)
4-chlorophenyl4-chlorobenzenesulfonate
4-Chlorophenyl-4-chlorobenzolsulphonate
p-chlorophenylp-chlorobenzenesulphonate
p-Chlorophenyl p-chlorobenzenesulphonate
CHLORFENSON PESTANAL (4-CHLOROPHENYL4- &
4-CHLOROPHENYL-4-CHLOROBENZENESULPHONATE
4-CHLORO-4-CHLOROPHENYLBENZENESULPHONATE
P-CHLOROPHENYL-P-CHLOROBENZENE SULFONATE
(4-Cloro-fenil)-4-cloro-venzol-solfonato
4-chlorobenzenesulfonatede4-chlorophenyle
(4-Chlor-phenyl)-4-chlor-benzol-sulfonate
parachlorophenylparachlorobenzenesulfonate
4-Chlorobenzenesulfonate de 4-chlorophenyle
(4-Chloor-fenyl)-4-chloor-benzeen-sulfonaat
Parachlorophenyl-parachlorobenzene-sulfonate
(4-chloor-fenyl)-4-chloor-benzeen-sulfonaate
PARA-CHLOROPHENYL-PARA-CHLOROBENZENESULPHONATE
p-chloro-benzenesulfonicacip-chlorophenylester
4-chloro-benzenesulfonicaci4-chlorophenylester
4-chlorobenzenesulfonicacid,4-chlorophenylester
4-Chlorobenzenesulfonicacid4-Chlorop-henylester
p-chlorobenzenesulfonicacid,p-chlorophenylester
p-chlorfenylesterkyselinyp-chlorbenzensulfonove
4-chlorobenzenesulfonatede4-chlorphenyle(french)
4-chlorobenzenesulfonatede4-chlorophenyle(french)
p-Chlorfenylester kyseliny p-chlorbenzensulfonove
p-Chlorobenzenesulfonic acid, p-chlorophenyl ester
Benzenesulfonic acid, 4-chloro-, 4-chlorophenyl ester
Benzenesulfonic acid, p-chloro-, p-chlorophenyl ester
chlorfenson (ISO) 4-chlorophenyl 4-chlorobenzenesulfonate
4-Chlorophenyl 4-chlorobenzenesulfonate, Difenson, Ovex | [EINECS(EC#)]
201-270-4 | [Molecular Formula]
C12H8Cl2O3S | [MDL Number]
MFCD00055266 | [MOL File]
80-33-1.mol | [Molecular Weight]
303.16 |
| Chemical Properties | Back Directory | [Melting point ]
86.5-86.8° | [Boiling point ]
429.6±45.0 °C(Predicted) | [density ]
1.4572 (estimate) | [storage temp. ]
0-6°C | [form ]
Crystalline | [biological source]
human blood | [BRN ]
2944674 | [Henry's Law Constant]
6.2×101 mol/(m3Pa) at 25℃, HSDB (2015) | [Major Application]
agriculture
environmental | [Cosmetics Ingredients Functions]
ANTIMICROBIAL | [InChI]
1S/C12H8Cl2O3S/c13-9-1-5-11(6-2-9)17-18(15,16)12-7-3-10(14)4-8-12/h1-8H | [InChIKey]
RZXLPPRPEOUENN-UHFFFAOYSA-N | [SMILES]
Clc1ccc(OS(=O)(=O)c2ccc(Cl)cc2)cc1 | [EPA Substance Registry System]
Chlorfenson (80-33-1) |
| Hazard Information | Back Directory | [Uses]
Miticide; control of powdery mildew. | [Description]
Chlorfenson is an obsolete insecticide. It has a low aqueous solubility and a low volatility. Data on its persistence in soil and water systems is missing. It has a low mammalian oral toxicity and thought to be a skin irritant. data on ecotoxicology is scant but it does appear to have a low toxicity to birds and a moderate toxicity to fish. | [Chemical Properties]
The pure product is white crystals. mp 86.5-86.8°C (commercial product 80°C). Solubility: ethylene dichloride 1000g/L, xylene 780g/L, ethanol 14g/L. Insoluble in water. Chemically stable, decomposes in strong alkali. | [Definition]
ChEBI: Chlorfenson is an arenesulfonic acid. | [Production Methods]
Commercial production details for chlorfenson are limited due to its discontinued use. Historically, chlorfenson was synthesised through chemical processes involving substituted benzene derivatives and sulfonate intermediates to form its active structure, 4-chlorophenyl methylsulfonylcarbamate. The production likely involved sulfonation and carbamoylation steps under controlled conditions to ensure purity and yield. | [General Description]
Chlorfenson is a pyrethroid pesticide effective against mites of citrus fruit, vegetable crops and ornamentals. It is a non-systemic acaricide with residual ovicidal activity. | [Mechanism of action]
Acts by inhibiting oxidative phosphorylation. Contact and stomach action and long residual ovicidal activity. | [Pesticide Type]
Acaricide; Miticide; Insecticide |
|
| Company Name: |
Sigma-Aldrich
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| Tel: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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