| Identification | Back Directory | [Name]
DICHLOFENTHION | [CAS]
97-17-6 | [Synonyms]
ECP
RNS3
vc13
VC 13
RNASE3
v-c-13
V-Cl 13
v-c1-13
hexnema
ent17470
Hexanema
VC-13(R)
tri-vc13
v-c 1-13
Mobilawn
Nemacide
Tri-vc 13
ENT 17470
ent17,470
ENT 17,470
ecp (jmaf)
MOBILAWN(R)
vc13nemacide
ECP Standard
vc-13nemacide
Dichlofention
nemacidevc-13
Diclofenthion
ichlofenthion
HILLVALEFLYDIP
VC-13 Nemacide
Nemacide vc-13
DICHLOFENTHION
Dichlorfenthion
FLOCKO.P.FLYDIP
DICHLORPHENTHION
Dichlorofenthion
NEMACIDE VC-13(R)
DICHLOFENTHION, 1GM, NEAT
Eosinophil cationic protein
Dichlofenthion 1g [97-17-6]
DICHLOFENTHION PESTANAL, 250 MG
Dichlofenthion Solution, 100ppm
Dichlofenthion@100 μg/mL in MeOH
Dichlofenthion
Solution, 1000ppm
Dichlofenthion@1000 μg/mL in MeOH
dichlofenthion (bsi,iso,ansi,ban)
Eosinophil Cationic Protein human
diethyl2,4-dichlorophenylphosphorothionate
Recombinant Human RNASE 3 Protein, His Tag
2,4-dichloro-phenyldiethylphosphorothionate
2,4-Dichlorophenyl diethyl phosphorothionate
o,o-diethylo-2,4-dichlorophenylthiophosphate
Diethyl 2,4-dichlorophenyl phosphorothionate
Recombinant Human ECP/RNASE3 Protein, Fc Tag
O,O-Dietil-O-(2,4-dicloro-fenil)-monotiofosfato
O,O-Diaethyl-O-2,4-dichlorphenyl-thionophosphat
O,O-Diethyl O-(2,4-dichlorophenyl) thiophosphate
ANTI-RNASE3 (C-TERM) antibody produced in rabbit
O-(2,4-Dichlorophenyl)-O,O-diethyl thiophosphate
O-2,4-DICHLOROPHENYL-O,O-DIETHYL-PHOSPHOROTHIOATE
(2,4-dichlorophenoxy)-diethoxy-thioxo-phosphorane
O,O-Diethyl-O-(2,4-dichloor-fenyl)-monothiofosfaat
o,o-diaethyl-o-2,4-dichlor-phenyl-monothiophosphat
O-(2 4-DICHLOROPHENYL) O O-DIETHYLPHOSPHOROTHIONATE
O,O-DIETHYL-O-(2,4-DICHLOROPHENYL)-PHOSPHOROTHIOATE
thiophosphatedeo-2,4-dichlorophenyleetdeo,o-diethyle
thiophosphatedeo-(dichloro-2,4phenyle)etdeo,o-diethyle
Phosphorothioic acid O,O-diethyl O-(2,4-dichlorophenyl)
Thiophosphate de o-2,4-dichlorophenyle et de O,O-diethyle
phenol,2,4-dichloro-,o-esterwitho,o-diethylphosphorothioate
thiophosphatedeo-2,4-dichlorophenyleetdeo,o-diethyle(french)
Thiophosphoric acid=O-(2,4-dichlorophenyl)=O,O-diethyl ester
(2,4-dichlorophenoxy)-diethoxy-sulfanylidene-$l^{5}-phosphane
PHOSPHOROTHIOIC ACID O-(2,4-DICHLOROPHENYL) O,O-DIETHYL ESTER
Phenol, 2,4-dichloro-, O-ester with O,O-diethyl phosphorothioate
dichlofenthion (ISO) O-2,4-dichlorophenyl O,O-diethyl phosphorothioate | [EINECS(EC#)]
202-564-5 | [Molecular Formula]
C10H13Cl2O3PS | [MDL Number]
MFCD00045182 | [MOL File]
97-17-6.mol | [Molecular Weight]
315.15 |
| Chemical Properties | Back Directory | [Boiling point ]
bp0.1 164-169° | [density ]
d20 1.300 | [refractive index ]
nD25 1.5291 | [Fp ]
100 °C | [storage temp. ]
0-6°C
| [solubility ]
Chloroform (Slightly), Ethyl Acetate (Slightly) | [form ]
Liquid | [biological source]
rabbit | [Water Solubility ]
245ug/L(25 ºC) | [Merck ]
13,3069 | [BRN ]
1993440 | [Henry's Law Constant]
1.0×10-2 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) | [EPA Substance Registry System]
Dichlofenthion (97-17-6) |
| Hazard Information | Back Directory | [Uses]
Nematocide, insecticide. | [Description]
Dichlofenthion is an organophosphate insecticide. It was previously used to control nematodes and cutworms mainly on ornamental crops, lawns and turf. It has a low aqueous solubility, is quite volatile and mobile in soil. Dichlofenthion is moderately toxic to mammals, a skin, eye and respiratory tract irritant and a sensitiser. It is highly toxic to fish and aquatic invertebrates. | [Chemical Properties]
Colorless liquid. Boiling point 164-169°C (1.33×10-2 kPa), relative density 1.320 (20/4°C). Easily soluble in most organic solvents and kerosene, with a solubility of 0.245 ppm in water. | [Definition]
ChEBI: Dichlofenthion is an organic thiophosphate. | [Production Methods]
Dichlofenthion is commercially synthesised through a multi-step process involving the formation of its phosphorothioate ester structure. The production typically begins with the reaction of 2,4-dichlorophenol with diethyl phosphorochloridothioate, forming the active compound. This reaction is carried out under controlled conditions using an organic solvent and a base to neutralise the hydrochloric acid byproduct. | [Mechanism of action]
Acetylcholinesterase (AchE) inhibitor | [Pesticide Type]
Insecticide |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,N | [Risk Statements ]
22-50/53 | [Safety Statements ]
60-61 | [RIDADR ]
2783 | [WGK Germany ]
3 | [RTECS ]
TF0350000 | [HazardClass ]
6.1(b) | [PackingGroup ]
III | [HS Code ]
29201900 | [Storage Class]
10 - Combustible liquids | [Safety Profile]
Poison by ingestion and
skin contact. A very toxic insecticide.
Mutation data reported. See also ESTERS
and PARATHION. When heated to
decomposition it emits very toxic fumes of
POx, SOx, and Cl-. | [Hazardous Substances Data]
97-17-6(Hazardous Substances Data) | [Toxicity]
LD50 in male, female rats (mg/kg): 185, 172 orally; 576, 355 dermally (Gaines, Linder) |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
|