| Identification | Back Directory | [Name]
CADUSAFOS | [CAS]
95465-99-9 | [Synonyms]
RUGBY
ebufos
APACHE
taredan
Toredan
fmc67825
codusafos
Hsdb 7139
CADUSAFOS
PMC 67825
CADUSAPHOS
Apache(TM)
Cadusafos [iso]
CADUSAFOS STANDARD
cadusafos (bsi,iso)
Cadusafos in Methanol
Cadusafos Solution, 100ppm
Cadusafos 100mg [95465-99-9]
CadusafosSolution,100mg/L,1ml
CadusafosSolution,10mg/L,10ml
Cadusafos@1000 μg/mL in Acetone
Cadusafos @100 μg/mL in Methanol
o-ethyl-s,s-di-sec-butylphosphorodithioate
o-Ethyl, S-bis(1-methylpropyl)phosphorodithioate
o-ethyl-s,s-bis(1-methylpropyl)phosphorodithioate
o-Ethyl S,S-bis(1-methylpropyl) phosphorodithioate (9ci)
phosphorodithioicacid,o-ethyl-,s,s-bis(1-methylpropyl)ester | [Molecular Formula]
C10H23O2PS2 | [MDL Number]
MFCD00072511 | [MOL File]
95465-99-9.mol | [Molecular Weight]
270.39 |
| Chemical Properties | Back Directory | [Melting point ]
<25 °C | [Boiling point ]
167°C | [density ]
1.069±0.06 g/cm3(Predicted) | [vapor pressure ]
0.12 Pa (25 °C) | [Fp ]
129℃ | [storage temp. ]
0-6°C | [form ]
neat | [Water Solubility ]
248 mg l-1 | [Specific Gravity]
1.05 | [BRN ]
8140049 | [Henry's Law Constant]
7.6×100 mol/(m3Pa) at 25℃, HSDB (2015) | [Major Application]
agriculture
environmental | [InChI]
1S/C10H23O2PS2/c1-6-9(4)14-13(11,12-8-3)15-10(5)7-2/h9-10H,6-8H2,1-5H3 | [InChIKey]
KXRPCFINVWWFHQ-UHFFFAOYSA-N | [SMILES]
CCOP(=O)(SC(C)CC)SC(C)CC | [EPA Substance Registry System]
Cadusafos (95465-99-9) |
| Hazard Information | Back Directory | [Description]
This nonsystemic organophosphate not registered for
U.S. usage is used to control nematodes and soil
insects on bananas and other crops in several countries.
The U.S. EPA has granted tolerances for cadusafos
in imported bananas, where it provides excellent control
of the burrowing nematode, Radopholus similis (22).
Cadusafos reportedly possesses reduced risk for contaminating
groundwater and provided good control of the citrus
nematode, Tylenchulus semipenetrans (23). Cadusafos is
commercially available in granular and microencapsulated
formulations. | [Uses]
CADUSAFOS is used in the agriculture industry
| [Uses]
Insecticide; nematocide. | [Definition]
ChEBI: Cadusafos is an organic thiophosphate and an organothiophosphate insecticide. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, a nematicide and an agrochemical. | [Production Methods]
Cadusafos, a synthetic organothiophosphate nematicide, is produced through a multi-step chemical synthesis involving the formation of its key phosphorodithioate structure. The process typically begins with the reaction of phosphorus compounds, such as phosphorus oxychloride or phosphorus pentasulfide, with alcohols and thiols to form the phosphorodithioate backbone. In the case of cadusafos, this includes the incorporation of sec-butyl mercaptan and ethyl alcohol to yield S,S-di-sec-butyl O-ethyl phosphorodithioate. | [General Description]
Cadusafos is a nematicide used in controlling nematodes, soil insects and cutworms in a variety of fruits and vegetables. Its mode of action involves the inhibition of acetylcholinesterase. | [Mechanism of action]
Broad-spectrum activity with contact and stomach action. Acetylcholinesterase (AchE) inhibitor. | [Metabolic pathway]
There is little published information on the metabolism of cadusafos.
What has been published suggests that the main route of metabolism in
animals is via hydrolysis to give 1-methyl-1-propanethiol which is then
thiooxidised. | [Metabolism]
The
acute oral LD50 values for rats and mice are 37.1 and
71.4 mg/kg, respectively. Inhalation LC50 (4 h) for rats
is 0.026 mg/L air. NOEL (2 yr) for rats is 1 mg/kg diet
(0.05 mg/kg/d) and ADI is 0.3 μg/kg. In mammals, it is
readily metabolized and is eliminated in the urine and
feces. The major metabolic route is hydrolysis to give
1-methyl-1-propanothiol, followed by oxidation. The halflife
in soils is 11–55 d. | [Pesticide Type]
Insecticide; Nematicide |
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