gptkbp:instanceOf
|
gptkb:chemical_compound
organophosphate insecticide
|
gptkbp:antidote
|
gptkb:pralidoxime
atropine
|
gptkbp:appearance
|
colorless to yellow-brown liquid
|
gptkbp:ATCCode
|
gptkb:P03AB03
|
gptkbp:boilingPoint
|
156 °C (at 0.1 mmHg)
|
gptkbp:CASNumber
|
121-75-5
|
gptkbp:category
|
gptkb:entomologist
gptkb:acetylcholinesterase_inhibitor
organophosphate ester
thioate ester
|
gptkbp:chemicalFormula
|
C10H19O6PS2
|
gptkbp:degradationProducts
|
gptkb:malaoxon
|
gptkbp:environmentalPersistence
|
low
|
gptkbp:firstSynthesized
|
1950s
|
https://www.w3.org/2000/01/rdf-schema#label
|
malathion
|
gptkbp:IUPACName
|
gptkb:diethyl_2-[(dimethoxyphosphorothioyl)sulfanyl]butanedioate
|
gptkbp:KEGGID
|
gptkb:C11193
|
gptkbp:mechanismOfAction
|
gptkb:acetylcholinesterase_inhibitor
|
gptkbp:meltingPoint
|
2 °C
|
gptkbp:MeSH_ID
|
gptkb:D008288
|
gptkbp:molecularWeight
|
330.35 g/mol
|
gptkbp:producer
|
gptkb:Bayer
gptkb:Cheminova
|
gptkbp:PubChem_CID
|
gptkb:ChEBI:6706
4004
|
gptkbp:regulates
|
approved for head lice treatment
approved for public health mosquito control
approved for use in agriculture
|
gptkbp:routeOfExposure
|
inhalation
ingestion
skin contact
|
gptkbp:sideEffect
|
nausea
respiratory distress
dizziness
headache
skin irritation
|
gptkbp:solubility
|
145 mg/L at 20 °C
|
gptkbp:toxicity
|
moderate
|
gptkbp:UNNumber
|
2783
|
gptkbp:uses
|
gptkb:entomologist
pediculicide
acaricide
|
gptkbp:WHOClassification
|
Class III (slightly hazardous)
|
gptkbp:bfsParent
|
gptkb:organophosphates
|
gptkbp:bfsLayer
|
7
|