gptkbp:instanceOf
|
nerve agent
|
gptkbp:antidote
|
gptkb:pralidoxime
atropine
|
gptkbp:aroma
|
faint fruity odor
|
gptkbp:boilingPoint
|
240°C
|
gptkbp:CASNumber
|
77-81-6
|
gptkbp:category
|
gptkb:G-series_nerve_agent
|
gptkbp:chemicalClass
|
organophosphate
|
gptkbp:chemicalFormula
|
C5H11N2O2P
|
gptkbp:color
|
colorless to brown
|
gptkbp:density
|
1.073 g/cm³
|
gptkbp:developedBy
|
gptkb:Nazi_Germany
|
gptkbp:discoveredBy
|
gptkb:Gerhard_Schrader
|
gptkbp:discoveredIn
|
1936
|
gptkbp:effectOnHumans
|
seizures
respiratory arrest
muscle paralysis
|
gptkbp:first_large-scale_production
|
1939
|
gptkbp:first_produced_at
|
gptkb:IG_Farben
|
gptkbp:hazard_class
|
extremely hazardous substance
|
https://www.w3.org/2000/01/rdf-schema#label
|
Tabun (nerve agent)
|
gptkbp:hydrolysis_product
|
gptkb:hydrogen_cyanide
diethyl phosphoramidate
|
gptkbp:IUPACName
|
gptkb:ethyl_N,N-dimethylphosphoramidocyanidate
|
gptkbp:lethal_dose_(LD50,_human,_inhalation)
|
400 mg·min/m³
|
gptkbp:lethal_dose_(LD50,_human,_skin)
|
1000 mg
|
gptkbp:mechanismOfAction
|
gptkb:acetylcholinesterase_inhibitor
|
gptkbp:meltingPoint
|
-50°C
|
gptkbp:militaryDesignation
|
GA
|
gptkbp:molecularWeight
|
162.13 g/mol
|
gptkbp:physical_state
|
gptkb:water
|
gptkbp:produced_during
|
gptkb:World_War_II
|
gptkbp:prohibits
|
gptkb:Chemical_Weapons_Convention
|
gptkbp:relatedTo
|
gptkb:VX
gptkb:Sarin
gptkb:Soman
|
gptkbp:riskFactor
|
causes convulsions, respiratory failure, death
|
gptkbp:routeOfExposure
|
inhalation
ingestion
skin absorption
|
gptkbp:solubility
|
soluble in water and organic solvents
|
gptkbp:storage
|
requires sealed containers
|
gptkbp:synthesisType
|
reaction of dimethylamine, phosphoryl chloride, and sodium cyanide
|
gptkbp:toxicity
|
highly toxic
|
gptkbp:UNNumber
|
N/A (prohibited substance)
|
gptkbp:used_in_warfare
|
no confirmed battlefield use
|
gptkbp:usedFor
|
chemical weapon
|
gptkbp:vaporPressure
|
0.07 mmHg at 25°C
|
gptkbp:bfsParent
|
gptkb:Otto_Ambros
|
gptkbp:bfsLayer
|
6
|