| Identification | Back Directory | [Name]
MALAOXON | [CAS]
1634-78-2 | [Synonyms]
maloxon
Liromat
Malaoxan
MALAOXON
Malaoxone
NCI-C08628
nci-co8628
Oxycarbophos
Malathon oxon
MALATHION-OXON
malaoxon (iso)
Malaoxon Standard
MALATHION-O-ANALOG
carbethoxymalaoxon
Carbethoxy malaoxon
malathion-o-analogue
MALAOXON PESTANAL
Malathion impurity B CRS
Malaoxon Solution, 100ppm
Malaoxon @100 μg/mL in MeOH
MalaoxonSolution,100mg/L,1ml
Malathion Impurity 11(Malaoxon)
Malaoxon@1000 μg/mL in Methanol
2-[(DiMethoxyphosphinyl)thio]butanedioic Acid
Diethyl [(Dimethoxyphosphino)thio]butanedioate
iethyl2-dimethoxyphosphorylsulfanylbutanedioate
diethyl 2-dimethoxyphosphorylsulfanylbutanedioate
Diethyl 2-[(dimethoxyphosphoryl)sulfanyl]succinate
O,O-DIMETHYL S-(1,2-DICARBETHOXYETHYL)-THIOPHOSPHATE
o,o-dimethyls-(1,2-dicarbethoxy)ethylphosphorothioate
o,o-dimethyl-s-(1,2-dicarbethoxy)ethylphosphorothioate
((dimethoxyphosphinyl)thio)-butanedioicacidiethylester
2-(dimethoxyphosphorylthio)succinic acid diethyl ester
O,O-Dimethyl-S-(1,2-dicarbethoxy)ethyl phosphorothioate
O,O-dimethylS-[1,2-bis(ethoxycarbonyl)ethyl]thiophosphate
s-(1,2-diethoxycarbonyl)ethylo,o-dimethylphosphorothioate
s-1,2-bis(ethoxycarbonyl)ethylo,o-dimethylphosphorothioate
o,o-dimethyls-1,2-bis(ethoxycarbonyl)ethylphosphorothioate
S-(1,2-Diethoxycarbonyl)ethyl O,O-dimethyl phosphorothioate
o,o-dimethyl-s-1,2-bis(ethoxycarbonyl)ethylphosphorothioate
O,O-Dimethyl S-1,2-bis(ethoxycarbonyl)ethyl phosphorothioate
Butanedioic acid, [(dimethoxyphosphinyl)thio]-, diethyl ester
diethylmercaptosuccinates-esterwitho,o-dimethylphosphorothioate
2-[(Dimethoxyphosphinyl)thio]butanedioic Acid 1,4-Diethyl Ester
Butanedioic acid, 2-[(dimethoxyphosphinyl)thio]-, 1,4-diethyl ester
Diethyl mercaptosuccinate S-ester with O,O-dimethyl phosphorothioate
Thiophosphoric acid O,O-dimethyl S-[1,2-di(ethoxycarbonyl)ethyl] ester
Thiophosphoric acid S-[1,2-bis(ethoxycarbonyl)ethyl]O,O-dimethyl ester
phosphorothioicacid,o,o-dimethylester,s-esterwith1,2-bis(ethoxycarbonyl
succinicacid,mercapto-,diethylester,s-esterwitho,o-dimethylphosphorothio
Succinic acid, mercapto-, diethyl ester, S-ester with O,O-dimethyl phosphorothioate
Phosphorothioic acid, O,O-dimethyl ester, S-ester with 1,2-bis(methoxycarbonyl)ethanethiol | [EINECS(EC#)]
634-923-0 | [Molecular Formula]
C10H19O7PS | [MDL Number]
MFCD00055461 | [MOL File]
1634-78-2.mol | [Molecular Weight]
314.29 |
| Chemical Properties | Back Directory | [Melting point ]
<20℃ | [Boiling point ]
114 °C | [density ]
1.248±0.06 g/cm3(Predicted) | [refractive index ]
1.4696 (589.3 nm 25℃) | [Fp ]
-18 °C | [storage temp. ]
0-6°C | [form ]
liquid | [color ]
Colorless oily liquid | [BRN ]
1804523 | [EPA Substance Registry System]
Malaoxon (1634-78-2) |
| Hazard Information | Back Directory | [Uses]
An active metabolite of Malathion. It is a widely used anticholinesterase phosphorothioate insecticide | [Definition]
ChEBI: Diethyl 2-[(dimethoxyphosphoryl)thio]succinate is a diester that is diethyl succinate in which position 2 is substituted by a (dimethoxyphosphoryl)thio group. It is a diester, an ethyl ester and an organic thiophosphate. | [General Description]
Colorless viscous oily liquid with a weak unpleasant odor. | [Air & Water Reactions]
MALAOXON may be sensitive to prolonged exposure to air. . Slightly water soluble. | [Reactivity Profile]
A thioorganophosphate, ester. Organophosphates are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. | [Fire Hazard]
MALAOXON is probably combustible. | [Safety Profile]
Poison by ingestion and intraperitoneal routes. Experimental reproductive effects. Mutation data reported. Whenheated to decomposition it emits toxic fumes of SOx and POx. |
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