| Identification | Back Directory | [Name]
DEMETON-S-METHYL SULFOXIDE | [CAS]
301-12-2 | [Synonyms]
r2170
B-21097
bay21097
ent24,964
NSC 370785
bayer21097
aimcosystox
metasystoxr
metasystox-r
metasystemox
OxydeMeton M
metasystemoxr
OxydeMeton-Methy
META SYSTOX-R(R)
OXYDEMETON-METHYL
OXYDEMETHONMETHYL
Oxidemeton-methyl
methyloxydemetons
oxydemeton-metile
Methyl oxydemeton
metilmercaptofosoksid
metaisosystoxsulfoxide
isomethylsystoxsulfoxide
DEMETON-S-METHYL SULFONE
demeton-methylsulphoxide
demeton-s-methyl-sulfoxid
methyldemeton-o-sulfoxide
oxydemeton-metile[italian]
DEMETON-S-METHYLSULPHOXIDE
DEMETON-S-METHYL SULFOXIDE
metilmercaptofosoksid(ussr)
OXYDEMETON-METHYL, 50MG, NEAT
Oxydemeton-methyl(content>90%)
Oxydemeton-methyl(content2%-90%)
demeton-s-methylsulfoxid[german]
Oxydemeton-methyl@1000 μg/mL in Methanol
dimethyls-(2-eththionylethyl)thiophosphate
Oxydemeton-methyl Solution in Methanol, 100μg/mL
o,o-dimethyls-(2-eththionylethyl)phosphorothioate
o,o-dimethyls-(2-ethylsulfinyl)ethylthiophosphate
o,o-dimethyls-(2-(ethylsufinyl)ethyl)thiophosphate
o,o-dimethyls-ethylsulphinylethylphosphorothiolate
o,o-dimetil-s-(2-etil-solfinil-etil)-monotiofosfato
1-dimethoxyphosphorylsulfanyl-2-ethylsulfinylethane
1-dimethoxyphosphorylsulfanyl-2-ethylsulfinyl-ethane
s-(2-(ethylsulfinyl)ethyl)o,o-dimethlphosphorothioate
o,o-dimethyl-s-(3-oxo-3-thia-pentyl)-monothiophosphat
o,o-dimethyl-s-(2-aethylsulfinyl-aethyl)-thiolphosphat
o,o-dimethyl-s-(2-ethylsulfinyl-ethyl)-monothiofosfaat
s-(2-(ethylsulfinyl)ethyl)o,o-dimethylphosphorothioate
O,O-DIMETHYL-S-(2-ETHYLSULFINYLETHYL)-PHOSPHOROTHIOATE
thiophosphatedeo,o-dimethyleetdes-2-ethylsulfinylethyle
S-(2-ethylsulphinylethyl) O,O-dimethyl phosphorothioate
o,o-dimethyls-(2-(ethylsulfinyl)ethyl)monothiophosphate
[(2-ethylsulfinylethylthio)-methoxy-phosphoryl]oxymethane
o-o-dimetil-s-(2-etil-solfinil-etil)-monotiofosfato[italian]
o,o-dimethyl-s-(2-ethylsulfinyl-ethyl)-monothiofosfaat[dutch]
o,o-dimethyl-s-(3-oxo-3-thia-pentyl)-monothiophosphat[german]
phosphorothioicacid,o,o-dimethyls-(2-(ethylsulfinyl)ethyl)ester
phosphorothioicacid,s-(2-(ethylsulfinyl)ethyl)o,o-dimethylester
S-[2-(Ethylsulfinyl)ethyl]phosphorothioic Acid O,O-DiMethyl Ester
Phosphorothioic acid, S-[2-(ethylsulfinyl)ethyl] O,O-dimethyl ester
ethanethiol,2-(ethylsulfinyl)-,s-esterwitho,o-dimethylphosphorothioate
S-2-(ethylsulphinyl)ethyl OO-dimethyl phosphorothioate,oxydemeton-methyl
oxydemeton-methyl S-2-(ethylsulphinyl)ethyl O,O-dimethyl phosphorothioate
Demeton-S-methyl sulfoxide, Methyl oxydemeton, S-[2-(Ethylsulfinyl)ethyl] O, O-dimethyl phosphorothioate | [EINECS(EC#)]
206-110-7 | [Molecular Formula]
C6H15O4PS2 | [MDL Number]
MFCD00055488 | [MOL File]
301-12-2.mol | [Molecular Weight]
246.28 |
| Chemical Properties | Back Directory | [Melting point ]
<-20℃ | [Boiling point ]
106 °C(Press: 0.01 Torr) | [density ]
1.289 g/cm3 (20 ºC) | [vapor pressure ]
3.8×10-3 Pa (20°C) | [refractive index ]
1.5216 (589.3 nm 20℃) | [storage temp. ]
0-6°C | [Water Solubility ]
Miscible | [EPA Substance Registry System]
Oxydemeton-methyl (301-12-2) |
| Hazard Information | Back Directory | [Uses]
A metabolite of Demeton-S-methyl (D231370). An organophosphorus pesticide biomarker. | [General Description]
Clear amber liquid. | [Air & Water Reactions]
Water soluble. DEMETON-S-METHYL SULFOXIDE may be rapidly hydrolyzed by alkali . | [Reactivity Profile]
Organophosphates such as DEMETON-S-METHYL SULFOXIDE 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. | [Fire Hazard]
DEMETON-S-METHYL SULFOXIDE is flammable. | [Description]
Oxydemeton-methyl, i.e., demeton-S-methyl sulfoxide,
is a colorless oil, bp 106 ?C/0.01 mm Hg, vp 3.8 mPa
(20 ?C). It is miscible with water and soluble in most
organic solvents, except petroleum ether. Log Kow =
?0.74(21 ?C). Oxydemeton-methyl is relatively stable in
acidic media but hydrolyzed in alkalinemedia;DT50 values
(22 ?C) at pH 4, 7, and 9 are 107, 46, and 2 d, respectively. | [Chemical Properties]
Oxydemeton methyl is a colorless to amber-colored liquid.
Oxydemeton methyl is relatively slowly hydrolyzed in acidic
media, but rapidly hydrolyzed in alkaline media.
Oxydemeton methyl is miscible with
water; readily soluble (10–100 g/
100 mL) in dichloromethane,
2-propanol, and toluene; and practically
insoluble (＜1 g/100 mL) in n-hexane. | [Definition]
ChEBI: Oxydemeton-methyl is an organic thiophosphate and an organothiophosphate insecticide. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, an acaricide and an agrochemical. It is functionally related to a 2-(ethanesulfinyl)ethanol. | [Environmental Fate]
Soil. The sulfoxide group is oxidized to the sulfone and oxidative and hydrolytic
cleavage of the side chain gives dimethylphosphoric and phosphoric acids (Hartley and
Kidd, 1987). Oxamyl was degraded by the microorganism Pseudomonas putida in a
laboratory study using cultured bacteria (Zeigler, 1980).
Plant. In asparagus, oxydemeton-methyl was converted to the corresponding sulfone
(Szeto and Brown, 1982).
Chemical/Physical. Oxydemeton-methyl can be converted to the corresponding sulfone
by hydrogen peroxide (Cremlyn, 1991). Emits toxic fumes of phosphorus and sulfur oxides
when heated to decomposition (Sax and Lewis, 1987). | [Metabolic pathway]
Oxydemeton-methyl is the primary thiooxidation metabolite of demeton-
S-methyl. It is further oxidised rapidly to demeton-Smethylsulfon in all
media. The major route of further metabolism of both sulfoxide and
sulfone is via hydrolysis to the sulfoxide and sulfone thiols. Stage I1
metabolism of these thiol hydrolysis products proceeds via oxidation
and conjugation and is different in soil, plants and animals. In plants the
thiols are conjugated, whereas in animals they are mainly methylated and
oxidised to sulfoxides, sulfones and sulfonic acids. Demethylation is an
important route in mammals; however, the compound is sufficiently polar
for much to be excreted in the urine unchanged. Demethylation has also
been reported to occur in plants. | [Metabolism]
Almost 99% of orally administered
oxydemeton-methyl to animals is excreted within 48 h
in the urine. It is oxidized to the sulfone, followed by
hydrolytic cleavage of the P?S bond. The thiol metabolites
are conjugated or methylated. O-Demethylation is also an
important degradation route both inmammals and plants.
Oxydemeton-methyl is rapidly degraded in soils. | [Degradation]
Oxydemeton-methyl is relatively slowly hydrolysed in acidic media but
rapidly hydrolysed under alkaline conditions. Half-lives at pH values 4,7
and 9 were 107,46 and 2 days respectively (PM). Under sterile aqueous
conditions oxydemeton-methyl was degraded to give the oxidised
hydrolysis product bis[2-(ethylsulfinyl)ethyl] disulfide (2) (Ziegler et
al., 1980) (Scheme 1). | [Toxicity evaluation]
The
acute oral LD50 for rats is about 50 mg/kg. Inhalation
LC50 (4 h) for rats is 0.47 mg/L air. NOEL (2 yr) for rats
is 1 mg/kg diet (0.05 mg/kg/d). ADI is 0.3 μg/kg b.w. for
the sum of oxydemeton-methyl, demeton-S-methylsulfone,
and demeton-S-methyl. |
| Safety Data | Back Directory | [Hazard Codes ]
T,N | [Risk Statements ]
24/25-50 | [Safety Statements ]
23-36/37-45-61 | [RIDADR ]
3018 | [RTECS ]
TG1420000 | [HazardClass ]
6.1(a) | [PackingGroup ]
II | [Safety Profile]
Poison by ingestion,
skin contact, intravenous, and
intraperitoneal routes. Human mutation data
reported. When heated to decomposition it
emits very toxic fumes of POx and SOx. See
also other demeton entries. | [Hazardous Substances Data]
301-12-2(Hazardous Substances Data) | [Toxicity]
LC50 (96-hour) for rainbow trout 4.0 mg/L (Walker, 1964); LC50 (24-hour) for
rainbow trout and bluegill sunfish 10 mg/L (Hartley and Kidd, 1987); acute oral LD50 for
rats 65–75 mg/kg (Hartley and Kidd, 1987), 30 mg/kg (RTECS, 1985). |
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