dimethoate
phosphorodithioic acid, O,O-dimethyl S-[2-(methylamino)-2-oxoethyl] ester

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CAS Number: 60-51-5 3D/inchi Other(deleted CASRN): 11003-53-5 ECHA EINECS - REACH Pre-Reg: 200-679-5 FDA UNII: W6U08B045O Nikkaji Web: J1.926G Beilstein Number: 1785339 MDL: MFCD00053676 XlogP3: 0.80 (est) Molecular Weight: 229.25900200 Formula: C5 H12 N O3 P S2 BioActivity Summary: listing NMR Predictor: Predict (works with chrome, Edge or firefox) Category:herbicides / pesticides   US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information: Google Scholar: Search Google Books: Search Google Scholar: with word "volatile" Search Google Scholar: with word "flavor" Search Google Scholar: with word "odor" Search Google Patents: Search US Patents: Search EU Patents: Search Pubchem Patents: Search PubMed: Search NCBI: Search   Physical Properties: Appearance: white crystalline solid (est) Assay: 95.00 to 100.00 Food Chemicals Codex Listed: No Melting Point: 52.00 °C. @ 760.00 mm Hg Boiling Point: 107.00 °C. @ 760.00 mm Hg (est) Vapor Pressure: 1.875000 mmHg @ 25.00 °C. (est) Flash Point: 32.00 °F. TCC ( 0.00 °C. ) (est) logP (o/w): 0.780 Soluble in:   water, 2.50E+04 mg/L @ 21C (exp)   water, 6626 mg/L @ 25 °C (est)   Organoleptic Properties: Odor and/or flavor descriptions from others (if found).   Cosmetic Information: None found   Suppliers: Sigma-Aldrich For experimental / research use only. Dimethoate PESTANAL®, analytical standard   Safety Information:   Hazards identification   Classification of the substance or mixture GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) None found. GHS Label elements, including precautionary statements   Pictogram   Hazard statement(s) None found. Precautionary statement(s) None found. Oral/Parenteral Toxicity: oral-bird - wild LD50 6600 ug/kg Toxicology and Applied Pharmacology. Vol. 21, Pg. 315, 1972. oral-cat LD50 100 mg/kg BEHAVIORAL: EXCITEMENT Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 28(3), Pg. 21, 1963. oral-chicken LD50 25 mg/kg Journal of Agricultural and Food Chemistry. Vol. 11, Pg. 91, 1963. oral-dog LD50 400 mg/kg Special Publication of the Entomological Society of America. Vol. 78-1, Pg. 31, 1978. oral-duck LD50 42 mg/kg Down to Earth. Vol. 35, Pg. 25, 1979. intraperitoneal-guinea pig LD10 390 mg/kg Toxicology and Applied Pharmacology. Vol. 8, Pg. 259, 1966. oral-guinea pig LD50 350 mg/kg Pesticide Chemicals Official Compendium, Association of the American Pesticide Control Officials, Inc., 1966. Vol. -, Pg. 395, 1966. intraperitoneal-hamster LD50 160 mg/kg Archives of Toxicology. Vol. 58, Pg. 152, 1986. oral-hamster LD50 200 mg/kg GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE LUNGS, THORAX, OR RESPIRATION: DYSPNEA British Journal of Industrial Medicine. Vol. 21, Pg. 52, 1964. oral-human LD50 30 mg/kg Guide to the Chemicals Used in Crop Protection. Vol. 6, Pg. 209, 1973. oral-man TDLo 286 mg/kg LUNGS, THORAX, OR RESPIRATION: DYSPNEA PERIPHERAL NERVE AND SENSATION: FASCICULATIONS BEHAVIORAL: COMA Intensive Care Medicine. Vol. 12, Pg. 110, 1986. oral-man TDLo 300 mg/kg CARDIAC: PULSE RATE VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION BEHAVIORAL: COMA Journal of Toxicology, Clinical Toxicology. Vol. 24, Pg. 69, 1986. oral-man TDLo 357 mg/kg BRAIN AND COVERINGS: OTHER DEGENERATIVE CHANGES KIDNEY, URETER, AND BLADDER: "CHANGES IN TUBULES (INCLUDING ACUTE RENAL FAILURE, ACUTE TUBULAR NECROSIS)" CARDIAC: CARDIOMYOPATHY INCLUDING INFARCTION Journal of Toxicology, Clinical Toxicology. Vol. 32, Pg. 61, 1994. intraperitoneal-mouse LD50 45 mg/kg GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE LUNGS, THORAX, OR RESPIRATION: DYSPNEA British Journal of Industrial Medicine. Vol. 21, Pg. 52, 1964. oral-mouse LD50 60 mg/kg GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS LUNGS, THORAX, OR RESPIRATION: DYSPNEA SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE British Journal of Industrial Medicine. Vol. 21, Pg. 52, 1964. unreported-mouse LD50 158 mg/kg Rinsho Shinkeigaku. Clinical Neurology. Vol. 23, Pg. 101, 1983. oral-quail LD50 25 mg/kg Journal of Agricultural and Food Chemistry. Vol. 29, Pg. 772, 1981. oral-rabbit LD50 300 mg/kg Special Publication of the Entomological Society of America. Vol. 78-1, Pg. 31, 1978. intraperitoneal-rat LD50 100 mg/kg SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS LUNGS, THORAX, OR RESPIRATION: DYSPNEA British Journal of Industrial Medicine. Vol. 21, Pg. 52, 1964. intravenous-rat LD50 450 mg/kg SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE LUNGS, THORAX, OR RESPIRATION: DYSPNEA GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS British Journal of Industrial Medicine. Vol. 21, Pg. 52, 1964. oral-rat LD50 60 mg/kg Yakkyoku. Pharmacy. Vol. 30, Pg. 623, 1979. unreported-rat LD50 215 mg/kg Yakkyoku. Pharmacy. Vol. 28, Pg. 225, 1977. Dermal Toxicity: skin-guinea pig LD50 965 mg/kg Toxicology and Applied Pharmacology. Vol. 3, Pg. 210, 1961. subcutaneous-hamster LD50 60 mg/kg SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS LUNGS, THORAX, OR RESPIRATION: DYSPNEA British Journal of Industrial Medicine. Vol. 21, Pg. 52, 1964. skin-mouse LD50 1000 mg/kg Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 33(6), Pg. 6, 1968. subcutaneous-mouse LD50 60 mg/kg LUNGS, THORAX, OR RESPIRATION: DYSPNEA GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE British Journal of Industrial Medicine. Vol. 21, Pg. 52, 1964. skin-rabbit LD50 1000 mg/kg BEHAVIORAL: EXCITEMENT Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 28(3), Pg. 21, 1963. skin-rat LD50 353 mg/kg British Journal of Industrial Medicine. Vol. 26, Pg. 59, 1969. subcutaneous-rat LD50 350 mg/kg SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE LUNGS, THORAX, OR RESPIRATION: DYSPNEA GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS British Journal of Industrial Medicine. Vol. 21, Pg. 52, 1964. Inhalation Toxicity: Not determined   Safety in Use Information: Category: herbicides / pesticides Recommendation for dimethoate usage levels up to:   not for fragrance use.   Recommendation for dimethoate flavor usage levels up to:   not for flavor use.   Safety References: European Food Safety Authority (EFSA) reference(s): Conclusion on the peer review of the pesticide risk assessment of confirmatory data submitted for the active substance dimethoate View page or View pdf Retrospective analysis of the immunotoxic effects of plant protection products as reported in the Draft Assessment Reports for their peer review at EU level View page or View pdf Assessment of the risk to human health through the pesticide active substance dimethoate and its metabolites in food View page or View pdf Prioritised review of the existing maximum residue levels for dimethoate and omethoate according to Article 43 of Regulation (EC) No 396/2005 View page or View pdf Peer review of the pesticide risk assessment of the active substance dimethoate View page or View pdf EPI System: View EPA-Iris:IRIS NIOSH International Chemical Safety Cards:search Chemical Carcinogenesis Research Information System:Search AIDS Citations:Search Cancer Citations:Search Toxicology Citations:Search Carcinogenic Potency Database:Search EPA GENetic TOXicology:Search EPA Substance Registry Services (TSCA):60-51-5 EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :3082 National Institute of Allergy and Infectious Diseases:Data WGK Germany:3 2-dimethoxyphosphinothioylsulfanyl-N-methylacetamide Chemidplus:0000060515 EPA/NOAA CAMEO:hazardous materials RTECS:60-51-5   References:   2-dimethoxyphosphinothioylsulfanyl-N-methylacetamide NIST Chemistry WebBook: Search Inchi Pubchem (cid): 3082 Pubchem (sid): 134970544   Other Information: (IUPAC): Atomic Weights of the Elements 2011 (pdf) Videos: The Periodic Table of Videos tgsc: Atomic Weights use for this web site (IUPAC): Periodic Table of the Elements CHEBI: View CHEMBL: View KEGG (GenomeNet): C14326 HMDB (The Human Metabolome Database): Search ChemSpider: View Wikipedia: View Formulations/Preparations: •pratt cygon 2-e systemic insecticide active ingredient 23.4% dimethoate •de-fend e-267 dimethoate systemic insecticide active ingredient 30.5% dimethoate •emulsifiable concentrate dustable powder; aerosol; ulv ultra low vol liquid ... •these include: bio systemic insecticide (pan britannica ind), vitex (la littorale) ec (200, 400, or 600 g technicall); 'rogor as' ul (300 gl); turbair systemic insecticide (pan britannica ind), ul; wp (200 gkg); granules (50 gkg). •technical grade is 98% pure •trade names: digon, duragon, rebelate, dimate   Potential Blenders and core components note None Found   Potential Uses: None Found   Occurrence (nature, food, other):note   not found in nature   Synonyms:   aadimethoal   acetic acid, O,O-dimethyldithiophosphoryl-, N-monomethylamide salt   cekuthoate   cygon   de-fend   devigon   dimate   dimetate   dimethogen 2- dimethoxyphosphinothioylsulfanyl-N-methylacetamide O,O- dimethyl phosphorodithioate S-ester with 2-mercapto-N-methylacetamide (8CI)   dimethyl phosphorodithioate, S-ester with 2-mercapto-N-methylacetamide   dimethyl S-((methylcarbamoyl)methyl) phosphorodithioate O,O- dimethyl S-((methylcarbamoyl)methyl)phosphorodithioate O,O- dimethyl S-(2-(methylamino)-2-oxoethyl) phosphorodithioate   dimethyl S-(N-(methylcarbamoyl)methyl) phosphorodithioate O,O- dimethyl S-(N-methylcarbamoylmethyl) dithiophosphate O,O- dimethyl S-(N-Methylcarbamoylmethyl) Phosphorodithioate O,O- dimethyl S-(N-methylcarbamylmethyl) thiothionophosphate O,O- dimethyl S-[2-(methylamino)-2-oxoethyl] dithiophosphate O,O- dimethyl S-[2-(methylamino)-2-oxoethyl] phosphorodithioate O,O- dimethyl S-methylcarbamoylmethyl phosphorodithioate O,O- dimethyl S-methylcarbamoylmethylphosphorodithioate O,O- dimethyl-S-(N-monomethyl)-carbamyl methyl dithiophosphate   dimeton   dimevur   ferkethion   fosfamid   fosfotox   perfecthion   phosphorodithioic acid O,O-dimethyl ester ester with 2-mercapto-N-methylacetamide   phosphorodithioic acid O,O-dimethyl ester, ester with 2-mercapto-N-methylacetamide   phosphorodithioic acid O,O-dimethyl S-(2-(methylamino)-2-oxoethyl) ester   phosphorodithioic acid O,O-dimethyl S-[2-(methylamino)-2-oxoethyl] ester   phosphorodithioic acid, O,O-dimethyl ester, S-ester with 2-mercapto-N-methylacetamide   phosphorodithioic acid, O,O-dimethyl S-(2-(methylamino)-2-oxoethyl) ester   phosphorodithioic acid, O,O-dimethyl S-[2-(methylamino)-2-oxoethyl] ester   racusan   rogodan   rogor   roxion   sevigor   sinoratox   systoate   trimetion   Articles:   None found yet. 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Notes: an organothiophosphorus cholinesterase inhibitor that is used as a systemic and contact insecticide.

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