Revision as of 19:03, 18 April 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (← Previous edit |
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{{Chembox |
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{{Chembox |
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| Verifiedfields = changed |
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| verifiedrevid = 409106433 |
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| Watchedfields = changed |
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| Name = Mevinphos |
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| verifiedrevid = 424730608 |
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| ImageFile =Mevinphos.png |
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| Name = Mevinphos |
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| ImageSize = |
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| ImageFile =Mevinphos E,Z Isomers Formulae V.1.svg |
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| IUPACName_hidden = yes |
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| ImageSize = |
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| IUPACName = 2-methoxycarbonyl-1-methylvinyl dimethyl phosphate |
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| IUPACName = 2-methoxycarbonyl-1-methylvinyl dimethyl phosphate |
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| SystematicName = |
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| OtherNames = |
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| SystematicName = |
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| OtherNames = |
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| Section1 = {{Chembox Identifiers |
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|Section1={{Chembox Identifiers |
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| Abbreviations = |
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| Abbreviations = |
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| CASNo = 26718-65-0 |
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| CASNo = 7786-34-7 |
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| CASNo_Comment = |
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| CASNo_Comment = |
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| CASNo_Ref = <ref name=agrochem>{{cite book|editor=Muller, Franz|title=Agrochemicals: Composition, Production, Toxicology, Applications|year=2000|publisher=Wiley-VCH|location=Toronto|isbn=3-527-29852-5}}</ref> |
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| CASNo_Ref = {{cascite|correct|??}} |
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| PubChem =5355863 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| PubChem_Comment = |
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| UNII = 14ZYO4IKXT |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| PubChem = 9560 |
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| ChemSpiderID = |
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| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
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| EINECS = |
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| ChemSpiderID = 9185 |
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| SMILES = |
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| InChI = 1/C7H13O6P/c1-6(5-7(8)10-2)13-14(9,11-3)12-4/h5H,1-4H3 |
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| InChI = |
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| InChIKey = GEPDYQSQVLXLEU-UHFFFAOYAN |
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| Beilstein = |
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| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
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| Gmelin = |
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| StdInChI = 1S/C7H13O6P/c1-6(5-7(8)10-2)13-14(9,11-3)12-4/h5H,1-4H3 |
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| 3DMet =}} |
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| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
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| Section2 = {{Chembox Properties |
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| StdInChIKey = GEPDYQSQVLXLEU-UHFFFAOYSA-N |
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| Formula =C<sub>7</sub>H<sub>13</sub>O<sub></sub>6P |
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| MolarMass =224.1 |
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| EINECS = |
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| SMILES =CC(=CC(=O)OC)OP(=O)(OC)OC |
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| Appearance = colourless liquid<ref name=agrochem /> |
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| Density = |
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| Beilstein = |
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| MeltingPt = |
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| Gmelin = |
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| 3DMet =}} |
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| Melting_notes = |
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|Section2={{Chembox Properties |
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| BoilingPt =21 °C (''E'' isomer); 6.9 °C (''Z'' isomer) |
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| C=7 | H=13 | O=6 | P=1 |
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| pKa = |
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| Appearance = Colorless liquid<ref name=agrochem>{{cite book|editor=Muller, Franz|title=Agrochemicals: Composition, Production, Toxicology, Applications|year=2000|publisher=Wiley-VCH|location=Toronto|isbn=3-527-29852-5}}</ref> |
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| pKb = }} |
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| Density = 1.25 g/mL<ref name=PGCH/> |
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| Section3 = {{Chembox Structure |
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| MeltingPtC = 21 |
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| CrystalStruct = |
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| MeltingPt_notes = (''E'' isomer); 6.9 °C (''Z'' isomer) |
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| Coordination = |
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| MolShape = }} |
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| BoilingPtC = |
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| BoilingPt_notes = |
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| Section4 = {{Chembox Thermochemistry |
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| pKa = |
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| pKb = |
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| Solubility = miscible<ref name=PGCH/> |
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| VaporPressure = 0.003 mmHg (20°C)<ref name=PGCH/> |
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}} |
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}} |
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| Section5 = {{Chembox Pharmacology |
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|Section3={{Chembox Structure |
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| AdminRoutes = |
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| CrystalStruct = |
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| Bioavail = |
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| Coordination = |
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| Metabolism = |
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| MolShape = }} |
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|Section4={{Chembox Thermochemistry |
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| HalfLife = |
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}} |
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| ProteinBound = |
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|Section5={{Chembox Pharmacology |
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| Excretion = |
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| Legal_status = |
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| AdminRoutes = |
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| Legal_US = |
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| Bioavail = |
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| Legal_UK = |
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| Metabolism = |
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| Legal_AU = |
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| HalfLife = |
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| Legal_CA = |
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| ProteinBound = |
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| PregCat = |
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| Excretion = |
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| PregCat_AU = |
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| Legal_status = |
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| PregCat_US = }} |
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| Legal_US = |
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| Legal_UK = |
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| Section6 = {{Chembox Explosive |
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| ShockSens = |
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| Legal_AU = |
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| FrictionSens = |
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| Legal_CA = |
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| ExplosiveV = |
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| PregCat = |
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| REFactor = }} |
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| PregCat_AU = |
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| PregCat_US = }} |
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| Section7 = {{Chembox Hazards |
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|Section6={{Chembox Explosive |
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| ExternalMSDS = |
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| EUClass = |
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| ShockSens = |
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| EUIndex = |
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| FrictionSens = |
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| MainHazards = |
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| DetonationV = |
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| NFPA-H = |
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| REFactor = }} |
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|Section7={{Chembox Hazards |
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| NFPA-F = |
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| NFPA-R = |
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| ExternalSDS = |
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| NFPA-O = |
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| MainHazards = |
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| RPhrases = |
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| NFPA-H = |
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| SPhrases = |
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| NFPA-F = |
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| RSPhrases = |
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| NFPA-R = |
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| FlashPt = |
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| NFPA-S = |
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| FlashPtF = 347 |
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| Autoignition = |
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| FlashPt_ref = <ref name=PGCH/> |
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| ExploLimits = |
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| AutoignitionPt = |
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| LD50 =3.7 - 7 mg/kg (rat, oral)<ref name=agrochem /> |
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| PEL = }} |
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| ExploLimits = |
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| PEL = TWA 0.1 mg/m<sup>3</sup> <ref name=PGCH>{{PGCH|0503}}</ref> |
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| Section8 = {{Chembox Related |
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| IDLH = 4 ppm<ref name=PGCH/> |
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| OtherAnions = |
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| LC50 = 14 ppm (rat, 1 hr)<ref name=IDLH>{{IDLH|7786347|Phosdrin}}</ref> |
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| OtherCations = |
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| LD50 = 3 mg/kg (rat, oral)<br/>4 mg/kg (mouse, oral)<br/>6-7 mg/kg (rat, oral)<ref name=IDLH/> |
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| OtherFunctn = |
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| REL = TWA 0.01 ppm (0.1 mg/m<sup>3</sup>) ST 0.03 ppm (0.3 mg/m<sup>3</sup>) <ref name=PGCH/> |
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| Function = |
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}} |
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| OtherCpds = }} |
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|Section8={{Chembox Related |
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| OtherAnions = |
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}} |
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}} |
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'''Mevinphos''' is an ] ] that acts as an ] inhibitor to control insects in a wide range of crops. It is most commonly used for the control of chewing and sucking insects, as well as ]. |
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'''Mevinphos''' is a toxic ] ] that acts as an ] to control insects in a wide range of crops. It was most commonly used for the control of chewing and sucking insects, as well as ]. Common synonym names are duraphos, fosdrin, menite, mevinfos, mevinox, phosdrin, and phosdrine. It is not allowed in the ] anymore.<ref>{{PPDB|471}}</ref> |
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==Manufacture== |
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==Manufacture== |
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{{reflist}} |
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{{reflist}} |
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==Further reading== |
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{{insecticides}} |
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* {{cite book|editor=Wolverton, B.C.|title=Aquatic Plants for Removal of Mevinphos from the Aquatic Environment; Volume 72720 of NASA Technical memorandum|year=1975|publisher=National Space Technology Laboratories (U.S.)|location=Mississippi}} |
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==External links == |
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* {{PPDB|471}} |
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{{Insecticides}} |
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{{Acetylcholine metabolism and transport modulators}} |
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