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Mevinphos: Difference between revisions

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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 Latest revision as of 13:29, 23 September 2024 edit undo5.178.188.143 (talk)No edit summaryTag: Visual edit 
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{{Chembox {{Chembox
| Verifiedfields = changed
| verifiedrevid = 409106433
| Watchedfields = changed
| Name = Mevinphos
| verifiedrevid = 424730608
| ImageFile =Mevinphos.png
| Name = Mevinphos
| ImageSize =
| ImageFile =Mevinphos E,Z Isomers Formulae V.1.svg
| IUPACName_hidden = yes
| ImageSize =
| IUPACName = 2-methoxycarbonyl-1-methylvinyl dimethyl phosphate
| IUPACName = 2-methoxycarbonyl-1-methylvinyl dimethyl phosphate
| SystematicName =
| OtherNames = | SystematicName =
| OtherNames =
| Section1 = {{Chembox Identifiers
|Section1={{Chembox Identifiers
| Abbreviations =
| Abbreviations =
| CASNo = 26718-65-0
| CASNo = 7786-34-7
| CASNo_Comment =
| CASNo_Comment =
| 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>
| CASNo_Ref = {{cascite|correct|??}}
| PubChem =5355863
| UNII_Ref = {{fdacite|correct|FDA}}
| PubChem_Comment =
| UNII = 14ZYO4IKXT
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| PubChem = 9560
| ChemSpiderID =
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| EINECS =
| ChemSpiderID = 9185
| SMILES =
| InChI = 1/C7H13O6P/c1-6(5-7(8)10-2)13-14(9,11-3)12-4/h5H,1-4H3
| InChI =
| InChIKey = GEPDYQSQVLXLEU-UHFFFAOYAN
| Beilstein =
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| Gmelin =
| StdInChI = 1S/C7H13O6P/c1-6(5-7(8)10-2)13-14(9,11-3)12-4/h5H,1-4H3
| 3DMet =}}
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| Section2 = {{Chembox Properties
| StdInChIKey = GEPDYQSQVLXLEU-UHFFFAOYSA-N
| Formula =C<sub>7</sub>H<sub>13</sub>O<sub></sub>6P
| MolarMass =224.1 | EINECS =
| SMILES =CC(=CC(=O)OC)OP(=O)(OC)OC
| Appearance = colourless liquid<ref name=agrochem />
| Density = | Beilstein =
| MeltingPt = | Gmelin =
| 3DMet =}}
| Melting_notes =
|Section2={{Chembox Properties
| BoilingPt =21 °C (''E'' isomer); 6.9 °C (''Z'' isomer)
| C=7 | H=13 | O=6 | P=1
| pKa =
| 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>
| pKb = }}
| Density = 1.25 g/mL<ref name=PGCH/>
| Section3 = {{Chembox Structure
| MeltingPtC = 21
| CrystalStruct =
| MeltingPt_notes = (''E'' isomer); 6.9 °C (''Z'' isomer)
| Coordination =
| MolShape = }} | BoilingPtC =
| BoilingPt_notes =
| Section4 = {{Chembox Thermochemistry
| pKa =
| pKb =
| Solubility = miscible<ref name=PGCH/>
| VaporPressure = 0.003 mmHg (20°C)<ref name=PGCH/>
}} }}
| Section5 = {{Chembox Pharmacology |Section3={{Chembox Structure
| AdminRoutes = | CrystalStruct =
| Bioavail = | Coordination =
| Metabolism = | MolShape = }}
|Section4={{Chembox Thermochemistry
| HalfLife =
}}
| ProteinBound =
|Section5={{Chembox Pharmacology
| Excretion =
| Legal_status = | AdminRoutes =
| Legal_US = | Bioavail =
| Legal_UK = | Metabolism =
| Legal_AU = | HalfLife =
| Legal_CA = | ProteinBound =
| PregCat = | Excretion =
| PregCat_AU = | Legal_status =
| PregCat_US = }} | Legal_US =
| Legal_UK =
| Section6 = {{Chembox Explosive
| ShockSens = | Legal_AU =
| FrictionSens = | Legal_CA =
| ExplosiveV = | PregCat =
| REFactor = }} | PregCat_AU =
| PregCat_US = }}
| Section7 = {{Chembox Hazards
|Section6={{Chembox Explosive
| ExternalMSDS =
| EUClass = | ShockSens =
| EUIndex = | FrictionSens =
| MainHazards = | DetonationV =
| NFPA-H = | REFactor = }}
|Section7={{Chembox Hazards
| NFPA-F =
| NFPA-R = | ExternalSDS =
| NFPA-O = | MainHazards =
| RPhrases = | NFPA-H =
| SPhrases = | NFPA-F =
| RSPhrases = | NFPA-R =
| FlashPt = | NFPA-S =
| FlashPtF = 347
| Autoignition =
| FlashPt_ref = <ref name=PGCH/>
| ExploLimits =
| AutoignitionPt =
| LD50 =3.7 - 7 mg/kg (rat, oral)<ref name=agrochem />
| PEL = }} | ExploLimits =
| PEL = TWA 0.1 mg/m<sup>3</sup> <ref name=PGCH>{{PGCH|0503}}</ref>
| Section8 = {{Chembox Related
| IDLH = 4 ppm<ref name=PGCH/>
| OtherAnions =
| LC50 = 14 ppm (rat, 1 hr)<ref name=IDLH>{{IDLH|7786347|Phosdrin}}</ref>
| OtherCations =
| LD50 = 3 mg/kg (rat, oral)<br/>4 mg/kg (mouse, oral)<br/>6-7 mg/kg (rat, oral)<ref name=IDLH/>
| OtherFunctn =
| 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/>
| Function =
}}
| OtherCpds = }}
|Section8={{Chembox Related
| OtherAnions =
| OtherCations =
| OtherFunction =
| OtherFunction_label =
| OtherCompounds =
}}
}} }}


'''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 ]. '''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>


==Manufacture== ==Manufacture==
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{{reflist}} {{reflist}}


==Further reading==
{{insecticides}}
* {{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}}

==External links ==
* {{PPDB|471}}

{{Insecticides}}
{{Acetylcholine metabolism and transport modulators}}


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