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| verifiedrevid = 431632775 | | verifiedrevid = 431632775 | ||
|Reference=<ref>''Merck Index'', 11th Edition, '''5666'''.</ref> | |Reference=<ref>''Merck Index'', 11th Edition, '''5666'''.</ref> | ||
|ImageFile= |
|ImageFile=Mecoprop-2D-skeletal.png | ||
|ImageSize= |
|ImageSize=200px | ||
⚫ | |IUPACName=(''RS'')-2-(4-Chloro-2-methylphenoxy)propanoic acid | ||
|ImageFile1 = Mecoprop-racemic-dimer-from-xtal-labelled-3D-balls.png | |||
|ImageSize1=250px | |||
⚫ | |IUPACName=(''RS'')-2-(4- |
||
|OtherNames= | |OtherNames= | ||
|Section1= {{Chembox Identifiers | |Section1= {{Chembox Identifiers | ||
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}} | }} | ||
|Section2= {{Chembox Properties | |Section2= {{Chembox Properties | ||
| C=10|H=11|Cl=1|O=3 | |||
| Formula=C<sub>10</sub>H<sub>11</sub>ClO<sub>3</sub> | |||
| MolarMass=214.646 | |||
| Appearance=Solid | | Appearance=Solid | ||
| Density= | | Density= | ||
| MeltingPt= 94–95 °C <ref name="GESTIS">{{GESTIS|ZVG=510276|Name=Mecoprop|Date=8 September 2008}}</ref> | | MeltingPt= 94–95 °C <ref name="GESTIS">{{GESTIS|ZVG=510276|Name=Mecoprop|Date=8 September 2008}}</ref> | ||
| BoilingPt= decomposes <ref name="GESTIS"/> | | BoilingPt= decomposes <ref name="GESTIS"/> | ||
| Solubility= 900 mg/ |
| Solubility= 900 mg/L(20 °C) <ref name="GESTIS"/> | ||
}} | }} | ||
|Section3= {{Chembox Hazards | |Section3= {{Chembox Hazards |
Revision as of 11:44, 17 May 2013
Names | |
---|---|
IUPAC name (RS)-2-(4-Chloro-2-methylphenoxy)propanoic acid | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ECHA InfoCard | 100.002.060 |
KEGG | |
PubChem CID | |
CompTox Dashboard (EPA) | |
SMILES
| |
Properties | |
Chemical formula | C10H11ClO3 |
Molar mass | 214.65 g·mol |
Appearance | Solid |
Melting point | 94–95 °C |
Boiling point | decomposes |
Solubility in water | 900 mg/L(20 °C) |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards | Xn, N |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Mecoprop, or methylchlorophenoxypropionic acid (MCPP), is a common general use herbicide found in many household weed killers and "weed-and-feed" type lawn fertilizers. It is primarily used to control broadleaf weeds. It is often used in combination with other chemically related herbicides such as 2,4-D, dicamba, and MCPA.
Mecoprop is a mixture of two stereoisomers, with the (R)-(+)-enantiomer ("Mecoprop-P", "Duplosan KV") possessing the herbicidal activity.
The United States Environmental Protection Agency has classified mecoprop as toxicity class III - slightly toxic.
See also
References
- Merck Index, 11th Edition, 5666.
- ^ Record of Mecoprop in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 8 September 2008.
- Template:HPD
- ^ Mecoprop at EXTOXNET
- G. Smith, C. H. L. Kennard, A. H. White and P. G. Hodgson (1980). "(+-)-2-(4-Chloro-2-methylphenoxy)propionic acid (mecoprop)". Acta Cryst. B36 (4): 992–994. doi:10.1107/S0567740880005134.
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External links
- Mecoprop Pesticide Information Profile - Extension Toxicology Network
- Mecoprop at AlanWood.net
- Mecoprop at pesticideinfo.org
- Mecoprop at coastalwiki.org