Mecoprop
Names | |
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IUPAC name
(RS)-2-(4-Chloro-2-methylphenoxy)propanoic acid | |
Identifiers | |
93-65-2 | |
3D model (Jmol) | Interactive image |
ChEBI | CHEBI:75704 |
ChEMBL | ChEMBL2145254 |
ChemSpider | 6886 |
ECHA InfoCard | 100.002.060 |
EC Number | 230-386-8 |
KEGG | C18742 |
PubChem | 7153 |
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Properties | |
C10H11ClO3 | |
Molar mass | 214.65 g·mol−1 |
Appearance | Solid |
Melting point | 94 to 95 °C (201 to 203 °F; 367 to 368 K) [2] |
Boiling point | decomposes [2] |
900 mg/L(20 °C) [2] | |
Hazards | |
Main hazards | Xn, N [2] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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.[3] It is primarily used to control broadleaf weeds.[4] It is often used in combination with other chemically related herbicides such as 2,4-D, dicamba, and MCPA.
The United States Environmental Protection Agency has classified mecoprop as toxicity class III - slightly toxic.[4]
Mecoprop is a mixture of two stereoisomers, with the (R)-(+)-enantiomer ("Mecoprop-P", "Duplosan KV") possessing the herbicidal activity.[5]
See also
References
- ↑ Merck Index, 11th Edition, 5666.
- 1 2 3 4 Record of Mecoprop in the GESTIS Substance Database of the IFA, accessed on 8 September 2008
- ↑ Record in the Household Products Database of NLM
- 1 2 Mecoprop at EXTOXNET
- ↑ G. Smith, C. H. L. Kennard, A. H. White and P. G. Hodgson (April 1980). "(±)-2-(4-Chloro-2-methylphenoxy)propionic acid (mecoprop)". Acta Crystallogr. B. 36 (4): 992–994. doi:10.1107/S0567740880005134.
External links
- Mecoprop Pesticide Information Profile - Extension Toxicology Network
- Mecoprop at AlanWood.net
- Mecoprop at pesticideinfo.org
- Mecoprop at coastalwiki.org
- Mecoprop in the Pesticide Properties DataBase (PPDB)
- Mecoprop-P in the Pesticide Properties DataBase (PPDB)
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