Mecoprop
From Self-sufficiency
Mecoprop[1] | |
---|---|
File:(±)-Mecoprop Enantiomers Formulae.png | |
File:Mecoprop-racemic-dimer-from-xtal-labelled-3D-balls.png | |
(RS)-2-(4-chloro-2-methylphenoxy)propanoic acid | |
style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
CAS number | 93-65-2 |
PubChem | 7153 |
SMILES | Script error: No such module "collapsible list". |
style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
Molecular formula | C10H11ClO3 |
Molar mass | 214.646 |
Appearance | Solid |
Melting point |
94–95 °C [2] |
Boiling point |
decomposes [2] |
Solubility in water | 900 mg/l (20 °C) [2] |
style="background: #F8EABA; text-align: center;" colspan="2" | Hazards | |
Main hazards | Xn, N [2] |
(what is this?) (verify) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
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.
Mecoprop is a mixture of two stereoisomers, with the (R)-(+)-enantiomer ("Mecoprop-P", "Duplosan KV") possessing the herbicidal activity[5].
The United States Environmental Protection Agency has classified mecoprop as toxicity class III - slightly toxic.[4]
See also
References
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External links
- Mecoprop Pesticide Information Profile - Extension Toxicology Network
- Mecoprop at AlanWood.net
- Mecoprop at pesticideinfo.org
- Mecoprop at coastalwiki.orgde:Mecoprop
- ↑ Merck Index, 11th Edition, 5666.
- ↑ 2.0 2.1 2.2 2.3 Record of Mecoprop in the GESTIS Substance Database from the IFA, accessed on 8 September 2008
- ↑ Record in the Household Products Database of NLM
- ↑ 4.0 4.1 Mecoprop at EXTOXNET
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.