Monolinuron
Appearance
Names | |
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Preferred IUPAC name
3-(4-Chlorophenyl)-1-methoxy-1-methylurea | |
Systematic IUPAC name
1-(4-Chlorophenyl)-3-methoxy-3-methylurea | |
Other names
N′-(4-Chlorophenyl)-N-methoxy-N-methylurea
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Identifiers | |
3D model (JSmol)
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2212523 | |
ChemSpider | |
ECHA InfoCard | 100.015.572 |
EC Number |
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KEGG | |
MeSH | Monolinuron |
PubChem CID
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RTECS number |
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C9H11ClN2O2 | |
Molar mass | 214.65 g·mol−1 |
Melting point | 80 to 83 °C (176 to 181 °F; 353 to 356 K) |
0.735 g/L | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Monolinuron is a pesticide,[1] more specifically a selective systemic herbicide[2] and an algaecide.[3] As an herbicide, it is used to control broad-leaved weeds and annual grasses in vegetable crops such as leeks, potatoes,[2] and dwarf French beans.[4] Monolinuron affects the photosynthesis in weeds. Following uptake of monolinuron through roots and leaves of weeds, monolinuron causes early symptoms of yellowing and die-back of the leaves, eventually resulting in weed death.[4] In fishkeeping it is used to control blanketweed and hair algae.[3]
References
- ^ Rossoff; Irving S. (2002). Encyclopedia of clinical toxicology. p. 718.
{{cite book}}
: CS1 maint: multiple names: authors list (link) - ^ a b Milne; George W. A. (2005). Gardner's commercially important chemicals. p. 44.
{{cite book}}
: CS1 maint: multiple names: authors list (link) - ^ a b "Pesticides: HSE registered products". Retrieved 2009-07-31.
- ^ a b "Department for Environment, Food and Rural Affairs, Evaluation of Fully Approved or Provisionally Approved Products, Evaluation on: Monolinuron, May 1995" (PDF). Retrieved 2011-08-19.
External links
- Monolinuron - Identification, toxicity, use, water pollution potential, ecological toxicity and regulatory information
- Monolinuron at the Compendium of Pesticide Common Names
- Monolinuron in the Pesticide Properties DataBase (PPDB)