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Monolinuron

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Monolinuron
Skeletal formula of monolinuron
Ball-and-stick model of the monolinuron molecule
Names
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
Identifiers
3D model (JSmol)
2212523
ChemSpider
ECHA InfoCard 100.015.572 Edit this at Wikidata
EC Number
  • 217-129-5
KEGG
MeSH Monolinuron
RTECS number
  • YS6425000
UNII
  • InChI=1S/C9H11ClN2O2/c1-12(14-2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13) checkY
    Key: LKJPSUCKSLORMF-UHFFFAOYSA-N checkY
  • Clc1ccc(NC(=O)N(OC)C)cc1
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).
checkY verify (what is checkY☒N ?)

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

  1. ^ Rossoff; Irving S. (2002). Encyclopedia of clinical toxicology. p. 718.{{cite book}}: CS1 maint: multiple names: authors list (link)
  2. ^ a b Milne; George W. A. (2005). Gardner's commercially important chemicals. p. 44.{{cite book}}: CS1 maint: multiple names: authors list (link)
  3. ^ a b "Pesticides: HSE registered products". Retrieved 2009-07-31.
  4. ^ 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.