Monolinuron
From Infogalactic: the planetary knowledge core
Skeletal formula of monolinuron | |
Ball-and-stick model of the monolinuron molecule | |
Names | |
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Preferred IUPAC name
3-(4-chlorophenyl)-1-methoxy-1-methylurea
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Systematic IUPAC name
1-(4-Chlorophenyl)-3-methoxy-3-methylurea
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Other names
N′-(4-Chlorophenyl)-N-methoxy-N-methylurea
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Identifiers | |
1746-81-2 ![]() |
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2212523 | |
ChemSpider | 14868 ![]() |
EC Number | 217-129-5 |
Jmol 3D model | Interactive image |
KEGG | C18794 ![]() |
MeSH | Monolinuron |
PubChem | 15629 |
RTECS number | YS6425000 |
UNII | 6KJJ4XAD6M ![]() |
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Properties | |
C9H11ClN2O2 | |
Molar mass | 214.6 g/mol |
Melting point | 80 to 83 °C (176 to 181 °F; 353 to 356 K) |
0.735 g/L | |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Monolinuron is a pesticide,[1] more specifically a selective systemic herbicide[2] and an algaecide.[3] As a 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
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)
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