332992
3-(4-Chlorophenyl)-1,1-dimethylurea
99%
Synonym(s):
Monuron
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About This Item
Linear Formula:
ClC6H4NHCON(CH3)2
CAS Number:
Molecular Weight:
198.65
EC Number:
205-766-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
2097922
MDL number:
Assay:
99%
InChI key
BMLIZLVNXIYGCK-UHFFFAOYSA-N
InChI
1S/C9H11ClN2O/c1-12(2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)
SMILES string
CN(C)C(=O)Nc1ccc(Cl)cc1
assay
99%
mp
173-174 °C (lit.)
Gene Information
human ... EPHX2(2053)
mouse ... Ephx2(13850)
General description
3-(4-Chlorophenyl)-1,1-dimethylurea is an inhibitor of photophosphorylation. The kinetics of photo-induced transformation of 3-(4-chlorophenyl)-1,1-dimethylurea has been investigated in aqueous solution containing nitrates and nitrites at 310nm and 365nm. Degradation of Monuron (3-(4-chlorophenyl)-1,1-dimethylurea) photoinduced by Fe(III) in aqueous solution has been reported.
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Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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STOMATAL RESPONSES TO CHANGES IN CARBON DIOXIDE CONCENTRATION IN LEAVES TREATED WITH 3-(4-CHLOROPHENYL)-1, 1-DIMETHYLUREA.
Allaway WG and Mansfield TA.
The New phytologist, 66(1), 57-63 (1967)
W Chu et al.
Chemosphere, 86(11), 1079-1086 (2011-12-30)
A comprehensive study of the degradation of monuron, one of the phenylurea herbicides, was conducted by UV-Vis/WO(3) process. It was found that hydroxyl radicals played a major role in the decay of monuron while other radicals (e.g. superoxide) and hole
Hui Li et al.
Environmental science & technology, 38(20), 5393-5399 (2004-11-17)
Pesticide adsorption by soil clays can be dramatically influenced by the exchangeable cations present. Among the common exchangeable base cations in soils (Ca2+, Mg2+, K+, and Na+), K+-saturated clays frequently demonstrate the strongest affinity for pesticides. In the presence of
Malathi Srinivasan et al.
Journal of biosciences, 31(5), 599-605 (2007-02-16)
Various urea-derived herbicides and different cytokinin analogues were used to determine their effects on callusing response and shoot regenerating capacity of alfalfa (Medicago sativa L.) and Coleus (Coleus forskohlii Briq.). The herbicides monuron and diuron evoked profuse callusing response from
Hana Mest'ánková et al.
Chemosphere, 57(10), 1307-1315 (2004-11-03)
The degradation of Monuron (3-(4-chlorophenyl)-1,1-dimethylurea) photoinduced by Fe(III) in aqueous solution has been investigated. The rate of degradation depends on the concentration of Fe(OH)2+, the most photoreactive species in terms of *OH radical formation. These *OH radicals are able to
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