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Details

Stereochemistry ACHIRAL
Molecular Formula C9H11ClN2O2
Molecular Weight 214.649
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MONOLINURON

SMILES

CON(C)C(=O)NC1=CC=C(Cl)C=C1

InChI

InChIKey=LKJPSUCKSLORMF-UHFFFAOYSA-N
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)

HIDE SMILES / InChI

Molecular Formula C9H11ClN2O2
Molecular Weight 214.649
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Efficient biotransformation of herbicide diuron by bacterial strain Micrococcus sp. PS-1.
2010-11
Determination of phenylurea and triazine herbicides in milk by microwave assisted ionic liquid microextraction high-performance liquid chromatography.
2010-09-15
Mineralisation of the herbicide linuron by Variovorax sp. strain RA8 isolated from Japanese river sediment using an ecosystem model (microcosm).
2010-08
Determination of phenylurea herbicides in aqueous samples using partitioned dispersive liquid-liquid microextraction.
2009-12-15
Simultaneous determination of 15 phenylurea herbicides in rice and corn using HPLC with fluorescence detection combined with UV decomposition and post-column derivatization.
2008-11-15
Comparison of four extraction methods for the analysis of 24 pesticides in soil samples with gas chromatography-mass spectrometry and liquid chromatography-ion trap-mass spectrometry.
2008-03-15
Application of the Doehlert design to optimize the signal obtained in photochemically induced fluorescence for the determination of eight phenylureas.
2008-03
Analysis of carbamate and phenylurea pesticide residues in fruit juices by solid-phase microextraction and liquid chromatography-mass spectrometry.
2007-04-20
Coupled-column liquid chromatography combined with postcolumn photochemical derivatization and fluorescence detection for the determination of herbicides in groundwater.
2007-03
Leaching potential of some phenylureas and their main metabolites through laboratory studies.
2006-10
Biomimetic approach to biomembrane models studies: medium influence on the interaction kinetics of some phenylurea derivatives herbicides.
2006-04-01
Monitoring of triazine and phenylurea herbicides in the surface waters of Greece.
2006
Isolation and characterisation of an isoproturon-mineralising Methylopila sp. TES from French agricultural soil.
2004-10-01
Application of solid-phase microextraction for determining phenylurea herbicides and their homologous anilines from vegetables.
2004-07-09
Application of solid-phase extraction and micellar electrokinetic capillary chromatography to the study of hydrolytic and photolytic degradation of phenoxy acid and phenylurea herbicides.
2004-01-23
Solid-phase microextraction coupled with high-performance liquid chromatography for the determination of phenylurea herbicides in aqueous samples.
2003-09-12
Direct determination of monolinuron, linuron and chlorbromuron residues in potato samples by gas chromatography with nitrogen-phosphorus detection.
2003-09-05
Analysis of phenylurea herbicides from plants by GC/MS.
2002-03-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:52:40 GMT 2025
Edited
by admin
on Mon Mar 31 18:52:40 GMT 2025
Record UNII
6KJJ4XAD6M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MONOLINURON [HSDB]
Preferred Name English
MONOLINURON
HSDB   ISO  
Common Name English
3-(4-CHLOROPHENYL)-1-METHOXY-1-METHYLUREA
Systematic Name English
N'-(4-CHLOROPHENYL)-N-METHOXY-N-METHYLUREA
Systematic Name English
MONOLINURON [MI]
Common Name English
MONOLINURON [ISO]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 207500
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
Code System Code Type Description
MERCK INDEX
m12028
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY
MESH
C030651
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY
ALANWOOD
monolinuron
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY
WIKIPEDIA
MONOLINURON
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY
HSDB
5030
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY
ECHA (EC/EINECS)
217-129-5
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY
FDA UNII
6KJJ4XAD6M
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY
CAS
1746-81-2
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID0037576
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY
PUBCHEM
15629
Created by admin on Mon Mar 31 18:52:40 GMT 2025 , Edited by admin on Mon Mar 31 18:52:40 GMT 2025
PRIMARY