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Details

Stereochemistry ACHIRAL
Molecular Formula C15H11ClF3NO4
Molecular Weight 361.7
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXYFLUORFEN

SMILES

CCOC1=CC(OC2=CC=C(C=C2Cl)C(F)(F)F)=CC=C1[N+]([O-])=O

InChI

InChIKey=OQMBBFQZGJFLBU-UHFFFAOYSA-N
InChI=1S/C15H11ClF3NO4/c1-2-23-14-8-10(4-5-12(14)20(21)22)24-13-6-3-9(7-11(13)16)15(17,18)19/h3-8H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C15H11ClF3NO4
Molecular Weight 361.7
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Oxyfluorfen is a selective pre and post-emergent herbicide. It is a contact herbicide and light is required for it to affect target plants. Oxyfluorfen can be used on weed-free soil to prevent germination of a wide variety of weeds or it can be applied to existing weeds at seedling stage especially with a tank mix partner to increase the variety of weeds controlled and/or the length of residual control. Oxyfluorfen can also be added at a low rate as a ‘spike’ to glyphosate or paraquat and diquat/paraquat herbicides to improve knockdown. It is available in emulsifiable concentrate and granular formulations.

Approval Year

PubMed

PubMed

TitleDatePubMed
Assessment of possible carcinogenicity of oxyfluorfen to humans using mode of action analysis of rodent liver effects.
2012-08
Environmental impact on vascular development predicted by high-throughput screening.
2011-11
Comparative study of human and mouse pregnane X receptor agonistic activity in 200 pesticides using in vitro reporter gene assays.
2011-02-27
Overexpression of a specific soybean GmGSTU4 isoenzyme improves diphenyl ether and chloroacetanilide herbicide tolerance of transgenic tobacco plants.
2010-10-01
Impact of environmental chemicals on key transcription regulators and correlation to toxicity end points within EPA's ToxCast program.
2010-03-15
Persistence and bioaccumulation of oxyfluorfen residues in onion.
2010-03
Enhanced dissipation of oxyfluorfen, ethalfluralin, trifluralin, propyzamide, and pendimethalin in soil by solarization and biosolarization.
2010-02-24
Development of a sample preparation method for the analysis of current-use pesticides in sediment using gas chromatography.
2010-02
[Determination of biphenyl ether herbicides in water using HPLC with cloud-point extraction].
2010-01
Pesticide extraction from table grapes and plums using ionic liquid based dispersive liquid-liquid microextraction.
2009-12
Ionic liquid based dispersive liquid-liquid microextraction for the extraction of pesticides from bananas.
2009-10-23
Pendimethalin and oxyfluorfen degradation under two irrigation conditions over four years application.
2009-05
Metabolism of nitrodiphenyl ether herbicides by dioxin-degrading bacterium Sphingomonas wittichii RW1.
2008-10-08
Optimization of separation and detection conditions for the multiresidue analysis of pesticides in grapes by comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry.
2008-05-09
Evaluation of six pesticides leaching indexes using field data of herbicide application in Casablanca Valley, Chile.
2007
Determination of diphenylether herbicides in water samples by solid-phase microextraction coupled to liquid chromatography.
2006-11
Effect of systemic herbicides on N2-fixing and phosphate solubilizing microorganisms in relation to availability of nitrogen and phosphorus in paddy soils of West Bengal.
2006-11
[Experimental study on oxyfluorfen technical herbicides induced mutagenicity].
2006-06
Herbicidal and antioxidant responses of transgenic rice overexpressing Myxococcus xanthus protoporphyrinogen oxidase.
2005-05
Assessment of the plasma desorption time-of-flight mass spectrometry technique for pesticide adsorption and degradation on 'as-received' treated soil samples.
2005
Pesticide patch test series for the assessment of allergic contact dermatitis among banana plantation workers in panama.
2004-09
Surface retention and photochemical reactivity of the diphenylether herbicide oxyfluorfen.
2004-04-13
Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells.
2004-04
Weed control and persistence of two oxyfluorfen formulations in olive groves under non tillage conditions.
2004
Oxyfluorfen toxic effect on S. obliquus evaluated by different photosynthetic and enzymatic biomarkers.
2003-11
A point mutation of valine-311 to methionine in Bacillus subtilis protoporphyrinogen oxidase does not greatly increase resistance to the diphenyl ether herbicide oxyfluorfen.
2003-10
Effect of the herbicides oxadiazon and oxyfluorfen on phosphates solubilizing microorganisms and their persistence in rice fields.
2003-10
Dissipation of the herbicide oxyfluorfen in subtropical soils and its potential to contaminate groundwater.
2003-02
Weed control in rose-scented geranium (Pelargonium spp).
2002-12
Jasmonate is involved in the induction of tyrosine aminotransferase and tocopherol biosynthesis in Arabidopsis thaliana.
2002-11
[Determination of acetochlor and oxyfluorfen by capillary gas chromatography].
2002-09
Degradation of oxyfluorfen by Azotobacter chroococcum (Beijerink).
2002-08
Toxicological effects of the herbicide oxyfluorfen on acetylcholinesterase in two fish species: Oreochromis niloticus and Gambusia affinis.
2002
Resistance of a soybean cell line to oxyfluorfen by overproduction of mitochondrial protoporphyrinogen oxidase.
2001-08
Herbicide-induced experimental variegate porphyria in mice: tissue porphyrinogen accumulation and response to porphyrogenic drugs.
1998-02-12
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:15:21 GMT 2025
Edited
by admin
on Mon Mar 31 19:15:21 GMT 2025
Record UNII
46GY4Y6567
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OXYFLUORFEN
HSDB   ISO   MI  
Common Name English
GALIGAN
Preferred Name English
RH 2915
Code English
2-CHLORO-4-TRIFLUOROMETHYLPHENYL 3-ETHOXY-4-NITROPHENYL ETHER
Systematic Name English
2'-CHLORO-3-ETHOXY-4'-TRIFLUOROMETHYL-4-NITRODIPHENYL ETHER
Common Name English
GOAL
Brand Name English
OXYGOLD
Brand Name English
KOLTAR
Brand Name English
RH-2915
Code English
BENZENE, 2-CHLORO-1-(3-ETHOXY-4-NITROPHENOXY)-4-(TRIFLUOROMETHYL)-
Systematic Name English
OXYFLUORFEN [ISO]
Common Name English
OXYFLUORFEN [MI]
Common Name English
RH 2915D
Code English
4-TRIFLUOROMETHYL-2-CHLORO-3'-ETHOXY-4'-NITROPHENYL ETHER
Common Name English
RH-2915D
Code English
2-CHLORO-1-(3-ETHOXY-4-NITROPHENOXY)-4-(TRIFLUOROMETHYL)BENZENE
Systematic Name English
OXYFLUORFEN [HSDB]
Common Name English
2-CHLORO-.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-P-TOLYL 3-ETHOXY-4-NITROPHENYL ETHER
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 111601
Created by admin on Mon Mar 31 19:15:21 GMT 2025 , Edited by admin on Mon Mar 31 19:15:21 GMT 2025
Code System Code Type Description
ALANWOOD
oxyfluorfen
Created by admin on Mon Mar 31 19:15:21 GMT 2025 , Edited by admin on Mon Mar 31 19:15:21 GMT 2025
PRIMARY
FDA UNII
46GY4Y6567
Created by admin on Mon Mar 31 19:15:21 GMT 2025 , Edited by admin on Mon Mar 31 19:15:21 GMT 2025
PRIMARY
CAS
42874-03-3
Created by admin on Mon Mar 31 19:15:21 GMT 2025 , Edited by admin on Mon Mar 31 19:15:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID7024241
Created by admin on Mon Mar 31 19:15:21 GMT 2025 , Edited by admin on Mon Mar 31 19:15:21 GMT 2025
PRIMARY
HSDB
7507
Created by admin on Mon Mar 31 19:15:21 GMT 2025 , Edited by admin on Mon Mar 31 19:15:21 GMT 2025
PRIMARY
PUBCHEM
39327
Created by admin on Mon Mar 31 19:15:21 GMT 2025 , Edited by admin on Mon Mar 31 19:15:21 GMT 2025
PRIMARY
MERCK INDEX
m8332
Created by admin on Mon Mar 31 19:15:21 GMT 2025 , Edited by admin on Mon Mar 31 19:15:21 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
255-983-0
Created by admin on Mon Mar 31 19:15:21 GMT 2025 , Edited by admin on Mon Mar 31 19:15:21 GMT 2025
PRIMARY