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Details

Stereochemistry ACHIRAL
Molecular Formula C13H16F3N3O4
Molecular Weight 335.279
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIFLURALIN

SMILES

CCCN(CCC)C1=C(C=C(C=C1[N+]([O-])=O)C(F)(F)F)[N+]([O-])=O

InChI

InChIKey=ZSDSQXJSNMTJDA-UHFFFAOYSA-N
InChI=1S/C13H16F3N3O4/c1-3-5-17(6-4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C13H16F3N3O4
Molecular Weight 335.279
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Protective glove use and hygiene habits modify the associations of specific pesticides with Parkinson's disease.
2015-02
Comparative study of human and mouse pregnane X receptor agonistic activity in 200 pesticides using in vitro reporter gene assays.
2011-02-27
Body mass index, agricultural pesticide use, and cancer incidence in the Agricultural Health Study cohort.
2010-11
Synthesis and evaluation of oryzalin analogs against Toxoplasma gondii.
2010-09-01
Pesticide use and myocardial infarction incidence among farm women in the agricultural health study.
2010-07
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
2010-04
Toxicity of herbicides to cyanobacterial isolates.
2009-05
Mechanism of trifluralin-induced thyroid tumors in rats.
2008-07-30
Cancer incidence among pesticide applicators exposed to trifluralin in the Agricultural Health Study.
2008-06
In silico prediction of pregnane X receptor activators by machine learning approaches.
2007-01
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Antiparasitic activity of flavonoids and isoflavones against Cryptosporidium parvum and Encephalitozoon intestinalis.
2006-06
Cellular and molecular actions of dinitroaniline and phosphorothioamidate herbicides on Plasmodium falciparum: tubulin as a specific antimalarial target.
2006-02
Environmental fate of herbicides trifluralin, metazachlor, metamitron and sulcotrione compared with that of glyphosate, a substitute broad spectrum herbicide for different glyphosate-resistant crops.
2005-09
CAR and PXR: xenosensors of endocrine disrupters?
2005-08-15
Transgenic rice containing human CYP2B6 detoxifies various classes of herbicides.
2005-05-04
Genes similar to naphthalene dioxygenase genes in trifluralin-degrading bacteria.
2004-05
Endocrine disruptors induce cytochrome P450 by affecting transcriptional regulation via pregnane X receptor.
2003-11-15
Biodegradation of the herbicide trifluralin by bacteria isolated from soil.
2003-03-01
Fate of pesticides in tropical soils of Brazil under field conditions.
2002-02-12
Effect of nutritional and environmental conditions on the production and composition of rhamnolipids by P. aeruginosa UG2.
2001-03
Dinitroaniline herbicides against protozoan parasites: the case of Trypanosoma cruzi.
2001-03
A comparison of the effects of two dinitroanilines against Cryptosporidium parvum in vitro and in vivo in neonatal mice and rats.
1999-11
Improved efficacy of dinitroaniline analogs for use as anti-cryptosporidial drugs.
1999-10-16
Assessment of drugs against Cryptosporidium parvum using a simple in vitro screening method.
1999-09-15
Synthesis and evaluation of dinitroanilines for treatment of cryptosporidiosis.
1998-02
Inhibition of Toxoplasma gondii replication by dinitroaniline herbicides.
1996-12
In vitro evaluation of anticryptosporidial agents using MDCK cell culture and chemiluminescence immunoassay.
1996-09-01
In vitro anticryptosporidial activity of dinitroaniline herbicides.
1996-03-01
Efficacy of the herbicide trifluralin against four P-glycoprotein-expressing strains of Leishmania.
1995-07
Protective effects of trifluralin on benzo(a)pyrene-induced tumors in A/J mice.
1985-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:46:02 GMT 2025
Edited
by admin
on Mon Mar 31 17:46:02 GMT 2025
Record UNII
C8BX46QL7K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIFLURALIN
HSDB   ISO   MI  
Common Name English
.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-2,6-DINITRO-N,N-DIPROPYL-P-TOLUIDINE
Preferred Name English
2,6-DINITRO-N,N-DIPROPYL-4-(TRIFLUOROMETHYL)BENZENAMINE
Systematic Name English
TRIFLURALIN [MI]
Common Name English
TRIFLURALIN [HSDB]
Common Name English
TRIFLURALIN [IARC]
Common Name English
TRIFLURALIN [ISO]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 36101
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
Code System Code Type Description
CHEBI
35027
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY
CAS
1582-09-8
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY
MERCK INDEX
m11124
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID4021395
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY
PUBCHEM
5569
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
216-428-8
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY
WIKIPEDIA
TRIFLURALIN
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY
MESH
D014274
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY
ALANWOOD
trifluralin
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY
FDA UNII
C8BX46QL7K
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY
HSDB
1003
Created by admin on Mon Mar 31 17:46:02 GMT 2025 , Edited by admin on Mon Mar 31 17:46:02 GMT 2025
PRIMARY