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Details

Stereochemistry RACEMIC
Molecular Formula C15H10ClF3NO4.Na
Molecular Weight 383.682
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HALOXYFOP-SODIUM

SMILES

[Na+].CC(OC1=CC=C(OC2=NC=C(C=C2Cl)C(F)(F)F)C=C1)C([O-])=O

InChI

InChIKey=DUZVBQWEFKXWJM-UHFFFAOYSA-M
InChI=1S/C15H11ClF3NO4.Na/c1-8(14(21)22)23-10-2-4-11(5-3-10)24-13-12(16)6-9(7-20-13)15(17,18)19;/h2-8H,1H3,(H,21,22);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C15H10ClF3NO4
Molecular Weight 360.692
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Compositional safety of event DAS-40278-9 (AAD-1) herbicide-tolerant maize.
2011-08-17
Development of an enzyme-linked immunosorbent assay for the rapid detection of haloxyfop-P-methyl.
2010-07-28
Determination of 142 pesticides in fruit- and vegetable-based infant foods by liquid chromatography/electrospray ionization-tandem mass spectrometry and estimation of measurement uncertainty.
2009-04-23
Cross-resistance patterns to ACCase-inhibiting herbicides conferred by mutant ACCase isoforms in Alopecurus myosuroides Huds. (black-grass), re-examined at the recommended herbicide field rate.
2008-11
PPARalpha- and DEHP-Induced Cancers.
2008
Diversity of acetyl-coenzyme A carboxylase mutations in resistant Lolium populations: evaluation using clethodim.
2007-10
Chiral separation of three agrochemical toxins enantiomers by high-performance liquid chromatography on a vancomycin crystalline degradation products-chiral stationary phase.
2007-03
Enantioseparation of 2-aryloxypropionic acids on chiral porous monolithic columns by capillary electrochromatography. Evaluation of column performance and enantioselectivity.
2006-07-07
Use of tert-butylbenzoylated tartardiamide chiral stationary phase for the enantiomeric resolution of acidic compounds by nano-liquid chromatography.
2006-07
Toxoplasma gondii acyl-lipid metabolism: de novo synthesis from apicoplast-generated fatty acids versus scavenging of host cell precursors.
2006-02-15
Identification of a plastid acyl-acyl carrier protein synthetase in Arabidopsis and its role in the activation and elongation of exogenous fatty acids.
2005-11
Recurrent selection with reduced herbicide rates results in the rapid evolution of herbicide resistance in Lolium rigidum.
2005-04
[Determination of haloxyfop residue in cereals by GC].
2004-01
Crystal structure of the carboxyltransferase domain of acetyl-coenzyme A carboxylase.
2003-03-28
Off-line solid-phase microextraction and capillary electrophoresis mass spectrometry to determine acidic pesticides in fruits.
2003-02-01
PCR-based detection of resistance to acetyl-CoA carboxylase-inhibiting herbicides in black-grass (Alopecurus myosuroides Huds) and ryegrass (Lolium rigidum gaud).
2002-05
Growth of Toxoplasma gondii is inhibited by aryloxyphenoxypropionate herbicides targeting acetyl-CoA carboxylase.
1999-11-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:52:05 GMT 2025
Edited
by admin
on Mon Mar 31 21:52:05 GMT 2025
Record UNII
D8926AE2C4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HALOXYFOP-SODIUM [ISO]
Preferred Name English
HALOXYFOP-SODIUM
ISO  
Common Name English
PROPANOIC ACID, 2-(4-((3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL)OXY)PHENOXY)-, SODIUM SALT
Systematic Name English
PROPANOIC ACID, 2-(4-((3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL)OXY)PHENOXY)-, SODIUM SALT (1:1)
Systematic Name English
Code System Code Type Description
ALANWOOD
haloxyfop-sodium
Created by admin on Mon Mar 31 21:52:05 GMT 2025 , Edited by admin on Mon Mar 31 21:52:05 GMT 2025
PRIMARY
PUBCHEM
23681922
Created by admin on Mon Mar 31 21:52:05 GMT 2025 , Edited by admin on Mon Mar 31 21:52:05 GMT 2025
PRIMARY
FDA UNII
D8926AE2C4
Created by admin on Mon Mar 31 21:52:05 GMT 2025 , Edited by admin on Mon Mar 31 21:52:05 GMT 2025
PRIMARY
EPA CompTox
DTXSID20990075
Created by admin on Mon Mar 31 21:52:05 GMT 2025 , Edited by admin on Mon Mar 31 21:52:05 GMT 2025
PRIMARY
CAS
69806-86-6
Created by admin on Mon Mar 31 21:52:05 GMT 2025 , Edited by admin on Mon Mar 31 21:52:05 GMT 2025
PRIMARY