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Details

Stereochemistry RACEMIC
Molecular Formula C15H18N3O4.Na
Molecular Weight 327.3109
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Imazamox-Sodium

SMILES

[Na+].COCC1=CN=C(C2=NC(=O)C(C)(N2)C(C)C)C(=C1)C([O-])=O

InChI

InChIKey=LYXJJLQNVOKQBQ-UHFFFAOYSA-M
InChI=1S/C15H19N3O4.Na/c1-8(2)15(3)14(21)17-12(18-15)11-10(13(19)20)5-9(6-16-11)7-22-4;/h5-6,8H,7H2,1-4H3,(H,19,20)(H,17,18,21);/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 C15H18N3O4
Molecular Weight 304.3211
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays.
2013-06-17
Activity profiles of 309 ToxCastâ„¢ chemicals evaluated across 292 biochemical targets.
2011-03-28
[Isolation, identification and soil remediation of atrazine-degrading strain T3 AB1].
2010-12
Identification of a hybridization window that facilitates sizeable reductions of pollen-mediated gene flow in spring wheat.
2010-06
Isolation, characterization of a strain capable of degrading imazethapyr and its use in degradation of the herbicide in soil.
2009-10
Effectiveness of glyphosate and imazamox on the control of the invasive cordgrass Spartina densiflora.
2009-09
Are herbicide-resistant crops the answer to controlling Cuscuta?
2009-07
Resistance mechanism to bensulfuron-methyl in biotypes of Scirpus mucronatus L. collected in Chilean rice fields.
2009-05-27
Molecular and biochemical characterization of an induced mutation conferring imidazolinone resistance in sunflower.
2008-12
Comparative genotoxicity evaluation of imidazolinone herbicides in somatic cells of Drosophila melanogaster.
2008-01
Characterization of imazamox degradation by-products by using liquid chromatography mass spectrometry and high-resolution Fourier transform ion cyclotron resonance mass spectrometry.
2007-11
Sorption and predicted mobility of herbicides in Baltic soils.
2007-08
Cross-resistance profile of mesosulfuron-methyl-resistant Italian ryegrass in the southern United States.
2007-04
Introgression of an imidazolinone-resistance gene from winter wheat (Triticum aestivum L.) into jointed goatgrass (Aegilops cylindrica Host).
2006-12
Responses of enantioselective characteristics of imidazolinone herbicides and Chiralcel OJ column to temperature variations.
2006-10-27
High-performance liquid chromatographic separation of imidazolinone herbicide enantiomers and their methyl derivatives on polysaccharide-coated chiral stationary phases.
2006-06-09
Photochemical degradation of imazamox in aqueous solution: influence of metal ions and anionic species on the ultraviolet photolysis.
2006-05-17
A comparative risk assessment of genetically engineered, mutagenic, and conventional wheat production systems.
2005-12
Imidazolinone-tolerant crops: history, current status and future.
2005-03
Does the effect of herbicide pulse exposure on aquatic plants depend on Kow or mode of action?
2005-02-10
Quantitative analysis of imazamox herbicide in environmental water samples by capillary electrophoresis electrospray ionization mass spectrometry.
2004-05-21
Biomassbed: a biological system to reduce pesticide point contamination at farm level.
2004-05
Evaluation of resistance in Cyperus difformis populations to ALS inhibiting herbicides.
2004
Cross resistance to ALS-inhibiting herbicides in Euphorbia heterophylla L. biotypes resistant to imazethapyr.
2003
Evaluation of resistance in Amaranthus quitensis Kunth populations to imazethapyr and other imidazolinones.
2003
Haptens and monoclonal antibodies for immunoassay of imidazolinone herbicides.
2002-06-05
Patents

Patents

Substance Class Chemical
Created
by admin
on Wed Apr 02 17:20:22 GMT 2025
Edited
by admin
on Wed Apr 02 17:20:22 GMT 2025
Record UNII
U3NM8KFD9Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Imazamox-Sodium
Common Name English
3-Pyridinecarboxylic acid, 2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-5-(methoxymethyl)-, sodium salt (1:1)
Preferred Name English
Code System Code Type Description
EPA CompTox
DTXSID70904420
Created by admin on Wed Apr 02 17:20:22 GMT 2025 , Edited by admin on Wed Apr 02 17:20:22 GMT 2025
PRIMARY
CAS
1226788-26-6
Created by admin on Wed Apr 02 17:20:22 GMT 2025 , Edited by admin on Wed Apr 02 17:20:22 GMT 2025
PRIMARY
PUBCHEM
138394675
Created by admin on Wed Apr 02 17:20:22 GMT 2025 , Edited by admin on Wed Apr 02 17:20:22 GMT 2025
PRIMARY
FDA UNII
U3NM8KFD9Z
Created by admin on Wed Apr 02 17:20:22 GMT 2025 , Edited by admin on Wed Apr 02 17:20:22 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE