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Details

Stereochemistry ACHIRAL
Molecular Formula C6H4ClNO2
Molecular Weight 157.554
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6-Chloronicotinic acid

SMILES

OC(=O)C1=CN=C(Cl)C=C1

InChI

InChIKey=UAWMVMPAYRWUFX-UHFFFAOYSA-N
InChI=1S/C6H4ClNO2/c7-5-2-1-4(3-8-5)6(9)10/h1-3H,(H,9,10)

HIDE SMILES / InChI

Molecular Formula C6H4ClNO2
Molecular Weight 157.554
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Interactions between Nosema microspores and a neonicotinoid weaken honeybees (Apis mellifera).
2010-03
Reactivity of hydroxyl radicals with neonicotinoid insecticides: mechanism and changes in toxicity.
2009-07
Influence of pesticide residues on honey bee (Hymenoptera: Apidae) colony health in France.
2009-06
(E)-6-Chloro-N'-(3,5-dichloro-2-hydroxy-benzyl-idene)-nicotinohydrazide.
2009-03-06
Development of fluorescence polarization immunoassay for the rapid detection of 6-chloronicotinic acid: main metabolite of neonicotinoid insecticides.
2009-02-11
Acute human self-poisoning with imidacloprid compound: a neonicotinoid insecticide.
2009
Comparison of experimental and density functional study on the molecular structure, infrared and Raman spectra and vibrational assignments of 6-chloronicotinic acid.
2008-12-01
6-Chloro-N'-(2-hydr-oxy-1-naphthyl-methyl-ene)nicotinohydrazide.
2007-12-06
[Influential factors and degradation pathway of imidacloprid by homogeneous Co/PMS system].
2007-12
Synthesis of two potential NK1-receptor ligands using [1-11C]ethyl iodide and [1-11C]propyl iodide and initial PET-imaging.
2007-07-30
Biodegradation of imidacloprid by an isolated soil microorganism.
2007-06-15
Column switching liquid chromatography and post-column photochemically fluorescence detection to determine imidacloprid and 6-chloronicotinic acid in honeybees.
2007-04-13
Imidacloprid residues in fruits, vegetables and water samples from Palestine.
2007-02
Application of matrix solid phase dispersion to the determination of imidacloprid, carbaryl, aldicarb, and their main metabolites in honeybees by liquid chromatography-mass spectrometry detection.
2006-05-15
A survey of pesticide residues in pollen loads collected by honey bees in France.
2006-04
Efficient synthesis of novel NK1 receptor antagonists: selective 1,4-addition of grignard reagents to 6-chloronicotinic acid derivatives.
2006-03-03
In vivo metabolic fate of [14C]-acetamiprid in six biological compartments of the honeybee, Apis mellifera L.
2005-08
In vivo distribution and metabolisation of 14C-imidacloprid in different compartments of Apis mellifera L.
2004-11
Effects of neonicotinoid insecticides on the bionomics of twospotted spider mite (Acari: Tetranychidae).
2004-10
Determination of imidacloprid and its metabolite 6-chloronicotinic acid in greenhouse air by application of micellar electrokinetic capillary chromatography with solid-phase extraction.
2003-06-27
Discrepancy between acute and chronic toxicity induced by imidacloprid and its metabolites in Apis mellifera.
2001-11
Monitoring of 6-chloronicotinic acid in human urine by gas chromatography-tandem mass spectrometry as indicator of exposure to the pesticide imidacloprid.
2001-08
Toxicity and nicotinic acetylcholine receptor interaction of imidacloprid and its metabolites in Apis mellifera (Hymenoptera: Apidae).
2001-07
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:19:45 GMT 2025
Edited
by admin
on Mon Mar 31 19:19:45 GMT 2025
Record UNII
99V0U0120A
Record Status Validated (UNII)
Record Version
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Name Type Language
6-Chloronicotinic acid
Systematic Name English
NSC-277
Preferred Name English
Nicotinic acid, 6-chloro-
Common Name English
3-Pyridinecarboxylic acid, 6-chloro-
Systematic Name English
6-Chloro-3-pyridinecarboxylic acid
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
226-201-5
Created by admin on Mon Mar 31 19:19:45 GMT 2025 , Edited by admin on Mon Mar 31 19:19:45 GMT 2025
PRIMARY
MESH
C035953
Created by admin on Mon Mar 31 19:19:45 GMT 2025 , Edited by admin on Mon Mar 31 19:19:45 GMT 2025
PRIMARY
CAS
5326-23-8
Created by admin on Mon Mar 31 19:19:45 GMT 2025 , Edited by admin on Mon Mar 31 19:19:45 GMT 2025
PRIMARY
FDA UNII
99V0U0120A
Created by admin on Mon Mar 31 19:19:45 GMT 2025 , Edited by admin on Mon Mar 31 19:19:45 GMT 2025
PRIMARY
PUBCHEM
79222
Created by admin on Mon Mar 31 19:19:45 GMT 2025 , Edited by admin on Mon Mar 31 19:19:45 GMT 2025
PRIMARY
NSC
277
Created by admin on Mon Mar 31 19:19:45 GMT 2025 , Edited by admin on Mon Mar 31 19:19:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID6063775
Created by admin on Mon Mar 31 19:19:45 GMT 2025 , Edited by admin on Mon Mar 31 19:19:45 GMT 2025
PRIMARY
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