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156353

Sigma-Aldrich

6-Chloropyridine-3-carboxylic acid

99%

Synonym(s):

6-Chloronicotinic acid

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About This Item

Empirical Formula (Hill Notation):
C6H4ClNO2
CAS Number:
5326-23-8
Molecular Weight:
157.55
Beilstein:
115993
EC Number:
226-201-5
MDL number:
MFCD00006241
UNSPSC Code:
12352100
PubChem Substance ID:
24849608
NACRES:
NA.22

Assay

99%

mp

190 °C (dec.) (lit.)

solubility

deionized water: soluble

SMILES string

OC(=O)c1ccc(Cl)nc1

InChI

1S/C6H4ClNO2/c7-5-2-1-4(3-8-5)6(9)10/h1-3H,(H,9,10)

InChI key

UAWMVMPAYRWUFX-UHFFFAOYSA-N

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Application

6-Chloropyridine-3-carboxylic acid (6-chloronicotinic acid/6-CNA) has been used to study its photolytic and photocatalytic degradation. 6-CNA is a degradation product of neonicotinoid insecticides imidacloprid and acetamiprid and is known to appear in different environmental matrices. The product has been used as a media component during the isolation of 6-CNA degrading bacterial strain from imidacloprid-exposed soil samples.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Mahrous M Kandil et al.
Journal of agricultural and food chemistry, 63(19), 4721-4727 (2015-05-02)
Thus far, only a small number and types of bacteria with limited ability in degrading imidacloprid have been reported. Also, genes regulating imidacloprid (IMDA) degradation have yet to be discovered. To study this in more detail, an enrichment technique was
A Segura Carretero et al.
Journal of chromatography. A, 1003(1-2), 189-195 (2003-08-06)
A method is described for the analysis of the insecticide imidacloprid [1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine] and its metabolite 6-chloronicotinic acid by micellar electrokinetic chromatography with diode-array detection at 270 and 227 nm, respectively. The best results were obtained using sodium dodecyl sulphate at
Mehmet Karabacak et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(3), 876-883 (2008-03-25)
The experimental and theoretical study on the structures and vibrations of 6-chloronicotinic acid (6-CNA, C(6)H(4)ClNO(2)) are presented. The Fourier transform infrared spectra (4,000-50 cm(-1)) and the Fourier transform Raman spectra (3,500-50 cm(-1)) of the title molecule in solid phase have
Valéria Guzsvány et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 47(12), 1919-1929 (2012-07-05)
Two spectroscopic methods, (1)H NMR and FTIR, were developed for the monitoring of the photocatalytic degradation of acetamiprid, a widely used pyridine-based neonicotinoid insecticide, in UV-irradiated aqueous suspensions of O(2)/TiO(2). The (1)H NMR method allowed also the identification of the
Gretty Ettiene et al.
Electrophoresis, 33(19-20), 2969-2977 (2012-09-22)
A sensitive and reliable method based on MEKC has been developed and validated for trace determination of neonicotinoid insecticides (thiamethoxam, acetamiprid, and imidacloprid) and the metabolite 6-chloronicotinic acid in water and soil matrices. Optimum separation of the neonicotinoid insecticides was
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