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156353

6-Chloropyridine-3-carboxylic acid

99%

Synonym(s):

6-Chloronicotinic acid

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5 g

Available to ship TODAYfromMILWAUKEE

$51.20
25 g

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$63.10
100 g

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$79.90

About This Item

Empirical Formula (Hill Notation):
C6H4ClNO2
CAS Number:
Molecular Weight:
157.55
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-201-5
Beilstein/REAXYS Number:
115993
MDL number:
Assay:
99%

$51.20


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assay

99%

mp

190 °C (dec.) (lit.)

solubility

deionized water: soluble

functional group

carboxylic acid, chloro

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

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.[1] The product has been used as a media component during the isolation of 6-CNA degrading bacterial strain from imidacloprid-exposed soil samples.[2]

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This Item
150339658219656429
assay

99%

assay

99%

assay

97%

assay

97%

solubility

deionized water: soluble

solubility

-

solubility

-

solubility

-

Quality Level

200

Quality Level

100

Quality Level

-

Quality Level

100

mp

190 °C (dec.) (lit.)

mp

176-178 °C (dec.) (lit.)

mp

140-143 °C (lit.)

mp

190-194 °C (lit.)

functional group

carboxylic acid, chloro

functional group

carboxylic acid, chloro

functional group

carboxylic acid, chloro

functional group

carboxylic acid, nitrile


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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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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
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
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



Global Trade Item Number

SKUGTIN
CRM4734304061838188267
156353-5G04061832977317
156353-25G04061832977300
156353-100G04061832977294

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