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25345

6-Chloronicotinic acid

Name: 6-Chloronicotinic acid
Brand: SIAL

purum, ≥97.0% (T)

Sinónimos:

6-Chloropyridine-3-carboxylic acid, 6-Chloronicotinic acid

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About This Item

Fórmula empírica (notación de Hill):

C₆H₄ClNO₂

Número de CAS:

5326-23-8

Peso molecular:

157.55

Beilstein:

115993

Número CE:

226-201-5

Número MDL:

MFCD00006241

Código UNSPSC:

12352100

ID de la sustancia en PubChem:

329752734

grado

purum

Ensayo

≥97.0% (T)

mp

190 °C (dec.) (lit.)

cadena SMILES

OC(=O)c1ccc(Cl)nc1

InChI

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

Clave InChI

UAWMVMPAYRWUFX-UHFFFAOYSA-N

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Otras notas

This product has been replaced by 156353-ALDRICH | 6-Chloropyridine-3-carboxylic acid 99%

Pictogramas

GHS07

Palabra de señalización

Warning

Frases de peligro

H315,H319,H335

Consejos de prudencia

P261 - P305 + P351 + P338

Clasificaciones de peligro

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

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

13 - Non Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number

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Comparison of experimental and density functional study on the molecular structure, infrared and Raman spectra and vibrational assignments of 6-chloronicotinic acid.

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

Determination of imidacloprid and its metabolite 6-chloronicotinic acid in greenhouse air by application of micellar electrokinetic capillary chromatography with solid-phase extraction.

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

Column switching liquid chromatography and post-column photochemically fluorescence detection to determine imidacloprid and 6-chloronicotinic acid in honeybees.

M D Gil García et al.

Journal of chromatography. A, 1147(1), 17-23 (2007-02-28)

The determination of imidacloprid and its main metabolite (6-chloronicotinic acid) in honeybees was performed by liquid chromatography with post-column photochemical derivatisation in alkaline medium and fluorescence detection. The compounds were extracted from honeybees with acetone under ultrasound conditions prior to

Metabolic degradation of imidacloprid in paddy field soil.

Romila Akoijam et al.

Environmental monitoring and assessment, 186(10), 5977-5984 (2014-06-04)

The metabolic degradation and persistence of imidacloprid in paddy field soil were investigated following two applications of imidacloprid at 20 and 80 g a.i. ha(-1) at an interval of 10 days. The soil samples were collected at various time intervals.

Determination of neonicotinoid insecticides in environmental samples by micellar electrokinetic chromatography using solid-phase treatments.

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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