25345
6-Chloronicotinic acid
purum, ≥97.0% (T)
Synonym(s):
6-Chloropyridine-3-carboxylic acid, 6-Chloronicotinic acid
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About This Item
Empirical Formula (Hill Notation):
C6H4ClNO2
CAS Number:
Molecular Weight:
157.55
Beilstein:
115993
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
grade
purum
Assay
≥97.0% (T)
mp
190 °C (dec.) (lit.)
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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Other Notes
This product has been replaced by 156353-ALDRICH | 6-Chloropyridine-3-carboxylic acid 99%
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
13 - Non 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
Regulatory Information
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Kumiko Taira et al.
Chudoku kenkyu : Chudoku Kenkyukai jun kikanshi = The Japanese journal of toxicology, 24(3), 222-230 (2011-09-29)
Neonicotinoid is a recently developed insecticide with worldwide use that has been increasing. It acts as a nicotinic acetylcholine receptor agonist. Chloropyridinyl neonicotinoid is a subgroup of neonicotinoid, and are commercially available as imidacloprid, nitenpyram, acetamiprid, and thiacloprid. The maximum
Won-Bo Shim et al.
Journal of agricultural and food chemistry, 57(3), 791-796 (2009-01-15)
A fluorescence polarization immunoassay (FPIA) for the quantitative determination of 6-chloronicotinic acid (6-CNA) using polyclonal antibody was developed. The 6-CNA-protein (bovine serum albumin and soybean trypsin inhibitor) conjugates and fluorescein-labeled 6-CNA derivative (tracer) were prepared and used as the immunogens
Fabienne Hoffmann-Emery et al.
The Journal of organic chemistry, 71(5), 2000-2008 (2006-02-25)
A new efficient synthesis of two novel classes of NK1 receptor antagonists, among them befetupitant and netupitant, starting from 6-chloronicotinic acid is described. The introduction of the o-tolyl substituent at C4 of the pyridine ring was achieved by a one-pot
Romina Zabar et al.
Chemosphere, 85(5), 861-868 (2011-08-02)
This work describes for the first time the photolytic and photocatalytic degradation of 6-chloronicotinic acid (6CNA) in double deionised water, which is a degradation product of neonicotinoid insecticides imidacloprid and acetamiprid, and it is known to appear in different environmental
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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