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Merck

25345

Sigma-Aldrich

6-Chlor-nicotinsäure

purum, ≥97.0% (T)

Synonym(e):

6-Chlor-nicotinsäure, 6-Chlorpyridin-3-carbonsäure

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About This Item

Empirische Formel (Hill-System):
C6H4ClNO2
CAS-Nummer:
Molekulargewicht:
157.55
Beilstein:
115993
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:

Qualität

purum

Assay

≥97.0% (T)

mp (Schmelzpunkt)

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)

InChIKey

UAWMVMPAYRWUFX-UHFFFAOYSA-N

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Sonstige Hinweise

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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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
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
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
F J Uroz et al.
The Analyst, 126(8), 1355-1358 (2001-09-06)
A new analytical method for determining 6-chloronicotinic acid (6-ClNA) in human urine is proposed. 6-ClNA is the main metabolite in warm-blooded animals after exposure to the insecticide imidachloprid. 6-ClNA was extracted from human urine using solid phase extraction (SPE) with
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

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