6-Chloronicotinic Acid - ≥99% , CAS No.5326-23-8

CAS: 5326-23-8 Cat. No.: C128115 Peso molecular: 157.55 Beilstein Registry Number: 115993 Número EC: 226-201-5
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
6-Chloronicotinic acid, purum, >=97.0% (T) | NSC277 | NSC-277 | BDBM50486226 | BP-12853 | 2-chloro-5-pyridine carboxylic acid | MFCD00066635 | BUTYL3-MERCAPTOPROPIONATE | 6-Chloropyridine-3-carboxylic acid, analytical standard | PS-5330 | EN300-19925 | 6C
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
C128115-5g
8
9,90US$
10g
C128115-10g
5
10,90US$
25g
C128115-25g
6
11,90US$
100g
C128115-100g
3

19,90US$

29,90US$
Guardar 10,00 US$ (33.44%)
500g
C128115-500g
3

97,90US$

146,90US$
Guardar 49,00 US$ (33.36%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

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.

Specifications

Sinónimos
6-Chloronicotinic acid, purum, >=97.0% (T) | NSC277 | NSC-277 | BDBM50486226 | BP-12853 | 2-chloro-5-pyridine carboxylic acid | MFCD00066635 | BUTYL3-MERCAPTOPROPIONATE | 6-Chloropyridine-3-carboxylic acid, analytical standard | PS-5330 | EN300-19925 | 6C
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥99%
Nombres e identificadores
Pubchem Sid488185694
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488185694
Sonrisas canónicasC1=CC(=NC=C1C(=O)O)Cl
IUPAC Name6-chloropyridine-3-carboxylic acid
InChIKeyUAWMVMPAYRWUFX-UHFFFAOYSA-N
INCHI1S/C6H4ClNO2/c7-5-2-1-4(3-8-5)6(9)10/h1-3H,(H,9,10)
Isómeros SMILES C1=CC(=NC=C1C(=O)O)Cl
WGK Alemania 3
Peso molecular 157.55
Beilstein 115993
Reaxy-Rn 115993
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=115993&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasePyridines and derivatives
SubclassPyridinecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentPyridinecarboxylic acids
Alternative Parents 2-halopyridines  Aryl chlorides  Heteroaromatic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyridine carboxylic acid - 2-halopyridine - Aryl chloride - Aryl halide - Heteroaromatic compound - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as pyridinecarboxylic acids. These are compounds containing a pyridine ring bearing a carboxylic acid group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
NAPRT Tchem Nicotinate phosphoribosyltransferase (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AOX1 Tchem Aldehyde oxidase (429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLS Tchem Glutaminase kidney isoform, mitochondrial (16997 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
norA Quinolone resistance protein norA (2171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cat Catalase (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

14 results found

Lot NumberCertificate TypeFechaArticulo
K2126059Certificate of AnalysisSep 08, 2025 C128115
D2410255Certificate of AnalysisMar 20, 2024 C128115
D2410256Certificate of AnalysisMar 20, 2024 C128115
F23141002Certificate of AnalysisMay 11, 2023 C128115
F23141005Certificate of AnalysisMay 11, 2023 C128115
F23141006Certificate of AnalysisMay 11, 2023 C128115
F23141011Certificate of AnalysisMay 11, 2023 C128115
F23141016Certificate of AnalysisMay 11, 2023 C128115
F2314958Certificate of AnalysisMay 11, 2023 C128115
F2314977Certificate of AnalysisMay 11, 2023 C128115
F2314997Certificate of AnalysisMay 11, 2023 C128115
G1520053Certificate of AnalysisMar 08, 2023 C128115
C2329077Certificate of AnalysisOct 21, 2021 C128115
C2329235Certificate of AnalysisOct 21, 2021 C128115

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Propiedades químicas y físicas
SolubilidadSoluble in Methanol,Ether,Ethanol; Slightly soluble in Chloroform,Benzene
Peso molecular157.550 g/mol
XLogP32.700
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass156.993 Da
Monoisotopic Mass156.993 Da
Topological Polar Surface Area50.200 Ų
Heavy Atom Count10
Formal Charge0
Complexity140.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Dong Li, Chunran Zhou, Shuai Wang, Zhan Hu, Jia Xie, Canping Pan, Ranfeng Sun.  (2023)  Imidacloprid-induced stress affects the growth of pepper plants by disrupting rhizosphere-plant microbial and metabolite composition.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:37437628] [10.1016/j.scitotenv.2023.165395]
2. Jingwen Zhang, Junning Liu, Yuheng Wang, Yong Wang, Ruiqin Yang, Xinyang Zhou.  (2023)  Simultaneous determination of ten neonicotinoid insecticides and a metabolite in human whole blood by QuEChERS coupled with UPLC-Q Exactive orbitrap high-resolution mass spectrometry.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:37059012] [10.1016/j.jchromb.2023.123689]
3. Shi Zhoukun, Dong Weiliang, Xin Fengxue, Liu Jiawei, Zhou Xinhai, Xu Fanli, Lv Ziyao, Ma Jiangfeng, Zhang Wenming, Fang Yan, Jiang Min.  (2018)  Characteristics and metabolic pathway of acetamiprid biodegradation by Fusarium sp. strain CS-3 isolated from soil.  BIODEGRADATION,  29  (6): (593-603).  [PMID:30259232] [10.1007/s10532-018-9855-8]
4. Mengling Tu, Wen Ma, Jia Chen, Yunxiao Zhu, Yang Liu, Xiaoli Ni, Xianjiang Li.  (2025)  Machine learning driven decoding of impurity fingerprint in imidacloprid material.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.113399]
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