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经验公式(希尔记法):
C6H5NO3
化学文摘社编号:
分子量:
139.11
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
225-682-9
Beilstein/REAXYS Number:
115991
MDL number:
InChI
1S/C6H5NO3/c8-5-2-1-4(3-7-5)6(9)10/h1-3H,(H,7,8)(H,9,10)
SMILES string
OC(=O)c1ccc(O)nc1
InChI key
BLHCMGRVFXRYRN-UHFFFAOYSA-N
grade
analytical standard
product line
PESTANAL®
assay
≥98.0% (HPLC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
impurities
≤1.0% water
mp
>300 °C (lit.), 302-308 °C
application(s)
agriculture
environmental
format
neat
Quality Level
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General description
6-Hydroxypyridine-3-carboxylic acid has aliphatic carboxylate anions.
Find more information here: Neonicotinoids
Find more information here: Neonicotinoids
Application
It can be used as a good organic linker source for the construction of lanthanide coordination polymers. It was used in qualitative and quantitative analysis of substrates and metabolites of neonicotinoids using LC-MSD TOF, in a study performed to clone 6-chloronicotinic acid chlorohydrolase from newly isolated 6-chloronicotinic acid mineralizing Bradyrhizobiaceae strain SG-6C.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Two-and three-dimensional lanthanide?organic frameworks constructed using 1-hydro-6-oxopyridine-3-carboxylate and oxalate ligands.
Liu, Cai-Ming, et al.
Dalton Transactions, 29, 5666-5672 (2009)
Li Xu et al.
Wei sheng wu xue bao = Acta microbiologica Sinica, 46(1), 63-67 (2006-04-04)
The current technology for microbial hydroxylation of nicotinic acid is a procedure of resting cells transformation. Here it was reported that non-degradation of 6-hydroxynicotinic acid during hydroxylation of nicotinic acid by resting cells was due to existing of nicotinic acid
Ashish Gupta et al.
NMR in biomedicine, 18(5), 293-299 (2005-03-11)
The utility of (1)H NMR spectroscopy is suggested and demonstrated for the diagnosis of Pseudomonas aeruginosa in urinary tract infection (UTI). The specific property of P. aeruginosa of metabolizing nicotinic acid to 6-hydroxynicotinic acid (6-OHNA) is exploited. The quantity of
C L Kitts et al.
Journal of bacteriology, 174(23), 7791-7797 (1992-12-01)
A complete pathway for Azorhizobium caulinodans nicotinate catabolism has been determined from mutant phenotype analyses, isolation of metabolic intermediates, and structural studies. Nicotinate serves as a respiratory electron donor to O2 via a membrane-bound hydroxylase and a specific c-type cytochrome
José Ignacio Jiménez et al.
Environmental microbiology, 13(7), 1718-1732 (2011-04-01)
The biochemistry of nicotinic acid (NA) degradation is known but the transcriptional control of the genes involved is still poorly studied. We report here the transcriptional regulatory circuit of the nic genes responsible for the aerobic degradation of NA in
实验方案
Learn more about Neonicotinoids - active substances used in plant protection products to control harmful insects.
Analysis of banned neonicotinoid insecticides from dandelion blossoms using QuEChERS and LC-MS.
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