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About This Item
Empirical Formula (Hill Notation):
C6H5NO3
CAS Number:
Molecular Weight:
139.11
Beilstein/REAXYS Number:
115860
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
99%
mp
254-255 °C (dec.) (lit.)
solubility
benzene: insoluble
chloroform: insoluble
cold water: slightly soluble
ethanol: slightly soluble
functional group
carboxylic acid
SMILES string
OC(=O)c1ccc[n+]([O-])c1
InChI
1S/C6H5NO3/c8-6(9)5-2-1-3-7(10)4-5/h1-4H,(H,8,9)
Inchi Key
FJCFFCXMEXZEIM-UHFFFAOYSA-N
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General description
Nicotinic acid N-oxide acts as a ligand and forms lead-carboxylate complexes having phosphorescent properties.
Application
Nicotinic acid N-oxide was used in a study to develop liquid chromatographic method for determination of free nicotinic acid and its metabolites in plasma and urine. It was used to synthesize and characterize peroxo complexes of vanadium(V) and molybdenum (VI) with nicotinic acid and nicotinic acid N-oxide.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Two novel lead-carboxylate complexes based on nicotinic acid N-oxide: Synthesis, crystal structures and luminescent properties.
Zhao YH, et al.
Inorganic Chemistry Communications, 10(4), 410-414 (2007)
Preparation, spectroscopic properties, and characterization of novel peroxo complexes of vanadium (V) and molybdenum (VI) with nicotinic acid and nicotinic acid N-oxide.
Djordjevic C, et al.
Inorganic Chemistry, 27(17), 2926-2932 (1988)
N Hengen et al.
Clinical chemistry, 24(10), 1740-1743 (1978-10-01)
We report a liquid-chromatographic procedure for determining free nicotinic acid and a metabolite, nicotinuric acid, in plasma and urine. Five-tenths milliliter of urine or deproteinized plasma is evaporated and the residue analyzed isocratically by reversed-phase ion-pair chromatography, with measurement of
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