106194
Nicotinic acid N-oxide
99%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C6H5NO3
CAS Number:
Molecular Weight:
139.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-265-0
Beilstein/REAXYS Number:
115860
MDL number:
Product Name
Nicotinic acid N-oxide, 99%
InChI key
FJCFFCXMEXZEIM-UHFFFAOYSA-N
InChI
1S/C6H5NO3/c8-6(9)5-2-1-3-7(10)4-5/h1-4H,(H,8,9)
SMILES string
OC(=O)c1ccc[n+]([O-])c1
assay
99%
mp
254-255 °C (dec.) (lit.)
solubility
benzene: insoluble
chloroform: insoluble
cold water: slightly soluble
ethanol: slightly soluble
functional group
carboxylic acid
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
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.
General description
Nicotinic acid N-oxide acts as a ligand and forms lead-carboxylate complexes having phosphorescent properties.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
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)
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service