Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

106194

Sigma-Aldrich

Nicotinic acid N-oxide

99%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C6H5NO3
CAS Number:
Molecular Weight:
139.11
Beilstein:
115860
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

mp

254-255 °C (dec.) (lit.)

solubility

benzene: insoluble
chloroform: insoluble
cold water: slightly soluble
ethanol: slightly soluble

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

Looking for similar products? Visit Product Comparison Guide

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit 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