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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:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-265-0
Beilstein/REAXYS Number:
115860
MDL number:
产品名称
烟酸 N-氧化物, 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
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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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
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