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About This Item
Empirical Formula (Hill Notation):
C11H13N3O
CAS Number:
Molecular Weight:
203.24
EC Number:
201-452-3
UNSPSC Code:
12352103
MDL number:
Beilstein/REAXYS Number:
181635
InChI
1S/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3
InChI key
RLFWWDJHLFCNIJ-UHFFFAOYSA-N
SMILES string
CN1N(c2ccccc2)C(=O)C(N)=C1C
assay
98%
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Application
Reagent used in the colorimetric determination of phenols and the synthesis of transition metal and lanthanide ligands.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Transition Met. Chem. (London), 18, 279-279 (1993)
Analytical Letters, 26, 87-87 (1993)
Polyhedron, 12, 1227-1227 (1993)
Yue Teng et al.
Journal of hazardous materials, 190(1-3), 574-581 (2011-04-19)
4-Aminoantipyrine (AAP) is widely used in the pharmaceutical industry, in biochemical experiments and in environmental monitoring. AAP as an aromatic pollutant in the environment poses a great threat to human health. To evaluate the toxicity of AAP at the protein
N Raman et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 85(1), 223-234 (2011-10-25)
Few novel 4-aminoantipyrine derived Schiff bases and their metal complexes were synthesized and characterized. Their structural features and other properties were deduced from the elemental analysis, magnetic susceptibility and molar conductivity as well as from mass, IR, UV-vis, (1)H NMR
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