A4382
4-Aminoantipyrine
reagent grade
Synonym(s):
4-Amino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one, Ampyrone
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About This Item
Empirical Formula (Hill Notation):
C11H13N3O
CAS Number:
Molecular Weight:
203.24
UNSPSC Code:
51384603
NACRES:
NA.31
PubChem Substance ID:
EC Number:
201-452-3
Beilstein/REAXYS Number:
181635
MDL number:
grade
reagent grade
Quality Level
assay
≥97% (HPLC)
form
powder
mp
105-110 °C (lit.)
solubility
water: 50 mg/mL
SMILES string
CN1N(c2ccccc2)C(=O)C(N)=C1C
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
Application
Reagent for glucose determination in the presence of phenol and peroxidase.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Protocols
Enzymatic assay of lipase type XIII from Pseudomonas sp. using a coupled enzyme system of glycerol kinase and glycerophosphate oxidase (EC 3.1.1.3)
Qihui Wang et al.
Journal of hazardous materials, 186(2-3), 1076-1081 (2010-12-21)
In this work, the immobilization of 4-aminoantipyrine onto bentonite was carried out and it was then used to investigate the adsorption behavior of Cr(III), Hg(II) and Pb(II) ions from aqueous solutions. The separation and preconcentration conditions of analytes were investigated
Mohammad Sayed Alam et al.
Bioorganic & medicinal chemistry, 20(13), 4103-4108 (2012-05-26)
4-Aminoantipyrine (4-amino-1,5-dimethyl-2-phenylpyrazole-3-one) and its analogues have been found to be compounds of interest for their anti-inflammatory, analgesic, antiviral, antipyretic, antirheumatic and antimicrobial activities. In the present study, Schiff base analogues of 4-aminoantipyrine were synthesized by the condensation reaction with substituted
A Z El-Sonbati et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 104, 213-221 (2012-12-27)
A novel series of copper(II) and palladium(II) with 4-derivatives benzaldehyde pyrazolone (L(n)) were synthesized. The mixed ligand complexes were prepared by using 1,10-phenanthroline (Phen) as second ligand. The structure of these complexes was identified and confirm by elemental analysis, molar
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A4382-25G | 04061835326242 |
| A4382-50G | 04061835326259 |
| A4382-10G | 04061835326228 |
| A4382-100G | 04061835326211 |
| A4382-250G | 04061835326235 |