Skip to Content
Merck
All Photos(5)

Documents

A4382

Sigma-Aldrich

4-Aminoantipyrine

reagent grade

Synonym(s):

4-Amino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one, Ampyrone

Sign Into View Organizational & Contract Pricing
All Photos(5)

About This Item

Empirical Formula (Hill Notation):
C11H13N3O
CAS Number:
83-07-8
Molecular Weight:
203.24
Beilstein:
181635
EC Number:
201-452-3
MDL number:
MFCD00003145
UNSPSC Code:
51384603
PubChem Substance ID:
24890855
NACRES:
NA.31

grade

reagent grade

Quality Level

300

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

Looking for similar products? Visit Product Comparison Guide

Application

Reagent for glucose determination in the presence of phenol and peroxidase.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000401973
0000401974
0000399558
0000399563
0000399576

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

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
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
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
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
View All Related Papers

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)

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)

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