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A4382

Sigma-Aldrich

4-Aminoantipyrine

reagent grade

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C11H13N3O
Número de CAS:
83-07-8
Peso molecular:
203.24
Beilstein:
181635
Número CE:
201-452-3
Número MDL:
MFCD00003145
Código UNSPSC:
51384603
ID de la sustancia en PubChem:
24890855
NACRES:
NA.31

grado

reagent grade

Nivel de calidad

300

Análisis

≥97% (HPLC)

formulario

powder

mp

105-110 °C (lit.)

solubilidad

water: 50 mg/mL

cadena SMILES

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

Clave InChI

RLFWWDJHLFCNIJ-UHFFFAOYSA-N

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Categorías relacionadas

Aplicación

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

Pictogramas

Exclamation mark
GHS07

Palabra de señalización

Warning

Frases de peligro

H302

Clasificaciones de peligro

Acute Tox. 4 Oral

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
0000274527
0000275296
0000275296
0000274527
SLCL7856

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Amjad H El-Sheikh et al.
Talanta, 83(2), 667-673 (2010-11-30)
Molecularly imprinted polymer (MIP) may not selectively recognize small template of limited number of functional groups, such as 2-chlorophenol (2-CP). In this work, a novel method was proposed to improve the recognition ability of the molecularly imprinted solid phase extraction
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
Yue Teng et al.
Journal of hazardous materials, 192(3), 1766-1771 (2011-07-26)
The effects of 4-aminoantipyrine (AAP) on oxidative stress induced by glutathione (GSH) depletion in single human erythrocytes were investigated using microfluidic technique and fluorescence imaging. Most cell-based toxicity evaluations on GSH are performed with bulk experiments based on analysis of
C Leelavathy et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 113, 346-355 (2013-06-08)
Novel metal(II) complexes derived from furfurylidene-4-aminoantipyrine and 2-aminobenzothiazole were synthesized and characterized by spectroscopic (IR, (1)H NMR, UV-Vis., ESR and DART-MS) and other analytical methods. IR spectral studies indicate the binding sites of the ligand with the metal ion. Molar
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