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A4382

Sigma-Aldrich

4-Aminoantipyrine

reagent grade

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C11H13N3O
Numéro CAS:
83-07-8
Poids moléculaire :
203.24
Numéro Beilstein :
181635
Numéro CE :
201-452-3
Numéro MDL:
MFCD00003145
Code UNSPSC :
51384603
ID de substance PubChem :
24890855
Nomenclature NACRES :
NA.31

Qualité

reagent grade

Niveau de qualité

300

Pureté

≥97% (HPLC)

Forme

powder

Pf

105-110 °C (lit.)

Solubilité

water: 50 mg/mL

Chaîne 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

Clé InChI

RLFWWDJHLFCNIJ-UHFFFAOYSA-N

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Catégories apparentées

Application

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

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (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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Protocoles

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)

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