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4-Aminoantipyrine

for spectrophotometric det. of H2O2 and phenols, ≥98.0%

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

  • CAS Number 83-07-8

  • Empirical Formula (Hill Notation) C11H13N3O

  • Molecular Weight 203.24

  •  Beilstein Registry Number 181635

  •  EC Number 201-452-3

  •  MDL number MFCD00003145

  •  PubChem Substance ID 24845973

  • Popular Documents:  FTNMR (PDF)  

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Properties

Related Categories Analytical Reagents, Analytical/Chromatography, Derivatization Reagents, Derivatization Reagents HPLC, Derivatization Reagents TLC,
assay   ≥98.0% (NT)
  ≥98.0%
quality   for spectrophotometric det. of H2O2 and phenols
mp   105-110 °C(lit.)
  108-110 °C
solubility   H2O: soluble0.1 g/mL, clear

Description

Other Notes

Reagent for the determination of H2O21

Price and Availability

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3-(<I>N</I>-<WBR>Ethyl-<WBR>3-<WBR>methylanilino)<WBR>-<WBR>2-<WBR>hydroxypropanesulfonic acid sodium salt

for enzymic, spectrophotometric det. of H2O2

3-(<I>N</I>-<WBR>Ethyl-<WBR>3-<WBR>methylanilino)<WBR>-<WBR>2-<WBR>hydroxypropanesulfonic acid sodium salt

for enzymic, spectrophotometric determination of H2O2, ≥98.0%

4-Aminoantipyrine

reagent grade

4-Aminoantipyrine

puriss. p.a., Reag. Ph. Eur., ≥99%

4-Aminoantipyrine

analytical reference material

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
WGK Germany 
3
RTECS 
CD2480000

Protocols & Articles

Peer-Reviewed Papers

References

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1. Determination of hydrogen peroxide with N,N-diethylaniline and 4-aminoantipyrine by use of an anion-exchange resin modified with manganese-tetrakis(sulphophenyl)porphine, as a substitute for peroxidase. Y. Saito et al. Talanta 34, 667, (1987)

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[Flow injection analysis method for hygienic examination of volatile phenol compounds in the air of residential area]. Mao L, Chen H, Liu G, et al. Wei Sheng Yan Jiu 40(6), 773-5, (2011)

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Prevalence and underlying etiologies of neonatal hypoglycemia. Najati N and Saboktakin L Pak. J. Biol. Sci. 13(15), 753-6, (2010)

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Coupling reaction and complex formation for the spectrophotometric determination of physiologically active catecholamines in bulk, pharmaceutical preparations and urine samples of schizophrenic patients. Nour El-Dien FA, Frag EY, and Mohamed GG Drug Test. Anal. 2(5), 234-42, (2010)

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Adsorption of chromium(III), mercury(II) and lead(II) ions onto 4-aminoantipyrine immobilized bentonite. Wang Q, Chang X, Li D, et al. J. Hazard. Mater. 186(2-3), 1076-81, (2011)

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The interaction between 4-aminoantipyrine and bovine serum albumin: multiple spectroscopic and molecular docking investigations. Teng Y, Liu R, Li C, et al. J. Hazard. Mater. 190(1-3), 574-81, (2011)

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Novel bioactive metabolites of dipyrone (metamizol). Tobias Rogosch et al Bioorg. Med. Chem. 20, 101-7, (2012)

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Diffusion of peroxides through dentine in vitro with and without prior use of a desensitizing varnish. Hannig C, Weinhold HC, Becker K, et al. Clin. Oral Investig. 15(6), 863-8, (2011)

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CREBH determines the severity of sulpyrine-induced fatal shock. Kamiyama N, Yamamoto M, Saiga H, et al. PLoS ONE 8(2), e55800, (2013)

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Synthesis of novel Schiff base analogues of 4-amino-1,5-dimethyl-2-phenylpyrazol-3-one and their evaluation for antioxidant and anti-inflammatory activity. Alam MS, Choi JH, and Lee DU Bioorg. Med. Chem. 20(13), 4103-8, (2012)

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Enzymatic assessment of paraoxonase 1 activity on HDL subclasses: a practical zymogram method to assess HDL function. Gugliucci A, Caccavello R, Kotani K, et al. Clin. Chim. Acta 415, 162-8, (2013)

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Structural, thermal, morphological and biological studies of proton-transfer complexes formed from 4-aminoantipyrine with quinol and picric acid. Adam AM Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 104, 1-13, (2013)

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Dispersive liquid-liquid microextraction combined with microvolume spectrophotometry to turn green the 5530 APHA standard method for determining phenols in water and wastewater. Lavilla I, Gil S, Costas M, et al. Talanta 98, 197-202, (2012)

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Derivatization of 2-chlorophenol with 4-amino-anti-pyrine: a novel method for improving the selectivity of molecularly imprinted solid phase extraction of 2-chlorophenol from water. El-Sheikh AH, Al-Quse RW, El-Barghouthi MI, et al. Talanta 83(2), 667-73, (2010)

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Synthesis, spectral characterization and biological activity of metal(II) complexes with 4-aminoantipyrine derivatives. Leelavathy C and Arul Antony S Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 113, 346-55, (2013)

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Effect of 4-aminoantipyrine on oxidative stress induced by glutathione depletion in single human erythrocytes using a microfluidic device together with fluorescence imaging. Teng Y, Liu R, Li C, et al. J. Hazard. Mater. 192(3), 1766-71, (2011)

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Synthesis, crystal structure, vibration spectral, and DFT studies of 4-aminoantipyrine and its derivatives. Li Y, Liu Y, Wang H, et al. Molecules 18(1), 877-93, (2013)

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Exploring the DNA binding mode of transition metal based biologically active compounds. Raman N and Sobha S Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 85(1), 223-34, (2012)

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Scavenging activity of aminoantipyrines against hydroxyl radical. Pedro M P Santos et al Eur. J. Med. Chem. 45, 2258-64, (2010)

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Supramolecular coordination and antimicrobial activities of constructed mixed ligand complexes. El-Sonbati AZ, Diab MA, El-Bindary AA, et al. Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 104, 213-21, (2013)

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Molecular interaction between 4-aminoantipyrine and catalase reveals a potentially toxic mechanism of the drug. Teng Y, Zhang H, and Liu R Mol. Biosyst. 7(11), 3157-63, (2011)

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Graphene matrix for signal enhancement in ambient plasma assisted laser desorption ionization mass spectrometry. Chang C, Li X, Bai Y, et al. Talanta 114, 54-9, (2013)

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Spectroscopic and mycological studies of Co(II), Ni(II) and Cu(II) complexes with 4-aminoantipyrine derivative. Sharma AK and Chandra S Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 81(1), 424-30, (2011)

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A highly selective fluorescent probe for Al3+ based on 4-aminoantipyrine. Zhou Y, Zhang J, Zhou H, et al. Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 106, 68-72, (2013)

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Supramolecular and structural modification on conformational by mixed ligand. El-Sonbati AZ, Diab MA, El-Bindary AA, et al. Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 99, 211-7, (2012)

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DNA binding mode of novel tetradentate amino acid based 2-hydroxybenzylidene-4-aminoantipyrine complexes. Raman N, Sobha S, Selvaganapathy M, et al. Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 96, 698-708, (2012)

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High-performance liquid chromatographic assay for metamizol metabolites in rat plasma: application to pharmacokinetic studies. Domínguez-Ramírez AM, Calzadilla PC, Cortés-Arroyo AR, et al. J. Pharm. Biomed. Anal. 71, 173-8, (2012)

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DNA template-assisted modulation of horseradish peroxidase activity. Datta SG, Dou X, Shibley A, et al. Int. J. Biol. Macromol. 50(3), 552-7, (2012)

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Modified nanodiamonds obtained by detonation synthesis in constructing biochemical indication systems (As exemplified by the glucose determination system). Mamaeva ES, Baron AV, Puzyr AP, et al. Dokl. Biochem. Biophys. 439, 182-4, (2011)

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Merck 14,591

Beil. 25,IV,3554

Aldrich MSDS 1, 58:C / Corp MSDS 1 (1), 135:D / FT-IR 1 (2), 397:A / FT-IR 2 (2), 3059:A / FT-NMR 1 (2), 1443:C / IR-Spectra (3), 1095:E / IR-Spectra (2), 956:F / NMR-Reference 2 (2), 376:A / RegBook 1 (2), 2061:L / Sigma FT-IR 1 (2), 97:B / Structure Index 1, 327:D:7

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