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Merck
모든 사진(1)

주요 문서

33528

Sigma-Aldrich

4-Aminoantipyrine

puriss. p.a., reag. Ph. Eur., ≥99%

동의어(들):

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

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About This Item

실험식(Hill 표기법):
C11H13N3O
CAS Number:
Molecular Weight:
203.24
Beilstein:
181635
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.21

Agency

USP/NF
reag. Ph. Eur.

Quality Level

grade

puriss. p.a.

분석

≥99%

무기 잔류물

≤0.1%

손실

≤0.5% loss on drying

mp

105-110 °C (lit.)
107-109 °C

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

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일반 설명

4-Aminoantipyrine forms heterocyclic Schiff bases, by reaction with various aldehydes and oximes. These Schiff bases form stable complexes with transition metals.

애플리케이션

  • Phenol impurity and wastewater analysis: Research demonstrated the application of 4-Aminoantipyrine in spectrophotometric determination of phenol impurities in phenoxyethanol and for assessing phenol index in drinking water and municipal wastewater, utilizing salting-out assisted liquid phase microextraction (Roustaei et al., 2024).
  • Advanced sensor development for tea polyphenols: Utilization of 4-Aminoantipyrine in developing a novel hybrid sensor array, integrated with polyphenol oxidase and its nanozymes, aided by machine learning to identify tea polyphenols and Chinese teas, showcasing its role in innovative sensor technology (Yang et al., 2024).

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

예방조치 성명서

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

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

이미 열람한 고객

Lucas de Melo da Silva et al.
The Science of the total environment, 631-632, 1079-1088 (2018-05-08)
Electro-oxidation with electrogenerated H2O2 (EO-H2O2) was applied to treat acidic aqueous solutions of 4-aminoantipyrine (4-AA), a persistent drug metabolite of dipyrone, in sulfate medium. Trials were made using a boron-doped diamond anode in the presence of H2O2 electrogenerated on site.
Transition metal complexes with Schiff-base ligands: 4-aminoantipyrine based derivatives-a review.
Raman N, et al.
Journal of Coordination Chemistry, 62(5, 691-709 (2009)
Tao Sun et al.
Frontiers in bioengineering and biotechnology, 8, 237-237 (2020-04-09)
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Synthesis, structural determination and antibacterial activity of compounds derived from vanillin and 4-aminoantipyrine.
Vaghasiya YK, et al.
J. Serb. Chem. Soc., 69(12), 991-998 (2004)
K Stange et al.
Scientific reports, 10(1), 6149-6149 (2020-04-11)
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