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Merck
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01-3360

Sigma-Aldrich

4-Aminoantipyrine

≥99.0%, JIS special grade

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C11H13N3O
Numero CAS:
83-07-8
Peso molecolare:
203.24
Beilstein:
181635
Numero CE:
201-452-3
Numero MDL:
MFCD00003145
Codice UNSPSC:
12352005
ID PubChem:
329747252

Grado

JIS special grade

Saggio

≥99.0%

Disponibilità

available only in Japan

Punto di fusione

105-110 °C (lit.)

Stringa SMILE

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
RLFWWDJHLFCNIJ-UHFFFAOYSA-N

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Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
U2381
U2326
U4227
U2124
U4027

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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
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
Yue Teng et al.
Molecular bioSystems, 7(11), 3157-3163 (2011-09-22)
4-Aminoantipyrine (AAP) is scarcely administered as an analgesic drug because of the potential side effects. The residue of AAP in the environment possesses a potential threat to human health. In this article, the binding mode of AAP with the important
Yi Li et al.
Molecules (Basel, Switzerland), 18(1), 877-893 (2013-01-25)
Three compounds derived from 4-aminoantipyrine (AA) were synthesized and their structures confirmed by melting point, elemental analysis, FT-IR, and 1H-NMR. The molecular structures of the four compounds were characterized by single-crystal X-ray diffraction and calculated by using the density functional
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