| Weight | 203.245 g/mol |
|---|---|
| Formula | C11H13N3O |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
4-Aminoantipyrine (83-07-8)
Aminoantipyrine · 4 Amino 1,5 Dimethyl 2 Phenyl 3H Pyrazolone · 4-Amino-1,5-Dimethyl-2-Phenyl-3H-Pyrazolone
Score:
#3957 in Biology
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#4982 in Chemistry
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- 4-Aminoantipyrine as an inhibitor of mild steel corrosion in HCl solution (Journal of Applied Electrochemistry, 1999)
- Sensitive 4-Aminoantipyrine Method for Phenolic Compounds (Analytical Chemistry, 1951)
- THE CONDENSATION OF AMINOANTIPYRINE. II. A NEW COLOR TEST FOR PHENOLIC COMPOUNDS (Journal of Organic Chemistry, 1943)
- Transition metal complexes with Schiff-base ligands: 4-aminoantipyrine based derivativesa review (Journal of Coordination Chemistry, 2009)
- Coordination Modes of a Schiff Base Pentadentate Derivative of 4-Aminoantipyrine with Cobalt(II), Nickel(II) and Copper(II) Metal Ions: Synthesis, Spectroscopic and Antimicrobial Studies (Molecules, 2009)
- Synthesis, structural determination and antibacterial activity of compounds derived from vanillin and 4-aminoantipyrine (Journal of The Serbian Chemical Society, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Aminoantipyrine
- 4 Amino 1,5 Dimethyl 2 Phenyl 3H Pyrazolone
- 4-Amino-1,5-Dimethyl-2-Phenyl-3H-Pyrazolone
- 4-Aminophenazone
- 4 Aminoantipyrine
- 4 Aminophenazone
- Ampyrone
-
SMILESCC1=C(C(=O)N(N1C)C2=CC=CC=C2)N
-
InChIKeyRLFWWDJHLFCNIJ-UHFFFAOYSA-N
- Pubchem - 4-Aminoantipyrine
- Wikipedia - ampyrone
Ampyrone is a metabolite of aminopyrine with analgesic, anti-inflammatory, and antipyretic properties. Due to the risk of agranulocytosis its use as a drug is discouraged. It is used as a reagent for biochemical reactions producing peroxides or phenols.
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