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Ampyrone

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(Redirected from 4-Aminoantipyrine)
Ampyrone
Names
Preferred IUPAC name 4-Amino-1,5-dimethyl-2-phenyl-3H-pyrazol-3-one
Other names solvapyrin A, aminoazophene, aminoantipyrene, aminoantipyrine, metapyrazone
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.321 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3Key: RLFWWDJHLFCNIJ-UHFFFAOYSA-N
  • InChI=1/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3Key: RLFWWDJHLFCNIJ-UHFFFAOYAT
SMILES
  • O=C2\C(=C(/N(N2c1ccccc1)C)C)N
Properties
Chemical formula C11H13N3O1
Molar mass 203.24 g/mol
Density 1.207g/cm
Melting point 106 to 110 °C (223 to 230 °F; 379 to 383 K)
Boiling point 309 °C (588 °F; 582 K) @760mmHg
Hazards
Flash point 140.7 °C (285.3 °F; 413.8 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Ampyrone is a metabolite of aminopyrine with analgesic, anti-inflammatory, and antipyretic properties. While the parent drug, aminopyrine, has been discouraged due to the risk of agranulocytosis, ampyrone itself has significantly lower toxicity. It is used as a reagent for biochemical reactions producing peroxides or phenols. Ampyrone stimulates liver microsomes and is also used to measure extracellular water.

References

  1. PubChem (25 March 2005). "4-Aminoantipyrine". PubChem. Retrieved 2022-05-09.
  2. ^ "4-Aminoantipyrine". pubchem.ncbi.nlm.nih.gov. 25 March 2005. Retrieved 2022-05-09.
  3. Bailey, D. N. (1983). "The unusual occurrence of 4-aminoantipyrine (4-aminophenazone) in human biological fluids". Journal of Analytical Toxicology. 7 (2): 76–78. doi:10.1093/jat/7.2.76. ISSN 0146-4760. PMID 6855207.
  4. PubChem. "Aminopyrine". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-08-26.
  5. PubChem. "4-Aminoantipyrine". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-08-26.
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