Ampyrone information

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	83-07-8 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:59026 ;
ChEMBL	ChEMBL1165011 ;
ChemSpider	2066 ;
ECHA InfoCard	100.001.321
PubChem CID	2151;
UNII	0M0B7474RA ;
CompTox Dashboard (EPA)	DTXSID8048860 ;
	InChI InChI=1S/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3 Key: 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,12H2,1-2H3 Key: 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/cm3
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 [77 °F], 100 kPa). verify (what is ?) Infobox references

Ampyrone is a metabolite of aminopyrine with analgesic, anti-inflammatory, and antipyretic properties.^[2] Its use as a drug is discouraged due to the risk of agranulocytosis.^[3] It is used as a reagent for biochemical reactions producing peroxides or phenols.^[2] Ampyrone stimulates liver microsomes and is also used to measure extracellular water.^[2]

^ PubChem (25 March 2005). "4-Aminoantipyrine". PubChem. Retrieved 2022-05-09.
^ ^a ^b ^c ^d "4-Aminoantipyrine". pubchem.ncbi.nlm.nih.gov. 25 March 2005. Retrieved 2022-05-09.
^ "On-line encyklopedia PWN (in Polish)". Archived from the original on 2011-06-07. Retrieved 2008-10-17.

[1] PubChem (25 March 2005). "4-Aminoantipyrine". PubChem. Retrieved 2022-05-09.

[PubChem-2] "4-Aminoantipyrine". pubchem.ncbi.nlm.nih.gov. 25 March 2005. Retrieved 2022-05-09.

[3] "On-line encyklopedia PWN (in Polish)". Archived from the original on 2011-06-07. Retrieved 2008-10-17.

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