Misplaced Pages

Ampyrone: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively
Page 1
Page 2
← Previous editContent deleted Content addedVisualWikitext
Revision as of 18:59, 6 August 2011 editBeetstra (talk | contribs)Edit filter managers, Administrators172,055 edits Script assisted update of identifiers for the Chem/Drugbox validation project (updated: 'UNII', 'ChEBI').← Previous edit Latest revision as of 22:36, 10 January 2025 edit undoArthurfragoso (talk | contribs)Extended confirmed users, Template editors4,591 edits dark mode fix 
(36 intermediate revisions by 25 users not shown)
Line 1: Line 1:
{{chembox {{chembox
| Watchedfields = changed | Watchedfields = changed
| verifiedrevid = 413864023 | verifiedrevid = 443387760
| ImageFile_Ref = {{chemboximage|correct|??}} | ImageFile_Ref = {{chemboximage|correct|??}}
| ImageFile = Ampyrone structure.png | ImageFile = Ampyrone structure.png
| ImageClass = skin-invert-image
| ImageSize = | ImageSize =
| PIN = 4-Amino-1,5-dimethyl-2-phenyl-3''H''-pyrazol-3-one<ref>{{Cite web|last=PubChem|title=4-Aminoantipyrine|date=25 March 2005|url=https://pubchem.ncbi.nlm.nih.gov/compound/2151#section=IUPAC-Name|access-date=2022-05-09|website=PubChem|language=en}}</ref>
| IUPACName = 4-Amino- 1,5-dimethyl- 2-phenyl- pyrazol- 3-one
| OtherNames = solvapyrin A, aminoazophene, aminoantipyrene, metapyrazone | OtherNames = solvapyrin A, aminoazophene, aminoantipyrene, aminoantipyrine, metapyrazone
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| 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 | 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
| InChIKey = RLFWWDJHLFCNIJ-UHFFFAOYAT | InChIKey = RLFWWDJHLFCNIJ-UHFFFAOYAT
Line 21: Line 22:
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 2066 | ChemSpiderID = 2066
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 0M0B7474RA | UNII = 0M0B7474RA
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 59026 | ChEBI = 59026
| SMILES = O=C2\C(=C(/N(N2c1ccccc1)C)C)N | SMILES = O=C2\C(=C(/N(N2c1ccccc1)C)C)N
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| C=11 | H=13 | N=3 | O=1 | C=11 | H=13 | N=3 | O=1<ref name="PubChem"/>
| MolarMass = 203.24 g/mol | MolarMass = 203.24 g/mol
| Appearance = | Appearance =
| Density = 1.207g/cm<sup>3</sup> | Density = 1.207g/cm<sup>3</sup>
| MeltingPt = 106-110°C | MeltingPtC = 106 to 110
| MeltingPt_notes =
| BoilingPt = 309°C @760mmHg
| BoilingPtC = 309
| BoilingPt_notes = @760mmHg
| Solubility = }} | Solubility = }}
| Section3 = {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards = | MainHazards =
| FlashPt = 140.7°C | FlashPtC = 140.7
| Autoignition = }} | AutoignitionPtC =
}}
}} }}


'''Ampyrone''' is a ] of ] with ], ], and ] properties. Due to the risk of ] its use as a ] is discouraged.<ref></ref> Instead it is used as a ] for ] reactions producing ]s or ]. Ampyrone stimulates ] ]s and is also used to measure ] water. '''Ampyrone''' is a ] of ] with ], ], and ] properties.<ref name="PubChem"/> While the parent ], aminopyrine, has been discouraged due to the risk of ],<ref>{{Cite journal |last=Bailey |first=D. N. |date=1983 |title=The unusual occurrence of 4-aminoantipyrine (4-aminophenazone) in human biological fluids |url=https://pubmed.ncbi.nlm.nih.gov/6855207/ |journal=Journal of Analytical Toxicology |volume=7 |issue=2 |pages=76–78 |doi=10.1093/jat/7.2.76 |issn=0146-4760 |pmid=6855207}}</ref><ref>{{Cite web |last=PubChem |title=Aminopyrine |url=https://pubchem.ncbi.nlm.nih.gov/compound/6009 |access-date=2024-08-26 |website=pubchem.ncbi.nlm.nih.gov |language=en}}</ref> ampyrone itself has significantly lower toxicity.<ref>{{Cite web |last=PubChem |title=4-Aminoantipyrine |url=https://pubchem.ncbi.nlm.nih.gov/compound/2151 |access-date=2024-08-26 |website=pubchem.ncbi.nlm.nih.gov |language=en}}</ref> It is used as a ] for ] reactions producing ]s or ].<ref name="PubChem">{{Cite web|date=25 March 2005|title=4-Aminoantipyrine|url=https://pubchem.ncbi.nlm.nih.gov/compound/2151#:~:text=A%20metabolite%20of%20AMINOPYRINE%20with,water|access-date=2022-05-09|website=pubchem.ncbi.nlm.nih.gov|language=en}}</ref> Ampyrone stimulates ] ]s and is also used to measure ] water.<ref name="PubChem"/>


==References== ==References==
Line 45: Line 51:


{{Anti-inflammatory and antirheumatic products}} {{Anti-inflammatory and antirheumatic products}}
{{NSAIDs}}
{{Analgesics}} {{Analgesics}}


] ]
]
]
]




Line 54: Line 62:
{{analgesic-stub}} {{analgesic-stub}}
{{heterocyclic-stub}} {{heterocyclic-stub}}

]
]
Ampyrone: Difference between revisions Add topic