Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

4-Dimethylaminophenol

From Wikipedia, the free encyclopedia

Not to be confused with4-Dimethylaminopyridine.
4-Dimethylaminophenol
Names
Preferred IUPAC name
4-(Dimethylamino)phenol
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.009.642Edit this at Wikidata
UNII
  • InChI=1S/C8H11NO/c1-9(2)7-3-5-8(10)6-4-7/h3-6,10H,1-2H3 checkY
    Key: JVVRCYWZTJLJSG-UHFFFAOYSA-N checkY
  • InChI=1/C8H11NO/c1-9(2)7-3-5-8(10)6-4-7/h3-6,10H,1-2H3
    Key: JVVRCYWZTJLJSG-UHFFFAOYAU
  • Oc1ccc(N(C)C)cc1
Properties
C8H11NO
Molar mass137.179 g/mol
Boiling point165 °C (329 °F; 438 K) (0.040 bar)
Pharmacology
V03AB27 (WHO)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

4-Dimethylaminophenol (DMAP) is an aromatic compound containing bothphenol andamine functional groups. It has the molecular formula C8H11NO.

Uses

[edit]

4-Dimethylaminophenol has been used as anantidote forcyanide poisoning.[1] It has also been shown to be effective in treatinghydrogen sulfide toxicity.[2]

It works by generatingmethemoglobin.[3]

This is suitable as an emergency treatment only; treatment must be followed up withsodium thiosulfate orcobalamin.

In an animal model, it has shown effectiveness when givenintramuscularly.[4] Though,intramuscular injection should be avoid due to the probability ofmuscular necrosis after injection.Intravenous injection is recommended in a dose of 250 mg.[5]

See also

[edit]

References

[edit]
  1. ^Kampe S, Iffland R, Korenkov M, Diefenbach C (December 2000)."Survival from a lethal blood concentration of cyanide with associated alcohol intoxication: Case report".Anaesthesia.55 (12):1189–1191.doi:10.1046/j.1365-2044.2000.01628.x.PMID 11121929.S2CID 32892580.
  2. ^Lindenmann J, Matzi V, Neuboeck N, Ratzenhofer-Komenda B, Maier A, Smolle-Juettner FM (December 2010). "Severe hydrogen sulphide poisoning treated with 4-dimethylaminophenol and hyperbaric oxygen".Diving and Hyperbaric Medicine.40 (4):213–217.ISSN 1833-3516.PMID 23111938.
  3. ^Vick JA, Von Bredow JD (1996)."Effectiveness of intramuscularly administered cyanide antidotes on methemoglobin formation and survival".J Appl Toxicol.16 (6):509–16.doi:10.1002/(SICI)1099-1263(199611)16:6<509::AID-JAT382>3.0.CO;2-V.PMID 8956097.S2CID 36140034.
  4. ^Vick JA, Froehlich H (July 1991)."Treatment of cyanide poisoning".Mil Med.156 (7):330–9.doi:10.1093/milmed/156.7.330.PMID 1922842.
  5. ^Federation of American Scientists (1 February 1996).NATO HANDBOOK ON THE MEDICAL ASPECTS OF NBC DEFENSIVE OPERATIONS(PDF). p. 334.
Nervous
system
Alcohol intoxication
Barbiturate
overdose
Benzodiazepine
overdose
GHB overdose
Nerve agent /
Organophosphate
poisoning
Opioid overdose
Reversal of
neuromuscular blockade
Circulatory
system
Beta blocker
Digoxin toxicity
Anticoagulants
Other
Arsenic poisoning
Cyanide poisoning
Hydrofluoric acid
Methanol /
Ethylene glycol
poisoning
Paracetamol toxicity
(Acetaminophen)
Toxic metals (cadmium
Other
Emetic
Retrieved from "https://en.wikipedia.org/w/index.php?title=4-Dimethylaminophenol&oldid=1306083128"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp