9-Aminoacridine

9-Aminoacridine
Names
	Preferred IUPAC name Acridin-9-amine
	Other names Aminacrine
Identifiers
CAS Number	90-45-9 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:74789 ;
ChEMBL	ChEMBL43184 ;
ChemSpider	6752 ;
ECHA InfoCard	100.001.814
PubChem CID	7019;
UNII	78OY3Z0P7Z ;
CompTox Dashboard (EPA)	DTXSID2024456 ;
	InChI InChI=1S/C13H10N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1-8H,(H2,14,15) Key: XJGFWWJLMVZSIG-UHFFFAOYSA-N ; InChI=1/C13H10N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1-8H,(H2,14,15) Key: XJGFWWJLMVZSIG-UHFFFAOYAM;
	SMILES n1c3c(c(c2c1cccc2)N)cccc3;
Properties
Chemical formula	C13H10N2
Molar mass	194.237 g·mol−1
Appearance	Yellow powder
Melting point	300 °C (572 °F; 573 K)
Pharmacology
ATC code	D08AA02 (WHO)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). verify (what is ?) Infobox references

9-Aminoacridine is a synthetic dye used clinically as a topical antiseptic and experimentally as a mutagen, an intracellular pH indicator and a small molecule MALDI matrix.^[1]

References

^ Vermillion-Salsbury, Rachal L.; Hercules, David M. (13 June 2002). "9-Aminoacridine as a matrix for negative mode matrix-assisted laser desorption/ionization". Rapid Communications in Mass Spectrometry. 16 (16). Wiley Interscience: 1575–1581. Bibcode:2002RCMS...16.1575V. doi:10.1002/rcm.750.

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[1] Vermillion-Salsbury, Rachal L.; Hercules, David M. (13 June 2002). "9-Aminoacridine as a matrix for negative mode matrix-assisted laser desorption/ionization". Rapid Communications in Mass Spectrometry. 16 (16). Wiley Interscience: 1575–1581. Bibcode:2002RCMS...16.1575V. doi:10.1002/rcm.750.

[1]

v t e Antiseptics and disinfectants (D08)
Acridine derivatives	Ethacridine lactate 9-Aminoacridine Euflavine
Biguanides and amidines	Dibrompropamidine Chlorhexidine^# Propamidine Hexamidine Polihexanide
Phenol and derivatives	Hexachlorophene Policresulen Phenol Triclosan Triclocarban Chloroxylenol^# Biphenylol Fenticlor
Nitrofuran derivatives	Nitrofurazone
Iodine products	Iodine/octylphenoxypolyglycolether Povidone-iodine^# Diiodohydroxypropane
Quinoline derivatives	Dequalinium Chlorquinaldol Oxyquinoline Clioquinol
Quaternary ammonium compounds	Benzalkonium Benzethonium chloride Cetrimonium (bromide/chloride) Cetylpyridinium Cetrimide Benzoxonium chloride Didecyldimethylammonium chloride
Mercurial products	Mercuric amidochloride Phenylmercuric borate Mercuric chloride Merbromin Nitromersol Thiomersal Mercuric iodide
Silver compounds	Silver nitrate
Alcohols	Propanol (propyl alcohol) Isopropanol (isopropyl alcohol) Ethanol (ethyl alcohol)^#
Other	Potassium permanganate Sodium hypochlorite Halazone Monalazone Hydrogen peroxide Eosin Chloramine-T (tosylchloramide) Octenidine dihydrochloride
^#WHO-EM ^‡Withdrawn from market Clinical trials: ^†Phase III ^§Never to phase III

See also

References