Jump to content

9-Aminoacridine

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Marbletan (talk | contribs) at 18:23, 4 January 2024. The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

9-Aminoacridine
Names
Preferred IUPAC name
Acridin-9-amine
Other names
Aminacrine
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.814 Edit this at Wikidata
UNII
  • 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) checkY
    Key: XJGFWWJLMVZSIG-UHFFFAOYSA-N checkY
  • 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
  • n1c3c(c(c2c1cccc2)N)cccc3
Properties
C13H10N2
Molar mass 194.237 g·mol−1
Appearance Yellow powder
Melting point 300 °C (572 °F; 573 K)
Pharmacology
D08AA02 (WHO)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

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]

See also

References

  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. doi:10.1002/rcm.750.


Stub icon

This dermatologic drug article is a stub. You can help Wikipedia by expanding it.

Stub icon

This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=9-Aminoacridine&oldid=1193611591"