Quinacridone

Quinacridone
Names
	Preferred IUPAC name 5,12-Dihydroquinolino[2,3-b]acridine-7,14-dione
	Other names C.I.: 73900, Pigment Violet 19
Identifiers
CAS Number	1047-16-1 ;
3D model (JSmol)	Interactive image;
ChemSpider	13369 ;
ECHA InfoCard	100.012.618
EC Number	213-879-2;
PubChem CID	13976;
UNII	11P487375P ;
CompTox Dashboard (EPA)	DTXSID5027354 ;
	InChI InChI=1S/C20H12N2O2/c23-19-11-5-1-3-7-15(11)21-17-10-14-18(9-13(17)19)22-16-8-4-2-6-12(16)20(14)24/h1-10H,(H,21,23)(H,22,24) Key: NRCMAYZCPIVABH-UHFFFAOYSA-N ; InChI=1/C20H12N2O2/c23-19-11-5-1-3-7-15(11)21-17-10-14-18(9-13(17)19)22-16-8-4-2-6-12(16)20(14)24/h1-10H,(H,21,23)(H,22,24) Key: NRCMAYZCPIVABH-UHFFFAOYAK;
	SMILES O=C4c5ccccc5Nc3cc2C(=O)c1c(cccc1)Nc2cc34;
Properties
Chemical formula	C20H12N2O2
Molar mass	312.328 g·mol−1
Appearance	Red powder (nanoparticles)
Density	1.47 g/cm3
Solubility in water	Insoluble
	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

Quinacridone is an organic compound used as a pigment. Numerous derivatives constitute the quinacridone pigment family, which finds extensive use in industrial colorant applications such as robust outdoor paints, inkjet printer ink, tattoo inks, artists' watercolor paints, and color laser printer toner. As pigments, the quinacridones are insoluble.^[1]^[2] The development of this family of pigments supplanted the alizarin dyes.^{[citation needed]}

^ Hunger, K.; Herbst, W. (2012). "Pigments, Organic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a20_371. ISBN 978-3527306732.(subscription required)
^ Blundell, Jane. "Quinacridone Colours". Jane Blundell.com. Retrieved 1 August 2018.