Pigment Red 149
Names
Preferred IUPAC name
2,9-Bis(2,5-dimethylphenyl)anthradiisoquinoline-1,3,8,10(2H ,9H )-tetrone
Identifiers
CAS Number
3D model (JSmol )
ChemSpider
ECHA InfoCard
100.023.264
EC Number
PubChem CID
UNII
CompTox Dashboard (EPA )
InChI
InChI=1S/C40H26N2O4/c1-19-13-20(2)16-23(15-19)41-37(43)29-9-5-25-27-7-11-31-36-32(40(46)42(39(31)45)24-17-21(3)14-22(4)18-24)12-8-28(34(27)36)26-6-10-30(38(41)44)35(29)33(25)26/h5-18H,1-4H3Key: FDXVHZCFTCIKDD-UHFFFAOYSA-N InChI=1/C40H26N2O4/c1-19-13-20(2)16-23(15-19)41-37(43)29-9-5-25-27-7-11-31-36-32(40(46)42(39(31)45)24-17-21(3)14-22(4)18-24)12-8-28(34(27)36)26-6-10-30(38(41)44)35(29)33(25)26/h5-18H,1-4H3Key: FDXVHZCFTCIKDD-UHFFFAOYAH
SMILES
Cc1cc(cc(c1)N2C(=O)c3ccc4c5ccc6c7c5c(ccc7C(=O)N(C6=O)c8cc(cc(c8)C)C)c9c4c3c(cc9)C2=O)C
Properties
Chemical formula
C40 H26 N2 O4
Molar mass
598.65
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
Infobox references
Chemical compound
Pigment Red 149 is an organic compound that is used as a pigment . Structurally, it is a derivative of perylene , although it is produced from perylenetetracarboxylic dianhydride by derivatization with 3,5-dimethylaniline .
References
K. Hunger. W. Herbst "Pigments, Organic" in Ullmann's Encyclopedia of Industrial Chemistry , Wiley-VCH, Weinheim, 2012. doi :10.1002/14356007.a20_371
Greene, M. "Perylene Pigments" in High Performance Pigments, 2009, Wiley-VCH, Weinheim. doi :10.1002/9783527626915.ch16
pp. 261-274.
Dyeing Techniques
Types of dyes
Traditional textile dyes
History
Craft dyes
Reference
Categories :
Pigment Red 149
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