Indanthrone blue

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Indanthrone blue
Skeletal formula
Ball-and-stick model
Names
Other names
C.I. vat blue 4, carbon paper blue, blue O, carbanthrene blue 2R, fenan blue RSN, graphtol blue RL, medium blue, monolite fast blue 3R, indanthrene, indanthrone, pigment blue 60, C.I. 69800
Identifiers
81-77-6 YesY
367131
ChemSpider 6435 YesY
Jmol 3D model Interactive image
PubChem 6690
  • InChI=1S/C28H14N2O4/c31-25-13-5-1-3-7-15(13)27(33)21-17(25)9-11-19-23(21)29-20-12-10-18-22(24(20)30-19)28(34)16-8-4-2-6-14(16)26(18)32/h1-12,29-30H YesY
    Key: UHOKSCJSTAHBSO-UHFFFAOYSA-N YesY
  • InChI=1/C28H14N2O4/c31-25-13-5-1-3-7-15(13)27(33)21-17(25)9-11-19-23(21)29-20-12-10-18-22(24(20)30-19)28(34)16-8-4-2-6-14(16)26(18)32/h1-12,29-30H
    Key: UHOKSCJSTAHBSO-UHFFFAOYAY
  • O=C6c5c4Nc3c(c2C(=O)c1ccccc1C(=O)c2cc3)Nc4ccc5C(=O)c7ccccc67
Properties
C28H14N2O4
Molar mass 442.43 g·mol−1
Density 1.6 g/ml
Insoluble
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Indanthrone blue, also called indanthrene, is an organic dye made from 2-aminoanthraquinone treated with potassium hydroxide in the presence of a potassium salt. It is a pigment that can be used in the following mediums: acrylic, alkalyd, casein, encaustic, fresco, gouache, linseed oil, tempera, pastel, and watercolor painting. It is used to dye unmordanted cotton and as a pigment in quality paints and enamels. As a food dye, it has E number E130, but it is not approved for use in either the United States or the European Union.[1] [2] Indanthrene Blue RS was patented in 1901 by Rene Bohn as the first anthraquinone vat dye, one of the dyes with very good fastness to light and washing.

Properties

It has the appearance of blue needles with metallic luster and melting point of 470-500 °C. It has excellent light fastness, but may bleed in some organic solvents.

References