Indanthrone blue
Organic dye made from 2-aminoanthraquinone
From Wikipedia, the free encyclopedia
Indanthrone blue, also called indanthrene, is an organic compound with the formula (C14H6O2NH)2. It is a dark blue solid that is a common dye as well as a precursor to other dyes.[1]
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| Names | |
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| Preferred IUPAC name
6,15-Dihydrodinaphtho[2,3-a:2′,3′-h]phenazine-5,9,14,18-tetrone | |
| 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 | |
3D model (JSmol) |
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| 367131 | |
| ChemSpider | |
| ECHA InfoCard | 100.001.251 |
| E number | E130 (colours) |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C28H14N2O4 | |
| Molar mass | 442.430 g·mol−1 |
| Appearance | dark blue solid |
| Density | 1.6 g/ml |
| Melting point | 470-500 °C (decomposes) |
| Insoluble | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Preparation and structure
The compound is made by oxidation of 2-aminoanthraquinone in the presence of potassium hydroxide.
synthesis of indanthrone - Procedure for producing indanthrone from 2-aminoanthraquinone.
By dimerization of 2-aminoanthraquinone]] (1) under strongly alkaline conditions at 220-235 °C, the intermediate 3 is obtained in two steps, which cyclizes intramolecularly and is oxidized to indanthrone 5.[2]
Owing to intermolecular hydrogen bonding, indanthrone is insoluble. It can be modified by installing tert-butyloxycarbonyl groups in place of the N-H groups to give an organic-soluble "latent pigment." Processing of such derivatives has affording crystals of the parent pigment.[3]
Applications
Indanthrone is utilized as a blue pigment (C.I. Pigment Blue 60), primarily in the process of vat dyeing, often referred to as C.I. Vat Blue 4.[4] Indanthrone is a vat dye, synthesized to provide highest color fastness for the dyeing and printing of predominantly cellulose-based textile fibers. Fabrics dyed with indanthrene fulfill the highest standards and exhibit exceptional wash fastness, boil fastness, light fastness, weather fastness and chlorine fastness.
It is a pigment that can be used in the following media: acrylic, alkyd, 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 number 130, but it is not approved for use in either the United States or the European Union.[5][6] It has excellent light fastness, but may bleed in some organic solvents.
Indanthrone blue was the first example of the brand "Indanthren" (an acronym for Indigo from anthracene) introduced by BASF in 1901.[7][8][9] One result is that even now, in Japan vat dyes are commonly described as threne dyes (スレン染料), derived from the Japanese transliteration of the brand.[10][11]
Other studies
As an organic semiconductor, indanthrone has been considered as a photocatalyst for oxygen generation from water utilizing solar energy.[12][13] Indanthrone's characteristic as a nonlinear optics light absorber, allows for its use as an optical limiter, which can be employed, for instance, in laser protective filters.[14]
Related compounds
Indrathren Blue CLB (PubChem CID 5483458, registry number 6492-78-0) is a related blue dye.