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DIBENZANTHRONE | CAS 116-71-2

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DIBENZANTHRONE Basic information

Product Name:DIBENZANTHRONE
Synonyms:sandothrenedarkbluenbo;sandothrenedarkbluenboa;sandothrenedarkbluenmba;Solanthrene Dark Blue B;Solanthrene Dark Blue BA;Solanthrene Dark Blue F-BA;Vat Dark Blue BO UL Conc;VAT BLUE 20
CAS:116-71-2
MF:C34H16O2
MW:456.49
EINECS:204-152-0
Product Categories:Organics
Mol File:116-71-2.mol

DIBENZANTHRONE Chemical Properties

Melting point 338-339 °C
Boiling point 522.64°C (rough estimate)
density 1.1055 (rough estimate)
refractive index 1.4875 (estimate)
storage temp. Sealed in dry,Room Temperature
AppearanceBrown to black Solid
CAS DataBase Reference116-71-2(CAS DataBase Reference)
NIST Chemistry ReferenceDibenzanthrone(116-71-2)
EPA Substance Registry SystemViolanthrone (116-71-2)

Safety Information

MSDS Information

DIBENZANTHRONE Usage And Synthesis

General DescriptionFire HazardSynthesis
DescriptionViolanthrone, Indanthren DarkBlue BOA,is generated bypotash fusion of benzanthrone , .Direct potash fusion leads to side products, suchas isoviolanthrone and 4-hydroxybenzanthrone.The crude product may be used directly or inmixtures with other dyes in vat dyeing. It is alsoused to generate violanthrone derivatives. Severalprocesses have been developed to decreasethe amounts of undesirable side products of thedirect potash fusion of benzanthrone or to purifythe bibenzanthronyl or the crude violanthrone. Especially effective is the additionof high-boiling solvents such as naphthalene, theso-called low carbazole anthracene residues, orsodium acetate to the melt. The quality of theproducts prepared by these methods is satisfactoryfor the production of almost all violanthronedyes.
Bluish-black to black powder.
Air & Water ReactionsInsoluble in water.
Flash point data for DIBENZANTHRONE are not available. DIBENZANTHRONE is probably combustible.
Flammability and ExplosibilityNot classified
Violanthrone of high purity is obtainedfrom 4,4'-bibenzanthronyl (153) by alkaline oracid ring closure, preferably in the presenceof oxidizing agents , . If this ringclosure is carried out in sulfuric acid withan excess of manganese dioxide, the 16,17-violanthronequinone (155) is obtained. This canbe reduced readily with sodium hydrogen sulfiteto 16,17-dihydroxyviolanthrone (156). Subsequentalkylation of the hydroxy groups yieldsvery fast navy-blue to brilliant-green vat dyes.The dimethyl ether (157) is the well-knowndye Caledon Jade Green or Indanthren BrilliantGreen B and FFB (extremely pure form).
Properties and Applications

TEST ITEMS

SPECIFICATION

APPEARANCE

BLUE POWDER

SHADE

REDDISH

HEAT RESISTANCE

300 °C min

LIGHT FASTNESS

8

ACID RESISTANCE

5

ALKALI RESISTANCE

5

FASTNESS TO BLEEDING

5

OIL ABSORPTION

40-50%

SPECIFIC SURFACE

27 m 2 /g

DENSITY

1.60 g/cm 3

RESIDUE ON 80 MESH

5.0% max

WATER SOLUBLE

1.0% max

VOLATITE 105 °C

1.0% max

TINTING STRENGTH

100-105 %

DIBENZANTHRONE Preparation Products And Raw materials

Raw materialsPotassium hydroxide-->Nitrogen-->Sodium acetate-->Sodium acetate trihydrate-->Sodium chlorate-->Naphthalene-->Benzanthrone-->Diffusing agent-->Triethylene glycol-->[4,4'-bi-7H-benz[de]anthracene]-7,7'-dione-->7H-Benz[de]anthracen-7-one, 2-chloro--->[3,3'-bi-7H-benz[de]anthracene]-7,7'-dione-->Anthra[9,1,2-cde]benzo[rst]pentaphene-->4,4'-dibenzoyl-1,1'-binaphtyl-->Vat Violet 10-->3-Bromobenzanthrone-->Anthracen-9-ol-->4,4'-dibenzoyl-1,1'-binaphtyl
Preparation ProductsVat Black 9-->INDANTHRENE BLACK BBN-->Vat Dark Blue VB-->vat black 16-->Anthra[9,1,2-cde]benzo[rst]pentaphene-5,10-dione, chloro derivs.-->INDANTHRENE BLACK BBN-->vat black 16

Declaration: The products displayed on this website are intended exclusively for industrial applications or scientific research. They are not intended for medical, pharmaceutical, or food use. In accordance with applicable laws and regulations, purchasing organizations must hold valid qualifications and approvals.

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