7,14-Dibenzpyrenequinone

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7,14-Dibenzpyrenequinone
Skeletal formula
Ball-and-stick model
Names
Other names
Golden Yellow GK
Dibenzochrysenedione
Dibenzpyrenequinone
Tyrian Yellow I-GOK
C.I. 59100
Dibenzo[b,def]chrysene-7,14-dione
3,4:8,9-dibenzopyrene-5,10-dione
Identifiers
128-66-5 N
ChemSpider 29142 YesY
Jmol 3D model Interactive image
KEGG C19545 YesY
PubChem 31412
  • InChI=1S/C24H12O2/c25-23-17-7-3-1-5-13(17)15-9-11-20-22-16(10-12-19(23)21(15)22)14-6-2-4-8-18(14)24(20)26/h1-12H YesY
    Key: ZTWQZJLUUZHJGS-UHFFFAOYSA-N YesY
  • InChI=1/C24H12O2/c25-23-17-7-3-1-5-13(17)15-9-11-20-22-16(10-12-19(23)21(15)22)14-6-2-4-8-18(14)24(20)26/h1-12H
    Key: ZTWQZJLUUZHJGS-UHFFFAOYAD
  • O=C2c1ccccc1c6c5c2ccc4c3ccccc3C(=O)c(c45)cc6
Properties
C24H12O2
Molar mass 332.36 g·mol−1
Appearance yellow solid
Density 1.418g/cm3
Boiling point 606.7 °C (1,124.1 °F; 879.9 K) at 760 mmHg
soluble
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

7,14-Dibenzpyrenequinone is a yellow synthetic anthraquinone vat dye, known as Vat Yellow 4. It is a bright yellow solid. This dye is used mostly as a dye for textiles and paper. Together with benzanthrone, it is used in some older pyrotechnic compositions for green and yellow colored smokes. It is produced from 1,5-dibenzoylnaphthalene by oxidative (dehydrogenative) ring closure.[1]

Safety

Vat Yellow 4 is a Group 3 carcinogen according to the IARC, as the evidence of its carcinogenity to humans is inadequate.

References

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