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Pigment yellow 185

From Wikipedia, the free encyclopedia
Pigment yellow 185
Names
Preferred IUPAC name
(2Z)-2-Cyano-N-methyl-2-[3-(2,4,6-trioxo-1,3-diazinan-5-ylidene)-2,3-dihydro-1H-isoindol-1-ylidene]acetamide
Other names
  • Isoindolinone Yellow AS-AP
  • Isoindolinone Yellow AS-BH
  • Isoindolinone Yellow ASR-AG
  • Enceprint Yellow
  • Sico Fast Yellow D
Identifiers
3D model (JSmol)
ECHA InfoCard 100.071.241 Edit this at Wikidata
EC Number
  • 278-388-8
UNII
  • InChI=1S/C16H11N5O4/c1-18-13(22)9(6-17)11-7-4-2-3-5-8(7)12(19-11)10-14(23)20-16(25)21-15(10)24/h2-5,19H,1H3,(H,18,22)(H2,20,21,23,24,25)/b11-9-
    Key: ACUPDOXCXXCPIX-LUAWRHEFSA-N
  • CNC(=O)/C(C#N)=C1/c2ccccc2C(N1)=C3C(=O)NC(=O)NC3=O
Properties
C16H11N5O4
Molar mass 337.295 g·mol−1
Appearance yellow green solid
Density 1.576 g/cm3
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Pigment yellow 185 is an organic compound that is used as a green yellow pigment and optical brightener. It is classified as a derivative of isoindoline. This yellow green compound is prepared by addition of ammonia to phthalonitrile to give diiminoisoindole, which in turn condenses first with N-methylcyanoacetamide and then with barbituric acid.[1]

References

[edit]
  1. ^ Radtke, Volker; Erk, Peter; Sens, Benno (2009). "Isoindoline pigments". In Faulkner, Edwin B.; Schwartz, Russell J. (eds.). High Performance Pigments (2nd ed.). Wiley-VCH. pp. 221–241. doi:10.1002/9783527626915.ch14. ISBN 978-3-527-62691-5.