2005, 2003, English, Article edition: NSC12448; Acid Alizarine Bordeaux G; Acid Alizarine Garnet R; Acid Chrome Red RB; Alizarine Bordeaux A; Alizarine Chrome Garnet R; Alizarine Garnet; Amacid Chrome Garnet R; Anthracene Chrome Red A; Atlantichrome Garnet Y; Benzenesulfonic acid, 3-[(2, 4-dihydroxyphenyl)azo]-4-hydroxy-, monosodium salt (9CI); C.I. Mordant Red 5 (VAN); C.I. Mordant Red 5, monosodium salt (8CI); C.I. 14290; Chromacid Fast Bordeaux R; Chrome Bordeaux A; Chrome Fast Bordeaux BR; Chrome Fast Bordeaux BRN; Chrome Fast Bordeaux JR; Chrome Garnet R; Chrome Garnet Y; Diacromo Garnet A; Diadem Chrome Garnet G; Diadem Chrome Garnet S; Diamond Chrome Red A; Durochrome Red A; Eniacromo Garnet A; Erio Chrome Garnet L; Eriochrome Bordeaux A; Eriochrome Bordeaux AP; Hispacrom Garnet G; Magracrom Red RB; Omega Chrome Bordeaux BL; Omega Chrome Bordeaux BLN; Omega Chrome Bordeaux BR; Superchrome Garnet Y; Tertrochrome Red A US National Cancer Institute

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Bookmark: http://trove.nla.gov.au/version/33389
Physical Description
  • 6428 bytes, 6163 bytes, chemical/​x-cml
  • Other
Published
  • Unilever Center for Molecular Informatics, Cambridge University
  • 2005-01-24T11:14:23Z
  • 2003-02-01
Language
  • English

Edition details

Title
  • NSC12448; Acid Alizarine Bordeaux G; Acid Alizarine Garnet R; Acid Chrome Red RB; Alizarine Bordeaux A; Alizarine Chrome Garnet R; Alizarine Garnet; Amacid Chrome Garnet R; Anthracene Chrome Red A; Atlantichrome Garnet Y; Benzenesulfonic acid, 3-[(2, 4-dihydroxyphenyl)azo]-4-hydroxy-, monosodium salt (9CI); C.I. Mordant Red 5 (VAN); C.I. Mordant Red 5, monosodium salt (8CI); C.I. 14290; Chromacid Fast Bordeaux R; Chrome Bordeaux A; Chrome Fast Bordeaux BR; Chrome Fast Bordeaux BRN; Chrome Fast Bordeaux JR; Chrome Garnet R; Chrome Garnet Y; Diacromo Garnet A; Diadem Chrome Garnet G; Diadem Chrome Garnet S; Diamond Chrome Red A; Durochrome Red A; Eniacromo Garnet A; Erio Chrome Garnet L; Eriochrome Bordeaux A; Eriochrome Bordeaux AP; Hispacrom Garnet G; Magracrom Red RB; Omega Chrome Bordeaux BL; Omega Chrome Bordeaux BLN; Omega Chrome Bordeaux BR; Superchrome Garnet Y; Tertrochrome Red A
Author
  • US National Cancer Institute
Published
  • Unilever Center for Molecular Informatics, Cambridge University
  • 2005-01-24T11:14:23Z
  • 2003-02-01
Physical Description
  • 6428 bytes, 6163 bytes, chemical/​x-cml
  • Other
Notes
  • NSC12448
  • C12H10N2O6S,15-21(16,20H)8-2H-4H-11(18H)10(6H-8)14-13-9-3H-1H-7(17H)5H-12(9)19H
Language
  • English
Contributed by
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