Sudangelb G
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Sudangelb G | |||||||||||||||
other names |
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Molecular formula | C 16 H 14 N 4 O | |||||||||||||||
Brief description |
yellow odorless solid |
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properties | ||||||||||||||||
Molar mass | 278.31 g mol −1 | |||||||||||||||
Physical state |
firmly |
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Melting point |
156-158 ° C |
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solubility |
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safety instructions | ||||||||||||||||
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Toxicological data | ||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Sudangelb G is a synthetically produced chemical compound from the group of azo and Sudan dyes .
Extraction and presentation
Sudangelb G can be obtained by reacting 1-phenyl-3-methyl-5-pyrazolone with aniline .
properties
Sudangelb G is a yellow, odorless solid that is practically insoluble in water.
use
Sudangelb G is used as a coloring agent for cosmetics and printing inks.
Individual evidence
- ↑ a b c d e f g h Cloeren Technology: Safety data sheet Epofluor Yellow , accessed on December 27, 2019.
- ^ Gisbert Otterstätter: Coloring of foods, medicines, cosmetics . Behr's Verlag DE, 2007, ISBN 3-89947-958-0 , p. 191 ( limited preview in Google Book search).
- ↑ K. Venkataraman: The Chemistry of Synthetic Dyes . Elsevier, 2012, ISBN 978-0-323-14937-2 , pp. 90 ( limited preview in Google Book search).