|  | |
|  | |
| Names | |
|---|---|
| IUPAC name Sodium 4-[(2,4-dihydroxyphenyl)diazenyl]benzenesulfonate | |
| Other names Sodium p-(2,4-dihydroxyphenylazo)benzenesulfonate;  Chrysoine;  Resorcinol Yellow;  Gold Yellow;  Yellow T;  Tropaeolin O;  Tropaeolin R;  C.I. Food Yellow 8;  C.I. Acid Orange 6;  C.I. 14270 | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.008.114 | 
| EC Number | 
 | 
| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
| 
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| 
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| Properties | |
| C12H9N2NaO5S | |
| Molar mass | 316.26 g·mol−1 | 
| Appearance | Orange-yellow solid | 
| Partially soluble | |
| Hazards | |
| NFPA 704 (fire diamond) | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Chrysoine resorcinol is a synthetic azo dye which was formerly used as a food additive. In Europe, it was banned as a food additive in 1977.[1] In the US, it was banned in 1988.[2]
Chrysoine resorcinol can be used as a pH indicator with a color change between pH 11 and pH 12.7. In colorimetry, it has an absorption maximum of 387 nm.
| Chrysoine resorcinol (pH indicator) | ||
| below pH 11.0 | above pH 12.7 | |
| 11.0 | ⇌ | 12.7 | 
Preparation
Acid orange 6 can be synthesised via the azo coupling of sulfanilic acid and resorcinol,
Notes
- ↑ "EUR-Lex - Official Journal of the European Union".
- ↑ "Chrysoine Resorcinol Properties, Molecular Formula, Applications - WorldOfChemicals". www.worldofchemicals.com. Retrieved 2022-07-12.
External links
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