Naphthol yellow S
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| Names | |
|---|---|
| Preferred IUPAC name
Disodium 5,7-dinitro-8-oxidonaphthalene-2-sulfonate | |
| Other names
Acid Yellow 1; Food Yellow 1; Sodium flavianate; Flavianic acid, sodium salt; C.I. 10316, Acid Yellow S, Amacid Yellow S, C.I. 10316, C.I. Acid Yellow 1, C.I. Food Yellow 1 | |
| Identifiers | |
3D model (JSmol) |
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| 3839220 | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.011.537 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C10H4N2Na2O8S | |
| Molar mass | 358.19 g·mol−1 |
| Appearance | yellow solid |
| Hazards | |
| GHS labelling:[2] | |
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| Warning | |
| H317, H373 | |
| P260, P272, P280, P302+P352, P314, P333+P313, P363, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Naphthol yellow S is an organic compound with the formula C10H4(SO3Na)(ONa)(NO2)2. It is one of several isomers of sulfonated dinitro-1-naphthol. It is prepared by nitration of a trisulfonate of 1-naphthol, a process involving replacement of sulfonate groups with nitro.[3] It is a derivative of 1-naphthol. At one time it was a popular food colorant but it was delisted in 1959 in the U.S.[4]
References
- ↑ Naphthol Yellow S at Sigma-Aldrich
- ↑ "Naphthol Yellow S". pubchem.ncbi.nlm.nih.gov.
- ↑ Maarten R. van Bommel and Matthijs de Keijzer (2025). "The Nitro Dyes". In Maarten R. van Bommel and Matthijs de Keijzer (ed.). Bright Colours from the Past: The History, Chemistry, Characterisation and Application of Synthetic Dyes Between 1856 and 1914. Springer, Cultural Heritage Science series. doi:10.1007/978-3-031-88664-5.
- ↑ Sharma, Vinita; McKone, Harold T.; Markow, Peter G. (2011). "A Global Perspective on the History, Use, and Identification of Synthetic Food Dyes". Journal of Chemical Education. 88 (1): 24–28. Bibcode:2011JChEd..88...24S. doi:10.1021/ed100545v.


