Acid orange 20 (also Orange I) is an organic compound and an azo dye. It is one of the first water soluble dyes to be commercialized, and one of seven original food dyes allowed under the U.S. Pure Food and Drug Act of June 30, 1906. It is analyzed by HPLC.[1]
Use and discontinuation

At one time it was a popular food colorant but it was delisted in 1959 in the U.S.[2][3]
In the early 1950s, after several cases were reported of sickness in children who had eaten Halloween candy colored with the dye, the FDA conducted new, more thorough and rigorous testing on food dyes.[4] Orange 1 was outlawed for food use in 1956.[5]
In [late] 1950[,] our Kansas City District received a complaint that children became ill after eating this candy. Investigation of the manufacturing process by our Denver District revealed that the candy contained about 0.25% of dye [FD&C Orange No. 1 and FD&C Yellow No. 5, "Orange Blend"]. An unusually large amount of dye was used in order to obtain a deep orange color for Halloween. Our Division of Pharmacology found that the candy caused abdominal cramps and diarrhea in human volunteers. It was further shown that an amount of the Orange Blend contained in twelve kisses caused identical symptoms. Pharmacological re-investigation of all the certifiable food colors has been initiated. Since practically no information was available regarding the amount of coal-tar color used in various food products, it was decided to initiate an investigational program to assemble such data. It is expected that this information will be useful in evaluating the pharmacological data obtained.
Chemical structure

Although acid orange 20 is often drawn as an azo compound (with C-N=N-C linkage), it mainly exists as a tautomer with a hydrazone (C=N-NH-C) group.[6]
Related compounds
- Orange II (Acid Orange 7), an isomer
References
- ↑ Yoshioka, N.; Ichihashi, K. (2008). "Determinación de 40 colorantes alimentarios sintéticos en bebidas y caramelos mediante cromatografía líquida de alta resolución utilizando una columna corta con detección por matriz de fotodiodos". Talanta . 74 (5): 1408– 1413. doi : 10.1016/j.talanta.2007.09.015 . PMID 18371797 .
- ↑ Sharma, Vinita; McKone, Harold T.; Markow, Peter G. (2011). "Una perspectiva global sobre la historia, el uso y la identificación de colorantes alimentarios sintéticos". Journal of Chemical Education . 88 (1): 24– 28. Bibcode : 2011JChEd..88...24S . doi : 10.1021/ed100545v .
- ↑ "Noticias sobre alimentación; EE. UU. podría prohibir los colorantes utilizados para teñir naranjas y otros alimentos". The New York Times . 19 de enero de 1954.
- ↑ Malia Wollan (5 de octubre de 2016). "Un tono completamente nuevo: La búsqueda para crear un M&M azul auténtico" . The New York Times Magazine . Consultado el 8 de octubre de 2016 .
- ↑ Maga, Joseph A.; Anthony T. Tu (1995). Toxicología de los aditivos alimentarios . CRC Press. pág. 182. ISBN 0-8247-9245-9.
- ↑ Vannucci, Giulia; Cañamares, Maria Vega; Prati, Silvia; Sanchez-Cortes, Santiago (2020). "Estudio de la tautomería azo-hidrazona del Naranja Ácido 20 mediante técnicas espectroscópicas: UV-Visible, Raman y dispersión Raman intensificada en superficie". Journal of Raman Spectroscopy . 51 (8): 1295– 1304. Bibcode : 2020JRSp...51.1295V . doi : 10.1002/jrs.5906 . hdl : 11585/789451 .
- colorantes alimentarios
- Colorantes azoicos
- colorantes ácidos
- Controversias de 1956
- Controversias del siglo XX en Estados Unidos