SYNTHESIS OF AZO COMPOUNDS DERIVATIVE FROM EUGENOL AND ITS APPLICATION AS A TITRATION INDICATOR

https://doi.org/10.22146/ijc.21568

Bambang Purwono(1*), Catur Mahardiani(2)

(1) Laboratory of Organic Chemistry, Faculty of Mathematics and Natural Sciences, Gadjah Mada University, Sekip Utara, Yogyakarta, Indonesia 5281
(2) Laboratory of Organic Chemistry, Faculty of Mathematics and Natural Sciences, Gadjah Mada University, Sekip Utara, Yogyakarta, Indonesia 5281
(*) Corresponding Author

Abstract


The synthesis of azo compounds from eugenol has been carried out by diazotation reaction. The diazonium salt was produced by reaction of aniline and sodium nitrite in acid condition at 0-5 °C temperature to yield benzenediazonium chloride salt. The salt was then reacted with eugenol to produce the azo derivatives. The azo product was analyzed by IR, 1H-NMR, dan GC-MS spectrometer. The results showed that the reaction of benzenediazonium chloride with eugenol gave 4-allyl-2-methoxy-6-hydroxyazobenzene in 34.27% yield for 30 minutes reaction. The derivative of azo compound was dissolved in ethanol and then the color changing was observed in range of pH 9.8-11.1 from yellow to red. Application for titration indicator for acetic acid titrated with sodium hydroxide showed error less than 3.20% compared with phenol phtaline indicator.


Keywords


Eugenol; Azo compound; titration indicator

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References

[1] Curtwright, R.D., Rynearson, J.A., and Markwell, J., 1994, J. Chem., Educ, 71, 682.

[2] Rageh, N.M., Ismail, N.M., and Dean, A.M.K., 2004, Can. J. Anal. Sci. and Spectrosc., 49,4, 240.

[3] Guzman. M., Camean. A.M., and Baustista. J., 1982, Microchemical J., 27, 1.

[4] Flair, M.N. and Setzer, W.N., 1990, J. Chem. Educ., 67, 795.



DOI: https://doi.org/10.22146/ijc.21568

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Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

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