R. Cai et al., Structural changes of sinapic acid during alkali-induced air oxidation andthe development of colored substances, J AM OIL CH, 76(6), 1999, pp. 757-764
Structural changes of sinapic acid were induced by air oxidation in aqueous
solutions at pH 7-10 and followed by spectral and high-performance liquid
chromatographic (HPLC) analysis. Color properties of the sinapic acid solut
ions were determined by taking the transmittance spectra, calculating the C
ommission Internationale de l'Eclairage (CIE) 1931 tri-stimulus values, and
converting to Hunter L a b values. Reaction rate constants for sinapic aci
d were determined by a kinetic study based on the quantitative results from
HPLC analysis. These reactions were first order with respect to sinapic ac
id and fit the appropriate equation with a coefficient of R-2 > 0.97. Sinap
ic acid was converted to thomasidioic acid with reaction rate constants (k)
of 8.54 x 10(-6), 2.51 x 10(-5), and 4.87 x 10-5 (-1) in phosphate-boric a
cid buffers of pH 7, 8.5, and 10, respectively: Similar reactions in ammoni
um bicarbonate buffers were more than 10 times faster. With time, thomasidi
oic acid further converted to 2,6-dimethoxy-p-benzoquinone and 6-hydroxy-5,
7-dimethoxy-2-naphthoic acid. Air oxidation of sinapic acid aqueous solutio
ns caused darkening of the color for the system, with the 2,6-dimethoxy-p-b
enzoquinone as a major color contributor.