The experimental vapor-liquid equilibrium (VLE) data for a ternary system of beta-caryophyllene + dipentene + alpha-pinene and two binary systems composed of beta-caryophyllene (1) + dipentene (2) and dipentene (2) + alpha-pinene (3) were measured using a modified Ellis still in the temperature range from 428.4 to 529.1 K at 100.7 kPa. The thermodynamic consistency test of the VLE data was carried out using the van Ness test and the McDermott-Ellis method. The binary VLE data were correlated 46 using the Margules, Nonrandom Two-Liquid (NRTL), Wilson, and Universal Quasi Chemical (UNIQUAC) activity coefficient models. The mean absolute deviation values of vapor-phase mole fraction and temperature are 0.0103 and 1.11 K for the beta-caryophyllene (1) + dipentene (2) system and 0.0025 and 0.17 K for the dipentene (2) + alpha-pinene (3) system, respectively. The Wilson model parameters obtained from the binary systems were used to predict the ternary VLE data. By comparing the experimental values for the ternary system with the values calculated using the Wilson model, the mean absolute deviation value of the equilibrium temperature was determined to be 0.49 K; the absolute deviation values of the vapor-phase composition of beta-caryophyllene and dipentene were determined to be less than 0.0078 and 0.0062, respectively.