This study reports the characterization and organic vapor sensing properties of Langmuir-Blodgett (LB) thin films of calix[4]arene derivatives that contain different numbers of tert butyl groups on their upper rims. Surface pressure-area isotherms show that very stable monolayers are formed at the air-water interface. The LB films are deposited onto different substrates, which allowed us to characterize the films by contact angle measurements, quartz crystal microbalance (QCM), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The results indicate that good quality, uniform LB films can be prepared with transfer ratios of over 0.95. Meanwhile, our QCM results show that the deposition of LB film layers depends heavily on the number of p-tert-butyl groups and calix[4]arene with four p-tert-butyl groups yields the highest slope with a mass value of 1145 ng per layer. Furthermore, our AFM and SEM studies reveal a dense surface morphology for all prepared LB films. The kinetic response of calix[4]arenes containing p-tert-butyl groups and without p-tert-butyl groups as an LB film to chloroform, benzene, toluene, and ethanol vapors were investigated as a function of time. After attaching tert-butyl groups onto the calix[4]arene structure, the response of LB film to chloroform vapor increased. LB films of compounds 1-4 yield a response to all vapors and more often select chloroform with a larger, faster, and more reproducible response. We thus conclude that these calix[4]arenes could be applied to research concerning vapor sensing devices operating at room temperature. © 2013 Elsevier B.V. All rights reserved.