In this work, we assemble amphiphilic iron(III) corroles at airwater interfaces into well-defined quasi-two-dimensional molecular monolayers and theirs stacks for sensing of nitric oxide (NO). For this purpose, we use the Langmuir-Blodgett (LB) technique, which allows varying the packing density of iron(III) corroles anchored to the aqueous subphase via one molecular side. The stacks of ten down to three molecular monolayers on the front and back sides of the substrates are sufficiently optically dense to detect NO binding to the layers photometrically. This sensing with few layers demonstrates the potential for electronic detection, where very thin surface functionaliza-tions enable efficient electronic communication between the layer and the (semi)conductor. Despite increasing optical densities, the spectral responses to NO exposure become smaller with increasing packing density until the collapse point of the monolayers is reached. This demonstrates that the highest molecular efficiency for binding and detection of NO is achieved at the smallest packing densities. This finding is relevant to all molecular sensor films with axial binding of analytes to the sensor molecules and demonstrates the advantage of sensor molecule assembly into monolayers on water-air interfaces using the LB technique.