Self-organization of nanoparticles into one-dimensional (1D) nanochains leads to new unpredicted physiochemical properties, which are further exploited to develop photonic or electronic devices. Thus, the controlled fabrication of 1D nanochains requires nanotemplate, which acts as building blocks for the self-assembly of nanoparticles. To address this issue, we designed a hydrotrope (sodium salicylate)-based CTAB/n-hexanol/water/heptane reverse micellar system. Hydrotrope, herein, modulates electrostatic interactions between reverse micellar droplets and paves the way for the formation of self-assembled structures. Small-angle X-ray scattering studies were performed on the CTAB/heptane reverse micellar system by varying hydrotrope concentrations and water-to-surfactant ratios (W-x). The aqueous content of the reverse micellar pool is determined from the W-x value, where W-x = [H2O]/[CTAB] and [CTAB] = 0.05 M. SAXS studies were performed for CTAB/heptane reverse micellar systems at three different W-x values, that is, 6, 12, and 16 and represented by W-6, W-12, and W-16, respectively. All SAXS profiles were modeled with a spherical form factor and a Baxter sticky hard sphere structure factor. The interaction between droplets was predicted in terms of stickiness parameter. The effect of W-x on the formation of self-assembled structures and forces governing the assembly has been discussed in detail. For the W-6 system, the electrostatic repulsion between reverse micellar droplets decreases, resulting in the formation of the 1D chain-like assembly of nanodroplets. In the case of the W-12 system, the dual feature of the hydrotrope has been observed, it increases the size of the reverse micellar system and reduces electrostatic repulsion between droplets because of which the formation of chain-like assemblies cannot be determined with accuracy. For the W-16 system, the decrease in micellar size with the increase in the hydrotrope concentration has been observed. Thus, our reverse micellar templates may provide a comprehensive method for the fabrication of high aspect ratio 1D nanochains of a variety of materials and harnessing their collective properties for magnetic, catalytic, and opto-electronic applications.