5160-53-2

Usage

Uses

Used in Explosive Manufacturing:
2,4,6-trinitrophenol-naphthalene (1:1) is used as a key ingredient in the production of explosives due to the explosive properties of 2,4,6-trinitrophenol. Its integration with naphthalene enhances the compound's performance in explosive formulations, making it suitable for various blasting applications.
Used in Chemical Reactions:
In the chemical industry, 2,4,6-trinitrophenol-naphthalene (1:1) serves as a reactant or catalyst in specific chemical processes. The combination of these two chemicals may facilitate certain reactions or improve the yield of desired products, contributing to the efficiency of chemical synthesis.
Used in Pesticide Formulation:
Given the historical use of 2,4,6-trinitrophenol in the manufacture of pesticides, the 1:1 combination with naphthalene could be employed to develop new pesticides or improve the effectiveness of existing ones. The naphthalene may act as a carrier or solvent, enhancing the delivery and action of the pesticide.
Used in Dye Production:
2,4,6-trinitrophenol, one of the components of the mixture, has been used in the production of dyes. The combined properties of 2,4,6-trinitrophenol and naphthalene in a 1:1 ratio could potentially be utilized in the development of new dye formulations for various applications, including textiles and other industries.
It is crucial to handle and store 2,4,6-trinitrophenol-naphthalene (1:1) with extreme care due to its potential explosive and toxic properties, ensuring safety in all applications.

Upstream product

• 91-20-3 naphthalene 
• 88-89-1 2,4,6-Trinitrophenol 

Downstream Products

• 1152-90-5 pyridinium picrate 
• 91-20-3 naphthalene 
• 88-89-1 2,4,6-Trinitrophenol 

Relevant academic research and scientific papers

Synthesis, crystal growth, structural, thermal and optical properties of naphthalene picrate an organic NLO material

Crystalline substance of naphthalene picrate (NP) was synthesized and single crystals were grown using slow evaporation solution growth technique. The solubility of the naphthalene picrate complex was estimated using different solvents such as chloroform and benzene. The material was characterized by elemental analysis, powder X-ray diffraction (XRD), nuclear magnetic resonance (NMR) and fourier transform-infrared (FT-IR) techniques. The electronic absorption was studied through UV-vis spectrophotometer. Thermal behavior and stability of the crystal were studied using thermogravimetric (TG) and differential thermal analysis (DTA) techniques. The second harmonic generation (SHG) of the material was confirmed using Nd:YAG laser.

A Computerised Least Square Method for Determination of Stability Constants of 1:1 Molecular Complexes and Chemical Shift of Pure Complexes from Nuclear Magnetic Resonance Data

A computerised method utilising nuclear magnetic resonance data has been developed for the determination of stability constants of 1:1 molecular complexes.It is based on the principle of least squares in which the coefficients are adjusted under a constraint with the help of Lagrange's method of undetermined multipliers.The method utilises the complete expression for equilibrium constant and is mathematically rigorous, straightforward, non-iterative and requires very little computer time.

Preparation and IR-Spectroscopic Study of Charge Transfer Complexes of Naphthalene Derivatives with Some Tri- and Di-Nitrobenzenes

The charge transfer complexes of naphthalene and some of its derivatives with some trinitro- and dinitrobenzenes are prepared and investigated by ir-spectroscopy.The shifts in the bands due to functional groups as well as the γCH bands of both donor and acceptor are found to be indicative for the type of bonding in the charge transfer complex. - Keywords: Charge transfer complexes, synthesis and IR-spectra