151237-06-8

Usage

Uses

Used in Cosmetics and Personal Care Products:
1,2-Dihexadecyloxybenzene is used as a surfactant and emulsifier for its ability to stabilize mixtures of oil and water, which is essential in the formulation of creams, lotions, and other personal care products. Its emulsifying properties help to create smooth textures and improve the spreadability of these products on the skin.
Used in Household Cleaners:
In the household cleaning industry, 1,2-dihexadecyloxybenzene serves as a surfactant and emulsifier, enhancing the cleaning power of detergents and soaps by reducing the surface tension of water and allowing it to mix more effectively with dirt and grease.
Used in Polymer Production:
1,2-Dihexadecyloxybenzene is utilized in the production of polymers due to its chemical structure that can contribute to the formation of polymer chains, which can be tailored for specific properties such as flexibility, strength, or durability.
Used as a Lubricant Additive:
In the lubrication industry, 1,2-dihexadecyloxybenzene is used as an additive to improve the performance of lubricants. Its chemical properties can enhance the lubricity and reduce friction between moving parts, which is particularly useful in industrial machinery and automotive applications.
Recognized for Environmental Benefits:
1,2-Dihexadecyloxybenzene is known for its low toxicity and biodegradability, making it a more environmentally friendly option compared to some other chemical compounds used in similar applications. This characteristic is particularly valuable in industries where ecological impact is a concern.

InChI:InChI=1/C38H70O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-31-35-39-37-33-29-30-34-38(37)40-36-32-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h29-30,33-34H,3-28,31-32,35-36H2,1-2H3

Upstream product

• 6068-28-6 tosylate de n-hexadecyle 
• 34789-97-4 pyrocatechol monosodium salt 
• 120-80-9 benzene-1,2-diol 
• 112-82-3 hexadecanyl bromide 
• 36653-82-4 1-Hexadecanol 

Downstream Products

• 219993-02-9 3,4-dihexadecyloxyacetophenone 
• 923029-80-5 1,2-bis(hexadecyloxy)-4,5-diiodobenzene 
• 118132-07-3 1,2-dibromo-4,5-bis(hexadecyloxy)benzene 
• 1315454-16-0 C₅₂H₈₈N₂O₈ 
• 1315454-15-9 4,5-di(hexadecyloxy)-1,2-dinitrobenzene 
• 151237-02-4 3,4-di(hexadecyloxy)phenylamine 
• 923029-84-9 1,2-bis(hexadecyloxy)-4-iodo-5-(trimethylsilyl)ethynylbenzene 
• 923029-87-2 1-ethynyl-4,5-bis(hexadecyloxy)-2-iodobenzene 
• 118132-14-2 4,5-bis(hexadecyloxy)phthalonitrile 
• 151236-98-5 3,4-di(hexadecyloxy)nitrobenzene 

Relevant academic research and scientific papers

Influence of main chain on the phase behaviors of side-chain liquid-crystalline polymers with triphenylene mesogens of long alkyl tail substituents

A series of side-chain liquid-crystalline polymers (SCLCPs) containing triphenylene mesogen, in which the long alkyl tail Tp connected directly with main chain, were synthesized successfully. The chemical structures of the monomers were confirmed by

Amphiphilic iron(ii) spin crossover coordination polymers: Crystal structures and phase transition properties

Iron(ii) coordination polymers with an N2O2 coordinating Schiff base-like equatorial ligand bearing different alkyl chain lengths (C16, C18, C20, and C22) and 1,2-bis(4-pyridyl)ethyne, 1,2-bis(4-pyridyl)ethene or 1,2-bis(4-pyridyl)et

Hydrogen bond-driven columnar self-assembly of electroluminescent D-A-D configured cyanopyridones

Herein, we report the design and synthesis of a new series of flying bird-shaped liquid crystalline (LC) cyanopyridone derivatives with a D-A-D architecture, CPO-1 to CPO-4. Their mesomorphic, photophysical, electrochemical, and electroluminescence charac

Amphiphilic [tpy-MII-tpy] metallotriangles: synthesis, characterisation and hierarchical ordering

Long chain (C16) alkylated metallocycles are synthesised and characterised. Their ordered aggregation was studied via TEM to gauge to the effects of molecular topology, solvent, counterion and metal centre(s) on morphology and nanoscale structu

Columnar catenar bisoxazoles and bisthiazoles

Three new series of catenar liquid crystals 1a-c derived from heterocyclic bisoxazoles and bisthiazoles exhibiting columnar phases were reported. All compounds 1a-c exhibited hexagonal columnar phases, which were confirmed by powder XRD diffractometer. Co

New octahedral, head-tail iron(II) complexes with spin crossover properties

The synthesis and characterisation of four new Schiff base-like ligands with long alkyl chains in the outer periphery and their iron(II) complexes with methanol and pyridine as axial ligands is reported. Two of the methanol complexes crystallise in a lipi

Cooperative spin transition in a lipid layer like system

A novel iron(ii) mononuclear spin transition complex [FeL(py)2] displays an abrupt spin transition around 225 K accompanied by a very wide thermal hysteresis loop (～50 K) that spreads out over 100 K. Crystal structure analysis in both low-spin and high-spin states reveals a lipid layer-like arrangement of the complex molecules and provides insights into the spin switching mechanism.

H-Bonded metallomesogens: preparation, characterization, and mesomorphic studies of (3-hydroxypropylimino)propan-1,2-diols

Two series of new Schiff bases 2 (n=8, 12, 16) derived from (3-hydroxypropyl imino)propan-1, 2-diol with a hydroxyl group at C19/C20-position and their palladium complexes 1 were prepared and their mesomorphic properties investigated

Physicochemical characterization of octakis(alkyloxy)-substituted Zn(II)-phthalocyanines non-covalently incorporated into an organogel and their remarkable morphological effect on the nanoscale-fibers

A series of octakis(alkyloxy)-substituted Zn(II)-phthalocyanines were efficiently incorporated into an organogel made of (1R,2R)-trans-1,2- bis(dodecanoylamino)cyclohexane by means of multiple cooperative non-covalent interactions, and SEM revealed the fo

A new class of discotic mesogens derived from tris(N-salicylideneaniline)s existing in C3h and Cs keto-enamine forms

(Chemical Equation Presented) Two series of a unique class of columnar liquid crystals derived from tris(N-salicylideneaniline)s [TSANs] in which the proton and the electron interact with each other through the H-bonding environment are reported. The synt