3230-09-9

Basic information

• Product Name: 1,4-DI(DODECYLOXY)BENZENE
• Synonyms: 1,4-DI(DODECYLOXY)BENZENE
• CAS NO: 3230-09-9
• Molecular Formula: C₃₀H₅₄O₂
• Molecular Weight: 0
• Mol File: 3230-09-9.mol
• Article Data: 34

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4-DI(DODECYLOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-DI(DODECYLOXY)BENZENE(3230-09-9)
• EPA Substance Registry System: 1,4-DI(DODECYLOXY)BENZENE(3230-09-9)

Safety Data

• Hazardous Substances Data: 3230-09-9(Hazardous Substances Data)

Usage

Type

Synthetic chemical compound

Classification

Alkylaryloxybenzene sulfonate

Structure

Long hydrophobic tail of dodecyl groups attached to a benzene ring

Applications

Surfactant or co-surfactant in industrial and household products

Uses

Production of detergents, dishwashing liquids, and other cleaning products

Properties

a. Reduces surface tension
b. Increases solubility of non-polar substances in water

Environmental Impact

Considered a persistent organic pollutant

Health Concerns

Possible endocrine disruptor

Current Efforts

Seeking alternative, eco-friendly surfactants to replace DDB in various applications

Upstream product

• 10157-76-3 dodecyl 4-methylbenzenesulphonate 
• 30008-10-7 sodium 4-hydroxybenzen-1-olate 
• 151-21-3 sodium dodecyl-sulfate 
• 143-15-7 1-dodecylbromide 
• 123-31-9 hydroquinone 
• 112-52-7 1-chlorododecane 

Downstream Products

• 137436-30-7 2,5-dibromo-1,4-didodecyloxybenzene 
• 145483-66-5 1,4-bis(dodecyloxy)-2,5-diiodobenzene 
• 171368-73-3 2,5-bis(dodecyloxy)bromobenzene 
• 122996-59-2 1,4-bis(bromomethyl)-2,5-bis-(dodecyloxy)benzene 
• 737581-58-7 1,4-bis(cyanomethyl)-2,5-bis(dodecyloxy)benzene 
• 209050-49-7 1,4-bis(dodecyloxy)-2,5-divinylbenzene 
• 874115-26-1 1-Bromo-2,5-bis-dodecyloxy-4-(4-iodo-phenylethynyl)-benzene 
• 171368-81-3 2,5-bis(dodecyloxy)-4-bromo-1-nitrobenzene 
• 171368-82-4 2,5-bis(dodecyloxy)-4-bromo-1-aminobenzene 
• 152270-00-3 1,4-bis(dodecyloxy)-2,5-diethynylbenzene 
• 243835-38-3 1-(3-hydroxy-3-methyl-1-butynyl)-4-ethynyl-2,5-di(dodecyloxy)benzene 
• 243835-42-9 1-ethynyl-2,5-di(dodecyloxy)-4-[(2,6-bis(2-pyridinyl)pyridine-4-yl)ethynyl]benzene 
• 243835-41-8 1,4-[(2,6-(2-C₅H₄N)C₅H₂N-4-CC)]-2,5-(OC₁₂H₂₅-n)2 
• 243835-44-1 1-[(4-bromo-2,5-di(dodecyloxy)phenyl)ethynyl]-2,5-di(dodecyloxy)-4-[(2,6-bis(2-pyridinyl)pyridine-4-yl)ethynyl]benzene 

Relevant articles and documents

Synthesis of copillar[5]arene by co-oligomerization of different monomers and its application to supramolecular polymer gel

A copillar[5]arene derivative with different repeating units was synthesized by co-oligomerization of different alkyl ethers. Copillar[5]arene-based supramolecular polymer gel was formed by a self-inclusion complexing in acetonitrile. The supramolecular polymer gel was driven by the C-H· π interactions, and presented two phases as time went on, and finally, constructed the supramolecular organic framework. Notably, the supramolecular polymer gel showed reversible gel-sol phase transitions upon heating and cooling. Meanwhile, the transparent films formed by the supramloecular gel show the potential application in the field of anti-acid rain materials.

A photoluminescent molecular host with aggregation-induced emission enhancement, multi-stimuli responsive properties and tunable photoluminescence host-guest interaction in the solid state

The development of controllable multimodal luminescent materials that are responsive to external stimuli has been a challenge. In this study, a photoluminescent (PL) molecular host with aggregation-induced emission enhancement (AIEE) characteristic and mu

Photoswitchable J-aggregated processable organogel by integrating a photochromic acceptor

A novel αchromophoric 1,4-bis(anthracenylethynyl)benzene (BAB)-based highly emissive J-aggregated organogel has been synthesized and characterized. Single-crystal structure determination of asymmetric π-chromophoric bola-amphiphilic BAB1 (dodecyl and triethyleneglycolmonomethylether containing side chains of bis(anthracenylethynyl)benzene) supports J-aggregation. Further, a photochromic acceptor chromophore, 4,4′-(perfluorocyclopent-1-ene-1,2-diyl)bis(5-methylthiophene-2-carbaldehyde), is noncovalently encapsulated in the gel and photoswitching studies have been performed based on photochromic F?rster resonance energy transfer. The modulated emission of the processable soft material is further exploited for rewritable display. However, BAB2 (dodecyl side chain on both sides) does not show gelation property due to its low solubility.