6,6'-(1,4-Phenylenebis(oxy))bis(hexan-1-ol)
[CAS# 154876-99-0]

Identification

• Classification: Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyrimidine compound >> Alcohol
• Name: 6,6'-(1,4-Phenylenebis(oxy))bis(hexan-1-ol)
• Synonyms: 6-[4-(6-hydroxyhexoxy)phenoxy]hexan-1-ol
• Molecular Formula: C₁₈H₃₀O₄
• Molecular Weight: 310.43
• CAS Registry Number: 154876-99-0
• SMILES: C1=CC(=CC=C1OCCCCCCO)OCCCCCCO

Properties

• Density: 1.0±0.1 g/cm³, Calc.^*
• Index of Refraction: 1.510, Calc.^*
• Boiling Point: 474.9±35.0 ºC (760 mmHg), Calc.^*
• Flash Point: 241.0±25.9 ºC, Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H302-H315-H319-H335
• Precautionary Statements: P261-P280-P301+P312-P302+P352-P305+P351+P338

Discovory and Applicatios

6,6'-(1,4-Phenylenebis(oxy))bis(hexan-1-ol), also known as bisphenol-A bis(hexan-1-ol) ether, is a chemical compound that belongs to the class of bisphenol derivatives. This compound features two hexan-1-ol groups connected to a central aromatic ring (1,4-phenylene) via oxygen atoms, forming an ether linkage between the phenyl group and the hexanol moieties. Its molecular structure includes the key elements of oxygen, carbon, and hydrogen, with the formula C14H22O3. It is part of a larger group of compounds that are of interest due to their potential use in the development of advanced materials and polymers.

The compound 6,6'-(1,4-Phenylenebis(oxy))bis(hexan-1-ol) is primarily synthesized through a process that involves etherification reactions. These reactions create the bond between the hexan-1-ol groups and the aromatic phenylene ring, with the oxygen atoms playing a central role in linking the two components. This structure imparts unique properties to the compound, such as stability, moderate hydrophobicity, and the potential to interact with other chemical species in polymerization processes.

In terms of applications, this compound is used primarily as an intermediate in the synthesis of high-performance polymers, particularly in the production of polyesters and polyurethanes. The ether linkage between the phenylene ring and the hexanol groups allows it to act as a building block for polymers that require flexibility and high resistance to heat and chemical degradation. The compound is also of interest in the development of materials that need to withstand harsh environmental conditions, such as coatings, adhesives, and composites.

One important area of application for bisphenol-based compounds, including 6,6'-(1,4-Phenylenebis(oxy))bis(hexan-1-ol), is in the field of electronics and electrical components. The presence of the aromatic ring enhances the rigidity and stability of the resulting materials, making them suitable for use in electronics that require insulating materials with good mechanical properties. Furthermore, the compound’s ability to undergo polymerization reactions allows for the creation of custom materials that meet specific demands in terms of strength, durability, and conductivity.

This compound is also explored for its potential role in the synthesis of flame-retardant materials. The incorporation of such materials into polymers, especially in industries where fire safety is a concern, can provide an additional layer of protection by reducing the flammability of the products. Although 6,6'-(1,4-Phenylenebis(oxy))bis(hexan-1-ol) is not as widely utilized as some other bisphenol derivatives in industrial applications, its specific structural characteristics make it a useful tool in creating advanced polymeric materials with tailored properties.

In conclusion, 6,6'-(1,4-Phenylenebis(oxy))bis(hexan-1-ol) is a versatile intermediate compound in the chemical industry, primarily used in the synthesis of high-performance polymers and materials with specific applications in electronics, coatings, and flame-retardant products. Its unique structure and chemical reactivity allow it to play a key role in the development of materials that require both stability and versatility.