74774-61-1

Usage

Uses

Used in Polymer Production:
1,10-BIS(4-CARBOXYPHENOXY)DECANE is used as a building block for the production of high-performance polymers such as polyimides and polyesters. Its incorporation into these materials significantly improves their mechanical and thermal properties, making them suitable for a wide range of applications in various industries.
Used in Surfactant and Dispersing Agent Applications:
In addition to its role in polymer production, 1,10-BIS(4-CARBOXYPHENOXY)DECANE is also utilized as a surfactant and dispersing agent in various industrial processes. Its ability to reduce surface tension and promote the dispersion of substances makes it a valuable component in the formulation of products such as detergents, emulsifiers, and coatings.
Used in Chemical Industry:
1,10-BIS(4-CARBOXYPHENOXY)DECANE is used as a chemical intermediate for the synthesis of other compounds and materials. Its unique structure and properties make it a suitable candidate for further chemical reactions and modifications, contributing to the development of new products and technologies.
Safety Considerations:
While 1,10-BIS(4-CARBOXYPHENOXY)DECANE offers numerous benefits in various applications, it is crucial to handle this chemical with care and adhere to safety guidelines. Exposure to high concentrations of 1,10-BIS(4-CARBOXYPHENOXY)DECANE can pose risks to human health and the environment, necessitating proper handling, storage, and disposal practices to minimize potential hazards.

InChI:InChI=1/C24H30O6/c25-23(26)19-9-13-21(14-10-19)29-17-7-5-3-1-2-4-6-8-18-30-22-15-11-20(12-16-22)24(27)28/h9-16H,1-8,17-18H2,(H,25,26)(H,27,28)

Upstream product

• 4101-68-2 1,10-dibromodecane 
• 99-96-7 4-hydroxy-benzoic acid 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 103330-20-7 1,10-Bis(p-carbethoxyphenoxy)decane 

Downstream Products

• 70856-65-4 4,4'-(decane-1,1'-diylbis(oxy))dibenzoic acid 
• 102101-68-8 C₃₈H₄₂O₈ 
• 102101-67-7 C₄₀H₄₆O₈ 
• 102101-66-6 C₄₂H₅₀O₈ 
• 102101-65-5 C₄₄H₅₄O₈ 
• 102101-64-4 C₄₆H₅₈O₈ 
• 102101-63-3 C₄₈H₆₂O₈ 
• 1428977-06-3 4,4'-(decane-1,1'-diylbis(oxy))dibenzoic acid 
• 102101-62-2 C₅₀H₆₆O₈ 

Relevant academic research and scientific papers

Synthesis of multifunctional coupling agents and their selective reactions with hydroxy and amino groups in the melt

Three new coupling agents with different numbers of N-acyl lactam and 4H-3,1-benzoxazin-4-one groups were synthesized. A selective stepwise conversion of the coupling agents with 1-dodecanol and 1-dodecylamine was demonstrated by means of solvent-free model reactions in melt at 195 and 210 °C, respectively. These coupling agents are regarded as potential cores for the synthesis of novel star-like compounds and polymers with defined arms varying in type and lengths.

Biological evaluation of bisbenzaldehydes against four Mycobacterium species

A series of bisbenzaldehydes and structurally related analogs, conveniently synthesized via microwave-assisted reactions, were evaluated in vitro against drug susceptible and multi-drug resistant Mycobacterium tuberculosis, against virulent Mycobacterium bovis, against Mycobacterium ulcerans and against two Mycobacterium avium subspecies. Among the 33 substances that were tested, compound 12, i.e. 4,4′-[1,12-dodecanediyl(oxy)]bisbenzaldehyde, emerged as the most promising hit. Its activity was further confirmed in an intracellular growth inhibition assay of M. tb in murine J774 A.1 macrophages. None of the compounds showed significant cytotoxicity on human C3A hepatocytes in a neutral red dye uptake assay and no genotoxicity or mutagenicity was observed as demonstrated by a VITOTOX test and confirmed with a comet assay.

Synthesis and Thermotropic Properties of Twin Mesogens Containing a Polymethylene Spacer

DSC and microscopic data are presented for a thermotropic twin mesogen series.Deviations from normal trends were observed.