110126-93-7

Basic information

• Product Name: 1 4-BIS(2-ETHYLHEXYLOXY)BENZENE 97
• Synonyms: 1 4-BIS(2-ETHYLHEXYLOXY)BENZENE 97
• CAS NO: 110126-93-7
• Molecular Formula: C₂₂H₃₈O₂
• Molecular Weight: 334.54
• Mol File: 110126-93-7.mol
• Article Data: 28

Chemical Properties

• Boiling Point: 190-200 °C2 mm Hg(lit.)
• Flash Point: 180 °F
• Appearance: /
• Density: 0.919 g/mL at 25 °C(lit.)
• Vapor Pressure: 5.77E-07mmHg at 25°C
• Refractive Index: n20/D 1.4860(lit.)
• CAS DataBase Reference: 1 4-BIS(2-ETHYLHEXYLOXY)BENZENE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 1 4-BIS(2-ETHYLHEXYLOXY)BENZENE 97(110126-93-7)
• EPA Substance Registry System: 1 4-BIS(2-ETHYLHEXYLOXY)BENZENE 97(110126-93-7)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 110126-93-7(Hazardous Substances Data)

Usage

Description

1,4-Bis(2-ethylhexyloxy)benzene 97, also known as di(2-ethylhexyl) phthalate (DEHP), is a chemical compound with the molecular formula C28H46O2. It is a clear, colorless liquid with a slightly sweet odor and is commonly used in various industrial applications due to its versatile properties.

Uses

Used in Plastic Industry:
1,4-Bis(2-ethylhexyloxy)benzene 97 is used as a plasticizer for the production of PVC (polyvinyl chloride) products. It enhances the flexibility, workability, and durability of PVC materials, making it suitable for a wide range of applications such as vinyl flooring, cables, and wire insulation.
Used in Lubricant Applications:
In the industrial sector, 1,4-Bis(2-ethylhexyloxy)benzene 97 is utilized as a lubricant. Its ability to reduce friction and wear between moving parts makes it a valuable component in various mechanical systems and processes.
Used in Adhesive and Sealant Manufacturing:
1,4-Bis(2-ethylhexyloxy)benzene 97 is also employed as a solvent in the manufacturing of adhesives and sealants. Its solvent properties allow for the even distribution of other components within the adhesive or sealant formulation, ensuring optimal performance and effectiveness.
Safety Precautions:
1,4-Bis(2-ethylhexyloxy)benzene 97 is classified as a substance with low toxicity. However, it is essential to handle and use this chemical in industrial settings with appropriate safety precautions to minimize potential health and environmental risks.

InChI:InChI=1/C22H38O2/c1-5-9-11-19(7-3)17-23-21-13-15-22(16-14-21)24-18-20(8-4)12-10-6-2/h13-16,19-20H,5-12,17-18H2,1-4H3

Upstream product

• 18908-66-2 3-bromomethylheptane 
• 106-51-4 p-benzoquinone 
• 123-31-9 hydroquinone 
• 104-76-7 2-Ethylhexyl alcohol 

Downstream Products

• 353797-92-9 α,α'-dibromo-2,5-di(2'-ethylhexyloxy)-p-xylene 
• 945624-63-5 2,5-bis((2-ethylhexyl)oxy)-4-bromobenzaldehyde 
• 936339-56-9 4,4'-[(2,5-(2-ethylhexyl)oxy-1,4-phenylene)di(E)ethene-2,1-diyl]dibromobenzene 
• 1381926-86-8 2,5-bis((2-ethylhexyl)oxy)-4-iodobenzaldehyde 
• 1377972-66-1 [2,5-bis(2-ethylhexyloxy)-4-formylbenzyl]phosphonic acid diethyl ester 
• 1613377-56-2 [2,5-bis(2-ethylhexyloxy)benzyl]phosphonic acid diethylester 
• 1613377-55-1 2-bromomethyl-1,4-bis(2-ethylhexyloxy)benzene 

Relevant articles and documents

Green emitting PLED having polymeric host and dopant in emissive layer

Poly(1,1'-biphenyl-4,4'-ylene vinylene-alt-2,5-bis(2-ethylhexyl)-1,4- phenylene vinylene] [poly(BPV-alt-BEHPV)] as a polymeric dopant, was synthesized by Honer-Emmons condensation from corresponding dialdehyde and diphosphonate monomers. Synthesized alternating polymer was used to fabricate single layer (ITO/Host:Dopant/Al) PLEDs with poly(vinyl carbazole) (PVK) as a host. Conjugated poly(BPV-alt-BEHPV) showed green emission from single layer ITO/poly(BPV-alt-BEHPV)/Al device. Emission colors from doped PLEDs were changed by energy transfer from blue originated from PVK to green with increasing the content of poly(BPV-alt-BEHPV).

Polytriazole bridged with 2,5-diphenyl-1,3,4-oxadiazole moieties: A highly sensitive and selective fluorescence chemosensor for Ag+

Fluorescent conjugated polytriazoles (FCP 1-4) containing both 2,5-diphenyl-1,3,5-oxadiazole (OXD) and 1,2,3-triazole moieties in the main chain were synthesized from aromatic diazide (1) and dialkynes (2-5) via click polymerization, respectively. In the polymers, OXDs (fluorophores) and triazole rings (generated via CuAAC acting as metal ion ligands) comprise a fluorescent system. The polytriazoles displayed relatively strong emission with quantum yields in the range of 0.20-0.28 at room temperature in DMF. The study on their ion-responsive properties showed that, although all four FCPs have good selectivity for Ag+, the integration of alkoxy side groups (methoxy for FCP 2, hexyloxy for FCP 3 and 2-ethylhexyloxy for FCP 4) to the main chains of the polytriazoles decreased their sensitivity for Ag+via alteration of the polymer aggregation status and electron density of the main chains. Thus FCP 1 is highly sensitive for Ag+, where its Ksv is as high as 1.44 × 105 M-1 and its lowest detection limit is in the ppb range (4.22 × 10-7 M). This study provides an efficient click approach to the synthesis of a novel fluorescence sensor for Ag+ detection, which could expand the application of click polymerization in designing fluorescence sensors based on the triazole unit. This journal is

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Copolymers having thiophene based and vinylene based moieties. Methods of producing the copolymers, and methods of utilizing the copolymers as chromogenic sensors for selective detection of iodide anion are also provided.

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This invention relates to electrophoretic fluids, the use of these fluids for the preparation of an electrophoretic display device, and electrophoretic displays comprising such fluids.

Production of alkoxyphenol (by machine translation)

[Problem] The carbon number of 6 or higher aliphatic alcohol when used as a raw material, byproduct formation is suppressed, high yield, low cost method for manufacturing alkoxyphenol are obtained. [Solution] For the production of intense study alkoxyphenol, solvent and in the presence of an acid catalyst, a dihydric phenol with an aliphatic alcohol dehydration condensation reaction. [Drawing] no (by machine translation)