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4,4'-[Oxybis(ethyleneoxy)]dianiline, also known as ODA, is a diamine compound characterized by its two ether linkages. It is widely recognized for its role as a curing agent in epoxy resins, enhancing the mechanical and thermal properties of these resins. ODA's chemical structure, which includes the ethyleneoxy linkages, contributes to its high-performance capabilities in various applications.

6954-41-2

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6954-41-2 Usage

Uses

Used in Adhesives Industry:
4,4'-[Oxybis(ethyleneoxy)]dianiline is used as a curing agent for epoxy resins in the adhesives industry to improve the mechanical and thermal properties of the adhesives, ensuring strong bonds and durability in various applications.
Used in Coatings Industry:
In the coatings industry, 4,4'-[oxybis(ethyleneoxy)]dianiline is utilized as a curing agent to enhance the performance of epoxy coatings, providing excellent chemical and heat resistance, as well as improved mechanical properties.
Used in Composite Materials:
4,4'-[Oxybis(ethyleneoxy)]dianiline is used as a curing agent in composite materials to improve their overall performance, including increased strength and thermal stability, making them suitable for a wide range of applications.
Used in Electronic Materials:
ODA is employed in the manufacturing of electronic materials, where its excellent chemical and heat resistance properties are crucial for the production of reliable and high-performance electronic components.
Used in Laminates:
4,4'-[Oxybis(ethyleneoxy)]dianiline is used as a curing agent in the production of laminates, contributing to their enhanced mechanical and thermal properties, which are essential for various industrial applications.
Used in Structural Adhesives:
In structural adhesives, 4,4'-[oxybis(ethyleneoxy)]dianiline is used to improve the adhesive's performance, providing strong bonds and increased resistance to environmental factors.
Safety Precautions:

Check Digit Verification of cas no

The CAS Registry Mumber 6954-41-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6954-41:
(6*6)+(5*9)+(4*5)+(3*4)+(2*4)+(1*1)=122
122 % 10 = 2
So 6954-41-2 is a valid CAS Registry Number.

6954-41-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-[2-(4-aminophenoxy)ethoxy]ethoxy]aniline

1.2 Other means of identification

Product number -
Other names M and B 2540

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6954-41-2 SDS

6954-41-2Relevant academic research and scientific papers

Liquid crystal dimers having vary oxyethylene flexible spacers

Park, Joo Hoon,Singu, Bal Sydulu,Choi, Ok Byung,Lee, Hwan Myung,Lee, Jin Young,Kim, Sung Jo,Cha, Eun Hee,Park, Seon Nam,Kwak, Myeong Heon,So, Bong Keun,Kim, Ran Hee,Lee, Soo Min,Yoon, Kuk Ro

, p. 1 - 6 (2017/09/07)

In this article, we are prepared that the liquid crystal dimers have aromatic-ester type mesogenic units or aromatic-Schiff base type mesogonic units and confirmed by 1H-NMR spectrometry. The mesomorphic and optical properties of the resultant dimers were studied by differential scanning calorimetry and polarizing optical microscopy.

Synthesis and Properties of a New Series of Troegerophanes

Ibrahim, Alhussein A.,Matsumoto, Mutsumi,Miyahara, Yuji,Izumi, Kenji,Suenaga, Masahiko,Shimizu, Nobujiro,Inazu, Takahiko

, p. 209 - 215 (2007/10/03)

A new series of macrocyclic compounds with one or two Troeger base skeletons has been synthesized by condensing mono-, di-, tri-, and teraethyleneglycol bis(p-aminophenoxy) ethers with formalin in the presence of concentrated hydrochloric acid in ethanol at room temperature for 13 days. This simple one-step cyclization provided 19 in remarkably high yield (46%) and 17, 18, and 20 in yields reflecting the strain of the rings and statistical factors. Complexation with lithium thiocyanate was observed for 20, the structure of which was elucidated by X-ray crystallography.

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