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2-Propenoic acid, 2-(dibutylaMino)ethyl ester, also known as dibutylaminoethyl methacrylate, is a versatile chemical compound widely used in the production of polymers, coatings, adhesives, sealants, and various industrial products. It is recognized for its ability to enhance the adhesion and flexibility of coatings, as well as its resistance to water and chemicals. Additionally, it serves as a crosslinking agent in the production of thermosetting resins. However, it is crucial to handle this chemical with care due to its potential to cause irritation to the skin, eyes, and respiratory system if proper safety measures are not followed.

7709-10-6

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7709-10-6 Usage

Uses

Used in Polymer and Coating Production:
2-Propenoic acid, 2-(dibutylaMino)ethyl ester is used as a key component in the production of polymers and coatings, contributing to their enhanced adhesion and flexibility. Its resistance to water and chemicals makes it a valuable addition to these materials, improving their durability and performance in various applications.
Used in Adhesive and Sealant Manufacturing:
In the manufacturing of adhesives and sealants, 2-Propenoic acid, 2-(dibutylaMino)ethyl ester is utilized for its ability to improve the bonding strength and flexibility of these products. This results in more effective and long-lasting adhesion in a wide range of applications.
Used in Industrial Product Development:
2-Propenoic acid, 2-(dibutylaMino)ethyl ester is also employed in the development of various other industrial products, where its properties can be leveraged to enhance the performance and durability of the final product.
Used as a Crosslinking Agent in Thermosetting Resins:
In the production of thermosetting resins, 2-Propenoic acid, 2-(dibutylaMino)ethyl ester serves as a crosslinking agent, which is essential for creating a strong, stable, and heat-resistant material. This makes it suitable for applications that require high-performance materials capable of withstanding extreme conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 7709-10-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7709-10:
(6*7)+(5*7)+(4*0)+(3*9)+(2*1)+(1*0)=106
106 % 10 = 6
So 7709-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H25NO2/c1-4-7-9-14(10-8-5-2)11-12-16-13(15)6-3/h6H,3-5,7-12H2,1-2H3

7709-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dibutylamino)ethyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names -

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:7709-10-6 SDS

7709-10-6Downstream Products

7709-10-6Relevant academic research and scientific papers

2-(Dibutylamino)ethyl acrylate as a highly efficient co-reactant of Ru(bpy)3 2+ electrochemiluminescence for selective detection of cysteine

Yuan, Fan,Hao, Kai,Sheng, Shu,Fereja, Tadesse Haile,Ma, Xiangui,Liu, Feng,Zafar, Muhammad Nadeem,Lou, Baohua,Tian, Huayu,Xu, Guobao

, (2020)

A highly efficient co-reactant of Ru(bpy)3 2+ electrochemiluminescence (ECL), 2-(dibutylamino)ethyl acrylate(DBAEA), was successfully synthesized by a straightforward one-step reaction between dibutylaminoethanol and acrylyl chloride. On account of the interaction between the olefin group of DBAEA and Pt electrode, the ECL intensity utilizing DBAEA as the co-reactant was increased dramatically, nearly as 10 times and 17 times as conventional co-reactants dibutyaminoethanol and tripropylamine. Since cysteine can remove the acrylate group of DBAEA specifically through conjugated addition/cyclization reaction, the ECL intensity of Ru(bpy)3 2+/DBAEA was declined selectively. Therefore, cysteine was detected through this novel ECL system with high selectivity towards other amino acids. The linear range was between 10 μM and 200 μM with a limit of detection of 1.15 μM. The cysteine in Dulbecco's Modified Eagle Medium (DMEM) was detected and satisfying recovery was obtained.

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