7709-10-6

Basic information

• Product Name: 2-Propenoic acid, 2-(dibutylaMino)ethyl ester
• Synonyms: 2-Propenoic acid, 2-(dibutylaMino)ethyl ester
• CAS NO: 7709-10-6
• Molecular Formula: C13H25NO2
• Molecular Weight: 227.3431
• EINECS: -0
• Mol File: 7709-10-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 294.7°Cat760mmHg
• Flash Point: 92.5°C
• Appearance: /
• Density: 0.913g/cm³
• Vapor Pressure: 0.0016mmHg at 25°C
• Refractive Index: 1.454
• CAS DataBase Reference: 2-Propenoic acid, 2-(dibutylaMino)ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 2-(dibutylaMino)ethyl ester(7709-10-6)
• EPA Substance Registry System: 2-Propenoic acid, 2-(dibutylaMino)ethyl ester(7709-10-6)

Safety Data

• Hazardous Substances Data: 7709-10-6(Hazardous Substances Data)

Usage

General Description

2-Propenoic acid, 2-(dibutylaMino)ethyl ester, also known as dibutylaminoethyl methacrylate, is a chemical compound used in the production of polymers and coatings. It is commonly utilized in the manufacturing of adhesives, sealants, and various other industrial products. 2-Propenoic acid, 2-(dibutylaMino)ethyl ester is known for its ability to improve the adhesion and flexibility of coatings, as well as its resistance to water and chemicals. It is also used as a crosslinking agent in the production of thermosetting resins. However, it is important to handle this chemical with care, as it can be irritating to the skin, eyes, and respiratory system if proper safety precautions are not taken.

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

Upstream product

• 102-81-8 N,N-dibutyl amino-2 ethanol 
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Relevant articles and documents

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

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.