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化驗
95%
形狀
liquid
包含
MEHQ as inhibitor
SMILES 字串
CC(=C)C(=O)OCCN1CCOCC1
InChI
1S/C10H17NO3/c1-9(2)10(12)14-8-5-11-3-6-13-7-4-11/h1,3-8H2,2H3
InChI 密鑰
MNZNJOQNLFEAKG-UHFFFAOYSA-N
一般說明
2-N-Morpholinoethyl methacrylate (MEMA) is a methacrylate monomer featuring a morpholino group that enhances its reactivity and solubility in various solvents. Its hydrophilicity, attributed to the tertiary amine in the morpholino structure, makes MEMA suitable for numerous applications in polymer chemistry. It can undergo various polymerization techniques, including radical and anionic polymerization. MEMA is particularly valuable in biomedical applications, including drug delivery systems, medical adhesives, dental composites, tissue engineering, and controlled drug release. It is utilized in the development of biocompatible materials, polymer matrices, hydrogels, and scaffolds. Beyond biomedical uses, MEMA finds applications in coatings, electronics, optical materials, and the textile industry.
應用
2-N-Morpholinoethyl methacrylate can be used as:
- A monomer for synthesizing pH-responsive amphiphilic polymers. These polymers are particularly useful in controlled release drug delivery systems due to their ability to respond to changes in pH, which is a critical factor in various physiological environments.
- A crosslinking agent during the synthesis of the hydrogel nanocomposites. This crosslinking is vital for improving the mechanical stability and structural integrity of the hydrogels.
- A monomer for the synthesis of thermoresponsive polymers, which are used for the applications in smart coatings and responsive drug delivery systems.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
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Nanoprecipitation is a straightforward yet powerful technique to synthesize polymer nanoparticles loaded with various biologically active compounds or contrast agents. Particle formation in this approach is kinetically controlled, and various assembly parameters have been used to control the size distribution
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Journal of dentistry, 43(9), 1132-1139 (2015-07-07)
The objective of this work was to investigate the polymerization behavior, neutralization capability, and mechanical properties of dentin adhesive formulations with the addition of the tertiary amine co-monomer, 2-N-morpholinoethyl methacrylate (MEMA). A co-monomer mixture based on HEMA/BisGMA (45/55, w/w) was
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