6206-58-2Relevant academic research and scientific papers
DENTAL ADHESIVE
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Paragraph 0246-0249, (2019/01/04)
Provided herein is a self-etching dental adhesive that exhibits excellent adhesiveness not only to dentin untreated by phosphoric acid etching, but to dentin treated by phosphoric acid etching. The present invention relates to a dental adhesive containing a (meth)acrylamide compound (a), an asymmetric acrylamide-methacrylic acid ester compound (b), and an acid group-containing (meth)acrylic polymerizable monomer (c). The (meth)acrylamide compound (a) is at least one selected from the group consisting of compounds represented by general formula (1), and compounds represented by general formula (2). The asymmetric acrylamide-methacrylic acid ester compound (b) is a compound represented by general formula (3). (In the formulae, the meanings of the symbols are omitted.)
DENTAL ADHESIVE
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Paragraph 0194; 0195; 0196, (2017/08/01)
The present invention provides a dental adhesive exhibiting excellent initial bond strength and bond durability to both enamel and dentin. The present invention relates to a dental adhesive containing: an asymmetric acrylamide-methacrylic acid ester compound (a); an acid group-containing (meth)acrylic polymerizable monomer (b); and a water-soluble polymerizable monomer (c). The asymmetric acrylamide-methacrylic acid ester compound (a) is represented by the following general formula (1): where X is an optionally substituted, linear or branched C1 to C6 aliphatic group or an optionally substituted aromatic group, the aliphatic group is optionally interrupted by at least one linking group selected from the group consisting of —O—, —S—, —CO—, —CO—O—, —O—CO—, —NR1—, —CO—NR1—, —NR1—CO—, —CO—O—NR1—, —O—CO—NR1—, and —NR1—CO—NR1—, and R1 is a hydrogen atom or an optionally substituted, linear or branched C1 to C6 aliphatic group.
The synthesis of novel hybrid monomers
Chan, Grace Y.N.,Looney, Mark G.,Solomon, David H.,Veluayitham, Sheela
, p. 31 - 35 (2007/10/03)
Novel hybrid amide-ester crosslinking monomers were prepared by using methodology which utilizes the differential functionalities present within a convenient amino alcohol. Modification of the procedure to a simple one-pot reaction enables the generation of these unique monomers to be scaled to commercial levels.
