CAS 36837-97-5 Dithiodi-2,1-ethanediyl bismethacrylate

NAVIGATION

Dithiodi-2,1-ethanediyl bismethacrylate

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Catalog Number

ACM36837975-2

CAS Number

36837-97-5

Product Name

Dithiodi-2,1-ethanediyl bismethacrylate

Structure

Category

Self-Assembly Materials

Synonyms

dithiodi-2,1-ethanediyl bismethacrylate;Bis(methacrylic acid)dithiobis(ethylene) ester;Bis[2-(methacryloyloxy)ethyl] persulfide;Bismethacrylic acid dithiobis(ethylene) ester;Bismethacrylic acid dithiobisethylene ester;Bismethacrylic acid dithiodiethylene

IUPAC Name

2-[2-(2-methylprop-2-enoyloxy)ethyldisulfanyl]ethyl2-methylprop-2-enoate

Molecular Weight

458.54564

Molecular Formula

C₂₀H₂₆O₈S₂-2

Canonical SMILES

CC(=C)C(=O)OCCSSCCOC(=O)C(=C)C

InChI Key

CGDNFXSLPGLMHK-UHFFFAOYSA-N

Boiling Point

394.5ºC at 760mmHg

Flash Point

185.7ºC

Purity

96%

Density

1.155g/cm³

Appearance

Colorless to yellow liquid

Application

Dithiodi-2,1-ethanediyl bismethacrylate serves an important role as a versatile crosslinker in the creation of specialized polymers with unique properties, such as REDOX sensitivity and self-healing capabilities. Its disulfide bonds can be cleaved in specific environments, making it ideal for drug delivery systems by enabling controlled release and modulation of drug properties. It can also engage in mercaptan-disulfide exchange reactions to form covalent cross-links within polymers, leading to the development of structural networks and gels. This property is particularly beneficial in creating reduction-responsive molecularly imprinted polymer (MIP) nanogels for targeted drug delivery and enhancing self-healing properties in polymer nanocomposites used in industries like coatings and electronics. Additionally, it is instrumental in synthesizing redox-responsive zwitterionic hydrogels, which exhibit enhanced stability and responsiveness in biological settings, making them suitable for biomedical applications such as tissue-engineered scaffolds.

EC Number

253-234-2

Exact Mass

290.06500

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