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Dithiodi-2,1-ethanediyl bismethacrylate

Catalog NumberACM36837975-2

CAS Number36837-97-5

CategorySelf-Assembly Materials

Dithiodi-2,1-ethanediyl bismethacrylate
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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