Dithiol Monomers (208)

Dithiol monomers, featuring sulfur atoms in their structure, impart distinctive properties to the resulting polymers, including enhanced thermal stability and resistance to oxidation. These monomers are often utilized in the synthesis of polymers for electronics, where sulfur-containing materials demonstrate superior conductivity. Additionally, macromonomers can be integrated into copolymers to enhance the material's overall performance, such as greater durability and improved chemical resistance.

(perfluoro-1,4-phenylene)dimethanol structure diagram

Total: 121

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Dithiol Monomers (208)

(perfluoro-1,4-phenylene)dimethanol

2-cyanoethyl acrylate

3-(1,1,1,5,5,5-hexamethyl-3-((trimethylsilyl)oxy)trisiloxan-3-yl)propyl methacrylate

potassium acrylate

4,4'-(diphenylmethylene)diphenol

N-butylacrylamide

3-((3-acrylamidopropyl)dimethylammonio)propane-1-sulfonate

(dimethoxy(methyl)silyl)methyl methacrylate

2,4,6-trimethyl-2,4,6-trivinyl-1,3,5,2,4,6-trioxatrisilinane

N-phenylmethacrylamide

4-benzoylphenyl methacrylate

3-((2-(methacryloyloxy)ethyl)dimethylammonio)propanoate

4-vinyl-1,1'-biphenyl

N-(3-aminopropyl)methacrylamide hydrochloride

N-(2-hydroxypropyl)methacrylamide

bis(4-aminophenyl)methanone

2-(tert-butylamino)ethyl methacrylate

N-(2-Amino-2-oxoethyl)acrylamide

4,4'-([1,1'-biphenyl]-4,4'-diylbis(oxy))dianiline

4,4'-(1,3-phenylenebis(oxy))dianiline

2,2,6,6-tetramethyl-1-(l1-oxidaneyl)piperidin-4-yl methacrylate

5-propyldihydrofuran-2(3H)-one

1,4-phenylenedimethanamine

bis(3-aminophenyl)methanone

3-(4-aminophenoxy)aniline

naphthalene-1,6-diol

3,3'-(1,3-phenylenebis(oxy))dianiline

benzyl acrylate

dodecane-1,12-diyl bis(2-methylacrylate)

decane-1,10-diyl diacrylate