Bismaleimide Monomers (901)

Bismaleimide monomers are bifunctional compounds featuring two maleimide rings (C=CC(O)-NH-) and are renowned for their exceptional thermal stability and mechanical strength. Their primary application lies in manufacturing high-performance thermosetting resins used in aerospace and automotive industries. These monomers' capacity to form crosslinked networks makes them well-suited for composites demanding superior heat resistance and durability. Additional uses include adhesives, coatings, and electronics, where maintaining thermal stability is essential.

naphthalene-2,6-dicarboxylic acid structure diagram

Total: 550

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Bismaleimide Monomers (901)

naphthalene-2,6-dicarboxylic acid

tetrahydro-[3,3'-bifuran]-2,2',5,5'-tetraone

1,4-dioxan-2-one

9H-fluorene-2,7-diamine

9,10-dioxo-9,10-dihydroanthracene-2,3-dicarboxylic acid

(1s,4s)-cyclohexane-1,4-diol

(perfluoro-1,4-phenylene)dimethanol

((1r,4r)-cyclohexane-1,4-diyl)dimethanol

(1r,4r)-cyclohexane-1,4-diol

bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid

furan-2-ylmethyl methacrylate

1,3,5-trimethyl-2-vinylbenzene

diethyl vinylphosphonate

decyl acrylate

3-vinylbenzaldehyde

2-methyl-1,4-phenylene bis(4-(3-(acryloyloxy)propoxy)benzoate)

2-cyanoethyl acrylate

2-([1,1'-biphenyl]-2-yloxy)ethyl acrylate

4,4,5,5-tetramethyl-2-(4-vinylphenyl)-1,3,2-dioxaborolane

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

adamantane-1,3-dicarboxylic acid

N-methyloxetan-3-amine

acenaphthylene

(1R,2R)-cyclohexane-1,2-diol

cyclohexane-1,2-diol

adamantane-1,3,5-triol

HS-PEG-SH average Mw1000

1,4-phenylenedimethanol

oxetan-2-ylmethanol

oxetan-3-ylmethanol