BioSciences - Polysciences, Inc.

132
Monomers
Bis(2-methacryloxyethyl) phosphate [32435-46-4] U4d . . . . . . . . . . . . . . . . . . . . . . . . . . .
MW 322 .2 n 20
D 1 .469 TSCA
[H 2 C=C(CH 3 )CO 2 CH 2 CH 2 O] 2 P(O)OH
Crosslinking monomer . Adhesion promoter through free phosphoric acid group .
2,2-Bis(4-methacryloxyphenyl)propane [3253-39-2] H2g . . . . . . . . . . . . . . . . . . . . . . . . . .
MW 364 .4 mp 72-74º TSCA
[H 2 C=C(CH 3 )CO 2 C 6 H 4 ] 2 C(CH 3 ) 2
Rigid, hydrophobic, crosslinking monomer .
Bisphenol A [80-05-7] HO7g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
MW 228 .3 mp 158-159° bp 220°/4mm TSCA (CH ) C(C H OH) 3 2 6 4 2
Bisphenol A is a useful building block to form diacrylates or diglycidylethers
for polymerization into engineering plastics, biomedical materials
or used as host matrices for conductive materials . (i .e . carbon nanotubes) .
Used in epoxy resins and polyethers .
HO
OH
4,4’-Bisphenol A Bis-(N-Methylphthalimide) [54395-52-7] H4g . . . . . . . . . . . . . . . . . . . . .
MW 546 .4 Tg ~ 67°C
Useful in the production of heat resistant polyimides, thermoplastic
polyetherimides and special plasticizers .
4,4’-Bisphenol A Dianhydride [38103-06-9] H4g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
MW 520 .5 4,4’ isomer ~ 95% Solid
Used in the synthesis of high performance polyetherimides and for flame
retardant, electrically insulating coatings, non-linear optical applications, for
epoxy curing, heat curable, and thermosetting copolymers with silicones .
Bisphenol A hydrogenated [80-04-6] HV5g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Diol, could be used in preparation of all aliphatic epoxy resins, polyethers .
2-Bromoethyl acrylate, min. 95% [4823-47-6] H5d . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
MW 179 bp 52-53º/5mm n 20
D 1 .476 100 ppm MEHQ
BrCH 2 CH 2 OCOCH=CH 2
Reactive halogen, has potential use in curable and reactive polymers and in
synthesis of other monomers .
1,4-Butanediol diacrylate, min. 85% [1070-70-8] BH5d . . . . . . . . . . . . . . . . . . . . . . . . . . . .
MW 198 .2 bp 83º/0 .3mm n 20
D 1 .456 75 ppm MEHQ Tg 45º TSCA
(H 2 C=CHCO 2 CH 2 CH 2 -) 2
Crosslinking monomer .
1,4-Butanediol diglycidyl ether [2425-79-8] BO6g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
MW 202 .3 bp 260-266º n 20
D 1 .453 TSCA
For post-crosslinking reactions, preparation of aliphatic epoxy resins .
1,3-Butanediol dimethacrylate, 98% [1189-08-8] EHOV7d . . . . . . . . . . . . . . . . . . . . . . . . .
MW 226 .3 bp 73º/0 .1mm n 20
D 1 .452 100 ppm MEHQ TSCA
H 2 C=C(CH 3 )CO 2 CH 2 CH 2 CH(CH 3 )O 2 CC(CH 3 )=CH 2
Crosslinking monomer .
For more information please call (800) 523-2575 or visit: polysciences.com
O
O
R = H or CH 3 (~1:1)
O
O
Catalog Size
16041-10 10 g
01381-25 25 g
02548-100 100 g
24284-25 25 g
24283-25 25 g
03474-100 100 g
02015-10 10 g
02049-100 100 g
01795-50 50 g
02047-500 500 g