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BioSciences - Polysciences, Inc.

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136<br />

Monomers<br />

- D -<br />

1,10-Decanediol dimethacrylate [6701-13-9] EHOU6d . . . . . . . . . . . . . . . . . . . . . . . . . . . . .<br />

MW 310 .4 bp 170°/2mm n 20<br />

D 1 .458 270 ppm HQ TSCA<br />

[H 2 C=C(CH 3 )CO 2 (CH 2 ) 5 ] 2<br />

Hydrophobic, long-chain crosslinking monomer .<br />

iso-Decyl acrylate [1330-61-6] H4d . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .<br />

MW 212 .3 bp 121°/10mm n 20<br />

D 1 .440 50 ppm MEHQ Tg -55° TSCA<br />

H 2 C=CHCO 2 C 10 H 21<br />

Hydrophobic ester monomer . Forms hydrocarbon-soluble polymers .<br />

n-Decyl methacrylate, 99% [3179-47-3] U5d . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .<br />

MW 226 .4 bp 155-156°/22mm n 20<br />

D 1 .443 100 ppm MEHQ Tg -30° TSCA<br />

H 3 C(CH 2 ) 9 OCOC(CH 3 )=CH 2<br />

High-purity hydrophobic ester monomer, forms oil-soluble polymers .<br />

iso-Decyl methacrylate, min. 90% [29964-84-9] H5g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .<br />

MW 226 .3 bp 78°/1mm n 20<br />

D 1 .441 100ppm MEHQ inhibitor<br />

10 ppm HQ/MEHQ inhibitor TSCA<br />

Hydrophobic ester monomer, forms oil-soluble polymers .<br />

1,4-Diacryloylpiperazine [6342-17-2] H5d . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .<br />

MW 194 .2 mp 90-92°<br />

Acrylamide-based crosslinking monomer .<br />

Diallyl Maleate [999-21-3] HV4d . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .<br />

MW 196 .2 mp -47°C (lit .) bp 160 - 116°C/4mm Hg (lit .) n 20<br />

D 1 .469 d 1 .073g/<br />

ml (lit .) 230°C TSCA CH 2 =CHCH 2 OCOCH=CHCOOCH 2 CH=CH 2<br />

Reactive functional monomer . Polymers formed with the incorporation of Diallyl<br />

Maleate have pendant allyl groups . Applications for Diallyl Maleate include polyester<br />

resins, adhesives, and ion exchange resins . When used at low levels, Diallyl<br />

Maleate is an effective agent for the promotion of branching in emulsion polymers .<br />

Diallyl Maleate - 99% Active [999-21-3] H4d . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .<br />

MW 196 Clear Liquid<br />

CH 2 =CHCH 2 OCOCH=CHCOOCH 2 CH=CH 2<br />

Moisture (%): 0 .05 Diallyl ester of maleic acid . Once polymerized through the vinyl center adjacent<br />

to the ester groups, it provides multiple postfunctionalization target sites at the pendant allylic<br />

centers . This makes it particularly useful both in acrylic chemistry but also in combination with<br />

alkyd and polyester resins . When employed at very low levels it is an effective site for branching<br />

generation in emulsion polymers .<br />

Diallyl phthalate, practical [131-71-9] I7g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .<br />

MW 246 .3 bp 161-163°/5mm n 20<br />

D 1 .5190<br />

Crosslinking monomer producing considerable cyclic structures .<br />

N,N-Diallylacrylamide [3085-68-5] U7d . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .<br />

MW 151 .2 bp 108-110°/3mm n 20<br />

D 1 .489 100 ppm HQ<br />

(H 2 C=CHCH 2 ) 2 _NCOCH=CH 2<br />

Crosslinking monomer .<br />

For more information please call (800) 523-2575 or visit: polysciences.com<br />

Catalog Size<br />

02140-25 25 g<br />

03008-100 100 g<br />

23344-25 25 g<br />

22493-100 100 g<br />

21190-10 10 g<br />

02156-250 250 g<br />

24892-100 100 g<br />

02159-1 1 kg<br />

01848-10 10 g

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