HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713952Generated: October 31, 2026
N-Isopropylacrylamide → HCID 131728324, compound
https://huagongshe.com/reaction/1713952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Isopropylacrylamide | HCID 16637 | — |
| Reactant | Tridecyl methacrylate | HCID 17234 | — |
| Reactant | 2,2'-Azobis(2-methylbutyronitrile) | HCID 93079 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131728324 | HCID 131728324 | — |
Reaction Steps
A 25 ml reaction vessel was charged with 12 g ethyl acetate, 2.85 g (0.007 mol) TRIS, 0.95 g (0.008 mol) NIPAM, 0.21 g (0.0008 mol) tridecyl methacrylate, and 0.078 g. 2,2′-azobis(2-methylbutanenitrile). After nitrogen flushing for 3 minutes, the vessel was closed and placed in an oil bath. The polymerization was run for 17.5 hours at 76° C. The polymer was precipitated into deionized water, dried at room temperature (20° C.), dissolved in acetone and precipitated into deionized water. The purified polymer was heated at 50° C. to remove bound water. Upon mixing the polymer with HMDS and casting a film, the film had an elongation of 10%. Upon addition of 2 wt % sucrose acetate isobutyrate to the polymer (10 wt %) in HMDS, the cast films had an elongation of greater than 250% without an increase in tack.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07795326B2 |
|---|
| Source dataset | uspto-grants-2010_09 |
|---|
| ORD ID | ord-2b24e2f3aca645b899b6ce81cfd9b0fa |
|---|
| Source note | uspto-grants-2010_09 |
|---|