HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197021Generated: October 30, 2026
Acrylamide → N-Octylacrylamide Acrylamide DMA
https://huagongshe.com/reaction/1197021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | 2-Propenamide, N-octyl- | HCID 82370 | — |
| Reactant | Sodium Lauryl Sulfate | HCID 3423265 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | N-Octylacrylamide Acrylamide DMA | HCID 131716741 | — |
Reaction Steps
A solution was prepared of 15 g of sodium dodecylsulfate in 500 mL of deoxygenated water. N-1-octyl-acrylamide, 0.496 g, was dissolved in this solution followed by 15.2 g of acrylamide and 14.31 g of DMA. The resulting solution was carefully transferred to a 1 L Morton style resin kettle fitted with a chilled water condenser, thermometer, inert gas sparger and mechanical stirrer. The temperature was adjusted to 20° C. and polymerization was initiated by the addition of 0.0165 g of potassium persulfate, K2S2O8, and 0.0116 g of sodium bisulfite, Na2S2O5. After stirring for 22 hr at 20±0.2C., a 333 mL portion of the viscous solution was poured slowly into 3 L of acetone. The precipitated polymer was then masticated in a Waring blender with acetone, filtered and dried under vacuum at 30° C. The yield of polymer was 8.43 g. A similar procedure was used to prepare the polymers illustrated in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05116923 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-4ad811248011491da781443e63fdb4cd |
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| Source note | uspto-grants-1992_05 |
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