HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089095Generated: November 1, 2026
Azobisisobutyronitrile → HCID 168686, compound
https://huagongshe.com/reaction/1089095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | 1-Dodecanethiol | HCID 8195 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Butyl Acrylate | HCID 8846 | — |
| Product | HCID 168686 | HCID 168686 | — |
Reaction Steps
A starting solution of 45 g of ethylacrylate, 45 g of butylacrylate, 5 g of acrylic acid, 0.5 g of azo-bis-isobutyronitrile and 0.35 g of lauryl mercaptan was added in 5 portions to a stirred reaction kettle at a kettle temperature of 70° C. Each portion was only added after an exotherm had indicated that the previous portion had reacted. The reaction was continued over a period of three hours at a temperature between 80° and 105° C. with a solution of 442 g of ethylacrylate, 442 g of butylacrylate, 44 g of acrylic acid, 50 g of azo-bis-isobutyronitrile and 6.1 g of lauryl mercaptan. Because of the high viscosity of the product, stirring in the reaction vessel becomes difficult. The polymer material was removed from the reactor and heated without stirring for 2 hours at 120° C. The polymer material was rubbery with comonomer proportions of 47.6:47.6:4.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04965117 |
|---|
| Source dataset | uspto-grants-1990_10 |
|---|
| ORD ID | ord-cac5e3aa023645ae9816620b8c5f80bf |
|---|
| Source note | uspto-grants-1990_10 |
|---|