HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111853Generated: November 3, 2026
Isophorone diisocyanate → Isophorone diamine
https://huagongshe.com/reaction/1111853
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isophorone diisocyanate | HCID 169132 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Isophorone diamine | HCID 17857 | — |
Reaction Steps
In the same apparatus as described in Example 1, a preadduct is produced from 67.03 parts, by weight, of a polyester of adipic acid and 1,4-butane diol (hydroxyl number 52.2; acid number 0.6), 3.06 parts, by weight, of a polydimethyl siloxane containing terminal methylol groups and having a hydroxyl number of 198.0 and 24.06 parts, by weight, of 1-isocyanato-3-isocyanatomethyl-3,5,5-trimethylcyclohexane by heating the mixture for 2.5 hours at 100° C. After dilution with 141.5 parts, by weight, of toluene, the solution is maintained at a temperature of 80° C. The mixture is then reacted to form the polyurethane in the same way as in Example 1, 1.49 kg/h of 1-amino-3-aminomethyl-3,5,5-trimethyl cyclohexane being additionally introduced as further reaction component into the reaction mixture in a pinned-disc mixer following the preheater and the reactor being heated using steam under a pressure of 25 bars. A 25% solution in toluene-isopropanol (1:1) prepared immediately after production of the reaction product has a viscosity of 6390 cP/20° C. After storage for 1 week at room temperature, the final viscosity amounts to 7250 cP/20° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04119613 |
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| Source dataset | uspto-grants-1978_10 |
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| ORD ID | ord-4364fff87dd44392bfb2d5dcb5bd8821 |
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| Source note | uspto-grants-1978_10 |
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