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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111853Generated: November 3, 2026

Isophorone diisocyanate → Isophorone diamine

https://huagongshe.com/reaction/1111853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsophorone diisocyanateHCID 169132—
SolventTolueneHCID 1140—
ProductIsophorone diamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04119613
Source datasetuspto-grants-1978_10
ORD IDord-4364fff87dd44392bfb2d5dcb5bd8821
Source noteuspto-grants-1978_10