Compounds having a stabilizing effect, method for producing said compounds, composition containing said stabilizing compounds, method for stabilizing an organic component, and use of stabilizing compounds
US-2020361879-A1 · Nov 19, 2020 · US
US9873676B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9873676-B2 |
| Application number | US-201515123200-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 3, 2015 |
| Priority date | Mar 4, 2014 |
| Publication date | Jan 23, 2018 |
| Grant date | Jan 23, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The isocyanate composition consists essentially of an isocyanurate derivative of 1,3-xylylenediisocyanate, the isocyanurate derivative is modified with aliphatic alcohol, and the modification amount of the aliphatic alcohol is 0.5 mass % or more and 15 mass % or less.
Opening claim text (preview).
The invention claimed is: 1. An isocyanurate composition consisting essentially of an isocyanurate derivative of 1,3-xylylenediisocyanate, wherein the isocyanurate derivative includes a trimer of 1,3-xylylenediisocyanate, the isocyanurate derivative is modified with aliphatic alcohol, and the modification amount of the aliphatic alcohol is 0.5 mass % or more and 15 mass % or less. 2. The isocyanurate composition according to claim 1 , wherein the modification amount of the aliphatic alcohol is 3.0 mass % or more and 7.0 mass % or less. 3. The isocyanurate composition according to claim 1 , wherein the aliphatic alcohol has carbon atoms of 4 or more and 20 or less. 4. The isocyanurate composition according to claim 1 , wherein the aliphatic alcohol is dihydric aliphatic alcohol. 5. An isocyanurate composition consisting essentially of an isocyanurate and an aliphatic alcohol-modified isocyanurate, wherein the isocyanurate is at least one selected from a group consisting of a mononuclear isocyanurate which is a trimer of 1,3-xylylenediisocyanate and a polynuclear isocyanurate of two or more of the mononuclear isocyanurates, and the modification amount of the aliphatic alcohol is 0.5 mass % or more and 15 mass % or less relative to a total amount of the isocyanurate composition.
Compounds forming isocyanates or isothiocyanates in situ (C08G18/80 takes precedence) · CPC title
containing at least two isocyanate or isothiocyanate groups linked to the aromatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate groups, e.g. xylylene diisocyanate or homologues substituted on the aromatic ring · CPC title
the polymeric products containing isocyanurate groups · CPC title
on metal layer · CPC title
characterised by using adhesives · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.