Method for producing polyurethane rigid foams and polyisocyanurate rigid foams
US-2016347904-A1 · Dec 1, 2016 · US
US2017137366A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017137366-A1 |
| Application number | US-201615346855-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 9, 2016 |
| Priority date | Nov 16, 2015 |
| Publication date | May 18, 2017 |
| Grant date | — |
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 invention provides polyglycerol partial esters based on mono- and dicarboxylic acids and their use as solubilizers, particularly in cosmetics, for example for perfume oils and essential oils in aqueous systems.
Opening claim text (preview).
1 . A polyglycerol partial ester obtainable by esterification of a polyglycerol with a carboxylic acid mixture comprising: a) at least one short-chain dicarboxylic acid having 2 to 12 carbon atoms, and b) at least one saturated fatty acid having 6 to 14 carbon atoms, wherein the molar ratio of polyglycerol to dicarboxylic acid to saturated fatty acid is in a ratio of from 3.1:1.0:0.5 to 14:1.0:6.0. 2 . The polyglycerol partial ester according to claim 1 , wherein the polyglycerol has an average degree of condensation N of 1.5 to 9. 3 . The polyglycerol partial ester according to claim 1 , wherein the polyglycerol used has a hydroxyl number of 1500 to 900 mg KOH/g. 4 . The polyglycerol partial ester according to claim 1 , wherein the short-chain dicarboxylic acid is selected from aliphatic, linear dicarboxylic acids, in particular oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, and dodecanedioic acid. 5 . The polyglycerol partial ester according to claim 1 , wherein the saturated fatty acid is selected from unbranched, unsubstituted fatty acids. 6 . The polyglycerol partial ester according to claim 1 , wherein the esterification the molar ratio of a) to b) is from 1.0:0.7 to 1.0:3.0. 7 . The polyglycerol partial ester according to claim 1 , wherein at 1 bar it has a turbidity point of 45 to 75° C. 8 . The polyglycerol partial ester according to claim 1 , wherein it has an HLB value of 13 to 17. 9 . The polyglycerol partial ester according to claim 1 , wherein it has a surface tension of less than 28 mN/m in 1.0% aqueous solution at 20° C. 10 . The polyglycerol partial ester according to claim 1 , wherein it has a saponification number of 70 to 199 mg KOH/g. 11 . The use of at least one polyglycerol partial ester according to claim 1 as solubilizer, particularly in cosmetic or pharmaceutical preparations.
derived from polycarboxylic acids and polyhydroxy compounds · CPC title
Washing or bathing preparations · CPC title
the alcohol moiety containing more than one hydroxy group · CPC title
Preparations for cleaning the hair · CPC title
Anti-perspirants or body deodorants (deodorisation of air A61L9/00) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.