Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Fatty acyl amino acid polyhydroxy ester compound and preparation method thereof

A fatty acylamino acid, polyhydroxy compound technology, applied in the field of organic compound synthesis, can solve the problems that have not yet been seen, and achieve the effects of excellent low irritation, unique skin feel, and good affinity

Pending Publication Date: 2020-05-19
YUEYANG SECCO ROEDER CHEM IND CO LTD JOINTLY
View PDF10 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Making full use of the advantages of amide groups and amino acid structures, as well as the strong hydrophilicity and refreshing type of polyhydroxyl structures, will better meet people's high demand for cosmetic raw materials. Cosmetic emulsifiers and thickeners with polyhydroxy structure

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Fatty acyl amino acid polyhydroxy ester compound and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0034] A preparation method of the above-mentioned fatty acylamino acid polyhydroxy ester compound, comprising the following steps:

[0035] (1) Take the fatty acylamino acid and polyhydroxy compound in the formula amount, add the catalyst, put it in a vacuum environment, heat it to 120-140°C while stirring, and keep it warm for 2-6h;

[0036] (2) Warm up the mixture obtained in step (1) to 160-200° C., keep it warm for 15-60 minutes, and cool to room temperature;

[0037] (3) Add activated carbon to the substance obtained in step (2), and filter to obtain the fatty acylamino acid polyhydroxy ester compound.

[0038]The addition amount of the catalyst in the reaction system is 0.1-5% of the total mass of the fatty acyl amino acid and the polyhydroxy compound.

[0039] As a further preferred solution, the vacuum degree of the vacuum environment in step (1) is -0.095MPa; the temperature in step (1) is 145°C, and the holding time is 3h; the temperature in step (2) is 160°C, and ...

Embodiment 1

[0041] A fatty acylamino acid polyhydroxy ester compound prepared by the following method:

[0042] (1) Take 30g of lauroyl sarcosine and 20g of xylitol, add 0.05g of catalyst p-toluenesulfonic acid, place in a vacuum of -0.095MPa, heat to 145°C while stirring, and keep warm for 3h;

[0043] (2) The mixture obtained in step (1) is heated up to 160° C., and after being incubated for 15 minutes, the heating is stopped and cooled to room temperature;

[0044] (3) Add activated carbon to the substance obtained in step (2) for decolorization, and obtain the fatty acylamino acid polyhydroxy ester compound of this embodiment after filtration.

Embodiment 2

[0046] A fatty acylamino acid polyhydroxy ester compound prepared by the following method:

[0047] (1) Take 25g of palmitoyl sarcosine and 20g of propylene glycol, add 0.05g of catalytic phosphoric acid, place in a vacuum of -0.095MPa, heat to 145°C while stirring, and keep warm for 3h;

[0048] (2) The mixture obtained in step (1) is heated up to 160° C., and after being incubated for 30 minutes, the heating is stopped and cooled to room temperature;

[0049] (3) Add activated carbon to the substance obtained in step (2) for decolorization, and obtain the fatty acylamino acid polyhydroxy ester compound of this embodiment after filtration.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a fatty acyl amino acid polyhydroxy ester compound. The fatty acyl amino acid polyhydroxy compound is prepared from 25-50 parts by weight of fatty acyl amino acid and 20-30 parts by weight of a polyhydroxy compound under the action of a catalyst. The structure of the fatty acyl amino acid polyhydroxy ester compound contains an amino acid structure, an amide group brought byamino acid, and a plurality of hydroxyl structures brought by polyol or natural sugar alcohol or saccharides, so the compound provided by the invention has the advantages of lower irritation, lower toxicity, good biodegradability, good affinity to human bodies and the like, has a strong moisturizing function, can provide unique skin feeling, and can also relieve the irritation of other additivesto the skin. The invention also discloses a preparation method of the fatty acyl amino acid polyhydroxy ester compound. According to the preparation method, the raw materials are natural and non-irritant, operation is simple and easy, and the reaction process of dehydration condensation is easy to control.

Description

technical field [0001] The invention relates to the technical field of organic compound synthesis, in particular to a fatty acylamino acid polyhydroxy ester compound and a preparation method thereof. Background technique [0002] With the advancement of science and technology and the improvement of people's living standards, people have higher and higher requirements for the functionality, experience, mildness, and safety of cosmetic raw materials. Emulsifiers and hydrophilic ester excipients in the cosmetics field , The variety, quality and quantity of thickeners have developed by leaps and bounds. Although there are many types of cosmetic emulsifiers, hydrophilic ester excipients, and thickeners, the common ones are based on fatty acid esters or fatty alcohol chains as lipophilic groups, which have a strong sticky feeling. When blended in a large amount in cosmetics, the usability and texture of the cosmetics deteriorate. In addition, in the current new cosmetics, there ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C07C233/47C07C231/12C07H13/04C07H1/00A61K8/44A61Q19/00
CPCC07C233/47C07C231/12C07H13/04C07H1/00A61K8/44A61Q19/00A61Q19/005A61Q19/007
Inventor 孔悠华陈浩
Owner YUEYANG SECCO ROEDER CHEM IND CO LTD JOINTLY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com