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106292-55-1

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106292-55-1 Usage

Description

1-OLEOYL-2-LINOLEOYL-RAC-GLYCEROL (CONTAINS 2% 1,3-ISOMER) is a diacylglycerol derived from palm oil, characterized by its clear, colorless oil appearance. It is a type of glycerol with two fatty acid chains, oleoyl and linoleoyl, attached to the glycerol backbone, and contains a small percentage of the 1,3-isomer.

Uses

Used in Pharmaceutical Industry:
1-OLEOYL-2-LINOLEOYL-RAC-GLYCEROL (CONTAINS 2% 1,3-ISOMER) is used as an active ingredient for the development of pharmaceutical products, particularly in the area of lipid metabolism and energy regulation. Its unique structure allows it to play a role in modulating cellular processes and signaling pathways.
Used in Cosmetics Industry:
In the cosmetics industry, 1-OLEOYL-2-LINOLEOYL-RAC-GLYCEROL (CONTAINS 2% 1,3-ISOMER) is used as an emollient, skin conditioning agent, and moisturizer. Its ability to penetrate the skin and deliver beneficial fatty acids makes it a valuable component in various skincare formulations, promoting skin health and hydration.
Used in Food Industry:
1-OLEOYL-2-LINOLEOYL-RAC-GLYCEROL (CONTAINS 2% 1,3-ISOMER) is used as an additive in the food industry, where it serves as an emulsifier, stabilizer, and texture enhancer. Its properties help improve the overall quality, taste, and shelf life of various food products.
Used in Research Applications:
In the field of scientific research, 1-OLEOYL-2-LINOLEOYL-RAC-GLYCEROL (CONTAINS 2% 1,3-ISOMER) is utilized as a research tool to study the effects of diacylglycerols on cellular signaling and lipid metabolism. Its unique structure allows researchers to investigate the role of specific fatty acid chains in various biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 106292-55-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,2,9 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106292-55:
(8*1)+(7*0)+(6*6)+(5*2)+(4*9)+(3*2)+(2*5)+(1*5)=111
111 % 10 = 1
So 106292-55-1 is a valid CAS Registry Number.
InChI:InChI=1/C39H70O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(41)43-36-37(35-40)44-39(42)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h12,14,17-20,37,40H,3-11,13,15-16,21-36H2,1-2H3/b14-12-,19-17-,20-18-

106292-55-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name rac 1-Oleoyl-2-linoleoylglycerol

1.2 Other means of identification

Product number -
Other names 1-OLEOYL-2-LINOLEOYL-RAC-GLYCEROL (CONTAINS 2% 1,3-ISOMER)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:106292-55-1 SDS

106292-55-1Downstream Products

106292-55-1Relevant articles and documents

Chemical synthesis method for 1,2-fatty diglyceride with customizable structure

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Paragraph 0019, (2018/03/01)

The invention discloses a chemical synthesis method for 1,2-fatty diglyceride with a customizable structure. The method is characterized by comprising the following steps: (a) weighing a certain amount of 3-glycerol-chlorohydrin and sodium acetate and adding into a reactor with a reflux condensation apparatus so as to obtain gylcerol monoacetate; (b) selecting fatty acid methyl ester types of biodiesel according to customization needs in presence of a base catalyst, and heating and refluxing the gylcerol monoacetate with the biodiesel in an organic solvent so as to obtain triglyceride; and (c) dissolving the triglyceride obtained in the previous step in a proper amount of methanol, adding potassium carbonate to react at room temperature, extracting with an organic solvent, and recrystallizing, thereby obtaining the high-purity (more than 90%) 1,2-fatty diglyceride. The method disclosed by the invention is simple and convenient in synthetic route, simple in after-treatment and high in total yield (more than 75%), and the 1,2-fatty diglyceride can be effectively synthesized.

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