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rac 1,2-Dioleoyl-3-chloropropanediol is a synthetic lipid compound that consists of two oleoyl chains attached to a 3-chloropropanediol backbone. It is a chiral molecule, with both R and S enantiomers present in equal amounts, hence the term "racemic". rac 1,2-Dioleoyl-3-chloropropanediol has unique properties due to the presence of the chloro group, which can potentially form hydrogen bonds and interact with other molecules in various ways.

69161-73-5

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69161-73-5 Usage

Uses

Used in Food Industry:
rac 1,2-Dioleoyl-3-chloropropanediol is used as a novel lipid in food protein hydrolyzates for enhancing the functional properties of proteins. The incorporation of this lipid can improve the solubility, emulsifying capacity, and foaming properties of protein hydrolyzates, which are important for various food applications such as stabilizers, emulsifiers, and foaming agents.
Used in Dairy Industry:
rac 1,2-Dioleoyl-3-chloropropanediol is used as a component in the isolation of fatty acid esters of chloropropanediol from fresh goat milk. This application is relevant for the dairy industry, as it can contribute to the development of new products with improved nutritional profiles and health benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 69161-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,6 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69161-73:
(7*6)+(6*9)+(5*1)+(4*6)+(3*1)+(2*7)+(1*3)=145
145 % 10 = 5
So 69161-73-5 is a valid CAS Registry Number.

69161-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-chloro-2-[(Z)-octadec-9-enoyl]oxypropyl] (E)-octadec-9-enoate

1.2 Other means of identification

Product number -
Other names 1,2-Dioleoyl-3-chlor-1,2-propandiol

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:69161-73-5 SDS

69161-73-5Downstream Products

69161-73-5Relevant academic research and scientific papers

Direct determination of MCPD fatty acid esters and glycidyl fatty acid esters in vegetable oils by LC-TOFMS

Haines, Troy D.,Adlaf, Kevin J.,Pierceall, Robert M.,Lee, Inmok,Venkitasubramanian, Padmesh,Collison, Mark W.

experimental part, p. 1 - 14 (2011/10/04)

Analysis of MCPD esters and glycidyl esters in vegetable oils using the indirect method proposed by the DGF gave inconsistent results when salting out conditions were varied. Subsequent investigation showed that the method was destroying and reforming MCPD during the analysis. An LC time of flight MS method was developed for direct analysis of both MCPD esters and glycidyl esters in vegetable oils. The results of the LC-TOFMS method were compared with the DGF method. The DGF method consistently gave results that were greater than the LC-TOFMS method. The levels of MCPD esters and glycidyl esters found in a variety of vegetable oils are reported. MCPD monoesters were not found in any oil samples. MCPD diesters were found only in samples containing palm oil, and were not present in all palm oil samples. Glycidyl esters were found in a wide variety of oils. Some processing conditions that influence the concentration of MCPD esters and glycidyl esters are discussed.

O-Silylated C3-halohydrins as a novel class of protected building blocks for total, regio- and stereocontrolled synthesis of glycerolipid frameworks

Stamatov, Stephan D.,Stawinski, Jacek

supporting information; scheme or table, p. 463 - 477 (2010/02/16)

We propose O-silylated C3-halohydrins [1(3)-O-silyl-2-O-acyl-, 1,2(2,3)-O-bis(silyl)-, and 1(3)-O-acyl-2-O-silyl-3(1)-halo-sn-glycerides] as new chirons in the total synthesis of glycerolipid constructs. These are efficiently producible via opening of the

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