17598-94-6

Basic information

• Product Name: DILAURIN
• Synonyms: 1,2-DILAURIN;DILAURIN (C12:0);DILAURIN;DIDODECANOIN;1,3-dilaurate glycerol;1,2-didodecanoylglycerol;glyceryl 1,2-dilaurate;1,2,3-Propanetriol 1,2-didodecanoate
• CAS NO: 17598-94-6
• Molecular Formula: C₂₇H₅₂O₅
• Molecular Weight: 456.7
• Product Categories: A - HFluorescent Probes, Labels, Particles and Stains;Amino Acids;Amino acids and other organic acid conjugates;Fluorescent Conjugates;Modified Amino Acids
• Mol File: 17598-94-6.mol
• Article Data: 20

Chemical Properties

• Melting Point: 53-56 °C
• Boiling Point: 531°Cat760mmHg
• Flash Point: 158°C
• Appearance: /
• Density: 0.953g/cm³
• Storage Temp.: −20°C
• PKA: 13.69±0.10(Predicted)
• CAS DataBase Reference: DILAURIN(CAS DataBase Reference)
• NIST Chemistry Reference: DILAURIN(17598-94-6)
• EPA Substance Registry System: DILAURIN(17598-94-6)

Safety Data

• WGK Germany: 1
• Hazardous Substances Data: 17598-94-6(Hazardous Substances Data)

Usage

General Description

DILAURIN, also known as 1,3-Di(octanoyloxy)propan-2-yl decanoate, is a chemical compound consisting of a glycerol molecule linked to two lauric acid molecules. It is a type of medium-chain triglyceride (MCT) that has been studied for its potential health benefits, including its antimicrobial and antiviral properties. DILAURIN has been shown to have a protective effect against various bacterial and viral infections, and it is also believed to have potential therapeutic applications in the treatment of conditions such as acne, athlete's foot, and influenza. Additionally, it is used in some cosmetic and personal care products for its moisturizing and emulsifying properties.

InChI:InChI=1/C27H52O5/c1-3-5-7-9-11-13-15-17-19-21-26(29)31-24-25(23-28)32-27(30)22-20-18-16-14-12-10-8-6-4-2/h25,28H,3-24H2,1-2H3

Upstream product

• 40738-26-9 rac-1-monolauroylglycerol 
• 539-93-5 1,3-dilauroylglycerol 
• 143-07-7 lauric acid 
• 56-81-5 glycerol 
• 111-82-0 methyl n-dodecanoate 
• 538-24-9 tridodecanoylglycerol 
• 103397-09-7 1-O-benzyl-2,3-di-O-dodecanoyl-rac-glycerol 
• 67-56-1 methanol 
• 96-13-9 2,3-Dibromopropan-1-ol 

Downstream Products

• 40738-26-9 rac-1-monolauroylglycerol 
• 539-93-5 1,3-dilauroylglycerol 
• 1678-45-1 glycerol laurate 
• 56-81-5 glycerol 
• 18656-40-1 1,2-dilauroylphosphatidylcholine 
• 5683-55-6 1,2-dilauroyl-sn-glycero-3-phosphoethanolamine 
• 79806-85-2 dilauroylphosphatidic acid 
• 688021-81-0 2-O-benzyl-1,3-bis[(1,2-di-O-lauroyl-sn-glycero-3)-phosphoryl]glycerol di(2-cyanoethyl) ester 
• 106405-47-4 1.2-Di-O-lauroyl-glycerin-3- 

Relevant articles and documents

Biocatalytic esterification in supercritical carbon dioxide by using a lipid-coated lipase

A lipid-coated lipase is soluble and acts as a more efficient catalyst for triglyceride syntheses in supercritical carbon dioxide (scCO2) than in conventional organic solvents, and the reactivity can be controlled reversibly by changing pressure and temperature in scCO2.

4-O-Acetyl-3-O-tert-butyldimethylsilyl-l-rhamnal: a building block in the stereoselective synthesis of 2-deoxy-α-l-rhamnopyranosides

The stereoselective synthesis of 2-deoxy-α-l-glycosides by addition of various acceptors to 4-O-acetyl-3-O-tert-butyldimethylsilyl-l-rhamnal promoted by triphenylphosphine-hydrogen bromide is developed.

Enzymatic esterification of lauric acid to give monolaurin in a microreactor

Monolaurin is a naturally occurring compound widely utilized in food and cosmetics. In this paper, we present a new method for the synthesis of monolaurin by esterification between lauric acid and glycerol catalyzed by Novozym 435 using a microreactor. The conversion of lauric acid is 87.04% in 20 min, compared with 70.54% via the batch approach in 5 h. Using an optimized solvent system consisting of t-BuOH/tert-amyl alcohol (1:1, v/v), the selectivity using the microreactor method is enhanced to 90.63% and the space–time yield of the process is 380.91 g/h/L. This newly devised method has the potential for application to other multiphase and enzymatic reactions.

1,2-Diacrylglycerol and wherein the intermediate preparation method

The invention discloses a preparation method for diacylglycero and an intermediate thereof. The preparation method for diacylglycero comprises the following steps: in an ether solvent and/or an alcohol solvent, in the present of an alkali, performing hydrolysis reaction on a compound shown as a formula 5, so as to obtain diacylglycero which is 1 shown in a formula 1. R in the formula 5 and 5 is C14-C18 saturated or unsaturated aliphatic acyl. The preparation method is cheap in raw materials, mild in reaction conditions, safe in operation, simple in postprocessing operation, high in reaction conversion rate, high in yield and suitable for large-scale production.