106-08-1

Basic information

• Product Name: Dodecanoic acid,26-hydroxy-3,6,9,12,15,18,21,24-octaoxahexacos-1-yl ester
• Synonyms: Lauricacid, 2-[2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethylester (8CI); Lauric acid, ester with nonaethylene glycol (6CI); Nonaethyleneglycol, monolaurate (8CI); NSC 1249
• CAS NO: 106-08-1
• Molecular Formula: C₃₀H₆₀O₁₁
• Molecular Weight: 596.7908
• EINECS: 203-359-3
• Mol File: 106-08-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 630.3°Cat760mmHg
• Flash Point: 183.3°C
• Appearance: /
• Density: 1.036g/cm³
• Vapor Pressure: 1.57E-18mmHg at 25°C
• Refractive Index: 1.462
• CAS DataBase Reference: Dodecanoic acid,26-hydroxy-3,6,9,12,15,18,21,24-octaoxahexacos-1-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Dodecanoic acid,26-hydroxy-3,6,9,12,15,18,21,24-octaoxahexacos-1-yl ester(106-08-1)
• EPA Substance Registry System: Dodecanoic acid,26-hydroxy-3,6,9,12,15,18,21,24-octaoxahexacos-1-yl ester(106-08-1)

Safety Data

• Hazardous Substances Data: 106-08-1(Hazardous Substances Data)

Usage

General Description

Dodecanoic acid, 26-hydroxy-3,6,9,12,15,18,21,24-octaoxahexacos-1-yl ester is a complex chemical compound consisting of dodecanoic acid and 26-hydroxy-3,6,9,12,15,18,21,24-octaoxahexacos-1-yl ester. Dodecanoic acid, also known as lauric acid, is a saturated fatty acid commonly found in coconut oil and offers various potential health benefits, including antimicrobial and anti-inflammatory properties. The other component, 26-hydroxy-3,6,9,12,15,18,21,24-octaoxahexacos-1-yl ester, is an ester derived from a hydroxy compound and an acid, and its specific properties and uses would depend on the precise nature of the hydroxy compound and acid involved. The combination of these two chemicals may have applications in various fields, including pharmaceuticals, cosmetics, and food production.

InChI:InChI=1/C30H60O11/c1-2-3-4-5-6-7-8-9-10-11-30(32)41-29-28-40-27-26-39-25-24-38-23-22-37-21-20-36-19-18-35-17-16-34-15-14-33-13-12-31/h31H,2-29H2,1H3

Relevant articles and documents

Combinatorial synthesis of PEG oligomer libraries

A simple chain-extending approach was established for the scale-up of the monoprotected monodisperse PEG diol materials. Reactions of THP-(OCH2CH2)n—OMs (n=4, 8, 12) with a large excess of commercially available H—(OCH2CH2)n—OH (n=1-4) under basic conditions led to THP-(OCH2CH2)n—OH (n=5-15). Similarly, Me-(OCH2CH2)n—OH (n=4-11, 13) were prepared from Me-(OCH2CH2)n—OMs (n=3, 7, 11). For the chain elongation steps, 40-80% yields were achieved through extraction purification. PEG oligomer libraries I and II were generated in 50-95% overall yields by alkylation or acylation of THP-(OCH2CH2)n—OH (n=1-15) followed by deprotection. Alkylation of Me-(OCH2CH2)n—OH (n=1-11, 13) with X—(CH2)m—CO2R (X=Br or OMs) and subsequent hydrolysis led to PEG oligomer library III in 30-60% overall yields. Combinatorial purification techniques were adapted to the larger-scale library synthesis. A total of 498 compounds, each with a weight of 2-5 g and a minimum purity of 90%, were synthesized.