19327-40-3

Basic information

• Product Name: N-OCTYLPENTAOXYETHYLENE
• Synonyms: PENTAETHYLENEGLYCOLMONOOCTYL ETHER;POLYOXYETHYLENE 5 OCTYL ETHER;N-OCTYLPENTAOXYETHYLENE;C8E5;3,6,9,12,15-pentaoxatricosan-1-ol;pentaoxyethylenemonooctylether;C8E5, Octyl pentaethylene glycol ether, Octylpentaglycol;14-(Octyloxy)-3,6,9,12-tetraoxatetradecane-1-ol
• CAS NO: 19327-40-3
• Molecular Formula: C18H38O6
• Molecular Weight: 350.49
• Mol File: 19327-40-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 434.3°Cat760mmHg
• Flash Point: 216.5°C
• Appearance: /
• Density: 0.99 g/mL at 25 °C(lit.)
• Vapor Pressure: 2.29E-09mmHg at 25°C
• Refractive Index: 1.451
• Storage Temp.: -15°C
• PKA: 14.36±0.10(Predicted)
• BRN: 1711907
• CAS DataBase Reference: N-OCTYLPENTAOXYETHYLENE(CAS DataBase Reference)
• NIST Chemistry Reference: N-OCTYLPENTAOXYETHYLENE(19327-40-3)
• EPA Substance Registry System: N-OCTYLPENTAOXYETHYLENE(19327-40-3)

Safety Data

• WGK Germany: 3
• RTECS: SB0422500
• F: 10-23
• Hazardous Substances Data: 19327-40-3(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 19327-40-3 differently. You can refer to the following data:
1. N-OCTYLPENTAOXYETHYLENE has been used to study the size and morphology of aggregates. It has also been used in a study to investigate the sorption of monodisperse alcohol ethoxylates and their effects on the mobility of 2,4-D in isolated plan
2. Pentaethylene Glycol Monooctyl Ether has been used to study the size and morphology of aggregates.

InChI:InChI=1/C18H38O6/c1-2-3-4-5-6-7-9-20-11-13-22-15-17-24-18-16-23-14-12-21-10-8-19/h19H,2-18H2,1H3

Upstream product

• 19327-38-9 triethylene glycol monooctyl ether 
• 19327-37-8 diethylene glycol octyl ether 
• 75-21-8 oxirane 
• 111-87-5 octanol 
• 19327-39-0 2-{2-[2-(2-Octyloxy-ethoxy)-ethoxy]-ethoxy}-ethanol 

Relevant articles and documents

Nonionic Isatin Surfactants: Synthesis, Quantum Chemical Calculations, ADMET and Their Antimicrobial Activities

The most challenge task in the building up of surface-active molecules is maximizing their surface activity with good biological activity. A nonionic surfactant (N-isatin-EOm-Cn where m is 5, 7 and 9 ethylene glycol units and n is 8, 10 and 12) is achieved by first reacting isatin with chloroacetic acid and then with different types of ethoxylated (C8–C12) fatty alcohols that possess 5, 7 and 9 ethylene oxide units. The prepared surfactants were characterized by FTIR and 1H NMR to confirm the structure. The surface activity, biodegradability, antimicrobial, and antifungal activity of the surfactants were evaluated. In addition, quantum chemical calculations and computations of oral bioavailability were performed. The obtained data show that all the synthesized compounds had good surface activity, biodegradability and biological activity.