6196-58-3

Basic information

• Product Name: C5E1
• Synonyms: PENTYLGLYCOL;N-PENTYLMONOOXYETHYLENE;2-(PENTYLOXY)ETHANOL;ETHYLENEGLYCOLMONOPENTYL ETHER;C5E1;2-(Pentyloxy)ethanol, C5E1, Pentylglycol;3-Oxaoctane-1-ol;C5E1, n-PentylMonooxyethylene
• CAS NO: 6196-58-3
• Molecular Formula: C7H16O2
• Molecular Weight: 132.2
• Mol File: 6196-58-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: -15.45°C (estimate)
• Boiling Point: 179.14°C (rough estimate)
• Flash Point: 75 °C
• Appearance: /
• Density: 0.893 g/mL at 20 °C(lit.)
• Vapor Pressure: 0.171mmHg at 25°C
• Refractive Index: n20/D 1.424
• Storage Temp.: -15°C
• CAS DataBase Reference: C5E1(CAS DataBase Reference)
• NIST Chemistry Reference: C5E1(6196-58-3)
• EPA Substance Registry System: C5E1(6196-58-3)

Safety Data

• RIDADR: 2810
• WGK Germany: 3
• F: 10-23
• HazardClass: 6.1(b)
• PackingGroup: III
• Hazardous Substances Data: 6196-58-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H16O2/c1-2-3-4-6-9-7-5-8/h8H,2-7H2,1H3

Upstream product

• 75-21-8 oxirane 
• 71-41-0 pentan-1-ol 
• 107-21-1 ethylene glycol 
• 96-49-1 [1,3]-dioxolan-2-one 
• 109-52-4 valeric acid 
• 110-53-2 1-Bromopentane 

Downstream Products

• 18912-81-7 2-methylbutoxy ethoxyethanol 
• 1470371-17-5 2-(pentyloxy)ethyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate 

Relevant articles and documents

PYRROLO[2,3-B]PYRIDIN DERIVATIVES AS INHIBITORS OF INFLUENZA VIRUS REPLICATION

Provided herein are compounds of Formula A, B or C that can inhibit the replication of influenza viruses, reduce the amount of influenza viruses, and/or treat influenza.

METHOD FOR PREPARING GLYCEROL ETHER AND GLYCOL ETHER

The present invention concerns a method for preparing glycerol ether or glycol ether comprising the reaction of a compound of formula (II) with a compound of formula (III) in the presence of a heterogeneous acid catalyst of formulas (II) and (III).

Selective synthesis of 1-O-Alkyl(poly)glycerol ethers by catalytic reductive alkylation of carboxylic acids with a recyclable catalytic system

(Poly)glycerol monoethers were synthesized in good yield and selectivity by the catalytic reductive alkylation of glycerol, diglycerol, and triglycerol with readily available, cheap and/or bio-sourced carboxylic acids. The reaction was catalyzed by 1 mol % of Pd/C under 50 bar H2 using an acid ion-exchange resin as a recyclable cocatalyst. The catalytic system was recycled several times, and a mechanism is proposed for this transformation.