Ethanol, 2-(ethenyloxy)-

Product Information

Molecular Formula:
C4H8O2
Molecular Weight:
88.1
Description
Ethanol, 2-(ethenyloxy)- is an indispensable entity in the realm of biomedical sciences. Its principal application prevails in the fabrication of pharmaceutical agents, acting as a pivotal intermediary.
Synonyms
2-(ethenyloxy)-ethano; 2-(ethenyloxy)ethanol; 2-(ethenyloxy)-ethanol; 2-(vinyloxy)-ethano; 2-Hydroxyethyl vinyl ether; 2-hydroxyethylvinylether; Ethanol, 2-(ethenyloxy)-; Ethanol, 2-(vinyloxy)-
IUPAC Name
2-ethenoxyethanol
Canonical SMILES
C=COCCO
InChI
InChI=1S/C4H8O2/c1-2-6-4-3-5/h2,5H,1,3-4H2
InChI Key
VUIWJRYTWUGOOF-UHFFFAOYSA-N
Boiling Point
143 °C
Flash Point
49 °C
Purity
>95.0%(GC)
Density
0.942 g/cm3
Solubility
Soluble in ethanol, ether, and benzene
Appearance
Colorless to Almost colorless clear liquid
Application
Used to make plastics, lacquers, and protective coatings.
Refractive Index
n20/D 1.436 (lit.)
Decomposition
When heated to decomposition it emits acird smoke and irritating fumes.

Safety Information

Hazards
H226:
Flammable liquid and vapour.
Precautionary Statement
P210:
Keep away from heat, sparks, open flames, hot surfaces. No smoking.
P233:
Keep container tightly closed.
P303+P361+P353:
IF ON SKIN (or hair):
Take off immediately all contaminated clothing. [As modified by IV ATP].
Rinse skin with water/shower.
P370+P378:
In case of fire:
Use for extinction:
P403+P235:
Store in a well ventilated place.
Keep cool.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.

Computed Properties

XLogP3
0.1
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
3
Exact Mass
88.052429494 g/mol
Monoisotopic Mass
88.052429494 g/mol
Topological Polar Surface Area
29.5Ų
Heavy Atom Count
6
Formal Charge
0
Complexity
34.5
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114086385-A Modified fiber, bio-based degradable material and preparation method thereof 2022-01-21
CN-114133494-A High-performance polycarboxylic acid type water reducing agent, and normal-temperature preparation method, use method and application thereof 2021-12-21
JP-2022040149-A Adhesive composition and laminated film using it 2021-12-21
CN-114133743-A Addition type flame-retardant heat-resistant liquid silicone rubber composition and preparation method thereof 2021-12-15
JP-2022040133-A A photosensitive coloring composition for a color filter for a solid-state image sensor, a color filter, and a solid-state image sensor using the same. 2021-12-15
CN-113929910-A Hyperbranched polymer underwater adhesive based on polyfunctional group rigid hydrophobic component and preparation method and application thereof 2021-12-07
CN-113896842-A Synthetic method of polycarboxylate superplasticizer by taking polyether macromonomer as raw material 2021-11-30
CN-113979661-A Preparation method of nano calcium silicate suspension with high stability and good early strength effect 2021-11-30
CN-113930120-A High-strength explosion-proof protective coating and production process thereof 2021-11-29
CN-113973837-A Insecticidal composition containing diazinon and pymetrozine and preparation method thereof 2021-11-29

Literatures

PMID Publication Date Title Journal
22820448 2012-09-10 A library of strictly linear poly(ethylene glycol)-poly(ethylene imine) diblock copolymers to perform structure-function relationship of non-viral gene carriers Journal of controlled release : official journal of the Controlled Release Society
22807837 2012-07-01 rac-2-[(2-Chloro-phen-yl)(4-chloro-phen-yl)meth-yl]-1,3-dioxolane Acta crystallographica. Section E, Structure reports online
22530594 2012-05-03 On the perturbation of the H-bonding interaction in ethylene glycol clusters upon hydration The journal of physical chemistry. A
22024976 2011-12-28 Thermal dissociation of ethylene glycol vinyl ether Physical chemistry chemical physics : PCCP
19175334 2009-02-05 Rate coefficients for the gas-phase reactions of OH and NO3 radicals and O3 with ethyleneglycol monovinyl ether, ethyleneglycol divinyl ether, and diethyleneglycol divinyl ether The journal of physical chemistry. A
18323104 2008-02-01 CCN activity and hygroscopic growth of organic aerosols following reactive uptake of ammonia Environmental science & technology
21201270 2008-01-04 (Glycol-κO,O')nitros-yl(η-penta-methyl-cyclo-penta-dien-yl)ruthenium(II) bis-(tri-fluoro-methane-sulfonate) Acta crystallographica. Section E, Structure reports online
16417246 2006-01-01 Water-soluble dendrigrafts bearing saccharidic moieties: elaboration and application to enzyme linked OligoSorbent Assay (ELOSA) diagnostic tests Bioconjugate chemistry
14600391 2003-11-01 Controlled release of vitamin E from thermo-responsive polymeric physico-gel Chemical & pharmaceutical bulletin
12797616 2003-06-01 Expandable bioresorbable endovascular stent. I. Fabrication and properties Annals of biomedical engineering
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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