VINYL PROPIONATE

Product Information

Molecular Formula:
C5H8O2
Molecular Weight:
100.12
Description
Applications: Vinyl Propionate (stabilized with MEHQ) is a useful research chemical.
Synonyms
Ethenylpropanoate; Propanoicacid,ethenylester; vinyl; Vinylester kyseliny propionove; vinylesterkyselinypropionove; vinylpropanoate
IUPAC Name
ethenyl propanoate
Canonical SMILES
CCC(=O)OC=C
InChI
InChI=1S/C5H8O2/c1-3-5(6)7-4-2/h4H,2-3H2,1H3
InChI Key
UIWXSTHGICQLQT-UHFFFAOYSA-N
Boiling Point
93°C
Melting Point
-80°C(lit.)
Flash Point
8 °C
Purity
BP 93-94deg
Density
0.919 g/mL at 25 °C(lit.)
Appearance
Colorless to Almost colorless clear liquid
Storage
2-8°C
Refractive Index
n20/D 1.403 (lit.)

Safety Information

Hazards
H225:
Highly flammable liquid and vapour.
H319:
Causes serious eye irritation.
Precautionary Statement
P210:
Keep away from heat, sparks, open flames, hot surfaces. No smoking.
P233:
Keep container tightly closed.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P303+P361+P353:
IF ON SKIN (or hair):
Take off immediately all contaminated clothing. [As modified by IV ATP].
Rinse skin with water/shower.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P370+P378:
In case of fire:
Use for extinction:

Computed Properties

XLogP3
1.1
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
3
Exact Mass
100.052429494 g/mol
Monoisotopic Mass
100.052429494 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
76.1
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
WO-2015200015-A1 Stabilized moisture-curable polymeric compositions 2014-06-27
WO-2015200016-A1 Stabilized moisture-curable polymeric compositions 2014-06-27
US-2015375521-A1 Electrostatic printing of cyclodextrin compositions 2014-06-26
US-2015376310-A1 Ethylene acid copolymers, their ionomers, and their use in packaging films and injection molded articles 2014-06-26
US-2015378274-A1 Toner 2014-06-26
US-2015378275-A1 Method for producing toner particles 2014-06-26
WO-2015199750-A1 Ethylene acid copolymers, their ionomers, and their use in packaging films and injection molded articles 2014-06-26
WO-2015200647-A1 Electrostatic printing of cyclodextrin compositions 2014-06-26
WO-2015195355-A1 Adhesive compositions comprising a silsesquioxane polymer crosslinker, articles and methods 2014-06-20
WO-2015195391-A1 Adhesive compositions comprising a silsesquioxane polymer crosslinker, articles and methods 2014-06-20

Literatures

PMID Publication Date Title Journal
20888759 2011-01-01 Direct enzymatic acylation of cellulose pretreated in BMIMCl ionic liquid Bioresource technology
21811674 2011-01-01 Immobilization of a Commercial Lipase from Penicillium camembertii (Lipase G) by Different Strategies Enzyme research
20655391 2010-11-01 Non-lipolytic and lipolytic sequence-related carboxylesterases: a comparative study of the structure-function relationships of rabbit liver esterase 1 and bovine pancreatic bile-salt-activated lipase Biochimica et biophysica acta
17046305 2006-11-01 Purification and biochemical characterization of a turkey preduodenal esterase Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology
16567014 2006-07-25 Markedly improving Novozym 435-mediated regioselective acylation of 1-beta-D-arabinofuranosylcytosine by using co-solvent mixtures as the reaction media Journal of biotechnology
16842350 2006-07-01 Biochemical and molecular characterization of a lipase produced by Rhizopus oryzae FEMS microbiology letters
15055765 2004-02-01 Kinetic resolution of rac-2-pentanol catalyzed by Candida antarctica lipase B in the ionic liquid, 1-butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]amide Biotechnology letters
12216836 2002-07-01 Distinction between esterases and lipases: a kinetic study with vinyl esters and TAG Lipids
11750885 2001-11-30 Lipase-catalysed hydrolysis of short-chain substrates in solution and in emulsion: a kinetic study Biochimica et biophysica acta
11348121 2001-05-18 Activation of pig liver esterase in organic media with organic polymers: application to the enantioselective acylation of racemic functionalized secondary alcohols The Journal of organic chemistry
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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