2-ETHYLACRYLIC ACID 98

Product Information

Molecular Formula:
C5H8O2
Molecular Weight:
100.116
Description
2-ethylacrylic acid is an alpha,beta-unsaturated monocarboxylic acid that is acrylic acid in which the hydrogen at position 2 is substituted by an ethyl group. It has a role as a mammalian metabolite. It is functionally related to an acrylic acid. It is a conjugate acid of a 2-ethylacrylate.
Synonyms
2-Ethylpropenoic acid,2-Methylenebutanoic acid,2-Methylenebutyric acid
IUPAC Name
2-methylidenebutanoic acid
Canonical SMILES
CCC(=C)C(=O)O
InChI
InChI=1S/C5H8O2/c1-3-4(2)5(6)7/h2-3H2,1H3,(H,6,7)
InChI Key
WROUWQQRXUBECT-UHFFFAOYSA-N
Boiling Point
176 ℃ (lit.)
Flash Point
181.9 ℃F - closed cup
Purity
0.98
Density
0.986
Refractive Index
n20/D 1.437 (lit.)

Safety Information

Hazards
H314
Precautionary Statement
P280 - P305 + P351 + P338 - P310

Computed Properties

XLogP3
1.2
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
2
Exact Mass
100.052429494 g/mol
Monoisotopic Mass
100.052429494 g/mol
Topological Polar Surface Area
37.3Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
94.3
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-114149545-A Aqueous epoxy resin emulsion, its preparation method and application 2021-12-31
CN-114163581-A Concrete tackifier and preparation method thereof 2021-12-28
CN-114181682-A High-temperature-resistant salt-resistant cross-linked polymer filtrate reducer and preparation method and application thereof 2021-12-21
CN-113917577-A High-water-resistance and bending-resistance optical protective film, polarizer and liquid crystal display device 2021-12-13
CN-114058008-A Process for preparing semi-aromatic polyamides end-capped with monocarboxylic acids, semi-aromatic polyamides and molding compositions 2021-12-13
CN-114058009-A Process for preparing semi-aromatic polyamides with reduced loss of diamine monomer, semi-aromatic polyamides and molding compositions 2021-12-13
CN-114058010-A Process for preparing low-energy semiaromatic polyamides, semiaromatic polyamides and moulding compositions 2021-12-13
CN-114133559-A Process for preparing semiaromatic polyamides with reduced salt formation cycle, semiaromatic polyamides and moulding compositions 2021-12-13
CN-114133560-A Process for preparing semiaromatic polyamides with improved impact strength, semiaromatic polyamides and moulding compositions 2021-12-13
CN-114044856-A Mud-blocking type polycarboxylate superplasticizer and preparation method thereof 2021-11-25

Literatures

PMID Publication Date Title Journal
22321051 2012-03-20 Significance of xenobiotic metabolism for bioaccumulation kinetics of organic chemicals in Gammarus pulex Environmental science & technology
22280359 2012-03-01 Homopolymer self-assembly into stable nanoparticles: concerted action of hydrophobic association and hydrogen bonding in thermoresponsive poly(alkylacrylic acid)s The journal of physical chemistry. B
22227362 2012-02-17 Predicting the chromatographic retention of polymers: application of the polymer model to poly(styrene/ethylacrylate)copolymers Journal of chromatography. A
23028220 2012-01-01 Influence of polymer size, liposomal composition, surface charge, and temperature on the permeability of pH-sensitive liposomes containing lipid-anchored poly(2-ethylacrylic acid) International journal of nanomedicine
22068566 2011-12-01 Preparation and characterization of chitosan hybrid membranes containing polyethylacrylate and polybutylacrylate The Journal of membrane biology
21693131 2011-11-01 Graft copolymerization of ethylacrylate onto xanthan gum, using potassium peroxydisulfate as an initiator International journal of biological macromolecules
22454753 2011-10-01 Sustained release intraocular drug delivery devices for treatment of uveitis Journal of ophthalmic & vision research
20566656 2011-09-01 Three-dimensional scaffolds as a model system for neural and endothelial 'in vitro' culture Journal of biomaterials applications
21277322 2011-05-01 Preparation and characterization of chitosan-grafted-poly(2-amino-4,5-pentamethylene-thiophene-3-carboxylic acid N'-acryloyl-hydrazide) chelating resin for removal of Cu(II), Co(II) and Ni(II) metal ions from aqueous solutions International journal of biological macromolecules
21392493 2011-05-01 Acute toxicity of organic chemicals to Gammarus pulex correlates with sensitivity of Daphnia magna across most modes of action Aquatic toxicology (Amsterdam, Netherlands)
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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