2-Ethylhexyl methacrylate

Product Information

Molecular Formula:
C12H22O2
Molecular Weight:
198.30
Description
2-Ethylhexyl Methacrylate can be used as a release coating composition.
Synonyms
2-ethylhexyl 2-methylprop-2-enoate
IUPAC Name
2-ethylhexyl 2-methylprop-2-enoate
Canonical SMILES
CCCCC(CC)COC(=O)C(=C)C
InChI
InChI=1S/C12H22O2/c1-5-7-8-11(6-2)9-14-12(13)10(3)4/h11H,3,5-9H2,1-2,4H3
InChI Key
WDQMWEYDKDCEHT-UHFFFAOYSA-N
Boiling Point
88 °C / 3.5 mmHg
Melting Point
-50°C
Flash Point
100 °C
Purity
> 99.0 % (GC)
Density
0.884 g/cm3
Solubility
water, 5.922 mg/L @ 25 °C (est)
Appearance
Colorless liquid
Application
This product is suitable for scientific research.
Refractive Index
1.437-1.439
Stability
Stable, but may polymerize upon exposure to light. Heat sensitive. Incompatible with strong acids, strong oxidizing agents, strong bases.
LogP
3.32210
Vapor Pressure
0.076 mm Hg @ 25 °C /Estimated/;Vapor pressure, Pa at 20 °C: 133
Henry's Law Constant
1.1X10-3 atm-cu m/mol @ 25 °C /Estimated/

Safety Information

Hazards
H315:
Causes skin irritation.
H317:
May cause an allergic skin reaction.
H319:
Causes serious eye irritation.
H335:
May cause respiratory irritation.
H361:
Suspected of damaging fertility or the unborn child.
H412:
Harmful to aquatic life with long-lasting effects.
Precautionary Statement
P261, P264, P271, P272, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362, P363, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
4.5
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
8
Exact Mass
198.161979940 g/mol
Monoisotopic Mass
198.161979940 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
185
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
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
US-11015113-B1 Wet-coated proppant and methods of making and using same 2020-04-13
WO-2021122883-A1 Method for cleaning and care of an automatic dishwasher 2019-12-20
WO-2021122886-A1 Methods for cleaning and caring for an automatic dishwasher 2019-12-20
WO-2021122889-A1 Methods for cleaning and caring for an automatic dishwasher 2019-12-20
WO-2021122903-A1 Aqueous latex of vinylidene chloride copolymer 2019-12-20
WO-2021123196-A1 Seeded resin-stabilized high-solids emulsion polymers 2019-12-20
WO-2021125292-A1 Methacrylic copolymer, production method therefor, methacrylic copolymer composition, and molded body 2019-12-20
WO-2021126264-A1 Inkjet inks 2019-12-20
WO-2021126780-A1 Combination of crosslinkers to improve coating properties 2019-12-20
WO-2021127128-A1 Two part curable compositions 2019-12-20

Literatures

PMID Publication Date Title Journal
22789804 2012-10-01 The synthesis of translucent polymer nanolatexes via microemulsion polymerization Journal of colloid and interface science
22428724 2012-04-01 Facile synthesis of main-chain degradable block copolymers for performance enhanced dismantlable adhesion ACS applied materials & interfaces
20857956 2010-10-19 Hydrolysis of p-nitrophenyl esters promoted by semifluorinated quaternary ammonium polymer latexes and films Langmuir : the ACS journal of surfaces and colloids
19275177 2009-04-09 Hydrolysis of p-nitrophenyl esters in mixtures of water and a fluorous solvent Langmuir : the ACS journal of surfaces and colloids
18193406 2008-06-01 Glucose sensor using a phospholipid polymer-based enzyme immobilization method Analytical and bioanalytical chemistry
19697507 2008-06-01 Development of new bone cement utilizing low toxicity monomers Journal of medical and dental sciences
17382571 2008-01-01 Ultrasound initiated miniemulsion polymerization of methacrylate monomers Ultrasonics sonochemistry
16758458 2006-12-01 Stress response of adherent cells on a polymer blend surface composed of a segmented polyurethane and MPC copolymers Journal of biomedical materials research. Part A
12790674 2003-05-01 Use of salt hydrate pairs to control water activity for enzyme catalysis in ionic liquids Biotechnology progress
4631 1976-04-01 Studies of introital colonization in women with recurrent urinary infections. V. The inhibitory activity of normal vaginal fluid on Proteus mirabilis and Pseudomonas aeruginosa The Journal of urology
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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