Benzyl methacrylate

Product Information

Molecular Formula:
C11H12O2
Molecular Weight:
176.21
Description
Used to make polymers of high (1.5680) refractive index.
Synonyms
benzyl 2-methylprop-2-enoate
IUPAC Name
benzyl 2-methylprop-2-enoate
Canonical SMILES
CC(=C)C(=O)OCC1=CC=CC=C1
InChI
InChI=1S/C11H12O2/c1-9(2)11(12)13-8-10-6-4-3-5-7-10/h3-7H,1,8H2,2H3
InChI Key
AOJOEFVRHOZDFN-UHFFFAOYSA-N
Boiling Point
95-98 ℃ (4 mmHg)
Flash Point
115 ℃
Purity
95 %
Density
1.04 g/cm3
Appearance
Colorless liquid
Storage
Store at 4 degrees celsius
Refractive Index
n20/D 1.512
LogP
2.30590

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
H335:
May cause respiratory irritation.
Precautionary Statement
P261, P264, P271, P272, 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
2.9
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
4
Exact Mass
176.083729621 g/mol
Monoisotopic Mass
176.083729621 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
13
Formal Charge
0
Complexity
190
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
EP-3842798-A1 Colorimetric drug test strip using porous support material 2019-12-23
US-2021190697-A1 Colorimetric drug test strip using porous support material 2019-12-23
WO-2021123196-A1 Seeded resin-stabilized high-solids emulsion polymers 2019-12-20
WO-2021124043-A1 Adhesive article comprising polymer and polymerizable cyclic olefins, adhesive compositions and methods 2019-12-20
WO-2021124663-A1 Dental adhesive composition 2019-12-20
WO-2021125292-A1 Methacrylic copolymer, production method therefor, methacrylic copolymer composition, and molded body 2019-12-20
WO-2021126780-A1 Combination of crosslinkers to improve coating properties 2019-12-20
WO-2021120106-A1 Alkali-soluble resin, photosensitive resin composition, photosensitive element, method of forming resist pattern, and method of forming wiring pattern 2019-12-19
WO-2021122692-A1 Textile coated with malodor reducing polymers 2019-12-18
WO-2021126611-A1 Inkjet ink and primer fluid set 2019-12-18

Literatures

PMID Publication Date Title Journal
21974909 2012-11-01 pH-induced phase transition control of thermoresponsive nano-micelles possessing outermost surface sulfonamide moieties Colloids and surfaces. B, Biointerfaces
22847179 2012-09-21 Effect of multi-walled carbon nanotubes incorporation into benzyl methacrylate monolithic columns in capillary liquid chromatography The Analyst
22605479 2012-07-03 Efficient synthesis of sterically-stabilized nano-objects via RAFT dispersion polymerization of benzyl methacrylate in alcoholic media Advanced materials (Deerfield Beach, Fla.)
21816404 2012-03-09 Preparation of phenyl-silica hybrid monolithic column with 'one-pot' process for capillary liquid chromatography Journal of chromatography. A
22489178 2012-01-01 Photosensized controlling benzyl methacrylate-based matrix enhanced Eu(3+) narrow-band emission for fluorescence applications International journal of molecular sciences
20934905 2011-08-15 Brillouin spectroscopy studies of two-component polymerizable liquid system: 2,2-bis[4-(2-hydroxymethacryloxypropoxy)phenyl]propane/benzyl methacrylate Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
21433142 2011-01-17 Designer template initiator for sequence regulated polymerization: systems design for substrate-selective metal-catalyzed radical addition and living radical polymerization Macromolecular rapid communications
20394939 2010-05-28 Fast preparation of photopolymerized poly(benzyl methacrylate-co-bisphenol A dimethacrylate) monoliths for capillary electrochromatography Journal of chromatography. A
20019424 2009-11-01 Prediction of the reduced glutathione (GSH) reactivity of dental methacrylate monomers using NMR spectra - Relationship between toxicity and GSH reactivity Dental materials journal
19719210 2009-08-18 Photoisomerization-induced tunable LCST phase separation of azobenzene-containing polymers in an ionic liquid Langmuir : the ACS journal of surfaces and colloids
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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