BIS(2-METHACRYLOXYETHYL) PHOSPHATE

Product Information

Molecular Formula:
C12H19O8P
Molecular Weight:
322.25
Description
Crosslinking monomer. Adhesion promoter through free phosphoric acid group.
Synonyms
BIS(2-METHACRYLOXYETHYL) PHOSPHATE; MONOACRYLOXYETHYL PHOSPHATE; 2-Propenoicacid,2-methyl-,phosphinicobis(oxy-2,1-ethanediyl)ester; bis(methacryloyloxyethyl) hydrogen phosphate; Bismethacrylic acid (phosphinicobisoxybisethylene) ester; Bismethacrylic acid pho
IUPAC Name
2-[hydroxy-[2-(2-methylprop-2-enoyloxy)ethoxy]phosphoryl]oxyethyl 2-methylprop-2-enoate
Canonical SMILES
CC(=C)C(=O)OCCOP(=O)(O)OCCOC(=O)C(=C)C
InChI
InChI=1S/C12H19O8P/c1-9(2)11(13)17-5-7-19-21(15,16)20-8-6-18-12(14)10(3)4/h1,3,5-8H2,2,4H3,(H,15,16)
InChI Key
NXBXJOWBDCQIHF-UHFFFAOYSA-N
Boiling Point
221 °C(lit.)
Flash Point
>230 °CF
Density
1.28
Storage
Store at 4 degrees celsius
Refractive Index
n20/D 1.469

Safety Information

Hazards
Unknown

Computed Properties

XLogP3
0.7
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
8
Rotatable Bond Count
12
Exact Mass
322.08175456 g/mol
Monoisotopic Mass
322.08175456 g/mol
Topological Polar Surface Area
108Ų
Heavy Atom Count
21
Formal Charge
0
Complexity
418
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-114094102-A Secondary battery 2021-11-03
CN-113912788-A Early-strength polycarboxylate superplasticizer for subway segments and preparation method thereof 2021-09-26
CN-113662860-A Dental bonding pretreatment system based on iron and ferrous ions 2021-08-25
CN-113416477-A Photosensitive phytic acid doped polyaniline-based ultraviolet-curing anticorrosive paint and preparation method thereof 2021-07-02
CN-113429692-A Transparent perovskite/polymer composite scintillator material and preparation method thereof 2021-05-28
CN-113512396-A Bi-component structural adhesive and preparation method and application thereof 2021-05-18
KR-102303462-B1 Insulation material and insulation products manufactured using the same 2021-03-12
KR-102341077-B1 A booklet without backbone of bookbinding 2021-02-15
CN-112920326-A Degradable high polymer material and preparation method and application thereof 2021-02-05
CN-112341104-A High-performance road rubber concrete and preparation method thereof 2021-01-07

Literatures

PMID Publication Date Title Journal
23018084 2012-12-01 Effect of a non-thermal, atmospheric-pressure, plasma brush on conversion of model self-etch adhesive formulations compared to conventional photo-polymerization Dental materials : official publication of the Academy of Dental Materials
22277774 2012-04-01 Incorporation of phosphate group modulates bone cell attachment and differentiation on oligo(polyethylene glycol) fumarate hydrogel Acta biomaterialia
22032933 2012-03-01 The effect of hydroxyapatite presence on the degree of conversion and polymerization rate in a model self-etching adhesive Dental materials : official publication of the Academy of Dental Materials
22178281 2012-01-30 Matrix supported tailored polymer for solid phase extraction of fluoride from variety of aqueous streams Journal of hazardous materials
20978639 2011-08-01 Effect of water storage on the microtensile bond strength of composite resin to dentin using experimental rigid rod polymer modified primers The journal of adhesive dentistry
21652040 2011-07-15 Monolithic capillary columns synthesized from a single phosphate-containing dimethacrylate monomer for cation-exchange chromatography of peptides and proteins Journal of chromatography. A
21526807 2011-06-07 Surfactant-free miniemulsion polymerization as a simple synthetic route to a successful encapsulation of magnetite nanoparticles Langmuir : the ACS journal of surfaces and colloids
20447640 2010-06-11 Polymeric cation-exchange monolithic columns containing phosphoric acid functional groups for capillary liquid chromatography of peptides and proteins Journal of chromatography. A
20157671 2010-06-01 Bonding of composite resin to dentin using rigid rod polymer modified primers The journal of adhesive dentistry
18671261 2009-09-15 Effect of initiator on photopolymerization of acidic, aqueous dental model adhesives Journal of biomedical materials research. Part A
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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