O-Phenylphenoxyethyl Acrylate Property

vapor pressure 

0Pa at 20℃

Water Solubility 

30mg/L at 20℃

InChI

InChI=1S/C17H16O3/c1-2-17(18)20-13-12-19-16-11-7-6-10-15(16)14-8-4-3-5-9-14/h2-11H,1,12-13H2

InChIKey

VAZQKPWSBFZARZ-UHFFFAOYSA-N

SMILES

C(OCCOC1=CC=CC=C1C1=CC=CC=C1)(=O)C=C

LogP

3.68

EPA Substance Registry System

Poly(oxy-1,2-ethanediyl), .alpha.-(1-oxo-2-propenyl)-.omega.-([1,1'-biphenyl]-2-yloxy)- (72009-86-0)

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H317May cause an allergic skin reaction

H361Suspected of damaging fertility or the unborn child

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P272Contaminated work clothing should not be allowed out of the workplace.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P281Use personal protective equipment as required.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P308+P313IF exposed or concerned: Get medical advice/attention.

P321Specific treatment (see … on this label).

P333+P313IF SKIN irritation or rash occurs: Get medical advice/attention.

P363Wash contaminated clothing before reuse.

P405Store locked up.

P501Dispose of contents/container to..…

O-Phenylphenoxyethyl Acrylate Chemical Properties,Usage,Production

Description

The molecular structure of O-Phenylphenoxyethyl Acrylate contains an aromatic nucleus. Generally speaking, the acrylic ester polymer, or the multipolymer in molecular structure, contains an aromatic nucleus because it has excellent transparency and a high refractive index and is widely used in optical material in industries such as optical resin, optical coating, optical adhesive, optical lens, and glasses manufactures. Because these fields all need water-white goods, they need monomers that have low coloring and are even colorless.

Synthesis

2-(2-biphenylyloxy)ethanol and acrylic acid are subjected to an esterification reaction under the protection of nitrogen by adopting cyclohexane as a solvent and adopting an organic acid as a catalyst in the presence of a polymerization inhibitor and a reduction agent. After completing the esterification reaction, alkali washing, water washing drying, and reduced pressure solvent removal are adopted to obtain the O-Phenylphenoxyethyl Acrylate, wherein the amount of the reduction agent is 0.1-2 wt% of the total weight of 2-(2-biphenylyloxy)ethanol and acrylic acid.