benzyl acrylate

2-propenoic acid, phenylmethyl ester

CAS: 2495-35-4 C10 H10 O2 MW: 162.18810000

Identification

Namebenzyl acrylate
IUPACbenzyl prop-2-enoate
CAS Number2495-35-4
EINECS219-673-9
FDA UNIISearch
Molecular FormulaC10 H10 O2
Molecular Weight162.18810000
MDL NumberMFCD00048147
Nikkaji NumberJ71.666I
XlogP32.60 (est)

Regulatory

DG SANTE Food Contact Materialsacrylic acid benzyl ester

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 228.67 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.073000 mmHg @ 25.00 °C. (est)
Flash Point 240.00 °F. TCC ( 115.50 °C. ) (est)
logP (o/w) 2.109 (est)
Soluble in water, 556.3 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryindirect food additives: adhesives and components of coatings
Recommendation for benzyl acrylate usage levels up tonot for fragrance use.
Recommendation for benzyl acrylate flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

acrylic acid benzyl ester benzyl prop-2-enoate phenylmethyl prop-2-enoate 2- propenoic acid phenyl methyl ester 2- propenoic acid, phenylmethyl ester PubMed: Transition state analysis of enantioselective Brønsted base catalysis by chiral cyclopropenimines. PubMed: "Click" and Olefin Metathesis Chemistry in Water at Room Temperature Enabled by Biodegradable Micelles. PubMed: Complex nanostructured materials from segmented copolymers prepared by ATRP. PubMed: Period-doubling behavior in frontal polymerization of multifunctional acrylates. PubMed: The effect of convection on a propagating front with a liquid product: Comparison of theory and experiments. PubMed: Solid Phase Synthesis of beta-Peptoids: N-Substituted beta-Aminopropionic Acid Oligomers.