lauryl acrylate
acrylic acid, dodecyl ester
Identification
| Name | lauryl acrylate |
| CAS Number | 2156-97-0 |
| EINECS | 218-463-4 |
| FDA UNII | 90IK36WGVR |
| Molecular Formula | C15 H28 O2 |
| Molecular Weight | 240.38656000 |
| MDL Number | MFCD00042871 |
| Nikkaji Number | J107.540C |
| Beilstein | 1779069 |
| XlogP3 | 6.20 (est) |
Regulatory
| DG SANTE Food Contact Materials | acrylic acid, dodecyl ester |
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Specific Gravity | 0.87000 @ 25.00 °C. |
| Refractive Index | 1.44500 @ 20.00 °C. |
| Boiling Point | 306.17 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.001000 mmHg @ 25.00 °C. (est) |
| Flash Point | 181.00 °F. TCC ( 82.78 °C. ) |
| logP (o/w) | 6.393 (est) |
| Soluble in | water, 0.1556 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | pharmaceuticals / chemical synthisis |
| Recommendation for lauryl acrylate usage levels up to | not for fragrance use. |
| Recommendation for lauryl acrylate flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
acrylic acid dodecyl ester
acrylic acid, dodecyl ester
dodecyl acrylate
N-
dodecyl acrylate
dodecyl prop-2-enoate
N-
lauryl acrylate
2-
propenoic acid dodecyl ester
2-
propenoic acid, dodecyl ester
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Solvent Effects on Acrylate kp in Organic Media?-A Systematic PLP-SEC Study.
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Evaluation of the influence of homopolymerization on the removal of water-insoluble organics by grafted polypropylene fibers.
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Receptor-attached amphiphilic terpolymer for selective drug recognition in aqueous solutions.
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Peak parking determination of the obstruction factor in lauryl acrylate monolithic CEC columns.
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Chemical initiation for butyl and lauryl acrylate monolithic columns for CEC.
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Development of an acrylate monolith in a cyclo-olefin copolymer microfluidic device for chip electrochromatography separation.
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19F- and fluorescently labeled micelles as nanoscopic assemblies for chemotherapeutic delivery.
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Neutron scattering study of the structural change induced by photopolymerization of AOT/D2O/dodecyl acrylate inverse microemulsions.
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Amphiphilic hyperbranched fluoropolymers as nanoscopic 19F magnetic resonance imaging agent assemblies.
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Alkyl chain length effects on copolymerization kinetics of a monoacrylate with hexanediol diacrylate.
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Evidence for the existence of an effective interfacial tension between miscible fluids. 2. Dodecyl acrylate-poly(dodecyl acrylate) in a spinning drop tensiometer.
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Measuring the mutual diffusion coefficient for dodecyl acrylate in low molecular weight poly(dodecyl acrylate) with laser line deflection (Wiener's Method) and the fluorescence of pyrene.
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Fabrication of porous polymer monoliths in polymeric microfluidic chips as an electrospray emitter for direct coupling to mass spectrometry.
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Evaluation of acrylate-based block copolymers prepared by atom transfer radical polymerization as matrices for paclitaxel delivery from coronary stents.
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Capillary electrochromatography column behavior of butyl and lauryl acrylate porous polymer monoliths.
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Development and in situ synthesis of monolithic stationary phases for electrochromatographic separations.
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Artificial receptor-attached amphiphilic copolymer for barbiturate binding in aqueous media.
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Effect of pendent group structures on the chemical selectivity and performance of sulfonated copolymers as novel pseudophases in electrokinetic chromatography.
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Application of capillary electrochromatography using macroporous polyacrylamide columns for the analysis of lignans from seeds of Schisandra chinensis.