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  2. Ethyl acrylate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acrylate

    Ethyl acrylate reacts with amines catalyzed by Lewis acids in a Michael addition to β-alanine derivatives in high yields: [13]. The nucleophilic addition at ethyl acrylate as an α,β-unsaturated carbonyl compound is a frequent strategy in the synthesis of pharmaceutical intermediates.

  3. Acrylate polymer - Wikipedia

    en.wikipedia.org/wiki/Acrylate_polymer

    Acrylic elastomer is a general term for a type of synthetic rubber whose primary component is acrylic acid alkyl ester (ethyl or butyl ester). [3] Acrylic elastomer possesses characteristics of heat and oil resistance, with the ability to withstand temperatures of 170–180 °C. It is used primarily for producing oil seals and packaging related ...

  4. Ethyl cyanoacrylate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacrylate

    Ethyl cyanoacrylate (ECA), a cyanoacrylate ester, is an ethyl ester of 2-cyano-acrylic acid. It is a colorless liquid with low viscosity and a faint sweet smell in pure form. It is the main component of cyanoacrylate glues and can be encountered under many trade names . [ 2 ]

  5. Dimethylaminoethyl acrylate - Wikipedia

    en.wikipedia.org/wiki/Dimethylaminoethyl_acrylate

    When ethyl acrylate is used as a reactant, ethanol is formed; this forms with the ethyl acrylate an azeotrope of the composition ethanol/ethyl acrylate 72.7:26.3%, which boils at 77.5 °C under atmospheric pressure. [8] To achieve a high reaction yield, the ethanol is distilled off from the reaction mixture.

  6. Laboratory safety - Wikipedia

    en.wikipedia.org/wiki/Laboratory_safety

    Hazardous chemicals present physical and/or health threats to workers in clinical, industrial, and academic laboratories. Laboratory chemicals include cancer-causing agents (carcinogens), toxins (e.g., those affecting the liver, kidney, and nervous system), irritants, corrosives, sensitizers, as well as agents that act on the blood system or damage the lungs, skin, eyes, or mucous membranes.

  7. Acrylic acid - Wikipedia

    en.wikipedia.org/wiki/Acrylic_acid

    Ethyl acrylate was once used as synthetic food flavoring and was withdrawn by FDA possibly due to cancerogenic effects observed in lab animals. [13] Animal studies showed that high-doses of acrylic acid decreased weight gain. Acrylic acid can be converted to non-toxic lactic acid. [14] Acrylic acid is a constituent of tobacco smoke. [15]

  8. Health and safety hazards of nanomaterials - Wikipedia

    en.wikipedia.org/wiki/Health_and_safety_hazards...

    The health and safety hazards of nanomaterials include the potential toxicity of various types of nanomaterials, as well as fire and dust explosion hazards. Because nanotechnology is a recent development, the health and safety effects of exposures to nanomaterials, and what levels of exposure may be acceptable, are subjects of ongoing research.

  9. Poly(ethyl acrylate) - Wikipedia

    en.wikipedia.org/wiki/Poly(ethyl_acrylate)

    Poly(ethyl acrylate) (PEA) is a family of organic polymers with the formula (CH 2 CHCO 2 CH 2 CH 3) n. It is a synthetic acrylate polymer derived from ethyl acrylate monomer. The polymers are colorless. This homopolymer is far less important than copolymers derived from ethyl acrylate and other monomers.