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  2. Ethyl acetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acetate

    Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.

  3. Ethyl acetate (data page) - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acetate_(data_page)

    for Ethyl Acetate/Acetic acid [3] P = 740 mmHg BP Temp. °C % by mole C 4 H 8 O 2; liquid vapor 117.07: 0.0: ... 78.3 75.6: 90.8: 82.3 76.1: 93.2: 86.8 76.4: 94.2: 88 ...

  4. File:Ethyl-acetate-2D-skeletal.svg - Wikipedia

    en.wikipedia.org/wiki/File:Ethyl_acetate2.svg

    Skeletal formula of ethyl acetate. CAS ® Registry Number: 141-78-6. Image generated in ChemDraw Professional 22.2 and converted into SVG file using Scribus 1.5.4 + Inkscape 1.2.1 (drawn according to official Manual of Style guidelines) Date: 27 January 2024: Source: Own work: Author: Chem Sim 2001: Permission (Reusing this file)

  5. Ethyl acetoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acetoacetate

    At large scale, ethyl acetoacetate is industrially produced by treatment of diketene with ethanol. [2] The small scale preparation of ethyl acetoacetate is a classic laboratory procedure. [3] It involves Claisen condensation of ethyl acetate. Two moles of ethyl acetate condense to form one mole each of ethyl acetoacetate and ethanol. [4]

  6. Immediately dangerous to life or health - Wikipedia

    en.wikipedia.org/wiki/Immediately_dangerous_to...

    141-43-5: 0152: Ethanolamine: 75 mg/m 3: 30 ppm: 141435: 110-80-5: 0060: 2-Ethoxyethanol: 1845 mg/m 3: 500 ppm: 110805: 111-15-9: 0364: 2-Ethoxyethyl acetate: 2705 mg/m 3: 500 ppm: 111159: 141-78-6: 0367: Ethyl acetate: 7200 mg/m 3: 2000 ppm: 141786 (10% Lower explosive limit LEL) 140-88-5: 0267: Ethyl acrylate: 1227 mg/m 3: 500 ppm: 140885 ...

  7. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

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  9. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

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