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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 ... 78.3 75.6: 90.8: 82.3 76.1: 93.2: 86.8 76.4: 94.2: 88.0 77.7: 98.4: 96.5 ...

4. Immediately dangerous to life or health - Wikipedia

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

   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, carcinogenic substance 64-17-5: 0044: Ethyl alcohol: 6237 mg/m 3: 3300 ppm: 64175 (10% Lower explosive limit LEL) 75-04-7: 1482: Ethylamine: 1110 mg/m 3: 600 ppm: 75047: 100-41-4: 0268: Ethyl ...

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. List of compounds with carbon number 4 - Wikipedia

   en.wikipedia.org/wiki/List_of_compounds_with...

   C 4 H 8 N 2 O 3: ethyl allophanate: 626-36-8 C 4 H 8 N 2 O 4 S 2: dithiodiglycolicdihydroxamic acid: 764-29-4 C 4 H 8 N 2 S: allylthiourea: 109-57-9 C 4 H 8 O: butanal: 123-72-8 C 4 H 8 O: cyclobutanol: 2919-23-5 C 4 H 8 O: cyclopropyl carbinol: 2516-33-8 C 4 H 8 O: cyclopropyl methyl ether: 540-47-6 C 4 H 8 O 2: butyric acid: 107-92-6 C 4 H 8 ...

7. 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.

8. Phenylacetaldehyde - Wikipedia

   en.wikipedia.org/wiki/Phenylacetaldehyde

   Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers. [1] Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds.

9. 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 ...