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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.
As of 2022, Jubilant Ingrevia is the world's lowest cost producer of pyridine-based derivative products, one of the two producers of pyridine and a leader in 14 pyridine derivatives. [17] The company is one of the two largest manufactures of Vitamin B3 globally, one of India's largest manufactures of Vitamin B4 , one of the two largest ...
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Ethyl acetate is usually the original solvent for nail polish itself. Acetonitrile has been used as a nail polish remover, but it is more toxic than the aforementioned options. It has been banned in the European Economic Area for use in cosmetics since 17 March 2000.
A specially denatured alcohol is a combination of ethanol and another chemical substance, e.g., ethyl acetate in SDA 29, 35, and 35A, added to render the mixture unsuitable for drinking. [12] SDAs are often used in cosmetic products, and can also be used in chemical manufacturing, pharmaceuticals, and solvents. [13]
Organized crime groups operating in East and Southeast Asia have demonstrated significant sophistication in recent years, as well as their comparative advantage when it comes to sourcing precursors and specialized non-controlled precursor and pre-precursor chemicals for the illicit manufacture of drugs. [4]
Saponification is a process of cleaving esters into carboxylate salts and alcohols by the action of aqueous alkali.Typically aqueous sodium hydroxide solutions are used. [1] [2] It is an important type of alkaline hydrolysis.
The dianion of ethyl acetoacetate is also a useful building block, except that the electrophile adds to the terminal carbon. The strategy can be depicted in the following simplified form: [6] CH 3 C(O)CHNaCO 2 C 2 H 5 + BuLi → LiCH 2 C(O)CHNaCO 2 C 2 H 5 + BuH (Bu = butyl) Reduction of ethyl acetoacetate gives ethyl 3-hydroxybutyrate. [8]