Acrylic acid 2-ethyl hexyl ester

Compound Name Ethylene Diamine Tetracetic Acid Ethylene Oxide Ethyl Acetate Ethyl Ether Ethyl Formate Ethyl Formate Ethylhexaldehyde Ethylhexaldehyde Ethylhexaldehyde 2-Ethyl Hexanol 2-Ethyl Hexanol 2-Ethyl-3-Propylacbolein 2-Ethylhexyl Acrylate, Inhibited 2-Ethyl Hexanol 2-Ethylhexyl Acrylate, Inhibited Ethyl Hexyl Tallate 2,4,5-T(esters)... 

The earliest industrial developments of acrylic acid - 1.051mp = 13.5°C, bp,.013 = 141.6°C) date from 1925/1930. It is largely used as an intermediate in the manufacture of low molecular weight esters, especially the ethyl, butyl and 2-ethyl hexyl acrylates. As a rule, the same synthesis methods, with slight variations, serve to produce the add itself, or its esters directly. The most widespread and most economical, based on propylene conversion, nevertheless requires the intermediate production of acrylic add before obtaining its derivatives by esterification, in a distinct step. 

Hexanoic acid 1-Hexanok acid n-Hexanoic acid. See Caproic acid Hexanoic acid, 2-ethyl-, cobalt (2+) salt See Cobalt octoate Hexanoic acid, 2-ethyl-, hexadecyl ester. See Cetyl octanoate Hexanoic acid, 2-ethyl-, zinc salt See Zinc 2-ethylhexanoate Hexanol 1-Hexanol Hexan-1-ol n-Hexanol. See Hexyl alcohol 6-Hexanolactone. Seee-Caprolactone monomer 1-Hexanol, 2-ethyl. See2-Ethylhexanol 1-Hexanol, 2-etl l-, acrylate. See Octyl aciylate 1-Hexanol, 2-etl -, phosphate. SeeTrioclyl phosphate 1-Hexanol, 2-etl -, sebacate. See Dioctyl sebacate... 

Ethylhexyl phosphonic acid, mono 2-ethylhexyi ester. See 2-Ethyi hexyl 2-ethyl hexyl phosphonate Ethylhexyl phthalate 2-Ethylhexyl phthalate. See s-Dioctyl phthalate 2-Ethylhexyl propenoate 2-Ethylhexyl 2-propenoate. See Octyl acrylate... 

A wide variety of other specialty monomers are also used to provide specialized performance properties for coating applications. For example, amine functional monomers can be used to improve adhesion to aged alkyd substrates. Specialized monomers can also be used to improve exterior durability, for example VEOVA (vinyl ester of vesatic acid) monomers can improve the hydrolysis resistance of vinyl acetate polymers, and n-butyl methacrylate can be used to enhance the durabiHty of BA-MMA acrylics. Polymer hydrophobicity can be fine tuned by varying the levels of hydrophobic and hydrophilic monomers in the composition and styrene or ethyl hexyl acrylate are used to increase film hydrophobicity and reduce water permeability in BA-MMA systems. Specialty monomers are also used to provide specific chemical functionality to polymer compositions. For example, hydroxyethyl methacrylate can be used to provide hydroxyl functionality to acrylic resins, allowing these polymers to be used in cross-linkable thermoset coatings which cure via melamine chemistry. While specialty monomers are used at relatively low levels in polymer compositions, they frequently provide the performance features needed for the successful application of emulsion polymers in many coating areas. 

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