Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

2-Ethylhexanoate

Leaded tin bronze Leaded tin bronzes Leaded yellow brass Leaded zinc oxide Lead 2-ethylhexanoate... [Pg.557]

This group of aluminum carboxylates is characterized mainly by its abiUty to gel vegetable oils and hydrocarbons. Again, monocarboxylate, dicarboxylate, and tricarboxylate salts are important. The chemical, physical, and biological properties of the various types of aluminum stearates have been reviewed (29). Other products include aluminum palmitate and aluminum 2-ethylhexanoate (30). [Pg.143]

Dibutyltin and dioctyltin diacetate, dilaurate, and di-(2-ethylhexanoate) are used as catalysts for the curing of room-temperature-vulcanized (RTV) sihcone elastomers to produce flexible siUcone mbbers used as sealing compounds, insulators, and in a wide variety of other appHcations. Diorganotin carboxylates also catalyze the curing of thermosetting siHcone resins, which are widely used in paper-release coatings. [Pg.74]

Sta.nnous2-Ethylhexa.noa.te, Stannous 2-ethyIhexanoate, Sn(CgH 302)2 (sometimes referred to as stannous octanoate, mol wt 405.1, sp gr 1.26), is a clear, very light yellow, and somewhat viscous Hquid that is soluble in most organic solvents and in siHcone oils (166). It is prepared by the reaction of stannous chloride or oxide with 2-ethylhexanoic acid. [Pg.75]

Ethylhexanal, the reduced aldol condensation product of //-butyraldehyde, is converted into 2-ethylhexanoic acid [149-57-5] which is converted primarily into salts or metal soaps. These are used as paint driers and heat stabili2ers for poly(vinyl chloride). [Pg.379]

Many substituted, ie, branched, fatty acids, particularly methacryUc, 2-ethylhexanoic, and ricinoleic acids, are commercially significant. Several substituted fatty acids exist naturally (Table 5). Fatty acids with a methyl group in the penultimate position are called iso acids, and those with a methyl group in the antepenultimate position are called anteiso acids (1) (see Carboxylic acids, branched-CHAIN acids). However, the term iso is often used in a broader sense to mean branched or mixtures of branched-chain industrial acids. [Pg.80]

Some of the more prominent carboxyhc acids that are not fat- or oil-based include acetic, acryUc, and olefin-based propionic, butyric/isobutyric, 2-ethylhexanoic, heptanoic, pelargonic, neopentanoic, and neodecanoic. Table 1 summarizes the production, pricing, and primary producers of these acids. [Pg.94]

Butyric acid is made by air-oxidation of butyraldehyde, which is obtained by appHcation of the oxo synthesis to propylene. Isobutyric acid is made from isobutyraldehyde, a significant product in the synthesis of butyraldehyde (see Butyraldehydes). Butyraldehyde is also used to make 2-ethylhexanoic acid. [Pg.94]

Octoates were the next drier development. Because these driers are produced from synthetic 2-ethylhexanoic acid, the chemical composition can be controlled and uniformity assured. Also, other synthetic acids, eg, isononanoic and neodecanoic, became available and are used for metal soap production. Compared to naphthenic acid, these synthetic acids have high acid values, are more uniform, lighter in color, and do not have its characteristic odor. It is also possible to produce metal soaps with much higher metal content by using synthetic acids. [Pg.217]

Pd(Ph3P)4, RS02Na, CH2CI2 or THF/MeOH, 70-99% yield. These conditions were shown to be superior to the use of sodium 2-ethylhexanoate. Methallyl, crotyl, and cinnamyl ethers, the Alloc group, and allylamines are all efficiently cleaved by this method. ... [Pg.72]

Pd(Ph3P)4, 2-ethylhexanoic acid or barbituric acid (THF, 3 h, 93% yield). Tributylstannane can serve as an allyl scavenger. ... [Pg.410]


See other pages where 2-Ethylhexanoate is mentioned: [Pg.821]    [Pg.595]    [Pg.35]    [Pg.88]    [Pg.88]    [Pg.113]    [Pg.147]    [Pg.152]    [Pg.184]    [Pg.234]    [Pg.234]    [Pg.382]    [Pg.382]    [Pg.525]    [Pg.557]    [Pg.573]    [Pg.592]    [Pg.803]    [Pg.925]    [Pg.937]    [Pg.1086]    [Pg.1090]    [Pg.546]    [Pg.35]    [Pg.73]    [Pg.75]    [Pg.420]    [Pg.10]    [Pg.76]    [Pg.480]    [Pg.481]    [Pg.81]    [Pg.219]    [Pg.221]    [Pg.261]    [Pg.248]    [Pg.332]    [Pg.374]    [Pg.821]   
See also in sourсe #XX -- [ Pg.69 ]

See also in sourсe #XX -- [ Pg.69 ]

See also in sourсe #XX -- [ Pg.274 ]




SEARCH



2-Ethylhexanoic acid

2-Ethylhexanoic acid chloride

2-Ethylhexanoic acid structure

2-Ethylhexanoic acid, sodium salt

2-Ethylhexanoic add

Catalyst stannous 2-ethylhexanoate

Cobalt 2-ethylhexanoate as reagen

Copper 2-ethylhexanoate

Epichlorohydrin with 2-ethylhexanoic acid, reaction

Ethylene glycol 2-Ethylhexanoic acid

Iron 2-ethylhexanoate

Lead 2-ethylhexanoate

Neodymium 2-ethylhexanoate

Nickel 2-ethylhexanoate

Nickel 2-ethylhexanoate aromatization

Nickel 2-ethylhexanoate catalysts

Nickel 2-ethylhexanoate oxidation

Nickel 2-ethylhexanoate/triethylaluminum

Potassium 2-ethylhexanoate

Resolutions 2-amino-2-ethylhexanoic acid

Sn 2-ethylhexanoate

Sodium 2-ethylhexanoate

Stannous 2-ethylhexanoate

Tert-butyl peroxy-2-ethylhexanoate

Tin 2-ethylhexanoate

Zinc 2-ethylhexanoate

Zirconium 2-ethylhexanoate

© 2024 chempedia.info