Search results
Results from the WOW.Com Content Network
Tin(II) 2-ethylhexanoate or tin(II) octoate or stannous octoate (Sn(Oct) 2) [1] is a compound of tin. Produced by the reaction of tin(II) oxide and 2-ethylhexanoic acid, it is a clear colorless liquid at room temperature, though often appears yellow due to impurities, likely resulting from oxidation of Sn(II) to Sn(IV).
This page was last edited on 31 December 2022, at 00:01 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
acid-base reactions: L n MOR' + RCO 2 H → L n MO 2 CR + R'OH protonolysis: L n Malkyl + RCO 2 H → L n MO 2 CR + alkane oxidative addition: L n M + RCO 2 H → L n (H)MO 2 CR. From preformed carboxylate, salt metathesis reactions are common: L n MCl + RCO 2 Na → L n MO 2 CR + NaCl. Metal carboxylates can be prepared by carbonation of ...
2-Ethylhexanoic acid (2-EHA), commonly known as octoic acid, [2] is the organic compound with the formula CH 3 (CH 2) 3 CH(C 2 H 5)CO 2 H. It is a carboxylic acid that is widely used to prepare lipophilic metal derivatives that are soluble in nonpolar organic solvents. 2-Ethylhexanoic acid is a colorless viscous oil. It is supplied as a racemic ...
Chromium(III) 2-ethylhexanoate, C 24 H 45 CrO 6, is a coordination complex of chromium and ethylhexanoate. In combination with 2,5-dimethylpyrrole it forms the Phillips selective ethylene trimerisation catalyst [ 3 ] (not to be confused with Phillips catalyst ), used in the industrial production of linear alpha olefins , particularly 1-hexene ...
Potassium 2-ethylhexanoate, also known as potassium iso-octanoate, is a chemical used to convert the tert-butylammmonium salt of clavulanic acid into potassium clavulanate (clavulanate potassium). [ citation needed ] It is also used as a corrosion inhibitor in automotive antifreeze [ citation needed ] and as a catalyst for polyurethane systems.
Hydroxyl aluminium bis(2-ethylhexanoate) P. Potassium 2-ethylhexanoate; T. Tin(II) 2-ethylhexanoate
Dibutylmagnesium can be obtained by reaction of butyllithium with magnesium butylchloride and subsequent addition of magnesium 2-ethylhexanoate. [3] The compound can also be prepared by hydrogenation of magnesium, followed by reaction with 1-butene. [1]