1.0M in hexanes for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping
Store at 2-8°C,Argon charged Ships Wet ice,FedEx DG Service Check lot-specific COA for exact specifications.
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Quality documents
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof
Cited in 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general
Description
Triethylborane can be used:As a radical initiator and terminator of free-radical reactions in aqueous media.(1)To synthesize polymers such as poly(2-substituted-1-propenylene)s by reacting with 2-substituted allylic arsonium ylides.(2)Catalyst for:Allylation of aldehydesDecarboxylative C-C bond cleavage reactionsRhenium hydride / boron Lewis acid cocatalysis of alkene hydrogenationsRegioselective hydroxyalkylation of unsaturated oxime ethersReactant for radical reductions of alkyl bromides withN-heterocyclic carbene boranesReactant for synthesis of tetramethylammonium trialkylphenylborate salts with oxidation potential
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