Butyllithium (abbreviated n-BuLi) is the most prominent organolithium reagent. It enjoys wide use as a polymerisation initiator in the production of elastomers such as polybutadiene or styrene-butadiene-styrene (SBS).
Butyllithium is commercially available as solutions (15%, 25%, 2 M, 2.5 M, 10 M, etc.) in alkanes such as pentane, hexanes, and heptanes or in ethers as diethyl ether and THF.
Butyllithium is commercially available as solutions (15%, 25%, 2 M, 2.5 M, 10 M, etc.) in alkanes such as pentane, hexanes, and heptanes or in ethers as diethyl ether and THF.
Butyllithium is commercially available as solutions (15%, 25%, 2 M, 2.5 M, 10 M, etc.) in alkanes such as pentane, hexanes, and heptanes or in ethers as diethyl ether and THF.
Butyllithium is commercially available as solutions (15%, 25%, 2 M, 2.5 M, 10 M, etc.) in alkanes such as pentane, hexanes, and heptanes or in ethers as diethyl ether and THF.
sec-Butyllithium is the chemical compound with the formula CH3CHLiCH2CH3, abbreviated sec-BuLi or s-BuLi This organolithium reagent is used as a source of sec-butyl carbanion in organic synthesis.[
sec-Butyllithium is the chemical compound with the formula CH3CHLiCH2CH3, abbreviated sec-BuLi or s-BuLi This organolithium reagent is used as a source of sec-butyl carbanion in organic synthesis.[
sec-Butyllithium is the chemical compound with the formula CH3CHLiCH2CH3, abbreviated sec-BuLi or s-BuLi This organolithium reagent is used as a source of sec-butyl carbanion in organic synthesis.[
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