tert-Butyllithium solution

1.3 M solution in pentane, MkSeal

Reagent Code: #88705
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Alias 3-Butyllithium
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CAS Number 594-19-4

science Other reagents with same CAS 594-19-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 64.06 g/mol
Formula C₄H₉Li
badge Registry Numbers
MDL Number MFCD00008795
thermostat Physical Properties
Boiling Point 36-40 °C
inventory_2 Storage & Handling
Density 0.69 g/mL at 20 °C
Storage 2~8°C, combustible area

description Product Description

Primarily used as a strong base and nucleophile in organic synthesis, this chemical is essential for deprotonation reactions, enabling the formation of carbon-carbon bonds. It is widely employed in the preparation of organolithium compounds, which serve as intermediates in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Additionally, it is utilized in polymerization processes, particularly in the production of styrenic and diene polymers, contributing to the development of high-performance materials. Its reactivity makes it a valuable reagent in metalation reactions, where it facilitates the introduction of functional groups into aromatic and heteroaromatic compounds. Due to its highly reactive nature, it is handled under inert conditions to ensure safety and efficacy in industrial and laboratory settings.

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Test Parameter Specification
Appearance Colorless to light yellow liquid
Concentration 1.3 M in heptane

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Size Availability Unit Price Quantity
inventory 500ml
10-20 days ฿26,600.00

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tert-Butyllithium solution
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Primarily used as a strong base and nucleophile in organic synthesis, this chemical is essential for deprotonation reactions, enabling the formation of carbon-carbon bonds. It is widely employed in the preparation of organolithium compounds, which serve as intermediates in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Additionally, it is utilized in polymerization processes, particularly in the production of styrenic and diene polymers, contributing to the development of high-performance materials. Its reactivity makes it a valuable reagent in metalation reactions, where it facilitates the introduction of functional groups into aromatic and heteroaromatic compounds. Due to its highly reactive nature, it is handled under inert conditions to ensure safety and efficacy in industrial and laboratory settings.
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