tert-Butyllithium solution
1.3 M solution in pentane, MkSeal
- Product Code: 88705
Alias:
3-Butyllithium
CAS:
594-19-4
| Molecular Weight: | 64.06 g./mol | Molecular Formula: | C₄H₉Li |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00008795 | |
| Melting Point: | Boiling Point: | 36-40 °C | |
| Density: | 0.69 g/mL at 20 °C | Storage Condition: | 2~8°C, combustible area |
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.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to light yellow liquid |
| CONCENTRATION | 1.3M in heptane |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 500.000 | 10-20 days | $1,104.67 |
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tert-Butyllithium solution
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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