Lithium triethylborohydride
1.0 M solution in THF , MkSeal
- Product Code: 88698
Alias:
Lithium triethylborohydride solution; Lithium triethylborohydride
CAS:
22560-16-3
| Molecular Weight: | 105.94 g./mol | Molecular Formula: | C₆H₁₆BLi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00011703 | |
| Melting Point: | Boiling Point: | ||
| Density: | 0.892 g/mL at 25 °C | Storage Condition: | 2~8℃ |
Product Description:
Lithium triethylborohydride is widely used as a strong reducing agent in organic synthesis. It is particularly effective in the reduction of various functional groups, such as carbonyl compounds, including ketones and aldehydes, converting them into their corresponding alcohols. It is also employed in the reduction of esters, amides, and nitriles to their respective primary alcohols and amines. Additionally, it is utilized in the selective reduction of organohalides and epoxides, making it a valuable reagent in the preparation of complex organic molecules. Its high reactivity and selectivity make it a preferred choice in the synthesis of pharmaceuticals, fine chemicals, and other specialized organic compounds.
Product Specification:
| Test | Specification |
|---|---|
| CONCENTRATION | 0.95-1.1 |
| APPEARANCECOLOR | Colourless to light yellow |
| APPEARANCE | Clear slightly cloudy liquid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 100.000 | 10-20 days | €195.49 |
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| 500.000 | 10-20 days | €702.82 |
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Lithium triethylborohydride
Lithium triethylborohydride is widely used as a strong reducing agent in organic synthesis. It is particularly effective in the reduction of various functional groups, such as carbonyl compounds, including ketones and aldehydes, converting them into their corresponding alcohols. It is also employed in the reduction of esters, amides, and nitriles to their respective primary alcohols and amines. Additionally, it is utilized in the selective reduction of organohalides and epoxides, making it a valuable reagent in the preparation of complex organic molecules. Its high reactivity and selectivity make it a preferred choice in the synthesis of pharmaceuticals, fine chemicals, and other specialized organic compounds.
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