Lithium tert-butoxide
99%
- Product Code: 88729
Alias:
Lithium tert-butoxide
CAS:
1907-33-1
Properties:
Easy to absorb moisture
| Molecular Weight: | 80.05 g./mol | Molecular Formula: | C₄H₉LiO |
|---|---|---|---|
| EC Number: | 217-611-5 | MDL Number: | MFCD00050479 |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Lithium tert-butoxide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions. It is highly effective in generating carbanions from weakly acidic compounds, making it valuable in the formation of carbon-carbon bonds. This chemical is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it serves as a catalyst or reagent in various polymerization processes, aiding in the production of specialized polymers. Its sterically hindered nature also makes it useful in selective reactions where less bulky bases might lead to unwanted side products.
Product Specification:
| Test | Specification |
|---|---|
| CA | 0-0.01 |
| LI2CO3LIOH LIOH | 0-0.8 |
| IRONFE | 0 0.001% |
| PB | 0-0.005 |
| Purity | 98.5 101.5% |
| APPEARANCE | White or light yellow powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 25.000 | 10-20 days | Ft8,188.32 |
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| 100.000 | 10-20 days | Ft28,982.35 |
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| 500.000 | 10-20 days | Ft124,979.65 |
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| 2500.000 | 10-20 days | Ft511,877.87 |
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Lithium tert-butoxide
Lithium tert-butoxide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions. It is highly effective in generating carbanions from weakly acidic compounds, making it valuable in the formation of carbon-carbon bonds. This chemical is commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it serves as a catalyst or reagent in various polymerization processes, aiding in the production of specialized polymers. Its sterically hindered nature also makes it useful in selective reactions where less bulky bases might lead to unwanted side products.
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