Lithium amide
95%
- Product Code: 88737
Alias:
lithium amide
CAS:
7782-89-0
| Molecular Weight: | 22.96 g./mol | Molecular Formula: | LiNH₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00011093 | |
| Melting Point: | 373 °C | Boiling Point: | 430 °C |
| Density: | 1.178 g/mL | Storage Condition: | room temperature |
Product Description:
Lithium amide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is employed in the preparation of lithium enolates from carbonyl compounds, which are key intermediates in aldol reactions and other carbon-carbon bond-forming processes. In the pharmaceutical industry, it plays a crucial role in the synthesis of complex molecules, including active pharmaceutical ingredients (APIs). Additionally, it is utilized in the production of specialty chemicals, such as polymers and agrochemicals, where precise control over reactivity is essential. Its ability to act as a nucleophile also makes it valuable in the synthesis of organometallic compounds.
Product Specification:
| Test | Specification |
|---|---|
| PURITY TITRATION BY NAOH | 94 106% |
| Appearance | White to off-white powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft3,232.23 |
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| 5.000 | 10-20 days | Ft9,481.22 |
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| 25.000 | 10-20 days | Ft24,780.45 |
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| 100.000 | 10-20 days | Ft79,081.95 |
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Lithium amide
Lithium amide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is employed in the preparation of lithium enolates from carbonyl compounds, which are key intermediates in aldol reactions and other carbon-carbon bond-forming processes. In the pharmaceutical industry, it plays a crucial role in the synthesis of complex molecules, including active pharmaceutical ingredients (APIs). Additionally, it is utilized in the production of specialty chemicals, such as polymers and agrochemicals, where precise control over reactivity is essential. Its ability to act as a nucleophile also makes it valuable in the synthesis of organometallic compounds.
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