1-Iodo-2-methylbutane (stabilized with Copper chip)
≥95%(GC)
- Product Code: 68097
CAS:
616-14-8
| Molecular Weight: | 198.05 g./mol | Molecular Formula: | C₅H₁₁I |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01321177 | |
| Melting Point: | Boiling Point: | 148°C | |
| Density: | 1.51 | Storage Condition: | Room temperature, dry, inert gas storage |
Product Description:
Used primarily as an alkylating agent in organic synthesis, it facilitates the introduction of the 2-methylbutyl group into various molecules. It is particularly valuable in the preparation of complex organic compounds, including pharmaceuticals and agrochemicals. The stabilization with copper chips prevents the formation of iodine, ensuring the reagent's stability and effectiveness during reactions. It is also employed in nucleophilic substitution reactions, where it acts as a source of the 2-methylbutyl cation. Additionally, it finds use in research and development laboratories for exploring new chemical reactions and pathways.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Brown clear liquid |
| PURITYGC | 95-100 |
| SPECIFIC GRAVITY 2020 | 1.5040-1.5160 |
| Refractive index n20D | 1.4940-1.4980 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,520.00 |
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| 5.000 | 10-20 days | ฿6,660.00 |
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1-Iodo-2-methylbutane (stabilized with Copper chip)
Used primarily as an alkylating agent in organic synthesis, it facilitates the introduction of the 2-methylbutyl group into various molecules. It is particularly valuable in the preparation of complex organic compounds, including pharmaceuticals and agrochemicals. The stabilization with copper chips prevents the formation of iodine, ensuring the reagent's stability and effectiveness during reactions. It is also employed in nucleophilic substitution reactions, where it acts as a source of the 2-methylbutyl cation. Additionally, it finds use in research and development laboratories for exploring new chemical reactions and pathways.
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