tert-Butyl bromide
>98.0%(GC)
- Product Code: 122832
Alias:
tert-butyl bromide; 2-bromo-2-methylpropane, trimethylbromomethane, tert-butyl bromide, tert-butyl bromide, tert-butyl bromide, 2-methyl-2-bromopropane
CAS:
507-19-7
| Molecular Weight: | 137.02 g./mol | Molecular Formula: | C₄H₉Br |
|---|---|---|---|
| EC Number: | 208-065-9 | MDL Number: | MFCD00000125 |
| Melting Point: | -20 °C | Boiling Point: | 72 °C |
| Density: | 1.22 g/mL at 20 °C(lit.) | Storage Condition: | room temperature, flammable area |
Product Description:
Used primarily as an alkylating agent in organic synthesis, it introduces the tert-butyl group into various compounds. It is commonly employed in the production of pharmaceuticals, agrochemicals, and specialty chemicals. In research, it serves as a reagent for creating complex molecules and studying reaction mechanisms. Additionally, it is utilized in the preparation of polymers and as an intermediate in the synthesis of other organic compounds. Its reactivity makes it valuable in nucleophilic substitution reactions, particularly in the formation of carbon-carbon bonds.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 98-100 |
| Refractive Index N20/D | 1.426-1.429 |
| Appearance | Colorless To Orange Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | Ft3,232.23 |
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| 25.000 | 10-20 days | Ft7,757.36 |
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| 100.000 | 10-20 days | Ft22,948.85 |
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| 500.000 | 10-20 days | Ft81,775.48 |
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| 2500.000 | 10-20 days | Ft400,796.82 |
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tert-Butyl bromide
Used primarily as an alkylating agent in organic synthesis, it introduces the tert-butyl group into various compounds. It is commonly employed in the production of pharmaceuticals, agrochemicals, and specialty chemicals. In research, it serves as a reagent for creating complex molecules and studying reaction mechanisms. Additionally, it is utilized in the preparation of polymers and as an intermediate in the synthesis of other organic compounds. Its reactivity makes it valuable in nucleophilic substitution reactions, particularly in the formation of carbon-carbon bonds.
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