sec-Butyl bromide
98%
- Product Code: 122836
Alias:
2-bromobutane, 2-bromobutane, another butyl bromide, second butyl bromide, second butane bromide, sec-butyl bromide
CAS:
78-76-2
Molecular Weight: | 137.02 g./mol | Molecular Formula: | C₄H₉Br |
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EC Number: | 201-140-7 | MDL Number: | MFCD00000156 |
Melting Point: | -112 °C | Boiling Point: | 91 °C(lit.) |
Density: | 1.255 g/mL at 25 °C(lit.) | Storage Condition: | room temperature, flammable area |
Product Description:
Sec-butyl bromide is primarily used as an alkylating agent in organic synthesis, where it introduces the sec-butyl group into various molecules. It is commonly employed in the production of pharmaceuticals, agrochemicals, and other fine chemicals. The compound is also utilized in research and development for studying reaction mechanisms and developing new synthetic routes. Additionally, it serves as an intermediate in the manufacture of surfactants and specialty chemicals. Its reactivity makes it valuable in Grignard reactions and nucleophilic substitution processes.
Product Specification:
Test | Specification |
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Purity (GC) | 98 |
Refractive Index N20/D | 1.4355-1.4375 |
Specific Gravity (20/20 Degree Celsius) | 1.258-1.264 |
Appearance | Colorless To Yellow Brown Liquid |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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25.000 | 10-20 days | ฿350.00 |
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100.000 | 10-20 days | ฿590.00 |
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500.000 | 10-20 days | ฿1,960.00 |
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5000.000 | 10-20 days | ฿16,980.00 |
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sec-Butyl bromide
Sec-butyl bromide is primarily used as an alkylating agent in organic synthesis, where it introduces the sec-butyl group into various molecules. It is commonly employed in the production of pharmaceuticals, agrochemicals, and other fine chemicals. The compound is also utilized in research and development for studying reaction mechanisms and developing new synthetic routes. Additionally, it serves as an intermediate in the manufacture of surfactants and specialty chemicals. Its reactivity makes it valuable in Grignard reactions and nucleophilic substitution processes.
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