1-Iodobutane
Pharmaceutical Grade
- Product Code: 123022
Alias:
Iodobutane; 1-iodobutane, iodobutane, butyl iodide, iodobutane, n-butyl iodide
CAS:
542-69-8
| Molecular Weight: | 184.02 g./mol | Molecular Formula: | C₄H₉I |
|---|---|---|---|
| EC Number: | 208-824-4 | MDL Number: | MFCD00001098 |
| Melting Point: | −103 °C(lit.) | Boiling Point: | 130-131 °C(lit.) |
| Density: | 1.617 g/mL at 25 °C(lit.) | Storage Condition: | room temperature, flammable area, dry |
Product Description:
1-Iodobutane is primarily used in organic synthesis as an alkylating agent, where it introduces the butyl group into various chemical compounds. It is commonly employed in the preparation of pharmaceuticals, agrochemicals, and other organic intermediates. In research laboratories, it serves as a reagent for nucleophilic substitution reactions, particularly in the formation of carbon-carbon bonds. Additionally, it is utilized in the synthesis of organometallic compounds, such as Grignard reagents, which are essential in creating complex organic molecules. Its role in the production of surfactants and lubricant additives also highlights its industrial significance.
Product Specification:
| Test | Specification |
|---|---|
| Acidity | 0-0.05% |
| Ignition Residue (As Sulfate) | 0-0.01% |
| Refractive Index N20/D | 1.497-1.501 |
| Specific Gravity (20/20 Degree Celsius) | 1.613-1.618 |
| Purity | 97-100 |
| Boiling Range | 128-131 |
| Infrared Spectrum | Conforms To Structure |
| Appearance | Colorless To Light Yellow To Yellow To Light Orange To Light Pink Liquid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 50.000 | 10-20 days | $36.00 |
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| 100.000 | 10-20 days | $66.01 |
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| 2500.000 | 10-20 days | $1,615.96 |
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1-Iodobutane
1-Iodobutane is primarily used in organic synthesis as an alkylating agent, where it introduces the butyl group into various chemical compounds. It is commonly employed in the preparation of pharmaceuticals, agrochemicals, and other organic intermediates. In research laboratories, it serves as a reagent for nucleophilic substitution reactions, particularly in the formation of carbon-carbon bonds. Additionally, it is utilized in the synthesis of organometallic compounds, such as Grignard reagents, which are essential in creating complex organic molecules. Its role in the production of surfactants and lubricant additives also highlights its industrial significance.
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