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Iodobutane - 542-69-8

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ID: 2111

Product Description: Iodobutane

Synonym: butyl iodide

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CAS Number: 542-69-8

EC Number: 208-824-4

MDL: MFCD00001098

Beilstein: 1420755

MF: C4H9I

MW: 184.02

MOQ: 1kg

Minimum Purity: 98%

Pubchem: 10962

InChi Key: KMGBZBJJOKUPIA-UHFFFAOYSA-N

InChi: 1S/C4H9I/c1-2-3-4-5/h2-4H2,1H3

SMILES: CCCCI

Iodobutane

Iodobutane — also known as butyl iodide — is available for purchase from Iofina. This organic compound has various uses in experiments and applications as an alkylating agent in organic synthesis.

What Is Iodobutane?

Iodobutane is a high-purity alkyl halide used in organic synthesis, pharmaceuticals and chemical research. The Chemical Abstracts Service (CAS) number of iodobutane is 542-69-8, and it’s available in multiple isomeric forms — 1-iodobutane (n-butyl iodide) is the most common. This form offers excellent reactivity for alkylation and Grignard reactions.

Safety is essential when handling iodobutane due to its toxicity, volatility and potential environmental impact. It can irritate the eyes, skin and respiratory system if inhaled, swallowed or absorbed through the skin. 

Iodobutane/Butyl Iodide Applications

Iodobutane is a colorless to pale yellow liquid with a high density and relatively high boiling point around 130 degrees Celsius (266 degrees Fahrenheit), making it useful in a variety of chemical reactions requiring efficient alkylation. Key applications include:

  • Organic synthesis and alkylation reactions: Iodobutane is widely used as an alkylating agent to introduce butyl groups into various organic molecules, making it essential for chemical synthesis.
  • Grignard reagent formation: It serves as a precursor in Grignard reactions, where it reacts with magnesium to produce butyl magnesium iodide, an important reagent in organic chemistry. 
  • Pharmaceutical and agrochemical development: Iodobutane is the synthesis of active pharmaceutical ingredients (APIs) and agrochemicals, helping to create new medicinal and crop-protection compounds. 
  • Production of esters and ethers: This compound plays a key role in Williamson ether synthesis, where it reacts with alkoxides to form ethers and produces butyl esters in esterification processes. 
  • Material science and surface modification: Researchers use iodobutane to modify the surface properties of materials, improving their chemical compatibility and performance in specialized applications. 
  • Research and development: Iodobutane is a valuable reagent in laboratories for studying reaction mechanisms and synthesizing novel organic molecules. 

Why Choose Iofina?

At Iofina, we specialize in the exploration, extraction and manufacturing of iodine and its derivatives for industries worldwide. Our advanced technology ensures a reliable supply of high-quality iodine products, including customized iodides for specific applications. Unlike destructive extraction methods, we use an eco-friendly approach, partnering with oil companies to recover iodine from pre-drilled sites. As a leading producer in North America, we serve global markets in health, biocides, acetic acid manufacturing and more. We offer expert technical support and sustainable solutions for businesses globally. 

Get Our Specialized Line of Iodides, Chlorides, and Fluorides for Your Business Today!

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