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CAS 513-48-4

2-Iodobutane (stabilized with Copper chip) TCI B1093

2-Iodobutane (stabilized with Copper chip) TCI B1093

Chemical Identity

CAS No.
513-48-4
PubChem
CID 10559·SID 87564036
Formula
C4H9I
Molecular weight
184.02 g/mol
Purity
>98.0%(GC)
Reference databases
ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-iodobutane
SMILES
CCC(C)I
InChIKey
IQRUSQUYPCHEKN-UHFFFAOYSA-N
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2-Iodobutane (stabilized with Copper chip) is a chemical compound widely used in laboratory settings as a foundational building block for various organic synthesis reactions. Its simple molecular structure plays a crucial role in the formation of more complex chemical compounds. This reagent is particularly valuable in organic chemistry due to its reactivity and versatility in different types of chemical reactions. It is commonly employed in nucleophilic substitution, elimination, and addition reactions, making it an essential component in synthetic chemistry workflows.

The reactivity of 2-Iodobutane is largely attributed to the presence of iodine at the second carbon position, which provides a highly reactive site for chemical transformations. Iodine, being a halogen with high electron affinity, facilitates efficient and rapid chemical reactions. The stabilization with a copper chip enhances the compound’s stability, prolonging its shelf life and ensuring consistent performance in laboratory applications. This combination of reactivity and stability makes it a preferred choice for researchers and chemists.

In Indonesian laboratories, 2-Iodobutane is extensively used by chemists, students, and academic institutions for a wide range of experiments. Its ability to participate in various reaction mechanisms makes it indispensable in both educational and research environments. The compound is a key reagent in the development of new organic compounds and is frequently utilized in synthetic pathways that require high reactivity and controlled chemical transformations.

  • Organic synthesis reactions benefit from 2-Iodobutane due to its reactivity and ability to participate in nucleophilic substitution processes.
  • It is ideal for elimination reactions as it provides a stable and reactive iodinated carbon chain for efficient reaction pathways.
  • In addition, 2-Iodobutane is used in addition reactions where its iodine functionality enables selective and controlled chemical modifications.
  • Its versatility makes it suitable for educational purposes, allowing students to explore fundamental reaction mechanisms in organic chemistry.
  • The compound is also used in research settings to develop new synthetic methodologies and explore chemical transformation pathways.

Brand TCI
CAS number 513-48-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Liquid
Storage Store in a cool, dry place away from light and incompatible substances

2-Iodobutane should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed containers made of materials compatible with organic solvents to prevent evaporation and contamination. Due to its reactivity, it should be kept away from strong oxidizing agents and moisture. Always ensure proper ventilation when handling the compound to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is essential to maintain the compound's stability and effectiveness for laboratory use.

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