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CAS 31253-08-4

Ethyl 2-Iodopropionate TCI E1198

Ethyl 2-Iodopropionate TCI E1198

Chemical Identity

Other names
2-Iodopropionic Acid Ethyl Ester
CAS No.
31253-08-4
PubChem
CID 10922254·SID 354333693
Formula
C5H9IO2
Molecular weight
228.03 g/mol
Purity
>97.0%(GC)
Storage
<0°C
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
ethyl 2-iodopropanoate
SMILES
CCOC(=O)C(C)I
InChIKey
AVMMXNKUHBWIMU-UHFFFAOYSA-N
MDL
MDL02258628
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Ethyl 2-Iodopropionate is a chemical compound widely used in laboratory settings, particularly in organic synthesis reactions. It serves as a versatile reagent due to its functional groups, which include an iodide and an ester group. These groups contribute to its reactivity and make it suitable for various chemical transformations. In the laboratory, it is commonly employed in nucleophilic substitution reactions and polymerization processes, depending on the desired outcome of the experiment. Its ability to participate in multiple reaction types makes it a valuable tool for chemists working in both research and educational environments.

The compound's chemical properties make it a preferred choice for laboratory applications. Its iodide group provides electrophilic characteristics, enabling efficient substitution reactions under appropriate conditions. The ester functionality further enhances its reactivity, making it suitable for a range of synthetic pathways. Ethyl 2-Iodopropionate is stable under certain conditions but reacts vigorously with strong bases or organic solvents. These properties make it a reliable reagent for controlled chemical processes. Its versatility and reactivity are key factors in its widespread use across different laboratory disciplines.

In Indonesian laboratories, Ethyl 2-Iodopropionate is frequently used in organic chemistry research, especially in polymerization and the synthesis of complex compounds. It is also commonly utilized in higher education institutions for teaching purposes, where students gain hands-on experience with reactive organic compounds. The compound's role in both research and education underscores its importance in the chemical sciences within Indonesia.

TCI brochures (PDF)

  • Organic synthesis reactions where nucleophilic substitution and electrophilic reactivity are required.
  • Polymerization processes that benefit from the reactivity of iodide and ester functional groups.
  • Research in polymer science and macromolecular chemistry due to its compatibility with various reaction conditions.
  • Educational experiments focused on understanding the behavior of reactive organic compounds.
  • Development of new chemical compounds through controlled synthetic pathways involving iodinated esters.

Brand TCI
CAS number 31253-08-4
Molecular formula —
Purity —
Category Materials Science > Polymer/Macromolecule Reagents > Polymerization Reagents
Pack sizes Available in standard laboratory quantities as per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight and incompatible materials

Ethyl 2-Iodopropionate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to air and moisture. Due to its reactivity, it should be stored away from strong bases and organic solvents to avoid unwanted chemical interactions. Suitable containers for storage include glass or high-density polyethylene vessels that are resistant to chemical degradation. In laboratory settings, proper ventilation and personal protective equipment should be used when handling this compound to ensure safety. Regular monitoring of storage conditions is essential to maintain the integrity and effectiveness of the reagent.

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