2-Iodopropane (stabilized with Copper chip) TCI I0069

Chemical Identity

CAS No.: 75-30-9
PubChem: CID 6362·SID 87571473
Formula: C3H7I
Molecular weight: 169.99 g/mol
Purity: >99.0%(GC)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-iodopropane
SMILES: CC(C)I
InChIKey: FMKOJHQHASLBPH-UHFFFAOYSA-N

Rp 769.650,00

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2-Iodopropane (stabilized with Copper chip) is a chemical compound widely used in laboratory settings for its reactivity and versatility. As a building block in organic chemistry, it plays a crucial role in the synthesis of various organic compounds. Its simple molecular structure allows it to participate in multiple chemical reactions, making it an essential tool for researchers. This compound is particularly valuable in reactions that require high reactivity and the ability to form complex molecules through functional group transformations.

The reactivity of 2-iodopropane is attributed to the presence of iodine, a highly electronegative halogen atom. This property makes it ideal for nucleophilic substitution and alkylation reactions. The inclusion of a copper chip as a stabilizer enhances its safety by reducing the risk of decomposition and uncontrolled reactions. This stabilization ensures that the compound remains stable during storage and use, making it a reliable choice for laboratory applications.

In Indonesian laboratories, 2-Iodopropane is commonly used in organic chemistry research, especially in universities and research institutions. Its role in synthesizing complex molecules and its stability under controlled conditions make it a preferred material for both academic and industrial research. The compound's ability to react with various functional groups supports its use in a wide range of chemical processes and experimental designs.

TCI brochures (PDF)

Alkylation Reagents for Ester Synthesis 2026-04-06 · p. 4

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Organic synthesis reactions benefit from 2-Iodopropane due to its reactivity and ability to form complex molecules through nucleophilic substitution.
Alkylation processes often utilize this compound as a versatile reagent for introducing alkyl groups into organic frameworks.
Research in functional group transformations relies on 2-Iodopropane for its capacity to participate in diverse chemical mechanisms.
Stability under controlled conditions makes it suitable for long-term storage and repeated use in experimental setups.
It is commonly used in academic settings for teaching and research in organic chemistry, supporting both theoretical and practical learning.

Brand	TCI
CAS number	75-30-9
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 direct sunlight

2-Iodopropane should be stored in a cool, dry place away from direct sunlight to maintain its stability. It is recommended to use sealed containers to prevent exposure to air and moisture. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. The presence of a copper chip as a stabilizer reduces the risk of decomposition, but care should still be taken to avoid contact with incompatible substances. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling to ensure laboratory safety.

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