1-Iodoheptane (stabilized with Copper chip) TCI I0320

Chemical Identity

CAS No.: 4282-40-0
PubChem: CID 20274·SID 87571677
Formula: C7H15I
Molecular weight: 226.10 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-iodoheptane
SMILES: CCCCCCCI
InChIKey: LMHCYRULPLGEEZ-UHFFFAOYSA-N

Rp 557.550,00

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Berat 25g 500g

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1-Iodoheptane is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecular structures. As a building block, it serves as a fundamental component in the creation of larger, more intricate chemical compounds. This compound is essential in various laboratory processes, including nucleophilic substitution, coupling reactions, and alkylation. Its reactivity makes it a key player in organic chemistry research, enabling the formation of new chemical entities with precise structural control.

The unique properties of 1-Iodoheptane make it a preferred choice for laboratory applications. It is a stable yet reactive compound, with its iodide group being particularly reactive. The inclusion of a copper chip in the product enhances its stability during storage and usage, ensuring consistent performance. The compound is colorless and has a distinct odor, making it easily identifiable. Its resistance to degradation under normal laboratory conditions further supports its reliability in chemical synthesis.

In Indonesian laboratories, 1-Iodoheptane is extensively used in organic chemistry research conducted by universities and research institutions. It plays a vital role in projects related to synthetic chemistry, drug development, and material science. Its availability and reliability make it a standard reagent in many experimental setups, supporting both academic and industrial research efforts.

Related TCI products

Organic synthesis reactions benefit from 1-Iodoheptane due to its reactivity and ability to form new carbon-carbon bonds.
Coupling reactions often utilize this compound as a versatile alkylating agent, facilitating the formation of complex molecules.
Nucleophilic substitution reactions rely on 1-Iodoheptane's iodide group, which is highly reactive and suitable for substitution mechanisms.
Alkylation processes in synthetic chemistry use this compound to introduce alkyl groups into target molecules with high efficiency.
Research in drug development frequently incorporates 1-Iodoheptane for the synthesis of pharmaceutical intermediates and active compounds.

Brand	TCI
CAS number	4282-40-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Colorless liquid
Storage	—

1-Iodoheptane should be stored in a cool, dry, and well-ventilated area away from direct sunlight. It is recommended to use sealed containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its reactivity, it should be handled in a fume hood to minimize exposure. Avoid contact with moisture and incompatible substances such as strong oxidizing agents. Ensure proper labeling and storage conditions to maintain its stability and effectiveness in laboratory applications.

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