3-n-Octylthiophene TCI O0213

Chemical Identity

CAS No.: 65016-62-8
PubChem: CID 566852·SID 87574205
Formula: C12H20S
Molecular weight: 196.35 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-octylthiophene
SMILES: CCCCCCCCC1=CSC=C1
InChIKey: WQYWXQCOYRZFAV-UHFFFAOYSA-N

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3-n-Octylthiophene is a chemical compound widely used as a foundational building block in the synthesis of heterocyclic compounds. Its unique molecular structure consists of a thiophene ring linked to a nonyl alkyl chain, making it a versatile intermediate in organic chemistry. In laboratory settings, it plays a crucial role in the development of complex molecules with specific biological or chemical properties. This compound is particularly valuable for its ability to participate in various organic reactions, enabling the creation of compounds with tailored functionalities.

The reactivity of 3-n-Octylthiophene, combined with its capacity to bond with multiple functional groups, makes it a preferred choice for synthetic chemists. Its chemical stability under controlled conditions further enhances its utility in laboratory applications. However, it is sensitive to oxidation and light exposure, requiring careful handling and storage. These properties make it an essential component in the synthesis of bioactive compounds and materials with specialized chemical behavior.

In Indonesian laboratories, 3-n-Octylthiophene is commonly used in research focused on organic synthesis and the development of compounds with specific molecular interactions. Its application spans across various scientific fields, including pharmaceutical research and material science. The compound's structural versatility supports its use in creating molecules that can interact with proteins or participate in redox reactions, making it a key reagent in advanced chemical studies.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 2

Related TCI products

Organic synthesis of heterocyclic compounds due to its thiophene ring and alkyl chain structure.
Development of bioactive molecules for pharmaceutical research because of its reactivity and functional group compatibility.
Creation of materials with specific chemical properties for advanced material science applications.
Investigation of redox reactions as it can participate in electron transfer processes.
Synthesis of compounds that interact with proteins for biochemical and biotechnological studies.

Brand	TCI
CAS number	65016-62-8
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid or solid, depending on the specific formulation
Storage	Store in a cool, dark place away from oxidizing agents and light

3-n-Octylthiophene should be stored in a cool, dark environment to prevent oxidation and degradation. It is recommended to use airtight containers made of glass or inert polymer to minimize exposure to air and moisture. Due to its sensitivity to light, it should be kept in a closed container and stored away from direct sunlight. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. The compound should not be exposed to strong oxidizing agents or high temperatures to maintain its chemical integrity. Proper ventilation is also essential when working with this material to ensure a safe laboratory environment.

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