3,5,5-Trimethylhexanoyl Chloride TCI T0951

Chemical Identity

CAS No.: 36727-29-4
PubChem: CID 161929·SID 87576766
Formula: C9H17ClO
Molecular weight: 176.68 g/mol
Purity: >90.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3,5,5-trimethylhexanoyl chloride
SMILES: CC(CC(=O)Cl)CC(C)(C)C
InChIKey: GEKPNPPFAYJZRD-UHFFFAOYSA-N

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Volume 25mL

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3,5,5-Trimethylhexanoyl Chloride is a chemical compound widely used in organic laboratory reactions. It serves as a key reagent in various synthetic processes, particularly in the construction of complex organic molecules. This compound is part of the building blocks category, which includes essential components for the synthesis of more intricate chemical structures. Its versatility makes it a valuable tool for chemists working on a range of experimental applications.

The compound’s reactivity and structural features make it a preferred choice in laboratory settings. Its long carbon chain and chlorinated end group contribute to its ability to participate in nucleophilic substitution reactions and ester formation. These properties allow it to act as a source of the carboxyl group, enabling it to react with a variety of other reagents. Its high reactivity ensures that it can be effectively utilized in multiple synthetic pathways.

In Indonesian laboratories, 3,5,5-Trimethylhexanoyl Chloride is commonly used in organic chemistry research. It plays a significant role in the synthesis of complex compounds and the development of new materials. Many research institutions and universities rely on this compound to meet the demands of their experimental needs. Its consistent performance and reliability make it a trusted choice for both academic and industrial research.

Related TCI products

Organic synthesis applications benefit from this compound’s ability to participate in nucleophilic substitution reactions, enabling the formation of complex molecular structures.
Ester formation processes utilize its carboxyl group, making it ideal for creating ester derivatives in various chemical reactions.
Carbon chain extension reactions are supported by its long carbon backbone, allowing for the construction of more complex organic molecules.
Reagent compatibility in synthetic pathways is enhanced due to its reactivity with a wide range of functional groups.
Research in material development leverages its structural versatility for the creation of new chemical compounds and polymers.

Brand	TCI
CAS number	36727-29-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid
Storage	Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could lead to degradation. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with incompatible substances such as strong bases or reactive metals. Always wear appropriate personal protective equipment, including gloves and safety goggles, when handling this material. Proper storage and handling ensure the safety of laboratory personnel and the effectiveness of the compound in experimental applications.

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