3,3-Dimethylbutyryl Chloride TCI B1196

Chemical Identity

CAS No.: 7065-46-5
PubChem: CID 81514·SID 87564132
Formula: C6H11ClO
Molecular weight: 134.60 g/mol
Purity: >99.0%(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3,3-dimethylbutanoyl chloride
SMILES: CC(C)(C)CC(=O)Cl
InChIKey: BUTKIHRNYUEGKB-UHFFFAOYSA-N

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3,3-Dimethylbutyryl Chloride is a chemical compound widely used in organic reactions for the synthesis of complex molecules. It serves as a key building block in various chemical processes, particularly in the creation of both heterocyclic and non-heterocyclic compounds. This reagent is essential in laboratories where the development of new chemical structures is a priority. Its versatility makes it a valuable asset in synthetic chemistry, enabling researchers to explore a wide range of chemical transformations.

The compound's unique molecular structure, featuring an activated carboxyl group, makes it highly reactive in a variety of chemical reactions. It is particularly effective in Friedel-Crafts acylations, acyl transfer reactions, and esterification processes. Its solubility in organic solvents further enhances its utility, as it facilitates efficient separation and purification steps in laboratory workflows. These properties make it a preferred choice for chemists working on complex synthesis projects.

In Indonesian laboratories, 3,3-Dimethylbutyryl Chloride is commonly used in organic chemistry research, especially in the synthesis of complex compounds. It is also frequently employed in pharmaceutical and food chemistry projects due to its ability to participate in reactions that yield bioactive compounds. Its application spans across multiple research areas, supporting both academic and industrial chemical development efforts.

Related TCI products

Organic synthesis projects benefit from this compound's reactivity in acyl transfer and esterification reactions.
Pharmaceutical research utilizes it for the development of bioactive molecules through complex chemical transformations.
Food chemistry applications rely on its role in synthesizing compounds with specific functional properties.
It is ideal for Friedel-Crafts acylations due to its activated carboxyl group and reactivity.
Its solubility in organic solvents makes it suitable for purification and separation processes in chemical laboratories.

Brand	TCI
CAS number	7065-46-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid or solid, depending on supplier packaging
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 stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize inhalation risks. Avoid contact with incompatible materials such as strong bases or reducing agents. Proper personal protective equipment, including gloves and safety goggles, should always be worn when handling this substance. Regular monitoring of storage conditions is essential to ensure the integrity of the compound and the safety of laboratory personnel.

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