Stearoyl Chloride TCI S0404

Chemical Identity

CAS No.: 112-76-5
PubChem: CID 8212·SID 87575907
Formula: C18H35ClO
Molecular weight: 302.9 g/mol
Purity: >96.0%(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: octadecanoyl chloride
SMILES: CCCCCCCCCCCCCCCCCC(=O)Cl
InChIKey: WTBAHSZERDXKKZ-UHFFFAOYSA-N

Rp 1.881.600,00

~~Rp 1.331.400,00~~ Rp 1.881.600,00

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Berat 25g 250g

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Stearoyl Chloride (TCI S0404), with CAS number 112-76-5, is a chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. It serves as a key building block in chemical reactions, particularly in substitution and esterification processes. Its reactivity and versatility make it an essential reagent for organic chemists. This compound is commonly used in the preparation of esters and amides, which are fundamental in various chemical applications. Its ability to undergo chemical modifications makes it a valuable tool in synthetic chemistry.

Stearoyl Chloride is preferred due to its high reactivity and stability under controlled conditions. The presence of a chlorinated group at the end of the carbon chain allows it to react readily with bases, alcohols, and other functional groups. This reactivity enables it to participate in a wide range of chemical transformations, making it suitable for both research and industrial applications. Its stability ensures that it remains effective during synthesis processes, reducing the risk of degradation. These properties make it a reliable and efficient reagent in laboratory environments.

In Indonesian laboratories, Stearoyl Chloride is frequently used in organic chemistry research, particularly in pharmaceutical and material science fields. It plays a crucial role in the development of new drugs, polymers, and industrial chemicals. Its availability and consistent quality make it a preferred choice for researchers and chemists. The compound's ability to facilitate molecular modifications supports its widespread use in chemical synthesis and innovation.

TCI brochures (PDF)

Lipids 2025-12-17 · p. 7

Related TCI products

Organic synthesis applications benefit from Stearoyl Chloride due to its reactivity and ability to form esters and amides, which are essential in drug development and polymer science.
In pharmaceutical research, it is used to modify molecular structures, enabling the creation of new compounds with desired biological properties.
Material science laboratories utilize it for the synthesis of polymers and other advanced materials, leveraging its reactivity for functional group incorporation.
Industrial chemical production relies on Stearoyl Chloride for the creation of specialty chemicals, offering a reliable and efficient reagent for large-scale processes.
It is also applied in academic research settings for teaching and experimental purposes, supporting the study of organic reaction mechanisms and functional group chemistry.

Brand	TCI
CAS number	112-76-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Liquid
Storage	Store in a cool, dry place away from moisture and direct sunlight

Stearoyl Chloride 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, ideally with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong bases or reactive metals. Proper labeling and storage conditions ensure safe handling and long-term usability in laboratory settings. Always follow standard safety protocols when working with reactive chemical compounds.

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