p-Toluoyl Chloride TCI T0311

Chemical Identity

CAS No.: 874-60-2
PubChem: CID 13405·SID 87576286
Formula: C8H7ClO
Molecular weight: 154.59 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-methylbenzoyl chloride
SMILES: CC1=CC=C(C=C1)C(=O)Cl
InChIKey: NQUVCRCCRXRJCK-UHFFFAOYSA-N

Rp 610.050,00

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p-Toluoyl Chloride (TCI T0311), with CAS number 874-60-2, is a versatile organic compound widely used in laboratory settings for its reactivity and utility in chemical synthesis. This compound serves as a key building block in the development of complex organic molecules, particularly in substitution and coupling reactions. Its structural features, including the p-tolyl group attached to a chlorine atom, make it an essential reagent for chemists working in both academic and industrial environments. As a non-heterocyclic building block, it is categorized under Chemistry > Building Blocks > Non-Heterocyclic Building Blocks, reflecting its role in foundational organic chemistry.

One of the primary reasons p-Toluoyl Chloride is preferred is its solubility in common organic solvents such as ethyl acetate and chloroform. This property simplifies the process of dissolving and reacting the compound in various experimental setups. Additionally, its stability under controlled conditions ensures a longer shelf life and reduces the risk of degradation during storage. These characteristics make it a reliable and efficient choice for laboratory applications requiring consistent performance.

In Indonesian laboratories, p-Toluoyl Chloride is extensively used in chemical research, especially in organic synthesis and analytical chemistry. It is a valuable resource for universities, research institutions, and chemical development companies. Its availability in various packaging options ensures convenience for both small-scale and large-scale experiments, supporting a wide range of scientific activities.

TCI brochures (PDF)

Reagents for Glyco Chemistry & Biology 5th Edition · p. 149

Related TCI products

Organic synthesis is a primary application where p-Toluoyl Chloride is used for its reactivity in substitution and coupling reactions, making it ideal for creating complex aromatic compounds.
Analytical chemistry benefits from its solubility in organic solvents, allowing precise dissolution and analysis in various experimental setups.
Industrial chemical development relies on its stability and reactivity, supporting the creation of new compounds and materials in research and production environments.
Teaching laboratories use it as a fundamental building block for students to understand organic reaction mechanisms and synthetic pathways.
Research institutions incorporate it into projects focused on aromatic compound synthesis, leveraging its role in creating derivatives and functional groups.

Brand	TCI
CAS number	874-60-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various sizes to suit different laboratory needs
Physical form	—
Storage	Store in a cool, dry place away from moisture and direct sunlight

p-Toluoyl Chloride should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Since it is a chemical reagent, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid direct contact with skin or inhalation of vapors. Keep the material away from incompatible substances and ensure proper ventilation in the workspace. Regular monitoring of storage conditions is essential to maintain the integrity of the compound for extended use in research and development activities.

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