Benzoic Anhydride TCI B0078

Chemical Identity

CAS No.: 93-97-0
PubChem: CID 7167·SID 87563280
Formula: C14H10O3
Molecular weight: 226.23 g/mol
Purity: >97.0%(GC)(T)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: benzoyl benzoate
SMILES: C1=CC=C(C=C1)C(=O)OC(=O)C2=CC=CC=C2
InChIKey: CHIHQLCVLOXUJW-UHFFFAOYSA-N

Rp 637.350,00

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Benzoic Anhydride is a chemical compound widely used in laboratories for organic synthesis. It serves as a key reagent in various chemical reactions, particularly in the formation of esters and carboxylic acids. Its reactivity makes it an essential component in the development of pharmaceuticals, food additives, and industrial chemicals. In laboratory settings, benzoic anhydride plays a crucial role in esterification processes and in the synthesis of compounds with carboxylate structures. Its chemical properties allow it to participate in complex reactions, making it a versatile tool for chemists.

The compound is known for its stability under specific conditions, yet it is highly reactive towards water and bases. This reactivity, while beneficial in chemical reactions, also requires careful handling. Benzoic anhydride is corrosive and can cause irritation to the skin and eyes. These properties make it a preferred choice for applications that demand high reactivity and the ability to engage in intricate chemical transformations. Its effectiveness in organic synthesis is further enhanced by its compatibility with a variety of reaction conditions and reagents.

In Indonesian laboratories, benzoic anhydride is commonly used in organic chemistry research, particularly in universities and research institutions focused on synthesizing active compounds. It is a preferred material due to its availability and reliability in achieving desired chemical outcomes. Its role in both academic and industrial research underscores its importance in the chemical sciences within the region.

TCI brochures (PDF)

Powerful Condensation Organocatalysts 2018-01-25 · p. 2
Protecting Agents 2025-03-25 · p. 7
Nucleosides, Nucleotides, Nucleic Acids and Related Reagents 2026-03-23 · p. 13
Reagents for Glyco Chemistry & Biology 5th Edition · p. 129

Related TCI products

Organic synthesis reactions where esterification and carboxylic acid formation are required
Pharmaceutical development for the synthesis of active pharmaceutical ingredients
Food additive manufacturing for the creation of flavor and preservative compounds
Industrial chemical production for the development of specialty chemicals
Academic research in universities and research institutes focusing on chemical innovation

From the TCI brochure

Acyl donor (Bz2O) in the B2291-catalyzed esterification

Brand	TCI
CAS number	93-97-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and bases

Benzoic anhydride should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the material in a sealed container to prevent exposure to moisture and air. Due to its corrosive nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Avoid contact with water and bases to prevent unwanted reactions. In a laboratory setting, it is important to store the compound away from incompatible substances to ensure safety and maintain its effectiveness for use in chemical processes. Proper storage conditions are essential to preserve its reactivity and ensure safe handling during experiments.

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