3,4,5-Trimethoxybenzoic Anhydride TCI T1093

Chemical Identity

CAS No.: 1719-88-6
PubChem: CID 74398·SID 87576889
Formula: C20H22O9
Molecular weight: 406.4 g/mol
Purity: >95.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (3,4,5-trimethoxybenzoyl) 3,4,5-trimethoxybenzoate
SMILES: COC1=CC(=CC(=C1OC)OC)C(=O)OC(=O)C2=CC(=C(C(=C2)OC)OC)OC
InChIKey: LQJFTZJNDJDCKV-UHFFFAOYSA-N

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3,4,5-Trimethoxybenzoic Anhydride is a chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. As an anhydride of benzoic acid, it serves as a versatile building block in organic chemistry, enabling the formation of ester and amide bonds through various reaction mechanisms. Its reactivity makes it a valuable reagent in the development of aromatic and heterocyclic compounds, which are essential in pharmaceutical and material science research.

This compound is preferred for its chemical stability under controlled conditions, though it is highly sensitive to moisture and air exposure. The presence of methoxy groups at positions 3, 4, and 5 enhances its electron-donating properties, increasing its reactivity in multiple chemical reactions. These characteristics make it a reliable choice for researchers requiring precise and predictable chemical behavior in synthetic processes.

In Indonesian laboratories, 3,4,5-Trimethoxybenzoic Anhydride is commonly used in organic chemistry research and the synthesis of pharmacological compounds. It is a staple in academic and industrial research institutions where high reactivity and structural stability are critical. Its application spans various experimental setups, making it an essential component in the chemical toolkit of Indonesian laboratories.

Related TCI products

Synthesis of complex aromatic compounds due to its reactivity and structural stability
Esterification reactions for the formation of ester derivatives in organic synthesis
Development of heterocyclic structures in pharmaceutical research applications
Preparation of functionalized aromatic molecules for advanced chemical studies
Organic chemistry experiments requiring high reactivity and controlled reaction conditions

Brand	TCI
CAS number	1719-88-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid
Storage	Should be stored in a dry, cool, and airtight environment

This compound should be stored in a dry, cool, and airtight container to prevent moisture and air exposure, which can degrade its chemical integrity. It is recommended to use glass or sealed plastic containers that are resistant to chemical reactions. Due to its sensitivity, it should be handled in a controlled laboratory environment with proper ventilation. Always ensure that the container is tightly sealed when not in use. Avoid contact with moisture and keep it away from heat sources to maintain its stability and effectiveness in chemical reactions.

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