3-Hydroxy-4,5-dimethoxybenzaldehyde TCI H1179

Chemical Identity

CAS No.: 29865-90-5
PubChem: CID 141513·SID 125307774
Formula: C9H10O4
Molecular weight: 182.17 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-hydroxy-4,5-dimethoxybenzaldehyde
SMILES: COC1=CC(=CC(=C1OC)O)C=O
InChIKey: NVLTWXMZECWWPC-UHFFFAOYSA-N

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3-Hydroxy-4,5-dimethoxybenzaldehyde is a chemical compound widely used as a building block in the synthesis of complex molecules. It plays a crucial role in organic chemistry laboratories, where it serves as a versatile intermediate for the development of new compounds. This compound is commonly employed in reactions that require aromatic structures with functional groups, such as aldehydes and hydroxyl groups. Its ability to participate in various chemical transformations makes it an essential tool for researchers aiming to create pharmaceuticals, industrial chemicals, and dyes.

The compound’s structural stability and functional group reactivity make it a preferred choice for synthetic chemists. Its aromatic ring, combined with methoxy and hydroxyl groups, provides multiple sites for chemical modification. This versatility allows it to be used in substitution, reduction, and oxidation reactions. The high purity and solid form of 3-Hydroxy-4,5-dimethoxybenzaldehyde ensure consistent results in experimental settings. Its availability in standardized forms supports reproducibility and reliability in laboratory work.

In Indonesian laboratories, 3-Hydroxy-4,5-dimethoxybenzaldehyde is extensively used in organic chemistry research, particularly in academic and research institutions. It is frequently employed in projects involving the synthesis of bioactive compounds, chemical development, and molecular structure studies. Its widespread use reflects its importance in advancing scientific research and innovation in the field of chemistry.

Related TCI products

Organic synthesis of bioactive compounds due to its aromatic structure and functional groups.
Development of pharmaceuticals and industrial chemicals through substitution and oxidation reactions.
Research in molecular structure analysis due to its reactivity and stability in chemical environments.
Creation of dyes and pigments by modifying its functional groups for color and solubility properties.
Educational purposes in chemistry laboratories for teaching synthetic methods and reaction mechanisms.

Brand	TCI
CAS number	29865-90-5
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 light and moisture

3-Hydroxy-4,5-dimethoxybenzaldehyde should be stored in a cool, dry place, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. The compound is generally stable under normal laboratory conditions but should be handled with care to avoid contamination. Proper labeling and storage in a designated chemical storage area are essential for safety. Always ensure that the substance is kept in a secure location to prevent accidental spills or exposure. Regular monitoring of storage conditions helps maintain the integrity and purity of the compound for reliable experimental results.

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