4-Butoxybenzaldehyde TCI B0126

Chemical Identity

CAS No.: 5736-88-9
PubChem: CID 79813·SID 87563321
Formula: C11H14O2
Molecular weight: 178.23 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-butoxybenzaldehyde
SMILES: CCCCOC1=CC=C(C=C1)C=O
InChIKey: XHWMNHADTZZHGI-UHFFFAOYSA-N

Rp 3.021.900,00

~~Rp 2.112.600,00~~ Rp 3.021.900,00

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Volume 25mL

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4-Butoxybenzaldehyde is a chemical compound widely used in organic laboratory reactions. It serves as a fundamental building block in the synthesis of more complex chemical structures. This compound is essential for chemists seeking to create derivatives with specific functional groups. Its presence in the laboratory enables the exploration of various synthetic pathways and the development of new compounds. Due to its versatility, it is a valuable resource for both academic and industrial research settings.

The reactivity of 4-Butoxybenzaldehyde is a key factor in its popularity among laboratory professionals. It contains both an aldehyde group and a butoxy ether group, which contribute to its ability to participate in nucleophilic, substitution, and condensation reactions. These properties make it an ideal precursor for the synthesis of a wide range of organic compounds. Its chemical stability under controlled conditions further enhances its usability and reliability in laboratory environments.

In Indonesian laboratories, 4-Butoxybenzaldehyde is commonly used in organic chemistry research. It plays a critical role in the development of new compounds and the modification of existing ones. Researchers in universities and research institutions rely on this compound to advance their work in synthetic chemistry. Its availability and chemical properties make it a preferred choice for those engaged in chemical synthesis and analysis.

Related TCI products

Organic synthesis applications benefit from 4-Butoxybenzaldehyde due to its reactivity and functional group versatility.
It is ideal for nucleophilic substitution reactions because of its aldehyde functionality and ether group.
The compound supports condensation reactions, making it useful in the formation of complex organic molecules.
It is frequently used in the development of new pharmaceutical compounds due to its structural adaptability.
Research institutions use it for academic studies in synthetic chemistry and compound modification.

Brand	TCI
CAS number	5736-88-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight

4-Butoxybenzaldehyde should be stored in a cool, dry location, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air. The compound is best kept in a well-ventilated area to minimize inhalation risks. Avoid contact with skin and eyes during handling. Always wear appropriate personal protective equipment, such as gloves and safety goggles. Ensure that storage conditions are consistent to maintain the compound's stability and effectiveness in laboratory applications.

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