Ethyl 3,5-dihydroxybenzoate丨CAS 4142-98-7

Ethyl 3,5-dihydroxybenzoate丨CAS 4142-98-7
Product Introduction:
Catalog No.: SS129188
CAS No.: 4142-98-7
Purity(HPLC): 98.0%min
Product Name: Ethyl 3,5-dihydroxybenzoate
Molecular Formula: C9H10O4
Molecular Weight: 182.17
Synonym(s): 3,5-dihydroxybenzoic acid ethyl ester
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Technical Parameters
Description

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Specifications

 

Appearance Light brown solid
Purity (HPLC) 98.0% min
Water content 1.0% max

 

 

 

Applications

 

Ethyl 3,5-dihydroxybenzoate (CAS 4142-98-7) is an aromatic ester widely used as an intermediate in organic synthesis, pharmaceuticals, and cosmetic formulations. In medicinal chemistry, it serves as a building block for the synthesis of bioactive compounds, including anti-inflammatory, antioxidant, and antimicrobial agents. Its dihydroxy functional groups allow for further derivatization, such as esterification, etherification, or glycosylation, enabling the construction of complex molecules. Additionally, ethyl 3,5-dihydroxybenzoate is used in the synthesis of dyes, natural product analogs, and specialty chemicals, as well as in cosmetic formulations as a precursor for UV filters and antioxidant ingredients.

 

Benefits

 

The benefits of ethyl 3,5-dihydroxybenzoate stem from its dual hydroxyl groups and ester functionality, which provide high chemical versatility. The hydroxyl groups enable hydrogen bonding and functionalization, while the ethyl ester enhances solubility and facilitates ester-based reactions. Its stability under standard storage conditions and solubility in common organic solvents make it convenient for multi-step synthesis and incorporation into various formulations. The compound's reactive and modifiable structure allows for the creation of derivatives with tailored bioactivity, solubility, and physicochemical properties, making it highly valuable in pharmaceutical, cosmetic, and fine chemical applications.

 

Conclusion

 

Ethyl 3,5-dihydroxybenzoate is a versatile intermediate used in pharmaceuticals, cosmetics, and specialty chemical synthesis. Its combination of dihydroxy and ester functional groups provides reactivity, solubility, and derivatization potential. By enabling the synthesis of bioactive molecules, functional derivatives, and antioxidant compounds, ethyl 3,5-dihydroxybenzoate remains an important building block in modern organic and industrial chemistry.

 

 

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