5438-38-0

Usage

Uses

Used in Food Industry:
Ethyl gallate is used as an antioxidant in the food industry to prevent the degradation of fats and oils, thereby extending the shelf life of food products. Its strong antioxidant properties help maintain the quality and freshness of food items.
Used in Cosmetic Industry:
In the cosmetic industry, ethyl gallate is used as an antioxidant to protect products from oxidation, which can lead to spoilage or degradation. Its antimicrobial properties also contribute to the preservation of cosmetic products, ensuring their safety and efficacy.
Used in Pharmaceutical Industry:
Ethyl gallate is being studied for its potential therapeutic applications in the treatment of cancer, inflammation, and oxidative stress-related diseases. Its antioxidant properties make it a promising candidate for the development of pharmaceutical products that can combat these conditions.
Used in Antioxidant Formulations:
Due to its strong antioxidant properties, ethyl gallate is used in the formulation of various antioxidant products, including dietary supplements and health products. It helps neutralize free radicals and supports overall health by reducing oxidative stress in the body.

InChI:InChI=1/C24H22ClFN2O4/c1-2-30-22-13-17(14-27-32-16-23(29)28-19-9-4-3-5-10-19)12-20(25)24(22)31-15-18-8-6-7-11-21(18)26/h3-14H,2,15-16H2,1H3,(H,28,29)

Upstream product

• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 
• 72207-94-4 2-ethoxy-4-formylphenyl acetate 
• 5438-50-6 4-acetoxy-3-ethoxy-benzonitrile 
• 56681-62-0 4-acetoxy-3-ethoxy-benzoic acid 

Downstream Products

• 97966-51-3 3-ethoxy-4-hydroxy-benzoic acid methyl ester 
• 56681-62-0 4-acetoxy-3-ethoxy-benzoic acid 
• 671790-53-7 3-ethoxy-5-bromo-4-hydroxy-benzoic acid 
• 53948-38-2 2,4-dibromo-6-ethoxyphenol 
• 174674-93-2 3-ethoxy-4-hydroxy-benzoic acid ethyl ester 

Relevant academic research and scientific papers

Kinetics and mechanistic study of oxidation of ethyl vanillin by alkaline hexacyanoferrate(III)

The kinetics of oxidation of ethyl vanillin by hexacyanoferrate(III) in aqueous alkaline medium was studied. The reactions are found to be fractional order with respect to substrate & hydroxide ion and first order with respect to oxidant. The rate-determi

Benzothiazole, thiazolopyridine, benzooxazole and oxazolopyridine derivatives

This invention is concerned with compounds of the formula wherein A, B1, B2, R1, R2 and G are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The invention further relates to pharmaceutical compositions containing such compounds, to a process for their preparation and to their use for the treatment and/or prevention of diseases which are associated with the modulation of SST receptors subtype 5.

Substituted benzofurans and benzothiophenes

The compounds of this invention are substituted benzofurans and benzothiophenes having pharmacological activity. In particular, these compounds have coronary vasodilator activity and are useful in the treatment angina pectoris.