Online Database of Chemicals from Around the World

2-(3,4-Dihydroxyphenyl)ethyl acetate
[CAS# 69039-02-7]

List of Suppliers
China Kouting Group Limited China Inquire  
+86 (21) 5811-6475
+86 18930086157
sales@koutingchina.com
kane@koutingchina.com
Chemical manufacturer since 2009
chemBlink standard supplier since 2009
Nanjing Spring Pharma Tech Co., Ltd. China Inquire  
+86 (25) 6871-0897
sales@springpharma.net
QQ chat
Chemical manufacturer since 2011
chemBlink standard supplier since 2014
Shanghai Yuanye Bio-Technology Co., Ltd. China Inquire  
+86 (21) 6184-5781
+86 13585604150
shyysw053@163.com
QQ chat
Chemical manufacturer since 2009
chemBlink standard supplier since 2016
Chengdu Biopurify Phytochemicals Ltd. China Inquire  
+86 (28) 8263-3860
8263-3987
sales@biopurify.com
biopurify@gmail.com
Skype Chat
QQ chat
Chemical manufacturer
chemBlink standard supplier since 2017
Complete supplier list of 2-(3,4-Dihydroxyphenyl)ethyl acetate
Identification
Classification Flavors and spices >> Synthetic spice >> Phenols, ethers and epoxides >> Phenolic flavors
Name 2-(3,4-Dihydroxyphenyl)ethyl acetate
Synonyms 4-[2-(Acetyloxy)ethyl]-1,2-benzenediol; Hydroxytyrosol acetate
Molecular Structure CAS # 69039-02-7, 2-(3,4-Dihydroxyphenyl)ethyl acetate, 4-[2-(Acetyloxy)ethyl]-1,2-benzenediol, Hydroxytyrosol acetate
Molecular Formula C10H12O4
Molecular Weight 196.20
CAS Registry Number 69039-02-7
SMILES CC(=O)OCCC1=CC(=C(C=C1)O)O
Properties
Density 1.260
Boiling point 356 ºC
Flash point 142 ºC
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P305+351+338-P302+352    Details
SDS Available
up Discovory and Applicatios
2-(3,4-Dihydroxyphenyl)ethyl acetate, also known as dihydrocaffeic acid acetate or hydroxytyrosol acetate, is a naturally occurring phenolic compound. Its discovery dates back to the 20th century research on plant metabolites, when it was found in olives, olive oil, and other sources of hydroxytyrosol. The acetate form is believed to be a product of natural acetylation, which enhances the stability and lipophilicity of the compound.

The main application of 2-(3,4-dihydroxyphenyl)ethyl acetate is as an antioxidant. Its structure has dihydroxy groups that are effective in scavenging free radicals. This makes it valuable in food preservation, where it protects oils and other products from oxidation, extending shelf life and maintaining nutritional quality.

In the cosmetic industry, this compound is used to protect the skin from oxidative stress and environmental damage due to its antioxidant properties. It is used in anti-aging creams, serums, and lotions to help maintain the healthy appearance of the skin by neutralizing harmful free radicals.

In the pharmaceutical field, 2-(3,4-dihydroxyphenyl)ethyl acetate shows promise for its potential health benefits. Research suggests that it may have anti-inflammatory, anticancer, and cardioprotective properties similar to hydroxytyrosol. Its ability to modulate oxidative stress and inflammation suggests that it has potential for treating chronic diseases such as cardiovascular disease and neurodegenerative diseases.

The compound is also incorporated into functional foods and dietary supplements for its health-promoting benefits. As a derivative of hydroxytyrosol, it helps improve the antioxidant capacity of these products, supporting overall health and potentially reducing the risk of chronic disease.

In scientific studies, 2-(3,4-dihydroxyphenyl)ethyl acetate is used as a model compound to study antioxidant mechanisms and the effects of acetylation on biological activity. Its structure provides a foundation for the development of new antioxidants and exploring the relationship between structure and function of phenolic compounds.
Market Analysis Reports
List of Reports Available for 2-(3,4-Dihydroxyphenyl)ethyl acetate
Related Products
(E)-3-(3,4-Dihydroxyphenyl)-N-[2-(3,4-dihydroxyphenyl)ethyl]-2-propenamide  2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[(2-O-beta-D-xylopyranosyl-beta-D-galactopyranosyl)oxy]-1-benzopyrylium chloride  1-(3,4-Dihydroxyphenyl)-2-[(1,1-dimethylethyl)amino]ethanone  2-(3,4-Dihydroxyphenyl)-8-[(2E)-3,7-dimethyl-2,6-octadien-1-yl]-5,7-dihydroxy-3-methoxy-4H-1-benzopyran-4-one  2,4-Dihydroxyphenyldimethylsulfonium triflate  (2,5-Dihydroxyphenyl)diphenylphosphine oxide  3,4-Dihydroxyphenylethanol  4-[2-(3,5-Dihydroxyphenyl)ethenyl]-1,3-benzenediol  4-[(1E)-2-(3,5-Dihydroxyphenyl)ethenyl]-2-methoxy-1,3-benzenediol  beta-D-glucopyranoside  N-[2-(3,4-Dihydroxyphenyl)ethyl]-2-propenamide  2-(3,4-Dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5,7-dihydroxy-1-benzopyrylium chloride  2-(3,4-Dihydroxyphenyl)-3-(beta-D-glucopyranuronosyloxy)-5,7-dihydroxy-1-benzopyrylium  3,4-Dihydroxyphenylglycine  3,4-Dihydroxyphenylglycol  2-(3,5-Dihydroxyphenyl)-6-hydroxybenzofuran  (2,3-Dihydroxyphenyl)(2-hydroxy-4,6-dimethoxyphenyl)methanone  3-(3,4-Dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methyl-2-buten-1-yl)-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one  3-(3,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one  3-(2,4-Dihydroxyphenyl)-7-hydroxy-5-methoxy-2H-1-benzopyran-2-one