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2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, 2,3-dihydroxypropyl ester, also known as epigallocatechin gallate (EGCG), is a complex chemical compound derived from the leaves of the Camellia sinensis plant, commonly known as green tea. EGCG is a type of catechin, a group of polyphenolic compounds with antioxidant properties. It is the most abundant and biologically active catechin in green tea, accounting for up to 50% of the total catechin content. EGCG has been extensively studied for its potential health benefits, including its antioxidant, anti-inflammatory, and anticancer properties. It is also known for its ability to inhibit various enzymes and cellular pathways, which may contribute to its potential therapeutic effects. However, it is important to note that while EGCG has shown promise in laboratory studies, more research is needed to fully understand its effects in humans and to determine the appropriate dosage and safety profile.

2179-24-0

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2179-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2179-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2179-24:
(6*2)+(5*1)+(4*7)+(3*9)+(2*2)+(1*4)=80
80 % 10 = 0
So 2179-24-0 is a valid CAS Registry Number.

2179-24-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydroxypropyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names 3,4-Dihydroxyzimtsaeuremonoglycerylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2179-24-0 SDS

2179-24-0Downstream Products

2179-24-0Relevant academic research and scientific papers

Selective separation of mono glyceryl ferulate using water from an ionic liquid solution of enzymatic transesterification

Sun, Shangde,Chen, Xiaowei,Bi, Yanlan,Yang, Guolong

, p. 1339 - 1345 (2014)

Mono glyceryl ferulate (MFG), an all-natural derivative of ferulic acid, can be used as antioxidant and a UV filter in food and cosmetic formulations. However, the applications of MFG in these fields are limited due to its low availability in nature. In this work, a novel method for selective separation of MFG from a room temperature ionic liquid (RTIL) solution of enzymatic transesterification of ethyl ferulate with glycerol was investigated. The effects of different extractants and extraction conditions on the selective separation of MFG were also studied. High extraction yields of MFG (98.23 ± 1.09 %) and the relative content of MFG in the extracts (97.76 ± 1.25 %) were achieved using neutral deionized water as extractant under the following conditions: 0.5:1 volume ratio of water to RTIL solution, extraction time of 6 min, centrifugation time of 6 min, and extraction done eight times. The extraction thermodynamics showed that the extraction of MFG was an exothermic process. The purified MFG exhibited good UV adsorbing properties at 280-360 nm with a λ max at 322 nm.

Ultrasonic-promoted enzymatic preparation, identification and multi-active studies of nature-identical phenolic acid glycerol derivatives

Dong, Zhe,Liu, Zengshe,Sun, Teng,Zhang, Haiping,Zheng, Mingming

, p. 11139 - 11147 (2020/04/03)

Phenolic acid glycerols (PAGs) are a group of rare phytochemicals found from potato periderm, which show great potential in the food, cosmetic and pharmaceutical industries. In this study, seven PAGs were enzymatically synthesized via transesterification of ethyl phenates (EPs) with glycerol by ultrasonic promotion. The conversions of 88.1-98.5% could be obtained in 1-9 h. Compared with the conventional stirring methods, the catalytic efficiency was significantly increased 11.0-44.0 folds by ultrasound assistance. The lipid peroxidation inhibition activity increased 8.1-fold and 14.4-fold compared to the parent phenolic acids (PAs). Furthermore, caffeoyl glycerol and feruloyl glycerol exhibited excellent antimicrobial activity against Escherichia coli compared to the corresponding PAs with minimum inhibitory concentration (MIC) decreasing 4-16-fold. The PAGs can also absorb a much wider and higher amount of the harmful UV-B rays than the corresponding PAs. The present strategy for facile synthesis of multifunctional PAGs paves the way for the development and application of natural phytochemicals and novel ingredients.

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