195723-10-5

Basic information

• Product Name: Methyl 4-O-feruloylquinate
• Synonyms: Methyl 4-O-feruloylquinate;(1alpha,3R,4alpha,5R)-1,3,5-Trihydroxy-4-[[(2E)-3-(4-hydroxy-3-methoxyphenyl)-1-oxo-2-propen-1-yl]oxy]cyclohexanecarboxylic acid methyl ester
• CAS NO: 195723-10-5
• Molecular Formula: C18H22O9
• Molecular Weight: 382.36188
• Mol File: 195723-10-5.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl 4-O-feruloylquinate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 4-O-feruloylquinate(195723-10-5)
• EPA Substance Registry System: Methyl 4-O-feruloylquinate(195723-10-5)

Safety Data

• Hazardous Substances Data: 195723-10-5(Hazardous Substances Data)

Usage

Description

Methyl 4-O-feruloylquinate is a chemical compound that belongs to the class of esters, specifically the methyl esters. It is derived from ferulic acid, a phenolic compound found in plants, and quinic acid, a natural acid present in coffee and other plant products. Methyl 4-O-feruloylquinate possesses potential antioxidant properties and has been studied for its ability to inhibit the oxidation of lipids and proteins in cells.

Uses

Used in Food Industry:
Methyl 4-O-feruloylquinate is used as a natural ingredient for its potential health benefits and antioxidant properties, which can help in preserving the quality and extending the shelf life of food products.
Used in Cosmetic Industry:
In the cosmetic industry, Methyl 4-O-feruloylquinate is used as an active ingredient for its potential antioxidant properties, which can contribute to skin health and protection against environmental stressors.
Further research is needed to fully understand the potential uses and benefits of Methyl 4-O-feruloylquinate in various applications.

Upstream product

• 55882-65-0 4-acetoxyferuloyl chloride 
• 191916-39-9 methyl (-)-quinate 

Relevant articles and documents

How to identify and discriminate between the methyl quinates of chlorogenic acids by liquid chromatography-tandemmass spectrometry

The methyl esters of chlorogenic acids, methyl quinates, are widely distributed in plant materials and frequently appear as extraction artifacts in plant samples. This is the first time when liquid chromatography-tandem mass spectrometry methods have been used for the identification and characterization of the methyl quinates. For this purpose, methyl quinates of mono caffeoylquinic acids and mono feruloylquinic acids were synthesized as authentic standards. The methyl quinates of mono and diacyl chlorogenic acids have shown characteristic fragmentation pattern in their tandem mass spectra. MS n+1 spectra of the methyl quinates of diacyl chlorogenic acids were identical to MSn spectra of mono acyl derivatives. These quinates do not produce any methyl quinate peak at m/z 205 if compared with quinic acid peak at m/z 191 in negative ion mode. In the MSn spectra of these quinates, cinnamic acid part or cinnamoyl part was detected as a base peak in negative ionmode. The retention time, order of elution and fragmentation pattern were completely different if compared with LC-MSn methods developed for chlorogenic acids. These LC-MSn methods have been applied for the identification and regioisomeric characterization of the methyl quinates of chlorogenic acids in mate tea and woodruff (Galium odoratum). Twomethyl caffeoylquinates (2 and 4) were identified asmethyl 3-caffeoylquinate andmethyl 5-caffeoylquinate. Copyright