Related Experiment Video
Updated: Jan 27, 2026

Measurement of Carotenoids in Perifovea using the Macular Pigment Reflectometer
Published on: January 29, 2020
Marigold carotenoids: Much more than lutein esters
Daniele Bobrowski Rodrigues1, Adriana Zerlotti Mercadante1, Lilian Regina Barros Mariutti2
1Department of Food Science, Faculty of Food Engineering, University of Campinas, Campinas-SP, Campinas 13083-862, Brazil.
Marigold flowers contain many more carotenoid esters than previously known. This study identified 56 carotenoid esters, including novel types, using advanced liquid chromatography and mass spectrometry techniques.
Area of Science:
- * Plant biochemistry and metabolomics
- * Food science and nutraceuticals
Background:
- * Carotenoids are lipophilic pigments with recognized health benefits.
- * Hydroxy-carotenoids exist as free forms or fatty acid esters in plants.
- * Analyzing plant carotenoid esters is challenging, limiting understanding of native profiles.
Purpose of the Study:
- * To comprehensively identify carotenoids and their esters in marigold petals.
- * To investigate the native carotenoid profile without saponification.
- * To characterize novel carotenoid ester structures in marigold.
Main Methods:
- * Liquid chromatography with diode-array detection and atmospheric pressure chemical ionization tandem mass spectrometry (LC-DAD-(APCI+)MS/MS).
- * Analysis of marigold petal extracts with and without saponification.
- * Utilized C30 reversed-phase columns for enhanced separation.
Main Results:
- * Identified 56 carotenoid esters in marigold petals without saponification, compared to 18 carotenoids in saponified extracts.
- * Discovered 6 free carotenoids, 20 monoesters, and 30 diesters.
- * First-time identification of zeaxanthin, violaxanthin, auroxanthin, zeinoxanthin, and β-cryptoxanthin esters in marigold.
Conclusions:
- * The native carotenoid profile of marigold is significantly richer in ester forms than previously documented.
- * Advanced LC-DAD-(APCI+)MS/MS methods enable sensitive and selective analysis of diverse carotenoid esters.
- * This research expands the understanding of marigold's chemical composition and potential applications.
Related Concept Videos
Acid Halides to Esters: Alcoholysis
Esters to Alcohols: Hydride Reductions
Lithium aluminum hydride is a source of hydride ions and functions as a nucleophile. The mechanism proceeds in three steps. Firstly, the nucleophilic hydride ion attacks the carbonyl carbon of the ester to form a tetrahedral intermediate. Subsequently, the carbonyl group re-forms,...
Esters to Alcohols: Grignard Reaction
The reaction requires two equivalents of the Grignard reagent and introduces two identical alkyl groups, derived from the Grignard reagent, bonded to the hydroxyl-bearing carbon of the alcohol.
The reaction follows the typical nucleophilic acyl substitution mechanism. The Grignard...
Esters to Carboxylic Acids: Saponification
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Esters to β-Ketoesters: Claisen Condensation Mechanism

