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Dihydroxyacetone: A User Guide for a Challenging Bio-Based Synthon
1,3-dihydroxyacetone (DHA) is an underrated bio-based synthon, with a broad range of reactivities. It is produced for the revalorization of glycerol, a major side-product of the growing biodiesel industry. The overwhelming majority of DHA produced worldwide is intended for application as a self-tann...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052986/ https://www.ncbi.nlm.nih.gov/pubmed/36985712 http://dx.doi.org/10.3390/molecules28062724 |
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author | Bricotte, Léo Chougrani, Kamel Alard, Valérie Ladmiral, Vincent Caillol, Sylvain |
author_facet | Bricotte, Léo Chougrani, Kamel Alard, Valérie Ladmiral, Vincent Caillol, Sylvain |
author_sort | Bricotte, Léo |
collection | PubMed |
description | 1,3-dihydroxyacetone (DHA) is an underrated bio-based synthon, with a broad range of reactivities. It is produced for the revalorization of glycerol, a major side-product of the growing biodiesel industry. The overwhelming majority of DHA produced worldwide is intended for application as a self-tanning agent in cosmetic formulations. This review provides an overview of the discovery, physical and chemical properties of DHA, and of its industrial production routes from glycerol. Microbial fermentation is the only industrial-scaled route but advances in electrooxidation and aerobic oxidation are also reported. This review focuses on the plurality of reactivities of DHA to help chemists interested in bio-based building blocks see the potential of DHA for this application. The handling of DHA is delicate as it can undergo dimerization as well as isomerization reactions in aqueous solutions at room temperature. DHA can also be involved in further side-reactions, yielding original side-products, as well as compounds of interest. If this peculiar reactivity was harnessed, DHA could help address current sustainability challenges encountered in the synthesis of speciality polymers, ranging from biocompatible polymers to innovative polymers with cutting-edge properties and improved biodegradability. |
format | Online Article Text |
id | pubmed-10052986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100529862023-03-30 Dihydroxyacetone: A User Guide for a Challenging Bio-Based Synthon Bricotte, Léo Chougrani, Kamel Alard, Valérie Ladmiral, Vincent Caillol, Sylvain Molecules Perspective 1,3-dihydroxyacetone (DHA) is an underrated bio-based synthon, with a broad range of reactivities. It is produced for the revalorization of glycerol, a major side-product of the growing biodiesel industry. The overwhelming majority of DHA produced worldwide is intended for application as a self-tanning agent in cosmetic formulations. This review provides an overview of the discovery, physical and chemical properties of DHA, and of its industrial production routes from glycerol. Microbial fermentation is the only industrial-scaled route but advances in electrooxidation and aerobic oxidation are also reported. This review focuses on the plurality of reactivities of DHA to help chemists interested in bio-based building blocks see the potential of DHA for this application. The handling of DHA is delicate as it can undergo dimerization as well as isomerization reactions in aqueous solutions at room temperature. DHA can also be involved in further side-reactions, yielding original side-products, as well as compounds of interest. If this peculiar reactivity was harnessed, DHA could help address current sustainability challenges encountered in the synthesis of speciality polymers, ranging from biocompatible polymers to innovative polymers with cutting-edge properties and improved biodegradability. MDPI 2023-03-17 /pmc/articles/PMC10052986/ /pubmed/36985712 http://dx.doi.org/10.3390/molecules28062724 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Perspective Bricotte, Léo Chougrani, Kamel Alard, Valérie Ladmiral, Vincent Caillol, Sylvain Dihydroxyacetone: A User Guide for a Challenging Bio-Based Synthon |
title | Dihydroxyacetone: A User Guide for a Challenging Bio-Based Synthon |
title_full | Dihydroxyacetone: A User Guide for a Challenging Bio-Based Synthon |
title_fullStr | Dihydroxyacetone: A User Guide for a Challenging Bio-Based Synthon |
title_full_unstemmed | Dihydroxyacetone: A User Guide for a Challenging Bio-Based Synthon |
title_short | Dihydroxyacetone: A User Guide for a Challenging Bio-Based Synthon |
title_sort | dihydroxyacetone: a user guide for a challenging bio-based synthon |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052986/ https://www.ncbi.nlm.nih.gov/pubmed/36985712 http://dx.doi.org/10.3390/molecules28062724 |
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