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Persulfate Reaction in a Hair‐Bleaching Formula: Unveiling the Unconventional Reactivity of 1,13‐Diamino‐4,7,10‐Trioxatridecane
The stability and unconventional reactivity of 1,13‐diamino‐4,7,10‐trioxatridecane in the presence of NH(3), H(2)O(2), and (NH(4))(2)S(2)O(8) are described. The ether‐diamine is an ingredient marketed to hair salons and consumers for so‐called “plex” services to compensate for hair damage during ble...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931532/ https://www.ncbi.nlm.nih.gov/pubmed/29744283 http://dx.doi.org/10.1002/open.201800013 |
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author | Gargano, Emanuele M. Mangiatordi, Giuseppe F. Weber, Ingo Goebel, Carsten Alberga, Domenico Nicolotti, Orazio Ruess, Wolfgang Wierlacher, Stefan |
author_facet | Gargano, Emanuele M. Mangiatordi, Giuseppe F. Weber, Ingo Goebel, Carsten Alberga, Domenico Nicolotti, Orazio Ruess, Wolfgang Wierlacher, Stefan |
author_sort | Gargano, Emanuele M. |
collection | PubMed |
description | The stability and unconventional reactivity of 1,13‐diamino‐4,7,10‐trioxatridecane in the presence of NH(3), H(2)O(2), and (NH(4))(2)S(2)O(8) are described. The ether‐diamine is an ingredient marketed to hair salons and consumers for so‐called “plex” services to compensate for hair damage during bleaching. The main reaction product identified is an unexpected azanyl ester derivative. This is considered relevant for the safety evaluation when used in cosmetic products. The mechanism of reaction was explored through DFT calculations. This study represents the first attempt to assess the stability of a plex active in an oxidative environment. |
format | Online Article Text |
id | pubmed-5931532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59315322018-05-09 Persulfate Reaction in a Hair‐Bleaching Formula: Unveiling the Unconventional Reactivity of 1,13‐Diamino‐4,7,10‐Trioxatridecane Gargano, Emanuele M. Mangiatordi, Giuseppe F. Weber, Ingo Goebel, Carsten Alberga, Domenico Nicolotti, Orazio Ruess, Wolfgang Wierlacher, Stefan ChemistryOpen Communications The stability and unconventional reactivity of 1,13‐diamino‐4,7,10‐trioxatridecane in the presence of NH(3), H(2)O(2), and (NH(4))(2)S(2)O(8) are described. The ether‐diamine is an ingredient marketed to hair salons and consumers for so‐called “plex” services to compensate for hair damage during bleaching. The main reaction product identified is an unexpected azanyl ester derivative. This is considered relevant for the safety evaluation when used in cosmetic products. The mechanism of reaction was explored through DFT calculations. This study represents the first attempt to assess the stability of a plex active in an oxidative environment. John Wiley and Sons Inc. 2018-03-25 /pmc/articles/PMC5931532/ /pubmed/29744283 http://dx.doi.org/10.1002/open.201800013 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Gargano, Emanuele M. Mangiatordi, Giuseppe F. Weber, Ingo Goebel, Carsten Alberga, Domenico Nicolotti, Orazio Ruess, Wolfgang Wierlacher, Stefan Persulfate Reaction in a Hair‐Bleaching Formula: Unveiling the Unconventional Reactivity of 1,13‐Diamino‐4,7,10‐Trioxatridecane |
title | Persulfate Reaction in a Hair‐Bleaching Formula: Unveiling the Unconventional Reactivity of 1,13‐Diamino‐4,7,10‐Trioxatridecane |
title_full | Persulfate Reaction in a Hair‐Bleaching Formula: Unveiling the Unconventional Reactivity of 1,13‐Diamino‐4,7,10‐Trioxatridecane |
title_fullStr | Persulfate Reaction in a Hair‐Bleaching Formula: Unveiling the Unconventional Reactivity of 1,13‐Diamino‐4,7,10‐Trioxatridecane |
title_full_unstemmed | Persulfate Reaction in a Hair‐Bleaching Formula: Unveiling the Unconventional Reactivity of 1,13‐Diamino‐4,7,10‐Trioxatridecane |
title_short | Persulfate Reaction in a Hair‐Bleaching Formula: Unveiling the Unconventional Reactivity of 1,13‐Diamino‐4,7,10‐Trioxatridecane |
title_sort | persulfate reaction in a hair‐bleaching formula: unveiling the unconventional reactivity of 1,13‐diamino‐4,7,10‐trioxatridecane |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931532/ https://www.ncbi.nlm.nih.gov/pubmed/29744283 http://dx.doi.org/10.1002/open.201800013 |
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