{"title":"Hydrolysis-resistant esters","authors":"J. Imperante","doi":"10.1201/9781420016123.ch22","DOIUrl":null,"url":null,"abstract":"Hydrolytic instability of esters in cosmetic products can be reduced, compared to that of standard straight chain esters, by using non-hydrolyzable esters synthesized from a diol reaction sequence. Two commercial dimer diol di-esters, given as examples, enable stable formulations at extremes of pH.","PeriodicalId":10780,"journal":{"name":"Cosmetics and toiletries","volume":"20 1","pages":"51-58"},"PeriodicalIF":0.0000,"publicationDate":"2005-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cosmetics and toiletries","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1201/9781420016123.ch22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Hydrolytic instability of esters in cosmetic products can be reduced, compared to that of standard straight chain esters, by using non-hydrolyzable esters synthesized from a diol reaction sequence. Two commercial dimer diol di-esters, given as examples, enable stable formulations at extremes of pH.