Fatty acyl glycosides of mono- and disaccharides
Fatty acyl glycosides derived from mono- and disaccharides are a class of compounds that combine the hydrophobicity of fatty acids with the hydrophilicity of sugar moieties. These unique molecules have found extensive applications in various fields due to their excellent emulsifying properties, skin-friendly nature, and stable formulation characteristics.
Fatty acyl glycosides are synthesized by attaching fatty acid residues to mono- or disaccharide backbones, such as glucose, fructose, lactose, or sucrose. The resulting compounds possess both water-soluble and lipophilic properties, making them ideal for use in personal care products like shampoos, conditioners, and body washes. They not only enhance the cleansing ability but also provide a soft feel upon application.
Moreover, these glycosides are often used in cosmetic formulations to improve spreadability and texture. Their biodegradable nature and gentle skin compatibility make them suitable for sensitive skin care products. Additionally, they can serve as emollients and anti-irritants, contributing to the overall effectiveness of dermatological applications.
In summary, fatty acyl glycosides derived from mono- and disaccharides are versatile ingredients that offer multiple benefits in personal and dermatological care products due to their unique physical and chemical properties.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Glucosyl beta1-3-galactose | 75023-56-2 | C12H22O11 |
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Calcium bromolactobionate | 33659-28-8 | C24H42Br2Ca2O24 |
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Byssomeruliol A; 12'-O-D-Mannopyranoside | 83162-80-5 | C30H50O11 |
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Rosavin | 84954-92-7 | C20H28O10 |
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Tetradecyl-β-D-maltoside | 18449-82-6 | C26H50O11 |
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D-(+)-Melibiose | 585-99-9 | C12H22O11 |
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Maltose Hydrate | 6363-53-7 | C12H24O12 |
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Palatinose Monohydrate | 13718-94-0 | C12H22O11 |
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Trehalulose | 51411-23-5 | C12H22O11 |
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b-D-Glucopyranoside,(2E,6R)-6-hydroxy-2,6-dimethyl-2,7-octadien-1-yl | 64776-96-1 | C16H28O7 |
Related Literature
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
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Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
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Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
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