Alkyl polyglycosides (APGs) are a class of non-ionic surfactants widely used in a variety of cosmetic, household, and industrial applications. Biodegradable and plant-derived from sugars, these surfactants are usually derivatives of glucose and fatty alcohols.[1] The raw materials are typically starch and fat, and the final products are typically complex mixtures of compounds with different sugars comprising the hydrophilic end and alkyl groups of variable length comprising the hydrophobic end.[2] When derived from glucose, they are known as alkyl polyglucosides.
APGs exhibit good wetting, foaming, and detergency properties, making them effective in cleaning and personal care products.[3][4] They are also stable across a wide pH range and compatible with various other surfactants.[5]
Uses
editAPGs are used to enhance the formation of foams in detergents. They are also used in the personal care industry because they are biodegradable and safe for sensitive skin.[6]
Preparation
editAPGs are produced by combining a sugar such as glucose with a fatty alcohol in the presence of acid catalysts at elevated temperatures.[1][7]
References
edit- ^ a b Karlheinz Hill; Wolfgang von Rybinski; Gerhard Stoll, eds. (2008). Alkyl Polyglycosides. Wiley-VCH. ISBN 978-3-527-61468-4.
- ^ Iglauer, S.; Wu, Y.; Shuler, P.; Tang, Y.; Goddard, W. A. (2010). "Analysis of the Influence of Alkyl Polyglycoside Surfactant and Cosolvent Structure on Interfacial Tension in Aqueous Formulations versus n-Octane". Tenside Surfactants Detergents. 47 (2): 87–97. doi:10.3139/113.110056.
- ^ "Alkyl Polyglucoside surfactants (APG)". Stanford Chemicals. Retrieved Aug 29, 2024.
- ^ Rosen, Milton; Kunjappu, Joy (2012). Surfactants and Interfacial Phenomena. Wiley. p. 29. ISBN 9780470541944.
- ^ Ruiz, Cristobal (2008). Sugar-Based Surfactants: Fundamentals and Applications (1st ed.). CRC Press. p. 14. ISBN 978-1420051667.
- ^ W von Rybinski; K Hill (1998). "Alkyl Polyglycosides—Properties and Applications of a new Class of Surfactants". Angewandte Chemie International Edition. 37 (10): 1328–1345. doi:10.1002/(SICI)1521-3773(19980605)37:10<1328::AID-ANIE1328>3.0.CO;2-9. PMID 29710912.
- ^ Joshi, Vishal Y.; Sawant, Manohar R. (2007). "Novel stereo controlled glycosylation of 1,2,3,4,6-penta-O-acetyl-β-D-glucopyranoside using MgO–ZrO2 as an environmentally benign catalyst". Catalysis Communications. 8 (12): 1910–1916. doi:10.1016/j.catcom.2007.03.010.