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[av_heading heading=’Sarcosinlau PW’ tag=’h1′ style=’blockquote modern-quote’ size=” subheading_active=” subheading_size=’15’ padding=’10’ color=” custom_font=”][/av_heading]
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[av_row row_style=”][av_cell col_style=”]CAS-Nummer[/av_cell][av_cell col_style=”]137-16-6[/av_cell][/av_row]
[av_row row_style=”][av_cell col_style=”]Einecs-Nummer[/av_cell][av_cell col_style=”]205-281-5[/av_cell][/av_row]
[av_row row_style=”][av_cell col_style=”]INCI-Bezeichnung[/av_cell][av_cell col_style=”]Sodium lauroyl Sarcosinate[/av_cell][/av_row]
[av_row row_style=”][av_cell col_style=”]International nonpropietary name (INN)[/av_cell][av_cell col_style=”]-[/av_cell][/av_row]
[av_row row_style=”][av_cell col_style=”]Artikelnummer[/av_cell][av_cell col_style=”]100111[/av_cell][/av_row]
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Sodium [dodecanoyl(methyl)amino]acetate is an extremely mild amino-acid surfactant, with high foamability. It can reach excellent synergistic effect when combined with other surfactants, meanwhile reduce irritation and improve foamability. It’s widely used in facial cleanser and other personal care products.
This surfactant is amphiphilic due to the hydrophobic 12-carbon chain (lauroyl) and the hydrophilic carboxylate. Since the nitrogen atom is in an amide linkage, the nitrogen is not pH active and is neutrally charged in all aqueous solutions regardless of pH. The carboxylate has a pKa of about 3.6 and is therefore negatively charged in solutions of pH greater than about 5.5.
It has Good compatibility with anionic surfactant, good foamability while combined with other surfactants, good resistance to salty-water and hard-water, stabile in pH 5.5 to alkali, applicable for soap base and light acid facial cleansers.
pH-sensitive vesicles can be prepared using this surfactant with another cationic or water-insoluble amphiphiles such as 1-decanol.
Addition of an mixture of equal parts of sodium lauroyl sarcosinate and the non-ionic surfactant sorbitan monolaurate (S20) to water led to the formation of micelle-like aggregates, even though neither surfactant formed micelles when present alone. Such aggregates can help carry other small molecules, such as drugs, through the skin.
Literature:
Wallach, D.F.H; R. Mathur; G.J.M. Redziniak; J.F. Tranchant (1992).
Akter, N; S. Radiman; F. Mohamed; I.A. Rahman; M.I.H. Reza (2011).
Eur. J. Pharm Sci. 31: 1–7. doi:10.1016/j.ejps.2007.01.004.
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