78 FORMULATING FOR MILDNESS
Conclusion The growing awareness of environmental aspects increases the focus on the raw materials used in cosmetic products. More and more, ingredients are preferred that are made from natural substances. For surfactants this applies to the hydrophobic and the hydrophilic part. The amino acid surfactants shown in Figures 1 and 2a are an ideal choice as their components - fatty acids and amino acids - are part of nature. The linkage between them is also ‘natural’. Therefore, amino acid surfactants are excellent biodegradable. They are proven to be mild with good foaming properties. For natural cosmetics, cocoyl glutamate is of special interest as it is completely based on renewable raw materials. For some customers in particular propylene glycol- free cocoyl glutamate solutions are ideal candidates for natural cosmetic applications. The N-acyl derivatives of glutamate,
sarcosine and glycine are the most popular amino acid surfactants in Europe. Zschimmer & Schwarz offers surfactants based on these amino acids for all needs of customers. The latest developments are the propylene glycol-free Protelan AG 37 (INCI: Disodium Cocoyl Glutamate, Sodium Cocoyl Glutamate) and Protelan GC-D (INCI: Sodium Cocoyl Glycinate). Both have a very low content of salt and free amino acids (in sum: below 0.2%). AG 37 is approvable for natural cosmetic labels. All Zschimmer & Schwarz products mentioned in this article are preservative-free and also available in RSPO-MB quality. The usage of amino acid surfactants in
combination with other suitable surfactants is a highly attractive way to create viscous cosmetic products without using thickeners: Lowering the pH-value starting from about 7 causes a steady protonation of the anionic carboxylate group(s) of amino acid surfactants. As a result of the neutral carboxylic function the micelle architecture changes completely. By this, viscous aqueous surfactant solutions can be created. This is the case in the particularly attractive pH-range at around 5-6. Besides this, cocoyl glutamates can additionally serve as viscosity reducer and are excellent emulsifiers for cold-processable oil-in-water emulsions. “We still do not know one thousandth of
one percent of what nature has revealed to us” (Albert Einstein). Extrapolated to amino acid surfactants this means: probably there are even more attractive possibilities for them in cosmetic applications which we do not know today.
PC
References 1 Hentrich W, Keppler H, Hintzmann K. Amides,
US Patent 2047069 (1936) 2 Wagner AT, Krohn T. Syndet Cleansing Bars: PERSONAL CARE ASIA PACIFIC
Table 2: Very mild and creamy foaming Body Shampoo Ingredients
INCI PROTELAN GG AMPHOTENSID B 5
Polyquaternium-47 (20%) Perfume Water
Sodium Cocoyl Glycinate, Disodium Cocoyl Glutamate Cocamidopropyl Betaine
Sodium Lauryl Sulfoacetate Sodium Lauryl Sulfoacetate Polyquaternium-47 Parfum (Fragrance) Aqua (Water)
Procedure: 1. Stir to homogeneity until the solution is clear. 2. Adjust the pH value with citric acid to 6.0.
Table 3: Shower Gel for natural cosmetics Phase Ingredients A
Water
B C
Xanthan Gum
ZUTELAN GL 810 ZUTELAN GL 124 Perfume
D PROTELAN AG 37
Sodium Cocoyl Hydrolyzed Wheat Protein
Sodium PCA Glycerin
Lactic acid (80 %) Sodium Benzoate Potassium Sorbate
INCI
Aqua (Water) Xanthan Gum
Caprylyl/Capryl Glucoside Lauryl Glucoside Parfum (Fragrance)
Disodium Cocoyl Glutamate / Sodium Cocoyl Glutamate
Sodium Cocoyl Hydrolyzed Wheat Protein Sodium PCA
Glycerin Lactic Acid
Sodium Benzoate Potassium Sorbate
Procedure: 1. Add B to A and stir to a homogeneous gel. 2. Combine C and stir until it is clear and homogenous. 3. Add all components of D to C in the indicated sequence and stir to homogeneity. 4. Combine AB and CD and stir to homogeneity. 5. Control the pH value and adjust if necessary to 5.3 - 5.5 (original).
The better “Soaps”?, Personal Care Magazine 2019; 13(3): 111 – 114
3 Wagner AT. Sulfate-free Surfactants: What about Sulfonates?, Personal Care Magazine 2018; 12(2): 61 – 65
4 Raykundaliya N, Bordes R, Holmberg K, Wu J, Somasundaran P, Shah DO. The effect on solution properties of replacing a hydrogen atom with a methyl group in a surfactant. Tenside Surfactants Detergents 2015; 52(5): 369 – 374.
5 Jungermann E, Gerecht JF, and Krems IJ, The preparation of Long Chain N-Acylamino Acids. J. Am. Chem. Soc. 1956; 78:172 – 174.
6 Bordes R, Tropsch J, Holmberg K. Role of an amide bond for self-assembly of surfactants. Langmuir 2010, 26 (5): 3077 – 3083.
7 Kaneko A, Sehgal P, Doe H. Interfacial and aggregation properties of aqueous N- dodecanoyl sarcosinate solution at different pH, Colloid Polymer Sci 2012, 290: 323 – 330
8 Preisig N, Schad T, Jacomine L, Bordes R, Stubenrauch C. How promoting and breaking intersurfactant H-bonds impact foam stability, Langmuir 2019, 35: 1499 – 15008
9 Stubenrauch C, Hamann M, Preisig N, Chauhan V, Bordes R. On how hydrogen bonds affect
foam stability, Advances in Colloid and Interface Science 2017, 247: 435 – 443
10 Regan J, Mollica LM, Ananthapadmanabhan KP. A novel glycinate-based body wash, J. Clin. Aesthet Dermatol 2013, 6(6): 23 – 30
11 Zhang Y, Romsted LS, Zhuang L, de Jong S. Simultaneous Determination of Interfacial Molarities of Amide Bonds, Carboxylate Groups, and Water by Chemical Trapping Micelles of Amphiphiles Containing Peptide Bond Models, Langmuir 2013; 29: 534−544
12 Rosen MJ, Zhu BY. Synergism in binary mixtures of surfactants, Journal of Colloid and Interface Science 1984; 99(2): 427 – 434
13 Li Y, Holmberg K, Bordes R. Micellization of true amphoteric surfactants, Journal of Colloid and Interface Science 2013; 411: 47 – 52
14 Wagner AT. Lecture: New hydrotropic surfactants. CESIO World Surfactant Conference 2019.
15 Wagner AT, Bach A, Wehler S. New multifunctional hydrotropic surfactants, SOFW Journal 2016, 142(10): 4 – 8
16 Wagner AT. Powerful surfactants from renewable raw materials, Personal Care Magazine 2016; 9(2): 34 – 36
November 2020
w/w% 50.5
0.5
15.0 5.0 0.4
20.0
1.25 1.2
4.2 1.5 0.3
0.15
w/w% 20.0
15.0 3.0 1.0 0.5
60.5
Page 1 |
Page 2 |
Page 3 |
Page 4 |
Page 5 |
Page 6 |
Page 7 |
Page 8 |
Page 9 |
Page 10 |
Page 11 |
Page 12 |
Page 13 |
Page 14 |
Page 15 |
Page 16 |
Page 17 |
Page 18 |
Page 19 |
Page 20 |
Page 21 |
Page 22 |
Page 23 |
Page 24 |
Page 25 |
Page 26 |
Page 27 |
Page 28 |
Page 29 |
Page 30 |
Page 31 |
Page 32 |
Page 33 |
Page 34 |
Page 35 |
Page 36 |
Page 37 |
Page 38 |
Page 39 |
Page 40 |
Page 41 |
Page 42 |
Page 43 |
Page 44 |
Page 45 |
Page 46 |
Page 47 |
Page 48 |
Page 49 |
Page 50 |
Page 51 |
Page 52 |
Page 53 |
Page 54 |
Page 55 |
Page 56 |
Page 57 |
Page 58 |
Page 59 |
Page 60 |
Page 61 |
Page 62 |
Page 63 |
Page 64 |
Page 65 |
Page 66 |
Page 67 |
Page 68 |
Page 69 |
Page 70 |
Page 71 |
Page 72 |
Page 73 |
Page 74 |
Page 75 |
Page 76 |
Page 77 |
Page 78 |
Page 79 |
Page 80 |
Page 81 |
Page 82 |
Page 83 |
Page 84 |
Page 85 |
Page 86 |
Page 87 |
Page 88 |
Page 89 |
Page 90 |
Page 91 |
Page 92 |
Page 93 |
Page 94 |
Page 95 |
Page 96