Oxidative composition for treating keratin fibers comprising scleroglucan gum and phosphorus-based chelating agent
A technology for keratin fiber and sclerodextran glue is applied in the field of treating keratin fibers and cosmetic compositions for treating keratin fibers to achieve the effects of improving working quality, good dyeing or brightening properties, and improving cosmetic performance and quality
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Embodiment 1
[0345] Preparation of the composition
[0346] Compositions A and B were prepared with the ingredients and levels as indicated in Table I below.
[0347] Composition A was comparative and contained xanthan gum. Composition B is according to the invention and comprises sclerodextran gum.
[0348] Amounts are indicated in grams of active material unless otherwise indicated.
[0349] Table I
[0350]
[0351] To characterize the composition (see below), TO corresponds to the state of the system 24 hours after pH adjustment.
[0352] Characterization of the composition
[0353] Measure viscosity (at atmospheric pressure) as follows:
[0354] - ThermoHaake RS600 rheometer equipped with titanium C60 / 1° geometry (0.055mm gap)
[0355] - in 10s -1 flow in stages at 25 °C under a shear rate of
[0356] - The viscosity of the composition is measured weekly.
[0357] result
[0358] Figure 1a The change in viscosity of Composition A is shown as a function of time (indicated...
Embodiment 2
[0363] Preparation of the composition
[0364] Compositions C and D were prepared with the ingredients and levels as indicated in Table II below.
[0365] Composition C was comparative and contained a non-phosphorus-based chelating agent. Composition D is according to the present invention and contains a phosphorus-based chelating agent.
[0366] Amounts are indicated in grams of active material unless otherwise indicated.
[0367] Table II
[0368]
[0369] Characterization of the composition
[0370] macroscopic representation
[0371] Once Compositions C and D were prepared, they were stored at room temperature or at 45°C.
[0372] On the day after the preparation, the comparative composition C shows a significantly larger amount than in the composition D according to the invention, apparently due to the decomposition of hydrogen peroxide (release of oxygen), which occurs at both storage temperatures of air bubbles.
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