An intelligent temperature-sensitive hair dye that reduces the entry of aniline substances into the human body and its preparation method
A temperature-sensitive, hair dye technology, applied in the field of designing cosmetics, can solve the problems of scarcity of colors, long dyeing time, difficult extraction, etc., and achieve the effects of rich color selection, good color fastness, and short dyeing time
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Embodiment 1
[0048] Example 1: Study on the sustained release properties of Poosham hydrogel on phenylenediamine transdermal
[0049] The traditional hair dye formula [A agent (mass percent): deionized water 93.2%, 2% phenylenediamine, 1% emulsified silicon oil, 0.5% sodium sodium sulfate, EDTA; ammonia water; B dose: from 93.5%, hydrogen peroxide 6%, Carropham 0.5%], poloxham, and polithamimosham adding alginate to 2H transdermal experiments, and control the concentration of phenylenediamine 20 mg / ml, taking 2 mL under transdermal experiment at 32 ° C, the effect of removing oxidant, the experimental results figure 1 :
[0050] As can be seen from the experimental results of the above figure, the traditional hair dye has the largest transdermal amount of 1110 μg / cm2, and the amount of poloham hydrogel transdermal is decreased without adding the oalcate. It is 758μg / cm2, adding seaweed. The amount of water gel of sodium sodium is further reduced, and less than half of the transdermal amo...
Embodiment 2
[0051] Example 2: Preparation of cationic bonchri surfactants containing an amide group and an ester functional group
[0052] (1) Preparation of 1,2-bis (bromoacetoxy) ethane
[0053] The reaction was distilled with bromoacetic acid (0.21 mol) and ethylene glycol (0.1 mol) at 130 ° C without solvent conditions for 6 h. After the reaction is completed, the reactive crude mixture was first washed twice with 200 ml of deionized water, and then washed once with a mixed solution of 100 ml of methanol water (where 80 ml of methanol, 20 mL) was washed once, and the washed product was dissolved in trichloromethane. Then dry with anhydrous sodium sulfate, and finally evaporated to remove dichloromethane to give an oily liquid. The yield of the reaction was 47% by the total mass quality of the above-mentioned product was 47%, and by IR and 1 H NMR characterizes the purified target compound.
[0054]
[0055] (2) Preparation of N- [3- (dimethylamino) propyl] fatamide
[0056] First, fatty...
Embodiment 3
[0087] Example 3: The specific components of the prepared A agents and B agents are as follows:
[0088] A agent:
[0089]
[0090]
[0091] B dose:
[0092]
[0093] The above A and B binders are mixed together, stir well, apply it on a clean hair, attenuately maintained 30 minutes, and then clean the hair and clean it.
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