Patent Application
20170137372
Field of the Invention
The present invention relates to a medium-chain acyl basic amino acid derivative that suppresses gelation, and a cosmetic composition containing same.
Discussion of the Background
It has been reported that a compound represented by the following formula:
wherein Ra and Rb are each a hydrogen atom or an alkyl group, and n is an integer of 0 to 12, or a salt thereof (hereinafter to be also referred to as “lauroyl amino acid derivative”) is useful for gelling or solidifying water and a liquid organic medium (patent document 1, non-patent document 1 and non-patent document 2 etc.). Because of the properties of the lauroyl amino acid derivative as a surfactant, it improves affinity to the skin when blended in a cosmetic, and is also expected to exert a moisturizing ability.' Therefore, studies are ongoing as regards blending of the lauroyl amino acid derivative into cosmetics.
However, when the lauroyl amino acid derivative is blended in a liquid cosmetic such as skin lotion, skin milk and the like, a stable preparation is difficult to obtain due to the gelling ability of the lauroyl amino acid derivative per se, which problematically markedly restricts the usability thereof.
The present invention provides a medium-chain acyl basic amino acid derivative which, when blended in a liquid cosmetic such as skin lotion, skin milk and the like, suppresses gelation while maintaining affinity to the skin and the like and can afford a stable preparation.
The present inventors have conducted intensive studies in an attempt to solve the aforementioned problems and unexpectedly found that a medium-chain acyl basic amino acid derivative having a short acyl chain length suppresses gelation while maintaining affinity to the skin and the like, even when blended in a liquid cosmetic such as skin lotion, skin milk and the like, and the obtained preparation is stable, which resulted in the completion of the present invention.
Therefore, the present invention provides the following.
wherein
R1 and R2 are each independently an alkyl group having 5-7 carbon atoms or an alkenyl group having 5-7 carbon atoms,
R3 and R4 are each a hydrogen atom,
z is an integer of not less than 0, and
x and y are each independently an integer of 2 - 4,
or a salt thereof.
According to the present invention, a medium-chain acyl basic amino acid derivative which, when blended in a liquid cosmetic such as skin lotion, skin milk and the like, suppresses gelation while maintaining affinity to the skin and the like and can afford a stable preparation, can be provided.
The definition of each symbol of a compound represented by the formula (1) is described in the following.
R1 and R2 are each independently an alkyl group having 5-7 carbon atoms or an alkenyl group having 5-7 carbon atoms.
The alkyl group having 5-7 carbon atoms means a linear or branched alkyl group having 5-7 carbon atoms, and a pentyl group, an isopentyl group, a neopentyl group, a hexyl group, an isohexyl group, a neohexyl group, a heptyl group, an isoheptyl group, a neoheptyl group and the like can be specifically mentioned.
The alkenyl group having 5-7 carbon atoms means a linear or branched alkenyl group having 5-7 carbon atoms, and a pentenyl group, a hexenyl group, a heptenyl group and the like can be specifically mentioned.
R1 and R2 are preferably each independently an alkyl group having 5-7 carbon atoms, more preferably a pentyl group or a heptyl group.
R3 and R4 are each a hydrogen atom.
z is an integer of not less than 0.
z is preferably an integer of 0-10, more preferably 7 or 8.
x and y are each independently an integer of 2-4.
x and y are each preferably 4.
As a compound represented by the formula (1), the following compound can be preferably mentioned.
A compound wherein
R1 and R2 are each independently an alkyl group having 5-7 carbon atoms,
R3 and R4 are each a hydrogen atom,
z is an integer of 0-10, and
x and y are each 4.
A compound wherein
R1 and R2 are each a pentyl group or a heptyl group,
R3 and R4 are each a hydrogen atom,
z is 7 or 8, and
x and y are each 4.
Specific examples of a compound represented by the formula (1) include a compound selected from
bis(Nε-octanoyl-L-lysine)sebacoylamide,
bis(Nε-hexanoyl-L-lysine)azelaoylamide, and
bis(Nε-octanoyl-L-lysine)azelaoylamide,
and a salt thereof.
Examples of a salt of the medium-chain acyl basic amino acid derivative of the present invention include alkali metal salts such as a lithium salt, a sodium salt, a potassium salt and the like; alkali earth metal salts such as a calcium salt, a magnesium salt and the like; ammonium salts; a salt of an organic amine base such as methylamine, diethylamine, trimethylamine, triethylamine, ethanolamine, dethanolamine, triethanolamine, ethylenediamine, tris(hydroxymethyl)methylamine, dicyclohexylamine, N,N′-dibenzylethylenediamine, guanidine, pyridine, picoline, choline, cinchonine, meglumine and the like, and the like.
Of these, a sodium salt or a potassium salt is preferable, and a sodium salt is more preferable.
The medium-chain acyl basic amino acid derivative of the present invention can be produced by a conventionally-used method. For example, as shown in the following formula, symmetrical medium-chain acyl basic amino acid derivative (1′) can be produced by reacting Nω-acyl amino acid (2) and dicarboxylic acid dichloride (3) in an appropriate solvent.
wherein R1′ is an alkyl group having 5-7 carbon atoms or an alkenyl group having 5-7 carbon atoms, R3′ is a hydrogen atom, z′ is an integer of not less than 0, and x′ is an integer of 2-4.
Examples of the Nω-acyl amino acid (2) include Nε-acyl lysine (e.g., Nε-hexanoyl-L-lysine, Nε-octanoyl-L-lysine etc.), Nδ-acyl ornithine (e.g., Nδ-hexanoyl-L-ornithine etc.), Nγ-acyl-α,γ-diaminobutyric acid and the like.
Examples of the dicarboxylic acid dichloride (3) include oxalyl chloride, malonyl chloride, succinyl chloride, glutaryl chloride, adipoyl chloride, pimeloyl chloride, suberoyl chloride, azelaoyl chloride, sebacoyl chloride, dodecanedioyl chloride and the like. The amount of dicarboxylic acid dichloride (3) to be used is generally 0.4-0.6 equivalent relative to Nω-acyl amino acid (2).
While the solvent is not particularly limited as long as it is inert to the reaction, examples thereof include ethers such as diethyl ether, tetrahydrofuran and the like.
In addition, asymmetric medium-chain acyl basic amino acid derivative (1″) can be produced as follows. First, Nω-acyl amino acid (2) and dicarboxylic acid monochloride monoester (4) are reacted in an appropriate solvent to give compound (5) (step 1). Then, the ester moiety of the obtained compound (5) is hydrolyzed in the presence of a base such as sodium hydroxide, potassium hydroxide and the like, the carboxylic acid moiety is chlorinated with a chlorinating agent such as thionyl chloride and the like, and the compound is reacted with Nω-acyl amino acid (2′) which is different from Nω-acyl amino acid (2) used in the aforementioned step 1 (step 2), whereby derivative (1″) can be produced.
wherein R1′, R3′, z′ and x′ are as defined above, R2′ is an alkyl group having 5-7 carbon atoms or an alkenyl group having 5-7 carbon atoms, R4′ is a hydrogen atom, R5 is an alkyl group such as a methyl group, an ethyl group and the like, and y′ is an integer of 2-4.
As Nω-acyl amino acids (2) and (2′), Nωl-acyl amino acids similar to those mentioned above can be used.
As dicarboxylic acid monochloride monoester (4), a commercially available product can be used as is when it is commercially available, or one produced by a method known per se or a method analogous thereto can also be used.
A medium-chain acyl basic amino acid derivative obtained by the above-mentioned method can be converted to a salt of the medium-chain acyl basic amino acid derivative by a reaction with alkali metal hydroxide such as sodium hydroxide, potassium hydroxide and the like, alkali earth metal hydroxide such as calcium hydroxide and the like, organic amine base, or the like.
The present invention also relates to a cosmetic composition containing the above-mentioned medium-chain acyl basic amino acid derivative or a salt thereof.
The amount of the above-mentioned medium-chain acyl basic amino acid derivative or a salt thereof in the cosmetic composition of the present invention is preferably 0.01-10 wt %, more preferably 0.05-5 wt %.
Specific examples of the cosmetic composition of the present invention include facial cleanser, skin lotion, skin milk, cream, gel, beauty essence, facial mask, mask, face powder, foundation, lip rouge, cheek rouge, eyeliner, mascara, eye shadow, eyebrow pencil, shampoo, rinse, hair conditioner, hair styling agent, hair treatment and the like.
Of these, skin lotion or skin milk is preferable.
The cosmetic composition of the present invention may contain a component that can be generally added to cosmetics as long as the effect of the present invention is not inhibited. Specific examples include oil, chelating agent, surfactant, powder, amino acid, polyvalent alcohol, polyamino acid and salt thereof, water-soluble polymer, sugar alcohol and alkylene oxide adduct thereof, lower alcohol, animal and plant extract, nucleic acid, vitamin, enzyme, anti-inflammatory agent, antimicrobial agent, preservative, antioxidant, ultraviolet absorber, adiaphoretic, pigment, dye, oxidation dye, organic and inorganic powder, pH adjuster, pearly sheen agent, and wetting agent.
The present invention is explained in detail in the following by referring to Examples, which are not to be construed as limitative.
The instrument used for the measurement of the compound was as described below.
1H-NMR measurement: Bruker, AVANCE III HD NMR Spectrometer
Nε-octanoyl-L-lysine (6.8 g, 25 mmol) was dissolved in water (70 g) and 25% aqueous sodium hydroxide solution (10 g), and diethyl ether (80 g) was added. Sebacoyl chloride (3.3 g, 14 mmol) was slowly added to the ether layer. The two-layer solution was stirred for about 1 hr while maintaining at 0° C., and then at room temperature for 23 hr. Then, 75% sulfuric acid was added dropwise to adjust to pH 2, the obtained white precipitate was collected by filtration, washed well with water and dried. The obtained compound was dissolved in an aqueous sodium hydroxide solution to adjust to pH 6.0, evaporated to dryness and recrystallized from methanol-diethyl ether to give the title compound (8.6 g, 94%).
1H-NMR (400 MHz, CD3OD, TMS, 25° C.): δ 0.89 (t, J=6.9 Hz, 6H), 1.31 (br, 28H), 1.36-1.45 (m, 4H), 1.47-1.54 (m, 4H), 1.55-1.63 (m, 8H), 1.64-1.72 (m, 2H), 1.79-1.89 (m, 2H), 2.15 (t, J=7.4 Hz, 4H), 2.23 (t, J=7.4 Hz, 4H), 3.15 (t, J=6.9 Hz, 4H), 4.35 (m, 2H)
Nε-hexanoyl-L-lysine (12.2 g, 50 mmol) was dissolved in water (130 g) and 25% aqueous sodium hydroxide solution (20 g), and diethyl ether (150 g) was added. Azelaoyl chloride (6.2 g, 28 mmol) was slowly added to the ether layer. The two-layer solution was stirred for about 1 hr while maintaining at 0° C., and then at room temperature for 23 hr. Then, 75% sulfuric acid was added dropwise to adjust to pH 2, and the obtained oily viscous substance was extracted with 2-propanol. 2-Propanol was evaporated under reduced pressure, the obtained compound was dissolved in an aqueous sodium hydroxide solution to adjust to pH 6.0, evaporated to dryness and recrystallized from methanol-diethyl ether to give the title compound (7.8 g, 47%).
1H-NMR (400 MHz, CD3OD, TMS, 25° C.): δ 0.90 (t, J=6.9 Hz, 6H), 1.31 (br, 18H), 1.36-1.45 (m, 4H), 1.47-1.54 (m, 4H), 1.55-1.63 (m, 8H), 1.64-1.72 (m, 2H), 1.79-1.89 (m, 2H), 2.15 (t, J=7.5 Hz, 4H), 2.23 (t, J=7.5 Hz, 4H), 3.15 (m, 4H2), 4.30 (m, 2H)
Using Nε-octanoyl-L-lysine and azelaoyl chloride, the title compound (8.0 g, 89%) was synthesized by a method almost similar to Production Example 1.
1H-NMR (400 MHz, CD3OD, TMS, 25° C.): δ 0.89 (t, J=6.9 Hz, 6H), 1.31 (br, 26H), 1.36-1.45 (m, 4H), 1.47-1.54 (m, 4H), 1.55-1.63 (m, 8H), 1.64-1.72 (m, 2H), 1.79-1.89 (m, 2H), 2.15 (t, J=7.4 Hz, 4H), 2.23 (t, J=7.4 Hz, 4H), 3.15 (t, J=6.9 Hz, 4H), 4.30 (m, 2H)
Using Nε-lauroyl-L-lysine and sebacoyl chloride, the title compound was synthesized by a method almost similar to Production Example 1.
Using Nε-lauroyl-L-lysine and azelaoyl chloride, the title compound was synthesized by a method almost similar to Production Example 1.
A cosmetic composition (skin lotion) having the composition (unit: wt %) shown in the following Table 1 was prepared by the method described in the following 1, and the stability, coatability and affinity to the skin of the obtained cosmetic composition were evaluated by the method described in the following 2. and 3.
The compound synthesized in the above-mentioned Production Example, various additives shown in the following Table 1 and water were stirred at 70° C. and uniformly dissolved. The mixture was cooled to room temperature, and pH was adjusted to 6.0 with citric acid to give a cosmetic composition (skin lotion).
The cosmetic composition prepared in the above-mentioned 1. was filled in a glass bottle, and stood at room temperature for 12 hr. Then, the glass bottle was placed upside down, visually observed, and evaluated by the following criteria.
The coatability and affinity to the skin of the cosmetic composition prepared in the above-mentioned 1. were evaluated by 5 professional panelists according to the following criteria.
When a cosmetic composition is taken on a hand from a container and actually spread on the back of the hand,
An average score of the professional panelists of not less than 4 was marked with ⊙, not less than 3 and less than 4 was marked with ◯, not less than 2 and less than 3 was marked with Δ, and less than 2 was marked with ×.
When a cosmetic composition is spread on the back of a hand,
An average score of the professional panelists of not less than 4 was marked with ⊙, not less than 3 and less than 4 was marked with ◯, not less than 2 and less than 3 was marked with Δ, and less than 2 was marked with ×.
The results are shown in Table 1.
The cosmetic composition free of a medium-chain acyl basic amino acid derivative (Comparative Example 1) showed good stability but showed very bad affinity to the skin. The cosmetic compositions containing a lauroyl amino acid derivative (Comparative Examples 2-4) showed comparatively good affinity to the skin but showed bad stability due to gelation and were difficult to apply.
On the other hand, the cosmetic compositions containing the medium-chain acyl basic amino acid derivative of the present invention (Examples 1-4) were stable, easily applied, and very superior in the affinity to the skin.
The present invention can provide a medium-chain acyl basic amino acid derivative which, when blended in a liquid cosmetic such as skin lotion, skin milk and the like, suppresses gelation while maintaining affinity to the skin and the like and can afford a stable preparation.
Where a numerical limit or range is stated herein, the endpoints are included. Also, all values and subranges within a numerical limit or range are specifically included as if explicitly written out.
As used herein the words “a” and “an” and the like carry the meaning of “one or more.”
Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that, within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.
All patents and other references mentioned above are incorporated in full herein by this reference, the same as if set forth at length.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2014-154444 | Jul 2014 | JP | national |
This application is a continuation of International Patent Application No. PCT/JP2015/071431, filed on Jul. 29, 2015, and claims priority to Japanese Patent Application No. 2014-154444, filed on Jul. 30, 2014, both of which are incorporated herein by reference in their entireties.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/JP2015/071431 | Jul 2015 | US |
| Child | 15417628 | US |
