JP5297768B2 - Sweat odor generation inhibitor composition - Google Patents
Sweat odor generation inhibitor composition Download PDFInfo
- Publication number
- JP5297768B2 JP5297768B2 JP2008287606A JP2008287606A JP5297768B2 JP 5297768 B2 JP5297768 B2 JP 5297768B2 JP 2008287606 A JP2008287606 A JP 2008287606A JP 2008287606 A JP2008287606 A JP 2008287606A JP 5297768 B2 JP5297768 B2 JP 5297768B2
- Authority
- JP
- Japan
- Prior art keywords
- component
- sweat odor
- odor generation
- sweat
- carbon atoms
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
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Description
本発明は、汗臭発生抑制剤組成物、汗臭発生抑制剤物品及び汗臭発生抑制方法に関する。 The present invention relates to a sweat odor generation inhibitor composition, a sweat odor generation inhibitor article, and a sweat odor generation suppression method.
香料成分を用いて汗臭を消臭する技術として、特許文献1には、汗臭に消臭効果のある香料を含有する消臭剤が記載されている。また、特許文献2には、居住空間の消臭に好適な液体消臭剤組成物の技術が開示されており、特許文献3には、香料成分を配合した衣料用消臭防しわ剤の技術が開示されている。
汗は発汗した初期はほとんど臭いを発生しないが、適度な温度/湿度下で放置すると所謂汗臭として知られている悪臭を発生する。このような汗臭は、オーデコロンや香水などの芳香剤や、汗臭をマスキングする香料を含有した消臭剤で消臭することが一般的である。しかしながら、このような香料によるマスキング法では汗臭を消し去ることができるわけではなく、汗臭の発生そのものを抑制する技術が強く求められている。 In the early stage of sweating, sweat hardly generates odor, but if left under moderate temperature / humidity, a bad odor known as so-called sweat odor is generated. Such sweat odor is generally deodorized with a deodorant containing a fragrance such as a cologne or perfume or a fragrance that masks the sweat odor. However, such a masking method using a fragrance does not eliminate the sweat odor, and there is a strong demand for a technique for suppressing the generation of the sweat odor itself.
上記特許文献1〜3に記載されている消臭剤に関しても、実施例で具体的に使用している香料成分は、瞬時に悪臭をマスキングするための、比較的揮発性の高いトップノートやミドルノートの範疇に入るものが多く、また、エチルブラシレートのような大環状ムスク系香料を用いた例示もあるが、特定の大環状香料成分が汗臭の発生そのものを抑制し得ることについてはなんら示唆はない。 Regarding the deodorizers described in the above Patent Documents 1 to 3, the perfume ingredients specifically used in the examples are relatively highly volatile top notes and middles for instantly masking malodors. There are many that fall within the category of notes, and there are also examples using macrocyclic musk fragrances such as ethyl brushate, but there is nothing about the fact that specific macrocyclic fragrance ingredients can suppress the occurrence of sweat odor itself. There is no suggestion.
従って本発明の課題は、汗臭の発生そのものを抑制し得る汗臭発生抑制剤組成物及び汗臭発生抑制方法を提供することにある。 Accordingly, an object of the present invention is to provide a sweat odor generation inhibitor composition and a sweat odor generation suppression method capable of suppressing the generation of sweat odor itself.
本発明者らは、汗臭の発生メカニズムを詳細に検討したところ、一般的に汗臭の原因として考えられているアンモニアや脂肪酸よりも、フェノール系化合物やインドール類が、汗臭への寄与が高い成分であること、さらには、これらフェノール系化合物やインドール類は、菌体由来のβ−グルクロニダーゼが汗に作用することで発生することを見出した。 The present inventors have examined in detail the mechanism of sweat odor generation, and phenolic compounds and indoles contribute to sweat odor rather than ammonia and fatty acids, which are generally considered causes of sweat odor. It has been found that these phenolic compounds and indoles are high components and are generated by the action of β-glucuronidase derived from bacterial cells on sweat.
そして、これまで、保留性が高く揮発性が低いためにマスキング法による消臭技術において用いられてこなかった香料成分の中に、β−グルクロニダーゼの活性を阻害するものがあることを見出し、本発明に至ったものである。 And until now, it has been found that some of the perfume ingredients that have not been used in the deodorization technology by the masking method because of its high retention and low volatility inhibit the activity of β-glucuronidase, and the present invention. Has been reached.
即ち、本発明は、下記(a)成分及び(b)成分を含有する汗臭発生抑制剤組成物を提供する。
(a)成分:3−メチル−4−シクロペンタデセン−1−オン、3−メチル−5−シクロペンタデセン−1−オン、5−シクロヘキサデセン−1−オン、8−シクロヘキサデセン−1−オン、9−シクロヘプタデセン−1−オン、7−シクロヘキサデセノリド及び10−オキサ―16−ヘキサデカノリドから選ばれるβ−グルクロニダーゼ阻害剤の1種以上、
(b)成分:界面活性剤(b1)及び溶剤(b2)から選ばれる1種以上
また、本発明は、上記(a)成分、(b)成分、及び水を含有する汗臭発生抑制剤組成物を、トリガー式スプレーヤーを具備した容器に充填してなる汗臭発生抑制剤物品、並びに上記(a)成分、(b)成分、及び水を含有する汗臭発生抑制剤組成物を、汗の付着した繊維製品又は革製品に接触させる汗臭発生抑制方法を提供する。
That is, this invention provides the sweat odor generation inhibitor composition containing the following (a) component and (b) component.
Component (a): 3-methyl-4-cyclopentadecene-1-one, 3-methyl-5-cyclopentadecene-1-one, 5-cyclohexadecene-1-one, 8-cyclohexadecene-1-one , One or more β-glucuronidase inhibitors selected from 9-cycloheptadecen-1-one, 7-cyclohexadecenolide and 10-oxa-16-hexadecanolide,
Component (b): One or more selected from surfactant (b1) and solvent (b2) The present invention also relates to a sweat odor generation inhibitor composition containing the component (a), the component (b), and water. A sweat odor generation inhibitor article comprising a container filled with a trigger sprayer, and a sweat odor generation inhibitor composition containing the above components (a), (b) and water, The present invention provides a method for suppressing the generation of sweat odor by bringing it into contact with a textile product or leather product to which water adheres.
本発明の汗臭発生抑制剤組成物及び汗臭発生抑制剤物品により、汗臭の発生そのものを抑制することができる。 With the sweat odor generation inhibitor composition and sweat odor generation inhibitor article of the present invention, the generation of sweat odor itself can be suppressed.
[(a)成分]
本発明の(a)成分は、3−メチル−4−シクロペンタデセン−1−オン、3−メチル−5−シクロペンタデセン−1−オン、5−シクロヘキサデセン−1−オン、8−シクロヘキサデセン−1−オン、9−シクロヘプタデセン−1−オン、7−シクロヘキサデセノリド及び10−オキサ―16−ヘキサデカノリドから選ばれる15〜17員環の大環状化合物の1種以上である。これらの化合物は、β−グルクロニダーゼの活性を阻害する機能を有し、持続的にフェノール系化合物やインドール類の発生を抑制する効果を有する。本発明における「β−グルクロニダーゼ阻害剤」とは、下記に示す方法により測定したβ-グルクロニダーゼの相対活性阻害率が40%以上の化合物をいう。
[(A) component]
The component (a) of the present invention includes 3-methyl-4-cyclopentadecene-1-one, 3-methyl-5-cyclopentadecene-1-one, 5-cyclohexadecene-1-one, and 8-cyclohexadecene. It is at least one of 15 to 17-membered macrocyclic compounds selected from -1-one, 9-cycloheptadecen-1-one, 7-cyclohexadecenolide and 10-oxa-16-hexadecanolide. These compounds have a function of inhibiting the activity of β-glucuronidase and have an effect of continuously suppressing the generation of phenolic compounds and indoles. The “β-glucuronidase inhibitor” in the present invention refers to a compound having a relative activity inhibition rate of β-glucuronidase measured by the method shown below of 40% or more.
<β-グルクロニダーゼ相対活性阻害率の測定方法>
γ線滅菌済み容器中に、2mMのp-ニトロフェニル−β−D−グルクロニド水溶液100μL、0.5Mリン酸バッファー(pH6.8)40μL、イオン交換水38μL、サンプル化合物の10質量%DPG(ジプロピレングリコール)溶液2μLを混合し、続いて16units/mLに調整したβ-グルクロニダーゼ水溶液20μLを加えて、37℃恒温槽中で2時間酵素反応を行った。試験化合物の反応液中での濃度は0.1質量%であった。また、サンプル化合物の代わりにDPGを加えたものをコントロールとし、サンプル化合物及びコントロールごとに、酵素液の代わりにイオン交換水を加えたものをブランクとして、それぞれ同様に2時間反応を行った。上記反応液を0.2Mグリシンバッファー(pH10.4)を用いて希釈し、波長400nmにおける吸光度を測定した。得られた測定値より、次式に従ってβ-グルクロニダーゼの相対活性阻害率を求めた。
<Method of measuring relative activity inhibition rate of β-glucuronidase>
In a γ-ray sterilized container, 100 μL of 2 mM p-nitrophenyl-β-D-glucuronide aqueous solution, 40 μL of 0.5 M phosphate buffer (pH 6.8), 38 μL of ion-exchanged water, 10% by mass of DPG (di Propylene glycol) solution (2 μL) was mixed, followed by addition of 20 μL of β-glucuronidase aqueous solution adjusted to 16 units / mL, and an enzyme reaction was performed in a 37 ° C. constant temperature bath for 2 hours. The concentration of the test compound in the reaction solution was 0.1% by mass. Moreover, the thing which added DPG instead of the sample compound was made into the control, and what added ion-exchange water instead of the enzyme liquid was made into the blank for every sample compound and control, and it reacted similarly for 2 hours, respectively. The reaction solution was diluted with 0.2 M glycine buffer (pH 10.4), and the absorbance at a wavelength of 400 nm was measured. From the obtained measured value, the relative activity inhibition rate of β-glucuronidase was determined according to the following formula.
「コントロール吸光度変化」=コントロール吸光度−コントロールのブランクの吸光度
「サンプル吸光度変化」=サンプル吸光度−サンプルのブランクの吸光度
本発明に係わる(a)成分の化合物について、上記方法でβ-グルクロニダーゼの相対活性阻害率を求めた結果を表1に示す。
“Control Absorbance Change” = Control Absorbance−Control Blank Absorbance “Sample Absorbance Change” = Sample Absorbance−Sample Blank Absorbance Relative activity inhibition of β-glucuronidase by the above-described method with respect to the compound of component (a) according to the present invention The results of the rate are shown in Table 1.
本発明の(a)成分としては、特に8−シクロヘキサデセン−1−オンが好適である。 As the component (a) of the present invention, 8-cyclohexadecene-1-one is particularly preferable.
[(b)成分]
本発明の(b)成分は、界面活性剤(b1)及び溶剤(b2)から選ばれる1種以上である。これら(b)成分は、(a)成分を対象物に効果的に浸透させ、β−グルクロニダーゼ活性阻害効果を高める重要な作用を有する。これら(b)成分はまた、汗臭発生抑制剤組成物が水性組成物である場合には、(a)成分を組成物中に安定に配合する効果を有する。
[Component (b)]
The component (b) of the present invention is at least one selected from the surfactant (b1) and the solvent (b2). These (b) components have the important effect | action which permeate | transmits a (a) component effectively to a target object and improves the beta-glucuronidase activity inhibitory effect. These components (b) also have an effect of stably blending the component (a) into the composition when the sweat odor generation inhibitor composition is an aqueous composition.
界面活性剤(b1)としては、非イオン界面活性剤、両性界面活性剤、陽イオン界面活性剤、及び陰イオン界面活性剤から選ばれる化合物を用いることができる。 As the surfactant (b1), a compound selected from a nonionic surfactant, an amphoteric surfactant, a cationic surfactant, and an anionic surfactant can be used.
非イオン界面活性剤としては、下記一般式(Surf−1)で示されるポリオキシアルキレンアルキルエーテル型非イオン界面活性剤、下記一般式(Surf−2)で示されるアルキルグリコシド型非イオン界面活性剤を挙げることができる。 Examples of the nonionic surfactant include a polyoxyalkylene alkyl ether type nonionic surfactant represented by the following general formula (Surf-1) and an alkylglycoside type nonionic surfactant represented by the following general formula (Surf-2). Can be mentioned.
R4−(OR5)n−OH (Surf−1)
〔式中、R4は炭素数8〜16、好ましくは10〜14の炭化水素基、好ましくはアルキル基であり、R5は炭素数2又は3のアルキレン基、好ましくはエチレン基であり、nはオキシアルキレン基の平均付加モル数を示す4〜10の数であり、n個のR5は同一でも異なっていても良い。〕
R6−(OR7)pGq (Surf−2)
〔式中、R6は直鎖の炭素数8〜16、好ましくは10〜16、特に好ましくは10〜14のアルキル基、R7は炭素数2〜4のアルキレン基、好ましくはエチレン基又はプロピレン基、特にエチレン基であり、Gは還元糖に由来する残基、pはオキシアルキレン基の平均付加モル数を示す0〜6の数であり、p個のR7は同一でも異なっていても良い。qはグルコースの平均縮合度を示す1〜10、好ましくは1〜5、特に好ましくは1〜2の数である。〕
両性界面活性剤としては、アミンオキシド型両性界面活性剤、スルホベタイン型両性界面活性剤及びカルボベタイン型両性界面活性剤が好適であり、具体的には、下記一般式(Surf−3)、下記一般式(Surf−4)の化合物が好ましい。
R 4 - (OR 5) n -OH (Surf-1)
[Wherein R 4 is a hydrocarbon group having 8 to 16 carbon atoms, preferably 10 to 14 carbon atoms, preferably an alkyl group, R 5 is an alkylene group having 2 or 3 carbon atoms, preferably an ethylene group, n Is a number from 4 to 10 indicating the average number of moles added of the oxyalkylene group, and the n R 5 s may be the same or different. ]
R 6- (OR 7 ) pGq (Surf-2)
[Wherein R 6 is a linear alkyl group having 8 to 16 carbon atoms, preferably 10 to 16 carbon atoms, particularly preferably 10 to 14 carbon atoms, and R 7 is an alkylene group having 2 to 4 carbon atoms, preferably ethylene group or propylene. A group, particularly an ethylene group, G is a residue derived from a reducing sugar, p is a number from 0 to 6 indicating the average number of moles added of the oxyalkylene group, and p R 7 may be the same or different. good. q is a number of 1 to 10, preferably 1 to 5, particularly preferably 1 or 2, indicating the average degree of condensation of glucose. ]
As the amphoteric surfactants, amine oxide type amphoteric surfactants, sulfobetaine type amphoteric surfactants and carbobetaine type amphoteric surfactants are suitable. Specifically, the following general formula (Surf-3), Compounds of general formula (Surf-4) are preferred.
〔式中、R8は直鎖の炭素数8〜16、好ましくは10〜16、特に好ましくは10〜14のアルキル基、R9は炭素数2〜4のアルキレン基、好ましくはエチレン基又はプロピレン基であり、Xは−COO−又は−CONH−、rは0又は1の数であり、R10及びR11はそれぞれ独立に炭素数1〜3のアルキル基又はヒドロキシアルキル基であり、好ましくはメチル基である。〕 [Wherein R 8 is a linear alkyl group having 8 to 16, preferably 10 to 16, particularly preferably 10 to 14 carbon atoms, and R 9 is an alkylene group having 2 to 4 carbon atoms, preferably ethylene group or propylene. X is —COO— or —CONH—, r is a number of 0 or 1, and R 10 and R 11 are each independently an alkyl group or a hydroxyalkyl group having 1 to 3 carbon atoms, preferably It is a methyl group. ]
〔式中、R12は直鎖の炭素数8〜16、好ましくは10〜16、特に好ましくは10〜14のアルキル基、R13は炭素数2〜4のアルキレン基、好ましくはエチレン基又はプロピレン基であり、Yは−COO−又は−CONH−、sは0又は1の数、好ましくは1の数であり、R14及びR15はそれぞれ独立に炭素数1〜3のアルキル基又はヒドロキシアルキル基であり、好ましくはメチル基であり、R16はヒドロキシ基で置換されていてもよい炭素数1〜3のアルキレン基である。Z-は−SO3 -又は−COO-である。〕
陽イオン界面活性剤としては、下記一般式(Surf−5)の化合物が好ましい。
[Wherein R 12 is a linear alkyl group having 8 to 16, preferably 10 to 16, particularly preferably 10 to 14 carbon atoms, and R 13 is an alkylene group having 2 to 4 carbon atoms, preferably ethylene group or propylene. Y is —COO— or —CONH—, s is a number of 0 or 1, preferably a number of 1, and R 14 and R 15 are each independently an alkyl group or hydroxyalkyl having 1 to 3 carbon atoms. A group, preferably a methyl group, and R 16 is an alkylene group having 1 to 3 carbon atoms which may be substituted with a hydroxy group. Z − is —SO 3 — or —COO 2 — . ]
As the cationic surfactant, a compound represented by the following general formula (Surf-5) is preferable.
〔式中、R17は炭素数8〜12のアルキル基、R18は炭素数1〜3のアルキル基又は炭素数8〜12のアルキル基、R19は炭素数1〜3のアルキル基、好ましくはメチル基であり、R20は炭素数1〜3のアルキル基又はベンジル基である。ここで、R20が炭素数1〜3のアルキル基の場合にはR18は炭素数8〜12のアルキル基が好ましく、R20がベンジル基の場合にはR18は炭素数1〜3のアルキル基が好適である。〕
陰イオン界面活性剤としては、炭素数10〜18のアルキル基又はアルケニル基を有するアルキルベンゼンスルホン酸塩、ポリオキシアルキレンアルキルエーテル硫酸エステル塩、アルキル硫酸エステル塩、α−オレフィンスルホン酸塩、α−スルホ脂肪酸塩、α−スルホ脂肪酸低級アルキルエステル塩又は脂肪酸から選ばれる陰イオン界面活性剤を挙げることができる。
[Wherein R 17 is an alkyl group having 8 to 12 carbon atoms, R 18 is an alkyl group having 1 to 3 carbon atoms or an alkyl group having 8 to 12 carbon atoms, and R 19 is an alkyl group having 1 to 3 carbon atoms, preferably Is a methyl group, and R 20 is an alkyl group having 1 to 3 carbon atoms or a benzyl group. Here, when R 20 is an alkyl group having 1 to 3 carbon atoms, R 18 is preferably an alkyl group having 8 to 12 carbon atoms, and when R 20 is a benzyl group, R 18 is an alkyl group having 1 to 3 carbon atoms. Alkyl groups are preferred. ]
Examples of the anionic surfactant include alkylbenzene sulfonate having 10 to 18 carbon atoms or alkenyl group, polyoxyalkylene alkyl ether sulfate, alkyl sulfate, α-olefin sulfonate, α-sulfone. Mention may be made of an anionic surfactant selected from fatty acid salts, α-sulfo fatty acid lower alkyl ester salts or fatty acids.
本発明では、界面活性剤(b1)として、両性界面活性剤及び陽イオン界面活性剤が好ましく、一般式(Surf−3)のアミンオキシド型両性界面活性剤及び一般式(Surf−5)の陽イオン界面活性剤がより好ましく、特に一般式(Surf−3)のアミンオキシド型両性界面活性剤が好ましい。 In the present invention, as the surfactant (b1), an amphoteric surfactant and a cationic surfactant are preferable, and an amine oxide amphoteric surfactant of the general formula (Surf-3) and a positive formula of the general formula (Surf-5) are used. Ionic surfactants are more preferred, and amine oxide amphoteric surfactants of general formula (Surf-3) are particularly preferred.
溶剤(b2)としては、下記(i)〜(iii)から選ばれる化合物が好ましい。 As the solvent (b2), compounds selected from the following (i) to (iii) are preferable.
(i)炭素数1〜3の一級アルコール、
(ii)下記一般式(Solv-1)で示される化合物、
R1−(OR2)m−OR3 (Solv-1)
〔式中、R1及びR3はそれぞれ独立に水素原子又は炭素数1〜7の炭化水素基であり、R2は炭素数2又は3のアルキレン基であり、mは1〜6の数であり、m個のR2は同一でも異なっていても良い。〕
(iii)炭素数3〜10の1価アルコールにグリシドール及び/又はエピクロルヒドリンを平均1〜5モル付加させたアルキル(ポリ)グリセリルエーテル
(i)の化合物の具体的例としては、エタノール、プロパノール、イソプロパノールであり、(ii)の化合物の具体的例としてはエチレングリコール、プロピレングリコール、ジエチレングリコール、ジプロピレングリコール、トリエチレングリコール、トリプロピレングリコール、エチレングリコールモノブチルエーテル、ジプロピレングリコールジメチルエーテル、ジエチレングリコールモノエチルエーテル、ジエチレングリコールモノブチルエーテル、プロピレングリコールモノメチルエーテル、プロピレングリコールモノブチルエーテル、プロピレングリコールモノエチルエーテル、プロピレングリコールジメチルエーテル、ポリオキシエチレン(m1=2〜3)ポリオキシプロピレン(m2=2〜3)グリコールジメチルエーテル(m1及びm2はそれぞれ平均付加モル数を示す)、ポリオキシエチレン(m3=1〜5)グリコールフェニルエーテル、フェニルカルビトール、フェニルセロソルブ、ベンジルカルビトールを挙げることができる。また、(iii)の化合物としては炭素数4〜10のアルキルモノグリセリルエーテル、アルキルジグリセリルエーテル等が挙げられる。
(I) a primary alcohol having 1 to 3 carbon atoms,
(Ii) a compound represented by the following general formula (Solv-1),
R 1- (OR 2 ) m-OR 3 (Solv-1)
[Wherein, R 1 and R 3 are each independently a hydrogen atom or a hydrocarbon group having 1 to 7 carbon atoms, R 2 is an alkylene group having 2 or 3 carbon atoms, and m is a number of 1 to 6] Yes, m R 2 may be the same or different. ]
(Iii) Alkyl (poly) glyceryl ether obtained by adding 1 to 5 moles of glycidol and / or epichlorohydrin on average to a monohydric alcohol having 3 to 10 carbon atoms. Examples of the compound of (i) include ethanol, propanol and isopropanol. Specific examples of the compound (ii) include ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, triethylene glycol, tripropylene glycol, ethylene glycol monobutyl ether, dipropylene glycol dimethyl ether, diethylene glycol monoethyl ether, diethylene glycol. Monobutyl ether, propylene glycol monomethyl ether, propylene glycol monobutyl ether, propylene glycol monoethyl ether , Propylene glycol dimethyl ether, polyoxyethylene (m1 = 2 to 3), polyoxypropylene (m2 = 2 to 3) glycol dimethyl ether (m1 and m2 each represent an average number of moles added), polyoxyethylene (m3 = 1 to 5) ) Glycol phenyl ether, phenyl carbitol, phenyl cellosolve, benzyl carbitol. Moreover, as a compound of (iii), C4-C10 alkyl monoglyceryl ether, alkyl diglyceryl ether, etc. are mentioned.
本発明では、溶剤(b2)として、エタノール、イソプロパノール及び炭素数6〜10のアルキルモノグリセリルエーテルから選ばれる1種以上が好ましく、特にエタノール及び2−エチルヘキシルグリセリルエーテルから選ばれる1種以上が好ましい。 In the present invention, the solvent (b2) is preferably at least one selected from ethanol, isopropanol, and alkyl monoglyceryl ether having 6 to 10 carbon atoms, and more preferably at least one selected from ethanol and 2-ethylhexyl glyceryl ether.
[(c)成分]
本発明では、任意ではあるが、汗臭を抑制するとともに消臭効果を付与することが好ましく、その目的から(c)成分としてキレート化剤を含有することが好ましい。(c)成分としては、具体的には下記の化合物を挙げることができる。
(1)フィチン酸などのリン酸系化合物またはこれらのアルカリ金属塩もしくはアルカノールアミン塩。
(2)エタン−1,1−ジホスホン酸、エタン−1,1,2−トリホスホン酸、エタン−1−ヒドロキシ−1,1−ジホスホン酸及びその誘導体、エタンヒドロキシ−1,1,2−トリホスホン酸、エタン−1,2−ジカルボキシ−1,2−ジホスホン酸、メタンヒドロキシホスホン酸などのホスホン酸またはこれらのアルカリ金属塩もしくはアルカノールアミン塩。
(3)2-ホスホノブタン−1,2−ジカルボン酸、1-ホスホノブタン−2,3,4−トリカルボン酸、α−メチルホスホノコハク酸などのホスホノカルボン酸またはこれのアルカリ金属塩もしくはアルカノールアミン塩。
(4)アスパラギン酸、グルタミン酸、グリシンなどのアミノ酸またはこれらのアルカリ金属 塩もしくはアルカノールアミン塩。
(5)ニトリロ三酢酸、イミノ二酢酸、エチレンジアミン四酢酸、ジエチレントリアミン五酢酸、グリコールエーテルジアミン四酢酸、ヒドロキシエチルイミノ二酢酸、トリエチレンテトラミン六酢酸、ジエンコル酸、アルキルグリシン−N,N−ジ酢酸、アスパラギン酸−N,N−ジ酢酸、セリン−N,N−ジ酢酸、グルタミン酸二酢酸、エチレンジアミンコハク酸などのアミノポリ酢酸またはこれらの塩、好ましくはアルカリ金属塩、もしくはアルカノールアミン塩。
(6)ジグリコール酸、オキシジコハク酸、カルボキシメチルオキシコハク酸、クエン酸、乳酸、酒石酸、シュウ酸、リンゴ酸、オキシジコハク酸、グルコン酸、カルボキシメチルコハク酸、カルボキメチル酒石酸などの有機酸またはこれらのアルカリ金属塩、もしくはアルカノールアミン塩。
(7)アミノポリ(メチレンホスホン酸)もしくはそのアルカリ金属塩もしくはアルカノールアミン塩、またはポリエチレンポリアミンポリ(メチレンホスホン酸)もしくはアルカリ金属塩もしくはアルカノールアミン塩を挙げることができる。
[Component (c)]
In the present invention, it is optional but preferably suppresses sweat odor and imparts a deodorizing effect, and for that purpose, it is preferable to contain a chelating agent as the component (c). Specific examples of the component (c) include the following compounds.
(1) Phosphoric acid compounds such as phytic acid or alkali metal salts or alkanolamine salts thereof.
(2) ethane-1,1-diphosphonic acid, ethane-1,1,2-triphosphonic acid, ethane-1-hydroxy-1,1-diphosphonic acid and its derivatives, ethanehydroxy-1,1,2-triphosphonic acid Phosphonic acids such as ethane-1,2-dicarboxy-1,2-diphosphonic acid and methanehydroxyphosphonic acid, or alkali metal salts or alkanolamine salts thereof.
(3) Phosphonocarboxylic acids such as 2-phosphonobutane-1,2-dicarboxylic acid, 1-phosphonobutane-2,3,4-tricarboxylic acid, α-methylphosphonosuccinic acid, or alkali metal salts or alkanolamine salts thereof .
(4) Amino acids such as aspartic acid, glutamic acid and glycine, or alkali metal salts or alkanolamine salts thereof.
(5) nitrilotriacetic acid, iminodiacetic acid, ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, glycol etherdiaminetetraacetic acid, hydroxyethyliminodiacetic acid, triethylenetetraminehexaacetic acid, diencoric acid, alkylglycine-N, N-diacetic acid, Aminopolyacetic acid such as aspartic acid-N, N-diacetic acid, serine-N, N-diacetic acid, glutamic acid diacetic acid, ethylenediamine succinic acid, or a salt thereof, preferably an alkali metal salt or an alkanolamine salt.
(6) Organic acids such as diglycolic acid, oxydisuccinic acid, carboxymethyloxysuccinic acid, citric acid, lactic acid, tartaric acid, oxalic acid, malic acid, oxydisuccinic acid, gluconic acid, carboxymethyl succinic acid, carboxymethyl tartaric acid or the like Alkali metal salt or alkanolamine salt.
(7) Aminopoly (methylenephosphonic acid) or an alkali metal salt or alkanolamine salt thereof, or polyethylenepolyamine poly (methylenephosphonic acid) or an alkali metal salt or alkanolamine salt.
これらの中で、上記(2)、(5)及び(6)からなる群より選ばれる少なくとも1種が好ましく、上記(5)及び(6)からなる群より選ばれる少なくとも1種がさらに好ましい。最も好ましい(c)成分は、エチレンジアミン四酢酸(塩)、クエン酸(塩)である。 Among these, at least one selected from the group consisting of (2), (5) and (6) is preferable, and at least one selected from the group consisting of (5) and (6) is more preferable. The most preferred component (c) is ethylenediaminetetraacetic acid (salt) and citric acid (salt).
[(d)成分]
本発明では、任意ではあるが、(a)成分以外の香料成分〔以下、(d)成分という〕を併用することで、汗の付着した対象物に好ましい香りを着香させることができる。特に、保留効果の高いlogPowが3.0以上の香料成分〔以下、(d1)成分という〕を、(a)成分及び(d)成分の合計質量に対して好ましくは1.0質量%以上、より好ましくは5〜60質量%、更に好ましくは10〜50質量%含有することが好適である。このような(d1)成分を比較的多く併用することで、対象物への(a)成分の保留性が増し、β−グルクロニダーゼの阻害効果を持続させることができる。
[Component (d)]
In the present invention, although it is optional, a perfume component other than the component (a) [hereinafter referred to as the component (d)] can be used in combination to impart a preferred scent to the object to which sweat is attached. In particular, a perfume component [hereinafter referred to as (d1) component] having a log Pow of 3.0 or more with a high retention effect is preferably 1.0% by mass or more based on the total mass of the component (a) and the component (d), More preferably, it is 5-60 mass%, More preferably, it is suitable to contain 10-50 mass%. By using a relatively large amount of such a component (d1), the retention of the component (a) on the object is increased, and the inhibitory effect of β-glucuronidase can be maintained.
ここでlogPowとは、化学物質の1−オクタノール/水分配係数であり、f値法(疎水性フラグメント定数法)により算出された値をいう。具体的には、化合物の化学構造を、その構成要素に分解し、各フラグメントの有する疎水性フラグメント定数(f値)を積算して求めることができ、CLOGP3 Reference Manual Daylight Software 4.34, Albert Leo, David Weininger, Version1, March 1994を参考にすることができる。 Here, logPow is a 1-octanol / water partition coefficient of a chemical substance, and is a value calculated by the f-value method (hydrophobic fragment constant method). Specifically, the chemical structure of a compound can be determined by decomposing the chemical structure into its constituent components and integrating the hydrophobic fragment constants (f values) of each fragment. CLOGP3 Reference Manual Daylight Software 4.34, Albert Leo, David You can refer to Weininger, Version1, March 1994.
(d1)成分としては、i)α−ピネン(4.18)、β−ピネン(4.18)、カンフェン(4.18)、リモネン(4.35)、テルピノーレン(4.35)、ミルセン(4.33)、p−サイメン(4.07)及びβ−カリオフィレン(6.45)から選ばれる炭化水素系香料、ii)サンダルマイソールコア(3.9)、サンタロール(3.9)、l−メントール(3.2)、シトロネロール(3.25)、ジヒドロミルセノール(3.03)、エチルリナロール(3.08)、ムゴール(3.03)及びネロリドール(4.58)から選ばれるアルコール系香料、iii)アルデヒドC−111(4.05)、グリーナール(3.13)、マンダリンアルデヒド(4.99)、シトラール(3.12)、シトロネラール(3.26)、アミルシンナミックアルデヒド(4.32)、ヘキシルシンナミックアルデヒド(4.85)、リリアール(3.86)、シクラメンアルデヒド(3.5)、セトナール(4.86)、ボロナール(4.72)、マセアール(3.6)、ベルンアルデヒド(4.88)、マイラックアルデヒド(3.87)、ジヒドロジャスモン(3.13)、イオノンα(3.71)、メチルイオノンα(4.24)、メチルイオノンG(4.02)及びトリメチルウンデセナール(5.16)から選ばれるアルデヒド・ケトン系香料、iv)ヘプチルアセテート(3.36)、シトロネリルアセテート(4.20)、ゲラニルアセテート(3.72)、リナリルアセテート(3.50)、ヘキシルサリシレート(5.09)、エチルシンナメート(3.0)、ベンジルサリシレート(4.2)、イソブチルサリシレート(3.92)及びヘキシルサリシレート(5.09)から選ばれるエステル系香料、v)チモール(3.40)及びバニトロープ(3.11)から選ばれるフェノール系香料、vi)セドロキサイド(4.58)、シトロネリルエチルエーテル(4.36)、アネトール(3.31)、ネロリンヤラヤラ(3.24)、エステラゴール(3.1)、メチルイソオイゲノール(3.0)及びアンブロキサン(5.27)から選ばれるエーテル系香料、テンタローム(5.7)、及びパーライド(5.7)などを挙げることができる(括弧内の数値はlogPow値を示す)。 As the component (d1), i) α-pinene (4.18), β-pinene (4.18), camphene (4.18), limonene (4.35), terpinolene (4.35), myrcene (4.33), p-cymene (4.07) and Hydrocarbon fragrance selected from β-caryophyllene (6.45), ii) Sandalmysol core (3.9), Santalol (3.9), 1-menthol (3.2), Citronellol (3.25), Dihydromyrsenol (3.03), Ethyl Alcohol-based fragrance selected from linalool (3.08), mugor (3.03) and nerolidol (4.58), iii) aldehyde C-111 (4.05), greenal (3.13), mandarin aldehyde (4.99), citral (3.12), citronellal ( 3.26), amylcinnamic aldehyde (4.32), hexylcinnamic aldehyde (4.85), lyial (3.86), cyclamen aldehyde (3.5), Setneral (4.86), Boronal (4.72), Maceal (3.6), Bernaldehyde (4.88), Mylacaldehyde (3.87), Dihydrojasmon (3.13), Ionone α (3.71), Methylionone α (4.24), Aldehyde / ketone flavors selected from methylionone G (4.02) and trimethylundecenal (5.16), iv) heptyl acetate (3.36), citronellyl acetate (4.20), geranyl acetate (3.72), linalyl acetate (3.50), hexyl Selected from salicylate (5.09), ethyl cinnamate (3.0), benzyl salicylate (4.2), isobutyl salicylate (3.92) and hexyl salicylate (5.09), v) selected from thymol (3.40) and banitrop (3.11) Phenolic fragrance, vi) Cedroxide (4.58), Citro Ether-based fragrances selected from rylethyl ether (4.36), anethole (3.31), neroline yarayara (3.24), estellagol (3.1), methylisoeugenol (3.0) and ambroxan (5.27), tentalum (5.7), and parride ( 5.7), etc. (numbers in parentheses indicate logPow values).
本発明の(d)成分として使用できる他の香料成分〔以下、(d2)成分という〕としては、テルピネオール(2.6)、ゲラニオール(2.77)、リナロール(2.55)、ミルセノール(2.61)、ネロール(2.77)、シス−ジャスモン(2.64)、フェニルエチルアセテート(2.13)、アリルアミルグリコレート(2.51)、リファローム(2.26)、シス−3−ヘキシルアセテート(2.34)、スチラリルアセテート(2.27)、o−t−ブチルシクロヘキサノン(2.27)、p−t−ブチルシクロヘキサノン(2.27)、アセチルオイゲノール(2.83)、シンナミルアセテート(2.35)、オイゲノール(2.40)、イソオイゲノール(2.58)、モスシンス(2.94)、アニソール(2.06)及びメチルオイゲノール(2.78)を挙げることができる(括弧内の数値はlogPow値を示す)。 Other perfume ingredients that can be used as the component (d) of the present invention (hereinafter referred to as the component (d2)) include terpineol (2.6), geraniol (2.77), linalool (2.55), mirsenol (2.61), and nerol (2.77). , Cis-jasmon (2.64), phenylethyl acetate (2.13), allyl amyl glycolate (2.51), rifarom (2.26), cis-3-hexyl acetate (2.34), styrylyl acetate (2.27), ot-butyl Cyclohexanone (2.27), pt-butylcyclohexanone (2.27), acetyl eugenol (2.83), cinnamyl acetate (2.35), eugenol (2.40), isoeugenol (2.58), moth synth (2.94), anisole (2.06) and methyl Eugenol (2.78) can be mentioned (numbers in parentheses indicate logPow values).
なお、本発明で用いた香料成分の名称は、「香料と調香の基礎知識」中島基貴著、産業図書(株)発行 第2刷(1996年5月30日)の記載に従った。 In addition, the name of the fragrance | flavor component used by this invention followed the description of "Basic knowledge of a fragrance | flavor and fragrance | scent" written by Motoki Nakajima, the second printing (May 30, 1996) published by Sangyo Tosho.
[汗臭発生抑制剤組成物]
本発明の汗臭発生抑制剤組成物中の(a)成分の含有量は、0.0001〜1質量%が好ましく、0.001〜1質量%がより好ましい。また、(b)成分の含有量は、0.01〜10.0質量%が好ましく、0.01〜8.0質量%がより好ましく、0.01〜5.0質量%が更に好ましい。また、対象物への浸透性及び消臭/防臭効果の点から、本発明の汗臭発生抑制剤組成物における(b1)成分/(b2)成分の質量比は、好ましくは0.001〜0.5、より好ましくは0.005〜0.5、更に好ましくは0.005〜0.3である。
[Sweating odor generation inhibitor composition]
0.0001-1 mass% is preferable and, as for content of (a) component in the sweat odor generation inhibitor composition of this invention, 0.001-1 mass% is more preferable. Moreover, 0.01-10.0 mass% is preferable, as for content of (b) component, 0.01-8.0 mass% is more preferable, and 0.01-5.0 mass% is still more preferable. Moreover, from the point of the permeability to a target object and the deodorizing / deodorizing effect, the mass ratio of the (b1) component / (b2) component in the sweat odor generation inhibitor composition of the present invention is preferably 0.001 to 0. 0.5, more preferably 0.005 to 0.5, and still more preferably 0.005 to 0.3.
(c)成分は、任意ではあるが、本発明の汗臭発生抑制効果に加え、消臭効果を付与することができるため含有することが好ましく、組成物中に好ましくは0.001〜10質量%、より好ましくは0.005〜5.0質量%、更に好ましくは0.01〜2.0質量%含有することが好適である。(d)成分についても任意ではあるが、対象物に好ましい香りを着香でき、しかも(a)成分の保留性を高め、β−グルクロニダーゼ阻害効果の持続性を向上させることができるため含有することが好ましく、組成物中に好ましくは0.001〜5.0質量%、より好ましくは0.001〜1.0質量%、更に好ましくは0.001〜0.5質量%含有することが好適である。 The component (c) is optional, but is preferably contained because it can impart a deodorizing effect in addition to the sweat odor generation suppressing effect of the present invention, and preferably 0.001 to 10 mass in the composition. %, More preferably 0.005 to 5.0 mass%, still more preferably 0.01 to 2.0 mass%. The component (d) is optional, but can be added to the object because it can give a favorable scent, and the retention of the component (a) can be increased and the persistence of the β-glucuronidase inhibitory effect can be improved. The composition preferably contains 0.001 to 5.0% by mass, more preferably 0.001 to 1.0% by mass, and still more preferably 0.001 to 0.5% by mass. is there.
また、本発明では、(a)成分、(d1)成分及び(d2)成分を含有する香料組成物として用いることが好ましく、該香料組成物における(a)成分/〔(a)成分+(d1)成分+(d2)成分〕の質量比は好ましくは0.001〜0.5、より好ましくは0.01〜0.5であり、(a)成分/(d1)成分の質量比は好ましくは0.1〜0.9、より好ましくは0.1〜0.8である。 Moreover, in this invention, it is preferable to use as a fragrance | flavor composition containing (a) component, (d1) component, and (d2) component, (a) component / [(a) component + (d1) in this fragrance | flavor composition. ) Component + (d2) component] is preferably 0.001 to 0.5, more preferably 0.01 to 0.5, and the mass ratio of (a) component / (d1) component is preferably It is 0.1-0.9, More preferably, it is 0.1-0.8.
本発明の汗臭発生抑制剤組成物は、対象物への接触のさせ易さから、上記成分を水に溶解/分散/乳化させた水溶液等の液体組成物の形態が好適であり、水の含有量は、好ましくは80〜99.99質量%、より好ましくは90〜99.99質量%である。また、本発明の汗臭発生抑制剤組成物の25℃におけるpHは、好ましくは4〜10、より好ましくは7〜9、更に好ましくは7.5〜8.5である。なお、pHは、株式会社堀場製のpHメータ(D−52S、pH電極6367−10D)を用いて測定することができる。 The sweat odor generation inhibitor composition of the present invention is preferably in the form of a liquid composition such as an aqueous solution in which the above components are dissolved / dispersed / emulsified in water from the viewpoint of easy contact with an object. The content is preferably 80 to 99.99% by mass, more preferably 90 to 99.99% by mass. Moreover, pH at 25 degreeC of the sweat odor generation inhibitor composition of this invention becomes like this. Preferably it is 4-10, More preferably, it is 7-9, More preferably, it is 7.5-8.5. The pH can be measured using a pH meter (D-52S, pH electrode 6367-10D) manufactured by Horiba, Ltd.
[汗臭発生抑制剤物品]
本発明の汗臭発生抑制剤物品は、本発明の汗臭発生抑制剤組成物をスポンジや不織布などの可撓性材料に含浸させてなるものや、トリガー式スプレーヤーを具備した容器に充填してなるものである。簡便性及び効果/効率の点から、好適な汗臭発生抑制剤物品は、本発明の汗臭発生抑制剤組成物を、トリガー式スプレーヤーを具備した容器に充填してなるものである。
[Sweet odor generation inhibitor]
The sweat odor generation inhibitor article of the present invention is filled with a sweat odor generation inhibitor composition of the present invention impregnated in a flexible material such as sponge or nonwoven fabric, or in a container equipped with a trigger sprayer. It will be. From the viewpoint of simplicity and effect / efficiency, a suitable sweat odor generation inhibitor article is obtained by filling the sweat odor generation inhibitor composition of the present invention into a container equipped with a trigger sprayer.
本発明の汗臭発生抑制剤組成物を、トリガー式スプレーヤーを具備した容器に充填して用いる際には、本発明の組成物は、(a)成分を0.0001〜1質量%、(b)成分を0.01〜5.0質量%、及び水を含有することが好ましい。 When the sweat odor generation inhibitor composition of the present invention is used by filling a container equipped with a trigger sprayer, the composition of the present invention comprises (a) component at 0.0001 to 1% by mass, ( It is preferable to contain 0.01-5.0 mass% of component b) and water.
トリガー式スプレーヤーとしては、噴射口から噴射方向に10cm離れた地点における噴霧液滴の平均粒径が10〜200μmとなり、噴射口から噴射方向に15cm離れた地点における粒径200μmを超える液滴の数が噴霧液滴の総数の1%以下となり、噴射口から噴射方向に10cm離れた地点における粒径10μm未満の液滴の数が噴霧液滴の総数の1%以下となる噴霧手段を備えたものが好ましい。噴霧液滴の粒子径分布は、例えば、レーザー回折式粒度分布計(日本電子株式会社製)により測定することができる。 As a trigger type sprayer, the average particle diameter of the spray droplets at a point 10 cm away from the injection port in the injection direction is 10 to 200 μm, and the droplet size exceeding 200 μm at the point 15 cm away from the injection port in the injection direction. A spraying means is provided in which the number is 1% or less of the total number of spray droplets, and the number of droplets having a particle size of less than 10 μm at a point 10 cm away from the spray port in the spray direction is 1% or less of the total number of spray droplets. Those are preferred. The particle size distribution of the spray droplets can be measured by, for example, a laser diffraction particle size distribution meter (manufactured by JEOL Ltd.).
噴霧液滴の平均粒径を所望の範囲に調整する観点から、汗臭発生抑制剤組成物の20℃における粘度は、好ましくは15mPa・s以下、より好ましくは1〜10mPa・sに調整することが好適である。粘度の調整は、エタノール、イソプロピルアルコール等の溶媒を適当量添加する事によって行う事ができる。粘度は、東京計器株式会社製のB型粘度計(モデル形式BM)にローター番号No.1のローターを備え付けたものを準備し、試料をトールビーカーに充填して恒温槽内で20℃に調整した後、該試料を上記粘度計にセットして、ローター回転数60r/minにて回転開始60秒後に測定した粘度である。 From the viewpoint of adjusting the average particle diameter of the spray droplets to a desired range, the viscosity at 20 ° C. of the sweat odor generation inhibitor composition is preferably adjusted to 15 mPa · s or less, more preferably 1 to 10 mPa · s. Is preferred. The viscosity can be adjusted by adding an appropriate amount of a solvent such as ethanol or isopropyl alcohol. Viscosity was measured using a rotor type no. 1 was prepared, and the sample was filled in a tall beaker and adjusted to 20 ° C. in a thermostatic bath. Then, the sample was set in the viscometer and rotated at a rotor rotational speed of 60 r / min. It is the viscosity measured 60 seconds after the start.
スプレーヤーの噴霧口径は、好ましくは1mm以下、より好ましくは0.3mm〜0.7mmである。噴霧口の形状、材質等は特に限定されない。 The spray diameter of the sprayer is preferably 1 mm or less, more preferably 0.3 mm to 0.7 mm. There are no particular limitations on the shape, material, and the like of the spray port.
[汗臭発生抑制方法]
本発明の汗臭発生抑制剤組成物は、汗の付着した繊維製品又は革製品、好適には衣類や靴に直接接触させることで、汗臭の発生そのものを抑制することができる。汗臭発生抑制剤組成物を接触させる方法としては、汗の付着した対象物を汗臭発生抑制剤組成物に浸漬させる方法や、スポンジや不織布などの可撓性材料に汗臭発生抑制剤組成物を含浸させた物品を用いて対象物に擦り付ける方法などを挙げることができるが、簡便性及び効果/効率の点から、トリガー式スプレーヤーを用いて汗臭発生抑制剤組成物を対象物に直接噴霧する方法が好適である。トリガー式スプレーヤーを用いて本発明の汗臭発生抑制剤組成物を対象物に直接噴霧する際には、(a)成分の含有量が0.0001〜1質量%、(b)成分の含有量が0.01〜5.0質量%であり、更に水を含有する汗臭発生抑制剤組成物を用いることが好ましい。
[Suppression of sweat odor]
The sweat odor generation inhibitor composition of the present invention can suppress the generation of sweat odor itself by bringing it into direct contact with a textile or leather product to which sweat is attached, preferably clothing or shoes. As a method of bringing the sweat odor generation inhibitor composition into contact, a method of immersing a sweat-attached object in the sweat odor generation inhibitor composition, or a sweat odor generation inhibitor composition in a flexible material such as sponge or nonwoven fabric Examples of the method include rubbing against an object using an article impregnated with the object. From the viewpoint of simplicity and effect / efficiency, the sweat odor generation inhibitor composition is applied to the object using a trigger sprayer. Direct spraying is preferred. When the sweat odor generation inhibitor composition of the present invention is sprayed directly onto an object using a trigger sprayer, the content of the component (a) is 0.0001 to 1% by mass, the content of the component (b) It is preferable to use a sweat odor generation inhibitor composition having an amount of 0.01 to 5.0% by mass and further containing water.
本発明の汗臭発生抑制方法は、汗の付着した繊維製品又は革製品0.04m2当たり、本発明の汗臭発生抑制剤組成物を通常0.05〜20.0g、好ましくは0.10〜15.0g、より好ましくは0.2〜10.0g噴霧することが好適であり、特に、汗の付着した繊維製品又は革製品0.04m2当たり好ましくは0.00000025〜0.001g、より好ましくは0.000001〜0.0008g、更に好ましくは0.000002〜0.0005gの(a)成分が噴霧されるように本発明の汗臭発生抑制剤組成物を噴霧することが好ましい。 The sweat odor generation suppressing method of the present invention is usually 0.05 to 20.0 g, preferably 0.10 to 0.04 m 2 of the sweat odor generation suppressing composition of the present invention per 0.04 m 2 of a textile or leather product to which sweat is attached. It is suitable to spray 15.0 g, more preferably 0.2-10.0 g, in particular preferably 0.000000025-0.001 g per 0.04 m 2 of sweat-attached textile or leather product, more preferably It is preferable to spray the sweat odor generation inhibitor composition of the present invention so that 0.000001 to 0.0008 g, more preferably 0.000002 to 0.0005 g of component (a) is sprayed.
実施例1〜4及び比較例1〜6
下記の配合成分を用い、表2に示す組成の本発明及び比較の汗臭発生抑制剤組成物を調製した。なお、汗臭発生抑制剤組成物は、塩酸を用いてpH7.80(25℃)に調整した。
Examples 1-4 and Comparative Examples 1-6
Using the following blending components, the present invention having a composition shown in Table 2 and a comparative sweat odor generation inhibitor composition were prepared. The sweat odor generation inhibitor composition was adjusted to pH 7.80 (25 ° C.) using hydrochloric acid.
得られた汗臭発生抑制剤組成物について、下記方法で汗臭発生の抑制効果を評価した。結果を表2に示す。 About the obtained sweat odor generation inhibitor composition, the suppression effect of sweat odor generation was evaluated by the following method. The results are shown in Table 2.
<配合成分>
(a)成分
a−1:8−シクロヘキサデセン−1−オン
(a’)成分((a)成分の比較品)
a’−1:ETHYLENE BRASSYLATE(エチレントリデカンジオエート)
(b)成分
b1−1:APAO(ラウリルアミノプロピルジメチルアミンオキシド)
b1−2:Q−D10E(ジデシルジメチルアンモニウムクロリド)
b1−3:エマルゲン109P(ポリオキシエチレンラウリルエーテル)
b2−1:エタノール
b2−2:2−エチルヘキシルグリセリルエーテル
その他成分
Tris:2-アミノ-2−ヒドロキメチルプロパン-1,3-ジオール
<汗臭発生抑制効果の評価方法>
(1)評価用サンプルの調製
30分ほど適度な運動をし、汗がしみ込んだ肌着(グンゼYG 綿100%)を15cm×15cmのサイズに切り取り、試験布として使用した(評価に使用した肌着の汗量は45〜55%owf)。スプレーバイアル(No.6)に、表2に示す汗臭発生抑制剤組成物を入れ、汗が付着した試験布に50%owf量スプレーした。スプレー後、試験布をJPボトル(100ml)に入れ密閉し、40℃、60%RHの恒温恒湿の環境下(縦1.9m×横4.9m×高さ2.3m)で20時間保存し、保存後、JPボトルから試験布を取り出し、評価用サンプルを調製した。
<Blending ingredients>
(A) Component a-1: 8-cyclohexadecene-1-one (a ′) component (comparison product of component (a))
a′-1: ETHYLENE BRASSYLATE (ethylene tridecandioate)
(B) Component b1-1: APAO (laurylaminopropyldimethylamine oxide)
b1-2: Q-D10E (didecyldimethylammonium chloride)
b1-3: Emulgen 109P (polyoxyethylene lauryl ether)
b2-1: ethanol b2-2: 2-ethylhexyl glyceryl ether and other components
Tris: 2-amino-2-hydroxymethylpropane-1,3-diol <Evaluation method of sweat odor generation inhibiting effect>
(1) Preparation of sample for evaluation The underwear (Gunze YG 100% cotton) that had been exercised moderately for about 30 minutes and was soaked in sweat was cut into a size of 15 cm x 15 cm, and used as a test cloth (of the underwear used for the evaluation) Sweat volume is 45-55% owf). A sweat odor generation inhibitor composition shown in Table 2 was placed in a spray vial (No. 6), and sprayed onto a test cloth to which sweat was attached in an amount of 50% owf. After spraying, the test cloth is placed in a JP bottle (100 ml), sealed, and stored for 20 hours in a constant temperature and humidity environment of 40 ° C. and 60% RH (length 1.9 m × width 4.9 m × height 2.3 m). After storage, the test cloth was taken out from the JP bottle to prepare an evaluation sample.
(2)汗臭発生抑制効果の評価
(1)で調製した評価用サンプルを、JPボトルから取り出し、熟練した5人のパネラーにより汗臭の官能評価を行った。汗臭の強さについては、以下に示す臭気強度レベルを尺度として採点を行い、5人の平均値を示した。この平均値の0.3の相違は、有意な差として認識される。なお、汗が付着した試験布を、汗臭発生抑制剤組成物による処理を行うことなくJPボトルにて20時間保存した場合の臭気強度は3.1であった。
(2) Evaluation of sweat odor generation suppression effect
The evaluation sample prepared in (1) was taken out from the JP bottle, and sensory evaluation of sweat odor was performed by five skilled panelists. For the intensity of sweat odor, scoring was carried out using the following odor intensity level as a scale, and the average value of 5 persons was shown. This difference of 0.3 in the average value is recognized as a significant difference. In addition, the odor intensity | strength when the test cloth which sweat adhered was preserve | saved for 20 hours by a JP bottle, without performing the process by the sweat odor generation inhibitor composition was 3.1.
汗臭の臭気強度の評価基準
0:感じない
1:かすかに感じる
2:やや強く感じる
3:強く感じる
4:非常に強く感じる
5:極端に強く感じる
Evaluation criteria for odor intensity of sweat odor 0: Not felt 1: Feels faint 2: Feels slightly strong 3: Feels strong 4: Feels very strong 5: Feels extremely strong
Claims (4)
(a)成分:8−シクロヘキサデセン−1−オンであるβ−グルクロニダーゼ阻害剤、
(b)成分:界面活性剤(b1)及び溶剤(b2)
(b1)成分/(b2)成分の質量比が0.005〜0.3である汗臭発生抑制剤組成物を、汗の付着した繊維製品又は革製品に接触させる汗臭発生抑制方法。 The sweat odor generation inhibitor composition containing the following (a) component 0.001-1 mass%, (b) component 0.01-5.0 mass%, and water ,
(A) component : β-glucuronidase inhibitor which is 8-cyclohexadecen-1-one ,
Component (b): surfactant (b1) and solvent (b2)
A sweat odor generation suppressing method in which a sweat odor generation inhibitor composition having a mass ratio of (b1) component / (b2) component of 0.005 to 0.3 is brought into contact with a textile or leather product to which sweat is attached.
(i)炭素数1〜3の一級アルコール、
(ii)下記一般式(Solv-1)で示される化合物、
R1−(OR2)m−OR3 (Solv-1)
〔式中R1及びR3はそれぞれ独立に水素原子又は炭素数1〜7の炭化水素基であり、R2は炭素数2又は3のアルキレン基であり、mは1〜6の数であり、m個のR2は同一でも異なっていても良い。〕
(iii)炭素数3〜10の1価アルコールにグリシドール及び/又はエピクロルヒドリンを平均1〜5モル付加させたアルキル(ポリ)グリセリルエーテル The sweat odor generation suppressing method according to claim 1 or 2, wherein the solvent (b2) is at least one selected from the following compounds (i) to (iii).
(I) a primary alcohol having 1 to 3 carbon atoms,
(Ii) a compound represented by the following general formula (Solv-1),
R 1- (OR 2 ) m-OR 3 (Solv-1)
[Wherein R 1 and R 3 are each independently a hydrogen atom or a hydrocarbon group having 1 to 7 carbon atoms, R 2 is an alkylene group having 2 or 3 carbon atoms, and m is a number of 1 to 6] , M R 2 s may be the same or different. ]
(Iii) Alkyl (poly) glyceryl ether obtained by adding 1 to 5 moles of glycidol and / or epichlorohydrin on average to a monohydric alcohol having 3 to 10 carbon atoms
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