JPH05125073A - 生理的冷却効果をもつた組成物および該組成物の製造法 - Google Patents
生理的冷却効果をもつた組成物および該組成物の製造法Info
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Abstract
グリセリンケタールまたは3,3,5−トリメチルシク
ロヘキサノングリセリンケタール(III)を含有してい
る、生理的冷却効果をもった組成物。 〔式中、R1は−CH2−CH(CH2OH)−,−C
H2−CH(CH2CH2OH),−CH2−C(CH
3)(CH2OH)−CH2−等の、水酸基を1乃至3
個有しているC2〜6アルキレン基であり、R2,R3
はOH,NH2,ハロゲンから選ばれた置換基を1乃至
3個有するC1〜10アルキル等、あるいは両者が一緒
になってそれらが結合している炭素原子と共に5〜7員
環を形成するアルキレン基である〕 【効果】 従来から使用されている薄荷油、メントール
等に特有の強い匂いや苦味を有しない、広範な用途に適
した生理的冷却効果剤である。
Description
または粘膜に塗布した場合生理的冷却効果を生じる組成
物に関する。人に新鮮な感じを齎す効果は人の神経系の
対応するレセプターを刺激することによって生じると考
えられている。本発明はさらにこの効果を生じ得る新規
化合物に関する。
天然の化合物は疑いもなく(−)−メントールであり、
これは薄荷油[例えばメンタ・アルヴェンシス(Men
tha arvensis)]の成分である。これは例
えば歯磨き、口中洗滌剤、食品、飲料および化粧品の製
造に用いられる。しかし典型的な強い薄荷の匂いおよび
苦味が不快に感じられることも多い。
積極的な冷却効果を有する物質を見出だそうとする試み
がなされなかったわけではない。例えばドイツ特許公開
明細書第2,202,535号にはp−メンタン−3−
カルボキシアミドおよびp−メンタン−3−カルボン酸
のエステルが、ドイツ特許公開明細書第2,205,2
55号にはN−置換p−メンタン−3−カルボキシアミ
ドが、ドイツ特許公開明細書第2,317,538号に
は脂肪族アミドが、ドイツ特許公開明細書第2,33
4,985号には脂環式スルフォキシドおよびスルフォ
ンが、またドイツ特許公開明細書第2,345,156
号には脂肪族の置換フォスフィンオキシドが提案されて
いる。しかしこれらの化合物は天然には産出せず、また
人の器官で分解されて天然産の物質に変わることもな
い。従ってこのような化合物を食品に使用することには
疑問があると考えるべきである。
これらの誘導体は設定された要求に全く合致しない。例
えばドイツ特許公開明細書第2,022,364号に提
案されている炭酸l−メンチルエチルはオレンジの匂い
をもち、ドイツ特許公開明細書第2,433,165号
記載のN−アセチルグリシン酸メンチルおよびドイツ特
許公開明細書第2,339,661号記載の複素環式カ
ルボン酸のメントールエステルは苦味が強く、また米国
特許第3,830,930号記載のいくつかのメンチル
ケトエステルは長期間に亙って苦味をもち、冷却効果も
弱い。
6号には天然産のC2〜C6−ヒドロキシカルボン酸のメ
ントールエステル(これは随時そのヒドロキシル基をC
1〜C4−カルボン酸でエステル化することができる)が
記載されており、これは匂いおよび香りがなく、長期間
に亙る冷却効果をもっている。特に乳酸1−メンチルは
実用になることが判っている。しかしこの製品はアルカ
リに対して安定でなく、従ってあらゆる用途(例えば石
鹸)に適しているとは言えない。
2−ジオール(ヨーロッパ特許明細書第80,148
号)およびN−エチル−p−メンタン−3−カルボキシ
アミド(ドイツ特許公開明細書第2,205,255号
および同第2,413,639号)のような他の化合物
もすでに使用されているが、冷却効果の大きい組成物ま
たは価格/使用特性比の良好な組成物が求められてい
る。
以下のヒドロキシル基、好ましくは1−ヒドロキシル基
を有するC2〜C6−アルキレン基を表し、R2およびR3
は互いに独立に随時ヒドロキシル、アミノおよびハロゲ
ン(例えばフッ素、塩素、臭素またはヨウ素)から成る
群から選ばれる基を1〜3個置換したC1〜C10−アル
キル、またはC5〜C7−シクロアルキル、好ましくはシ
クロヘキシル、或いはC6〜C12−アリール、好ましく
はフェニルを表すが、R2およびR3はその炭素原子の全
数は3以上の基であるか、或いはR2およびR3は一緒に
なって基R2およびR3の炭素原子と共に5〜7員環を構
成するアルキレン基であり、このアルキレン基はC1〜
C6−アルキル基で置換されていることができる、のケ
タールを少なくとも1個含むことを特徴とする生理的冷
却効果をもった組成物に関する。
ピルおよびt−ブチルである。
影響を及ぼす。この基の長さが短いと、効果が直接的で
短くなり、長いと効果は遅くなるが長続きする。化粧品
工業における重要な特徴は水に対する溶解性である。基
R2およびR3が短い場合は特にそうである。
の2個の酸素原子が結合した炭素原子と共にジオキソラ
ンまたはジオキサン環をつくる1,2−および1,3−
アルキレン基である。
適な化合物Iは式
たはC1〜C6−アルキル、好ましくは水素またはC1〜
C4−アルキルを表し、mおよびnは互いに独立に0ま
たは1を表す。
の、即ち随時置換基をもつシクロヘキサノンのケタール
である。
基はメチル、イソプロピルおよびt−ブチルである。
も公知の同様な方法でつくることができる。例えばケタ
ールIは一般にケタールIのベースになるケトンを3個
以上5個以下、好ましくは3個のヒドロキシル基をもっ
た当量以上の量の脂肪族C3〜C6−アルコールと酸を触
媒として反応させることによりつくられる。一般にケタ
ールIのベースとなるケトンおよび0.5モル当量以
上、一般にこの量の1.2〜4倍、好ましくは1.5〜
3倍過剰の量のヒドロキシル基を3〜5個もったC3〜
C6−アルコールを用いる。使用できる酸触媒の例とし
てはp−トルエンスルフォン酸、燐酸または硫酸水素カ
リウムを触媒として有効な量(例えばケトン1モル当た
りp−トルエンスルフォン酸を0.1〜3g)用いる。
反応は好ましくは水と共沸混合物をつくりケタール生成
中に遊離される水を共沸混合物捕捉法により除去し得る
有機溶媒中で行うか、、または水を消費する試薬、例え
ばトリアルキルオルトエステルを用いて行う。好適な有
機溶媒はベンゼン、トルエン、キシレン、クロロフォル
ム、塩化メチレン、およびトリクロロエチレンである。
水が分離しなくなるか、またはエステル/アルコール混
合物が分離してこなくなったら、反応は完結したと見做
される。生成物を順次希薄アルカリおよび水で洗滌し、
有機相を分離して乾燥し、溶媒を分離し、適宜残留物を
例えば蒸溜により精製することが望ましい。
っていて、好ましくは
体が特に好ましい。
る。
非対称炭素原子をもっているから、光学的異性体が生じ
る。使用する原料および製造法に依存してケタールIは
光学的異性体の混合物または純粋な光学的異性体として
存在することができる。これらの異性体の冷却効果は異
なっているので、異性体のうちのどれかが好適である。
よび/または希釈剤を含んでいることができる。これら
の種類は組成物の用途によって変わる。
れるすべての目的に使用することができる。このような
冷却剤がしばしば使用される製品の例としては、チュー
インガム、噛みタバコ、タバコ、飲料、アイスクリーム
のような嗜好品、ウェーファーの製造に使用される脂
肪、医薬品組成物、ボディ・ケア製品または化粧品組成
物、、例えば歯磨き、口中洗滌剤、うがい薬、香料、粉
化粧、ローション、軟膏、オイル、クリーム、髭剃り用
発泡液、髭剃り後のローション、シャンプー等の組成物
がある。
の冷たい感覚を誘起するのに十分な量含んでいる。一般
にすぐ使用できる製品(例えば練り歯磨き、口中洗滌
剤)の重量に関し0.01〜3重量%、好ましくは0.
05〜1重量%使用される。
しない限りすべての割合は重量による。
シチュック(A.A.Svishchuk)、エヌ・カ
ー・マフノフスキー(N.K.Makhnovski
i)のN.Kh.Ukr.Khim.Zh.誌(ロシア
語版)43(2)号、173〜6頁1977年、ケミカ
ル・アブストラクツ(CA)誌87(5)号39667
u記載の化合物。
gのl−メントール(2モル)、276gのグリセリン
(3モル)および5gの硫酸水素カリウムのトルエン溶
液を加える。この混合物を水分離器中で還流させる。7
時間後42gの水が分離される。この混合物を中和して
蒸溜する。
441gの無色透明な液が蒸溜される。ガスクロマトグ
ラフによれば純度は99%以上であることが判った。N
MRスペクトルによれば得られた化合物は1,3−ジオ
キソラン環を含んでいた。
4.1°;d(25℃)= 1.0380。
タール 140gの3,3,5−トリメチルシクロヘキサノン
(1モル)、184gのグリセリン(2モル)および2
gのp−トルエンスルフォン酸のトルエン溶液の混合物
を実施例1と同様に処理する。
て235gの無色透明の液が蒸溜された。ガスクロマト
グラフによれば純度は99%以上であった。
1.0369;融点<−20℃。
ル)、529gのグリセリン(5.75モル)および4
gのp−トルエンスルフォン酸の混合物を反応容器に入
れ、次いで670gのオルト蟻酸トリメチル(6.32
モル)を滴下する。この工程中反応混合物の温度は約4
5〜50℃に上昇する。得られたメタノール/蟻酸メチ
ル混合物を大気圧下において塔底温度が100℃になる
まで蒸溜する。これを50℃に冷却し、徐々に真空をか
け、この混合物を高真空下で精溜する。全体:716
g;n20 D = 1.4439;d(25℃)= 1.02
94。
%であることが判った。
た。
り、実施例9は冷却効果をもたない物質を示す。
ル(7−イソプロピル−3,10−ジメチル−1,5−
ジオキサスピロ[5,5]ウンデカン−3−メタノー
ル)1−メントンおよび1,1,1−トリメチロールエ
タンを実施例1と同様の方法で反応させた。無色透明な
高粘性の油が得られた。その性質は下記のとおりであっ
た。
=1.4833;α25 D = −27.3゜ 実施例 11 1−メントン1,1,1−トリメチロールプロパンケタ
ノール(3−エチル−7−イソプロピル−10−メチル
−1,5−ジオキサスピロ[5,5]ウンデカン−3−
メタノール)1−メントンおよび1,1,1−トリメチ
ロールプロパンを実施例1と同様の方法で反応させた。
無色透明の高粘性の油が得られた。その性質は下記のと
おりであった。
=1.4850;α25 D = −29.1゜ 実施例 12 1−メントン1,2,4−ブタントリオールケタール
(6−イソプロピル−9−メチル−1,4−ジオキサス
ピロ[4,5]−デカン−2−エタノール)1−メント
ンおよび1,2,4−ブタントリオールを実施例1と同
様の方法で反応させた。
る。 1.式
以下のヒドロキシル基を有するC2〜C6−アルキレン基
を表し、R2およびR3は互いに独立に随時ヒドロキシ
ル、アミノおよびハロゲンから成る群から選ばれる基を
1〜3個置換したC1〜C10−アルキル、またはC5〜C
7−シクロアルキル、或いはC6〜C12−アリールを表す
が、R2およびR3はその炭素原子の全数は3以上の基で
あるか、或いはR2およびR3は一緒になって基R2およ
びR3の炭素原子と共に5〜7員環を構成するアルキレ
ン基であり、このアルキレン基はC1〜C6−アルキル基
で置換されていることができる、のケタールを少なくと
も1個含む生理的冷却効果をもった組成物。
レン基を表す上記第1項記載の組成物。
たはC1〜C6−アルキルであり、mおよびnは互いに独
立に0または1である、をもつ一つである上記第1項記
載の組成物。
の組成物。
ある、の化合物。
ノングリセリンケタール。
るために上記第1項記載の式(I)の化合物を使用する
方法。
Claims (4)
- 【請求項1】 式 【化1】 但し式中R1は少なくとも1個以上、3個以下のヒドロ
キシル基を有するC2〜C6−アルキレン基を表し、 R2およびR3は互いに独立に随時ヒドロキシル、アミノ
およびハロゲンから成る群から選ばれる基を1〜3個置
換したC1〜C10−アルキル、 またはC5〜C7−シクロアルキル、或いはC6〜C12−
アリールを表すが、R2およびR3はその炭素原子の全数
は3以上の基であるか、 或いはR2およびR3は一緒になって基R2およびR3の炭
素原子と共に5〜7員環を構成するアルキレン基であ
り、このアルキレン基はC1〜C6−アルキル基で置換さ
れていることができる、のケタールを少なくとも1個含
むことを特徴とする生理的冷却効果をもった組成物。 - 【請求項2】 式 【化2】 但し式中R1は特許請求の範囲第1項の定義の通りであ
る、の化合物。 - 【請求項3】 3,3,5−トリメチルシクロヘキサノ
ングリセリンケタール。 - 【請求項4】 人の皮膚または粘膜に冷却効果を与える
ために特許請求の範囲第1項記載の式(I)の化合物を
使用することを特徴とする方法。
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4110973A DE4110973A1 (de) | 1991-04-05 | 1991-04-05 | Mittel mit physiologischem kuehleffekt und fuer diese mittel geeignete wirksame verbindungen |
| DE4110973.2 | 1991-04-05 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05125073A true JPH05125073A (ja) | 1993-05-21 |
| JP3071030B2 JP3071030B2 (ja) | 2000-07-31 |
Family
ID=6428853
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4103526A Expired - Lifetime JP3071030B2 (ja) | 1991-04-05 | 1992-03-30 | 生理的冷却効果をもつた組成物および該組成物の製造法 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5266592A (ja) |
| EP (1) | EP0507190B1 (ja) |
| JP (1) | JP3071030B2 (ja) |
| AT (1) | ATE123936T1 (ja) |
| AU (1) | AU653999B2 (ja) |
| CA (1) | CA2064918A1 (ja) |
| DE (2) | DE4110973A1 (ja) |
| DK (1) | DK0507190T3 (ja) |
| ES (1) | ES2073205T3 (ja) |
| IE (1) | IE67879B1 (ja) |
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| US4059118A (en) * | 1972-01-28 | 1977-11-22 | Wilkinson Sword Limited | Tobacco and tobacco-containing manufactures containing an ingredient having physiological cooling activity |
| US4157384A (en) * | 1972-01-28 | 1979-06-05 | Wilkinson Sword Limited | Compositions having a physiological cooling effect |
| US4153679A (en) * | 1972-04-18 | 1979-05-08 | Wilkinson Sword Limited | Acyclic carboxamides having a physiological cooling effect |
| GB1421743A (en) * | 1972-04-18 | 1976-01-21 | Wilkinson Sword Ltd | Ingestible topical and other compositions |
| CA1027347A (en) * | 1972-07-20 | 1978-03-07 | David G. Rowsell | Compounds having a physiological cooling effect and compositions containing them |
| GB1436329A (en) * | 1972-08-07 | 1976-05-19 | Unilever Ltd | Esters of menthol and a heterocyclic carboxylic acid and their use in cosmetic preparations |
| GB1434728A (en) * | 1972-09-27 | 1976-05-05 | Wilkinson Sword Ltd | Compositions and articles containing phospine oxides having a physiological cooling effect and phosphine oxides for use therein |
| US4070449A (en) * | 1972-10-24 | 1978-01-24 | Wilkinson Sword Limited | Compounds having a physiological cooling effect and compositions containing them |
| GB1422998A (en) * | 1973-03-22 | 1976-01-28 | Wilkinson Sword Ltd | Cyclohexanecarboxamides having a physiological cooling effect and compositions containing them |
| US4296093A (en) * | 1973-04-16 | 1981-10-20 | Wilkinson Sword Limited | Cyclic carboxamides having a physiological cooling effect |
| LU68016A1 (ja) * | 1973-07-13 | 1975-04-11 | ||
| DE2608226A1 (de) * | 1976-02-28 | 1977-09-08 | Haarmann & Reimer Gmbh | Mittel mit physiologischer kuehlwirkung |
| JPS5888334A (ja) * | 1981-11-20 | 1983-05-26 | Takasago Corp | 3−l−メントキシプロパン−1、2−ジオ−ル |
| DE69112991T2 (de) * | 1990-11-06 | 1996-03-21 | Wrigley W M Jun Co | Verwendung von Menthon-Ketalen als Aromaverstärker. |
-
1991
- 1991-04-05 DE DE4110973A patent/DE4110973A1/de not_active Withdrawn
-
1992
- 1992-03-24 AT AT92105041T patent/ATE123936T1/de not_active IP Right Cessation
- 1992-03-24 ES ES92105041T patent/ES2073205T3/es not_active Expired - Lifetime
- 1992-03-24 DK DK92105041.5T patent/DK0507190T3/da active
- 1992-03-24 EP EP92105041A patent/EP0507190B1/de not_active Expired - Lifetime
- 1992-03-24 DE DE59202585T patent/DE59202585D1/de not_active Expired - Lifetime
- 1992-03-30 JP JP4103526A patent/JP3071030B2/ja not_active Expired - Lifetime
- 1992-03-30 AU AU13909/92A patent/AU653999B2/en not_active Expired
- 1992-04-02 CA CA002064918A patent/CA2064918A1/en not_active Abandoned
- 1992-04-03 US US07/862,851 patent/US5266592A/en not_active Expired - Lifetime
- 1992-04-03 IE IE921084A patent/IE67879B1/en not_active IP Right Cessation
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102844386A (zh) * | 2009-11-20 | 2012-12-26 | 西姆莱斯股份公司 | 生理学清凉的活性成分以及含有这类活性成分的物质的用途 |
| US9718839B2 (en) | 2009-11-20 | 2017-08-01 | Symrise Ag | Use of physiological cooling active ingredients, and agents containing such active ingredients |
| CN102844386B (zh) * | 2009-11-20 | 2020-01-21 | 西姆莱斯股份公司 | 生理学清凉的活性成分以及含有这类活性成分的物质的用途 |
| US10584134B2 (en) | 2009-11-20 | 2020-03-10 | Symrise Ag | Use of physiological cooling active ingredients, and agents containing such active ingredients |
| WO2016153011A1 (ja) * | 2015-03-25 | 2016-09-29 | 高砂香料工業株式会社 | メチルメントール誘導体およびそれを含有する冷感剤組成物 |
| JPWO2016153011A1 (ja) * | 2015-03-25 | 2018-01-18 | 高砂香料工業株式会社 | メチルメントール誘導体およびそれを含有する冷感剤組成物 |
| US10494330B2 (en) | 2015-03-25 | 2019-12-03 | Takasago International Corporation | Methyl menthol derivative and cooling agent composition containing same |
| US11434220B2 (en) | 2017-08-31 | 2022-09-06 | Basf Se | Use of physiological cooling active ingredients, and compositions comprising such active ingredients |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0507190B1 (de) | 1995-06-21 |
| JP3071030B2 (ja) | 2000-07-31 |
| AU1390992A (en) | 1992-10-08 |
| US5266592A (en) | 1993-11-30 |
| AU653999B2 (en) | 1994-10-20 |
| DE4110973A1 (de) | 1992-10-08 |
| ATE123936T1 (de) | 1995-07-15 |
| DE59202585D1 (de) | 1995-07-27 |
| CA2064918A1 (en) | 1992-10-06 |
| IE67879B1 (en) | 1996-05-01 |
| ES2073205T3 (es) | 1995-08-01 |
| EP0507190A1 (de) | 1992-10-07 |
| DK0507190T3 (da) | 1995-10-09 |
| IE921084A1 (en) | 1992-10-07 |
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