JPS5839620A - Alcohol composition - Google Patents

Alcohol composition

Info

Publication number
JPS5839620A
JPS5839620A JP56139274A JP13927481A JPS5839620A JP S5839620 A JPS5839620 A JP S5839620A JP 56139274 A JP56139274 A JP 56139274A JP 13927481 A JP13927481 A JP 13927481A JP S5839620 A JPS5839620 A JP S5839620A
Authority
JP
Japan
Prior art keywords
composition
alcohol
ethanol
test
present
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.)
Granted
Application number
JP56139274A
Other languages
Japanese (ja)
Other versions
JPH0340008B2 (en
Inventor
Tokio Matsui
松井 時朗
Meiko Wada
輪田 めい子
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP56139274A priority Critical patent/JPS5839620A/en
Publication of JPS5839620A publication Critical patent/JPS5839620A/en
Publication of JPH0340008B2 publication Critical patent/JPH0340008B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof

Abstract

PURPOSE:To provide the titled composition giving low stimulation to the body, by compounding ethanol and/or propanol with a food additive selected from polyhydric alcohol, specific amino acid and benzyl benzoate. CONSTITUTION:The objective alcohol composition is prepared by mixing ethanol and/or propanol with one or more compounds selected from (A) a polyhydric alcohol or its derivative permissible as a food additive or a drug additive (e.g. ethylene glycol, propylene glycol, etc.), (B) an amino acid having 1-2 carboxyl groups (e.g. glycine, alanine, etc.) and (C) benzyl benzoate. The addition of the above compounds eliminates the characteristic stimulation of alcohol to the skin and the oral mucosa, keeps the sterilizing effect of alcohol, and exhibits the effect for preventing the dental caries, cleaning the nicotine-stained tooth, and removing the oral odor.

Description

【発明の詳細な説明】 本発明は新規なアルコ−kIl成物、郭しくは皮膚、口
内1111[41に対して1ρプール特有O剃漱を消失
させ、しかもアルコール本来の殺菌消毒作用を発揮さ破
ると共に、虫歯予防、−車中にと)及び口臭Ik*勅果
を貴する析し−アルコール組成物に輿する。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a novel alcohol-kIl composition, which eliminates the O shavings characteristic of 1ρ pools against 1111 [41] in the skin and mouth, and exhibits the sterilizing and disinfecting action inherent to alcohol. At the same time, it is used to prevent tooth decay (in the car) and to remove bad breath (Ik*) and alcohol composition.

従来よ)エタノール及びプロパノールが殺薗消壽作用を
有す石こと社よく知られて−る。しかしtk−IIXら
之等のアルプールは口に入れた)傷口を消毒するIIK
皮膚、口内粘膜$に強V%稠歇を与えるという致命的欠
点を有して−る。
It is well known that ethanol and propanol have a sterilizing effect. However, tk-IIX et al. put it in their mouth) IIK to disinfect the wound.
It has the fatal drawback of imparting strong V% consistency to the skin and oral mucous membranes.

本発Ij1Oa陶は、上記軟菌消毒作用を有するアA/
:l−ルに見すれる刺激性を消失させて、殺薗滴―作用
は実質的に低下させな−アルコール組成物を提供する点
にある。
This Ij1Oa ceramic has the above-mentioned soft bacteria disinfection effect.
The object of the present invention is to provide an alcohol composition which eliminates the irritating properties of alcohol and does not substantially reduce the effect of the alcohol.

また本発明は、虫歯予防、煙草中に七り及び消臭効果を
有するアルコール組成物を提供することを他の目的とす
る。
Another object of the present invention is to provide an alcohol composition that prevents dental caries and has a deodorizing effect on cigarettes.

本発明者は、上記目的より種々研究を重ねえ結果下記特
定の化合物がアルコールO刺激を消失させる作用を有す
ることを見い出し、更に2等化合物を配合したアルコー
ル組成物は、虫歯予防効果、煙草中にとり効果及び消臭
効果を奏し得ることを見い出し九・ 本発明は、之等の新しめ知見に基づき完成され友もので
7h〕、その要旨とする所祉、エタノール及び(又#i
>プロパノールに、食品添加物又は医薬品添加物として
許容される多価アルコール類もしくはその誘導体、1又
は2個のカルボキシル基を有するアミノ酸及び安息香酸
ベンジルからなる群から選ばれた少なくとも1種を配合
し九ζ七を締機とする刺激性のないアルコール組成物に
係る。
The present inventor has conducted various studies for the above purpose, and as a result, has found that the following specific compound has the effect of eliminating the alcohol O stimulus, and furthermore, an alcohol composition containing a secondary compound has a caries preventive effect, The present invention has been completed based on these new findings, and the present invention has been completed based on these new findings.
> Propanol is blended with at least one selected from the group consisting of polyhydric alcohols or their derivatives that are acceptable as food additives or pharmaceutical additives, amino acids having one or two carboxyl groups, and benzyl benzoate. Pertains to non-irritating alcohol compositions using 9ζ7 as a tightening device.

本発明アルコール組成物において主成分として利用され
るエタノール及びプルパノールとしては、従来よ#殺菌
消毒剤として知られる日本薬局方所載のエタノール9 
&5 V/V%以上t4にむ無水エフ、/−#、I春用
エタノール、イソプロパツール及び朧−プロパノールを
例示できる・ また上記アルコールに配合され、本発明所期の効果を奏
し得る化合物は、本発明者が独自に広範な化合物から鋭
意研究の結果選択したものであ〕、特定O多価アルコー
ル類もしくはその1lIII体、1又は2個のカルボキ
シル基を有するアミノ酸及び安息香酸ベンジルから構成
される群に属する。上記多価アルコール類及びそのII
QF体並びにアミノ酸とシしてa具体的には以下の各化
合物を例示できる。
The ethanol and purpanol used as main components in the alcohol composition of the present invention include ethanol 9 listed in the Japanese Pharmacopoeia, which is conventionally known as a sterilizing disinfectant.
&5 V/V% or more at t4, anhydrous F, /-#, I spring ethanol, isopropanol, and oboro-propanol can be exemplified. Compounds that can be blended with the above alcohol and exhibit the effects intended by the present invention are , which was independently selected by the present inventor as a result of intensive research from a wide range of compounds], and is composed of a specific O polyhydric alcohol or its 1lIII form, an amino acid having one or two carboxyl groups, and benzyl benzoate. belongs to the group The above polyhydric alcohols and II
Specific examples of the QF form and amino acids include the following compounds.

く多価アルコール類及びその誘導体〉 エチレングリコール、ブリピレングリコール、1.8−
ブタンジオール、ポリオキシアルキレングリプール(ポ
リオキシエチレングリコール、ポリオキシプロピレング
リコール等)、ポリオキシアルキレントリオール(ポリ
オキシプロピレントリオール4I)、グリセリン、ペン
タエリスリトール、ソルビトール、グルコース、マンニ
ット、7ラクトース、しよ糖噂のアルコール並びにポリ
オキシエチレン毫ノオレエート、グリセリン七ノ脂肪酸
エステル、プロピレングリコール脂肪酸エステル、ポリ
オキシエチレンソルビタン峰ノオレエート、シよ糖脂肪
酸エステル臀のエステル類及びポリオキシエチレンノニ
ルフェノ−にニーPル臀のエータ+4’煩等。
Polyhydric alcohols and their derivatives> Ethylene glycol, pyrene glycol, 1.8-
Butanediol, polyoxyalkylene glycol (polyoxyethylene glycol, polyoxypropylene glycol, etc.), polyoxyalkylene triol (polyoxypropylene triol 4I), glycerin, pentaerythritol, sorbitol, glucose, mannitol, 7-lactose, Sugar rumored alcohol and polyoxyethylene glycol oleate, glycerin heptanofatty acid ester, propylene glycol fatty acid ester, polyoxyethylene sorbitan monooleate, sucrose fatty acid ester esters, and polyoxyethylene nonylphenol. Eta + 4' trouble etc.

くアミノ酸類〉 クリシン、アラニン、フェニルアツニン、アルギニン、
グルタミン酸、アスパラギン酸、ζエチレン等。
Amino acids> Chrysin, alanine, phenylatunine, arginine,
Glutamic acid, aspartic acid, ζethylene, etc.

上記各化合物は、通常入手される形II(m1体4しく
は液体)の1壕、その1種を単独で又は露種以上を、ア
ルコールに配合され本発明のアルコール組成物をされる
。配合割合は、用いる化金物の種類、形11によjli
r干相瀘するが液体のものでは、アルコールに対して0
.1−!6V/V%、好ましくはt−20V/V91p
@FlOfllBト8h、”*九WA体04e)”t’
はo、osw/v%以上怠5W/V**で又はそのもの
の飽和溶解度まで、好壕しく社a、iw/v%以上10
W/V*tで又鉱そ040の飽和溶解度までとするのが
よい。上記配合割合の上限は、特Kjl界的fk%ので
紘なく、これを越えて用いて4本発明所期の効果紘発揮
されゐが、通常上記化合物を多量配合すれば、それだけ
得られる組成物中のアルコール含有量が低下することと
な)、使用に当〕多量の組成物が必要となる不利があル
、を良溶解[0低いものでは、一部下溶分として析出す
るおそれがTo)、これは本l&IJiの所望の効果に
寄与せず無駄となるおそれがある。
Each of the above-mentioned compounds may be used alone or in combination with one or more of the commonly available Form II (M1-form or liquid) forms to form the alcohol composition of the present invention. The blending ratio depends on the type and shape of the metal compound used.
It is resistant to alcohol, but in liquid form, it is 0 against alcohol.
.. 1-! 6V/V%, preferably t-20V/V91p
@FlOfllB 8h, "*9WA body 04e)"t'
is preferably o, osw/v% or more at 5 W/V** or until the saturation solubility of the substance, a, iw/v% or more than 10
W/V*t is preferably up to the saturation solubility of ore 040. The upper limit of the above blending ratio is not limited to the specific Kjl limit fk%, and the desired effect of the present invention can be achieved by using it beyond this limit, but normally, the more the above compound is blended, the more the composition obtained. There is a disadvantage that a large amount of the composition is required for use (as the alcohol content in the alcohol content decreases), but there is a disadvantage that a large amount of the composition is required for use. , this may not contribute to the desired effect of this I&IJi and may be wasted.

かくして得られる本発IjIOI11r!1.物は、そ
の110腔内41に適用することがてきる。を九本発明
組成物は更にこれKWり索及びヨク化カリクムを添加し
てNクドチンキ剤の形態で皮膚の消11に用いることも
でき、特に刺激性がないことよ)創傷等の諺められる皮
膚に対しても有利KJI−得る。
The original IjIOI11r thus obtained! 1. The object can be applied within the 110 cavity 41 thereof. The composition of the present invention can also be used in the form of a tincture by adding KW and Calicum to the skin, and is not particularly irritating. It also benefits the skin from KJI.

また本発明組成物は、これを有効成分として、通常の製
剤担体(賦形剤、希釈剤)41と組み合せ更に必要に応
じて着色剤、香料、凰昧剤、甘味剤及び他の医薬品等を
添加後賦形して条種の製剤形態例えば顆粒剤、錠剤、ト
ロープ剤、ペースト剤、工、(工、□工3、界7.工、
In addition, the composition of the present invention uses this as an active ingredient in combination with ordinary pharmaceutical carriers (excipients, diluents) 41, and further contains colorants, fragrances, demulcents, sweeteners, and other pharmaceuticals as necessary. After addition, it is shaped into strips of formulations such as granules, tablets, tablets, pastes, etc.
.

磨形謹、チューインガム形l141とすることができる
。上記におiて用いられる担体及びその他の添加剤とし
ては、通常使用される各種のものでよく、その具体例七
しては、デンプン、炭酸力ルシクム、炭酸水素ナトリク
ム、結晶セルロース、ケイ酸、微粒子無水シリカ、カオ
リン、ベントナイト、タルク、ステアリン酸塩、カルボ
キシメチルセルロース、メチルセルロース、ゼラチン、
〆リビニルビロリドン、アルギン酸、リン酸カルシクム
、リン酸カリクム、多孔質メタケイ酸、アルミン酸マグ
ネシクム、酢酸ビニル樹脂、メントール、チ毫−ル、チ
Mクジ油、グイと姉、ハツカ波、メントール、デツカリ
ン等を例示できる。上記各種形態O製剤の調製方法は常
法に@うことができる。例えば顆粒剤、錠剤等は、本1
891組成物に賦形剤等を混合し賦形後、有効成分とす
るアルブーA/D揮欽を防ぐためにポリビニルアルコ−
ル等にて被覆し、更に必要に応じステアリン駿カルシク
ム等にて光沢をつけることができる。禽獣剤は、本発明
組成物に甘味料、着色料、香料等を添加混合し、水で適
当に希釈することによシ調製される。ペースト剤乃至歯
磨は、CMC410結合剤乃至糊剤と本発明組成物とを
混合し、これに充填剤、増量剤及びその他の添加剤を混
練することによ)調製される。またチューインガムは、
チューインガム基材例えば酢酸ビニル樹脂等、を予めエ
タノールで軟化させ、これと本発明組成物及び必要に応
じ甘味料、薔P+等を混合禽浸させた多孔質物質例えば
多孔質メタケイ酸、アルミン駿マグネシクム等とを混諌
後、板状KiE*L、得られる成形物表面をポリビニル
アルコールフィルム等で被覆及び適当な大きさに裁断す
るととによ)製造される。
It can be made into a chewing gum type l141. The carrier and other additives used in i above may be any of the commonly used ones, and specific examples include starch, lucicum carbonate, sodium bicarbonate, crystalline cellulose, silicic acid, Fine particle anhydrous silica, kaolin, bentonite, talc, stearate, carboxymethylcellulose, methylcellulose, gelatin,
〆Livinylpyrrolidone, alginic acid, calcium phosphate, potassium phosphate, porous metasilicic acid, magnesium aluminate, vinyl acetate resin, menthol, thiol, chimney oil, Gui and sister, Hatsuka wave, menthol , detsukarin, etc. can be exemplified. The above-mentioned various Form O preparations can be prepared by conventional methods. For example, granules, tablets, etc.
After mixing the 891 composition with excipients and shaping, polyvinyl alcohol is added to prevent Albu A/D, which is the active ingredient, from volatilizing.
If necessary, it can be coated with stearicum or the like to give a gloss. The poultry and veterinary preparation is prepared by adding and mixing sweeteners, colorants, fragrances, etc. to the composition of the present invention, and diluting the mixture appropriately with water. Pastes or dentifrices are prepared by mixing the CMC 410 binder or thickening agent with the composition of the present invention and kneading therein fillers, extenders and other additives. Also, chewing gum
A chewing gum base material, such as vinyl acetate resin, is softened in advance with ethanol, and the composition of the present invention and, if necessary, a sweetener, Bara P+, etc. are mixed and soaked to form a porous material, such as porous metasilicic acid, aluminium silica, etc. The surface of the resulting molded product is coated with a polyvinyl alcohol film or the like and cut into an appropriate size to produce a plate-shaped KiE*L.

上記各積形flKl1m!される製剤中の本発明組成物
の含有量紘、製剤の形態、使用方法、適用量、所望0@
果4IaICよ)適宜に決定され特に制限社ないが、通
常製剤1単位当〉釣60重量部以上好ましくは60〜9
0重量部li度とするのがよい。
Each of the above product shapes flKl1m! The content of the composition of the present invention in the preparation, the form of the preparation, the method of use, the amount of application, and the desired amount
Although it is determined as appropriate and there are no particular restrictions, it is usually 60 parts by weight or more per unit of preparation, preferably 60 to 9
It is preferable to set it to 0 parts by weight li degree.

かくして調製される各製剤は、その形111Kj6じて
以下の如くして適用される。例えば錠剤等の固剤は、こ
れを口中に食t−t、噛むことによって、口腔内の洗浄
殺菌効果、虫歯予防効果、煙草ヤにと勤等の歯牙清#l
効果及び二ン二り奥等の口臭除去効果を奏し得る。かか
る固剤は通常的1〜8f“0゛単位形−で所菫の作用効
果を要求される時に適宜に適用すればよい。液剤は通常
の殺菌消毒剤と同$にこれを皮膚等に塗布することKよ
niu’r的に適用され、殺曹清毒効果及び体臭除去効
果を奏し得ると共にこれを例えば水虫治療作用のめる医
薬品等と併用するか又は該医薬品有効成分と混合した彫
型で適用すれば、患部K11l激を与えない水虫治療剤
として有効で参る。かかる殺菌消毒剤等は、通常アルコ
ール濃度が約lO〜80重量形の希釈液の形態で皮膚1
d当!IKIII約6〜10sJ程度の範囲で適用され
得る。また禽獣割箸の液剤は1度に約80dを1回に8
度、1日8回前後舎獣することによ如、口腔内沈浸作用
によって、例えば扁桃腺腫等の治癒、歯fil掃、煙草
やにとシ、口臭除去、虫歯予防410効果を奏し得る。
Each formulation thus prepared is applied in its form as follows. For example, a solid drug such as a tablet can be eaten or chewed in the mouth to have a cleaning and sterilizing effect on the oral cavity, a cavity prevention effect, and a dental cleaning effect for smoking, smoking, etc.
It has the effect of removing bad breath from the back of the mouth and the like. Such a solid agent is usually in the form of a unit of 1 to 8 f"0" and can be applied as appropriate when the desired effect is required.The liquid agent can be applied to the skin, etc. at the same cost as an ordinary sterilizing disinfectant. It can be applied in a regular manner, and has a soda-killing and body odor removal effect, and is used in combination with, for example, medicines that have a therapeutic effect on athlete's foot, or is applied in the form of a mixture with the active pharmaceutical ingredients. If so, it will be effective as a treatment for athlete's foot that does not cause irritation to the affected area.Such bactericidal disinfectants are usually applied to the skin in the form of a diluted solution with an alcohol concentration of about 10 to 80% by weight.
d right! IKIII can be applied in a range of about 6 to 10 sJ. In addition, the liquid agent for chopsticks for birds and animals is about 80 d at a time.
By rinsing around 8 times a day, it can have 410 effects, such as curing tonsilloma, cleaning teeth, removing bad breath, and preventing cavities due to its intraoral sinking action.

歯磨形−の薬剤社通常1回に約2〜8fを歯ブラシ9に
つけ1日8115Lはそれ以上歯を磨くことKよ)適用
され、虫歯予防、煙草中にとシ効果を奏し得ると崗誇に
口臭除去をも計p得る。更にチューインガム形態の薬剤
は、1回当〉その1〜s1枚を1日数回噛むことによ如
、上記歯磨と同様の効果を奏し得る。
Toothpaste-type pharmaceutical companies usually apply about 2 to 8 f on a toothbrush 9 at a time (you should not brush your teeth more than 8115 L a day), and are proud that it can prevent cavities and have a soothing effect while smoking. It also helps remove bad breath. Furthermore, the medicine in the form of chewing gum can produce the same effect as the above-mentioned toothpaste by chewing 1 to 1 piece of it several times a day.

以下本発明のアルコール組成物につき行なわれた各種試
験例を挙げる。尚各試験に用い九アルコール組成物廷、
日本薬局方所載の消毒用エタノール(エタノール880
ydK精製水を加え全量を1000s(として製したも
の)の100sZKs下記化合物N&1−46の夫々所
定量を添加溶解させて調製した。尚上記all!に当シ
、完全に溶解しない化合物にりいては湯浴によシso”
ctc加熊後放冷しP遇して析出物を除去し九飽和液の
形lで用いたものケ6る・ 〈供試化合物〉 ゛  □ 嵐    種鎖 1   l、3−ブタンジオール、 2   プロビンングリコール 8   プロピレングリフールモノオレエート4   
ポリオキシエチレングリコール6   ポリオキシプル
ピレングリコール6   ポリオキシプロピレントリオ
ール7   ポリオキシエチレンモノオレエート・8 
  ポリオキシエチレンノニルフェノールエーテル 9   グリセリンモノオレエート 10   k、リメチロールプロパン脂肪酸エステル1
1  ベンクエリスリトール 12  ソルビトール 18  マンニット 14  ポリオキシエチレンソルビタンモノオレエート 16  しよ糖 16  1、よ糖脂肪酸エステル 17  カップリングシュガー 18  グルコー7 19  フラクトース 20  グリシン 21  アラニン 22   L−アスパラギン酸 23  グルタミン酸 24′ アルギン酸 26   L−アルギニン・L−グルタミン酸塩26 
 安息香酸ベンジル 上記供試化合物鬼9.11〜18.16% 16、及び
20〜24の飽和溶解度は夫々法あ通シである。
Various test examples conducted on the alcohol composition of the present invention are listed below. In addition, nine alcohol compositions used in each test,
Ethanol for disinfection (Ethanol 880) listed in the Japanese Pharmacopoeia
ydK purified water was added to the total amount, and predetermined amounts of each of the following compounds N & 1-46 were added and dissolved in 100s ZKs (prepared as 1000s). All of the above! However, if there are compounds that do not dissolve completely, please take a hot water bath.
After heating with CTC, the precipitates were removed by allowing it to cool and then using it in the form of a saturated liquid.<Test compound> ゛ □ Arashi seed chain 1 l,3-butanediol, 2 Bing Glycol 8 Propylene Glyfur Monooleate 4
Polyoxyethylene glycol 6 Polyoxypropylene glycol 6 Polyoxypropylene triol 7 Polyoxyethylene monooleate 8
Polyoxyethylene nonylphenol ether 9 Glycerin monooleate 10 K, Limethylolpropane fatty acid ester 1
1 benquerythritol 12 sorbitol 18 mannitol 14 polyoxyethylene sorbitan monooleate 16 sucrose 16 1, sucrose fatty acid ester 17 coupling sugar 18 glucose 7 19 fructose 20 glycine 21 alanine 22 L-aspartic acid 23 glutamic acid 24' alginic acid 26 L-arginine/L-glutamate 26
Benzyl benzoate The saturation solubility of the above test compounds 9.11 to 18.16% 16 and 20 to 24 was standard.

供試化合物地    溶解度(96) 9       0.16 −11       ’1.11 131       1.67 18       1.60 16       1.67 16            0.6420     
       0.4011            
 0.4922             0.172
8            0.16j!4     
       0.10試験I   味覚試験(口内刺
激試験)上記各供試化合物を配合し九本発明組成物産1
〜26(番号は供試化合物翫と対応する)の夫々1回約
5gZ宛を、男性6人及び女性6人から構成される各被
検者の口に含ませ、之等各被検者に′)゛き口内1激の
有無を調べる。試験はひとつの組成物につき各人8回づ
つ行ない、夫々以下の基準に従い結果を求め、10人の
平均の価で下記@1表に示す。
Test compound solubility (96) 9 0.16 -11 '1.11 131 1.67 18 1.60 16 1.67 16 0.6420
0.4011
0.4922 0.172
8 0.16j! 4
0.10 Test I Taste test (oral irritation test) Nine inventive composition products 1 were prepared by blending each of the above test compounds.
~26 (numbers correspond to the test compound) were put into the mouths of each test subject, consisting of 6 men and 6 women, and ') Check for presence of 1-geki in the mouth. The test was conducted 8 times for each person for each composition, and the results were determined according to the following criteria, and the average value of the 10 people is shown in Table 1 below.

帯 ・・・・・・ 刺激強し 廿 ・・・・・・ 刺激有り + ・・・・・・ 刺激少々有如 ± −・−・ 刺激極めて少ない −・・・・・・ 刺激なし 111表 上記第1表よ)供試化合物凪l乃至!!6は、いずれ4
hこれを消毒用エタノールKl舎溶解することkよって
該アルコールの口内刺激性を消失させ得ることが判る。
Obi... Strong stimulation... Stimulation + ... Slight stimulation ± --- Very little stimulation --- No stimulation 111 table above No. 1 Table) Test compound Nagil~! ! 6 will eventually become 4
It is found that the oral irritation of the alcohol can be eliminated by dissolving it in disinfectant ethanol.

試験■ 傷に対する利激試験 傷にアルコールを塗布し消壽するとアルコールの傷に対
する刺激所閾傷にし−ること社よく知られている。この
試験は、上記本発明の供試組成物の傷に対する刺激性の
有無を調べ九4のである。
Test ■ Stimulus test on wounds It is well known that applying alcohol to a wound and letting it disappear will make the wound more sensitive to alcohol. This test was conducted to determine whether or not the sample composition of the present invention has irritation to wounds.

綿を用i指又は足O創偏部ti回拭き、偏部へ刺激を観
察した結果を下記第2表に示す。
The results of wiping the uneven part of the finger or foot with cotton ti times and observing the irritation to the uneven part are shown in Table 2 below.

;゛       ・ 、゛1パ1.ゼ−ニ −1− I^14−4 第2表 同−試験をインプロパツール50s/と糟製氷60−と
OII波に、供試化合物の所定量を配合した本発明組成
物N11丁〜84に’:)論行なつえ結果を下記*S表
に示す・ 第  sl 上記!I2表及びIN8表よ)、本発明組成物は、傷に
対する刺激性も消失されてお〕、シ与ることのないこと
が判ゐ。
;゛・、゛1Pa1. Zeni -1- I^14-4 Table 2 The same test was carried out for compositions of the present invention N11 to 84, in which a predetermined amount of the test compound was blended with Impropatool 50s/, Ice-making 60-, and OII wave. ni':) The results of the discussion are shown in the *S table below.・Chapter sl Above! Tables I2 and IN8 show that the composition of the present invention also eliminates irritation to wounds and does not cause any irritation.

試験■  殺菌作用試験 本発明組成物の下記各種微生物に対すゐ殺菌効果をlぺ
た。
Test ■ Bactericidal effect test The bactericidal effect of the composition of the present invention on the following various microorganisms was tested.

〈供試微生物〉 A ・・・ ストレプトコッカス ミュータンス(St
r@ptococcus ’    mutams )
B  −・  スタフィロコッカス オーレタス(St
iphylococcws     aurews )
町 C・・・ ミオパクテリクム チューベルカロシス (Mycobact*r1w  tubercules
ig )D ・・・ エシェリヒア プリー (lEschsrlckla    call  )K
  =  ’)フロコツカス ニューモニア工(Dlp
lococcus     pm@umo跪ia*)F
  −・・ プルモネラ  テイフイ(Silmome
l1m    typki  )本発明組成物の大々1
0Wtを試験管に採り、これに上記供試微生物O犬々を
培養し九培養液is/を入れ、l器秒後試験管よ#)1
白金耳を採り、とれを別の第1試験管内の培地に移植し
、更に16秒傷に、供試微生物を培養している最初の試
験管内培養液よ〉l白金耳づつをと〕これを集雪、第8
・・・O試験管内の培地に移植し、各試験管を順次87
℃にで2日間培養して微生物の発育の有無を調べ、発育
が阻止された時間(秒)即ち殺菌時間(秒)を求める。
<Test microorganism> A... Streptococcus mutans (St
r@ptococcus 'mutams)
B - Staphylococcus au lettuce (St
iphylococcws aurews)
Town C... Myopactericum tuberculosis (Mycobact*r1w tubercules
ig )D... Escherichia Puri (lEschsrlckla call)K
= ') Flokotsucus pneumoniae (Dlp)
lococcus pm@umo kneeling ia*)F
--- Pulmonella teifui (Silmome)
l1m typki) Large scale 1 of the composition of the present invention
Take 0Wt in a test tube, culture the above test microorganisms in it, add the culture solution is/, and after 1 second, transfer to the test tube.
Take a platinum loop, transfer it to the culture medium in another first test tube, and apply one platinum loop at a time to the wound for another 16 seconds with the culture medium in the first test tube in which the test microorganism is cultured. Snow collection, 8th
...Transplant into the culture medium in O test tube, and transfer each test tube sequentially to 87
The sample is incubated at ℃ for 2 days, and the presence or absence of growth of microorganisms is examined, and the time (seconds) during which growth is inhibited, that is, the sterilization time (seconds), is determined.

結果を同一試験を8度繰返した平均値にて下記第4表に
示す、崗本発明組成物における各供試化合物記会量は、
第1表における刺激性の消失が見られる一定量(6〜l
5g5Z、6fまた紘飽和溶解量)とした。
The amounts of each test compound in the composition of the present invention are shown in Table 4 below based on the average value obtained by repeating the same test 8 times.
A certain amount (6 to 1
5g 5Z, 6f (also saturated dissolved amount).

[4表 尚上記試験においてアルコールを単独で用いた場合、供
試微生物AK対する殺曹時閏は、消毒用工fi/−#ノ
場合80秒、i19.5%(V/V)エチルアルコール
即ち無水エタノールの場合soe、60%イソプロピル
アルコールの場680秒、60%n−プロピルアルコー
ルの場合46秒であった。
[Table 4] When alcohol was used alone in the above test, the time required to kill the sample microorganism AK was 80 seconds in the case of disinfectant fi/-#; 680 seconds for 60% isopropyl alcohol and 46 seconds for 60% n-propyl alcohol.

上記@4表よ)本発明組成物は、いずれも供試微生物に
対して強力な殺菌力を有することが明らかである。
It is clear that all of the compositions of the present invention (see @Table 4 above) have strong bactericidal activity against the test microorganisms.

試験■ 鍾草中に除去作用試験 内4118■のガラス管の一端を1紙にて閉じ、他端よ
珈紙巻煙草rピース」8本の燃焼によシ発生する煙をナ
ベで該ガラス管内を通して上記1紙を通過させる。1紙
は褐色となる。この褐変した1紙をii!=15111
の円形に!EJIII試験片とする。
Test ■ Removal effect during test One end of the glass tube of No. 4118 ■ was closed with a piece of paper, and the smoke generated by the combustion of 8 pieces of cigarettes was passed through the glass tube using a pan at the other end. Pass the paper above. 1 paper becomes brown. This browned paper ii! =15111
In a circular shape! This is an EJIII test piece.

上記試験片を内径1!eggの試験管に入れ、これに本
発明組成物の61dを入れ振巾50 ws 1分間12
0回0@41′e振盪して意O分後試験片O脱色程度及
び*0着着色度を観察する。結果を下記第6麦に示す。
The above test piece has an inner diameter of 1! Put 61d of the composition of the present invention into an egg test tube and shake at a shaking width of 50 ws for 1 minute.
Shake 0 times at 41'e and observe the degree of decolorization of the test piece and the degree of coloration after 0 minutes. The results are shown in the 6th barley below.

IIs表に社対照としてアルコールを単独で用V&九場
合及び比較のため従来よ)やにと〉効果があるとして提
案されているp−アミ7安息薔駿メチル及びナリチル酸
エチルを用いた場合の結果を併記する。
Table IIs shows the case of using alcohol alone as a control and the case of using p-ami7benzenbarashun methyl and ethyl nalicylate, which have been proposed to be effective (conventional) for comparison. Also include the results.

第6表 上記第6表よ〕本発明組成物は煙草やくと夛妨果を有す
ることが明らかである。
Table 6 [Table 6 above] It is clear that the composition of the present invention has a harmful effect when burning tobacco.

試験マ  消臭作用試験 市販ギ曹りデを食した直後の強いニンニク臭を感じられ
るヒトに、本発明組成物の8−を用い歯ブラシで1分間
歯を磨かせた。その結果1(11の距離をおいてニンニ
ク臭は諺められなかった。
Test Ma: Deodorizing Effect Test A person who can smell a strong garlic odor immediately after eating a commercially available Gisoori De was asked to brush his/her teeth for 1 minute with a toothbrush using Composition 8- of the present invention. As a result, there was no smell of garlic at a distance of 1 (11 meters).

★良同様に、市販ギWfデを食し強いニンニク臭を感じ
られるヒトWc′)@、本発明組成物の80dでIlM
うがいをし先後には、lQs以内の距離に近づくもニン
ニク臭は全(感知されなかった。
★Similarly, human Wc') who can feel a strong garlic odor after eating commercially available gi Wf de, IlM with 80d of the composition of the present invention
After gargling, I could not detect any garlic odor even though I got within 1Qs of it.

上記試験マよ〉本発明組成物は、口臭除去効果を有する
ことが明らかでslゐ。
From the above test, it is clear that the composition of the present invention has a bad breath removal effect.

以下本発明アルコール組成物0I81万例を実施例とし
て挙げる。
Below, 810,000 examples of the alcohol composition 0I of the present invention are listed as examples.

実施例1 消毒用エタノール     1000@tプロピレング
リコール     601消毒用エタノールにプロピレ
ングリコールヲ添加溶解して液剤形態の本発明組成物を
得る。
Example 1 Ethanol for Disinfection 1000@t Propylene Glycol 601 Propylene glycol was added and dissolved in ethanol for disinfection to obtain the composition of the present invention in a liquid form.

実施例! 消毒用エタノール      100 G+wJL−ア
ラニン         50F消毒用エタノールKL
−アラニンを加え湯浴上80℃に加温し溶解させ、室温
に冷却後不溶分をP去し、液剤形態の本発明組成物を得
る。
Example! Disinfecting ethanol 100 G+wJL-Alanine 50F Disinfecting ethanol KL
- Add alanine and dissolve by heating to 80° C. on a hot water bath, and after cooling to room temperature, insoluble matter is removed to obtain a composition of the present invention in a liquid form.

実施例8 消毒用エタノ、−ル       no(Is+Jしよ
糖脂肪酸エステ#       601寅施例2と同I
Kして液剤形態の本発明組成物を得る。
Example 8 Disinfectant Ethanol No. (Is+J Saccharide Fatty Acid Aesthetic #601 Same as Example 2)
The composition of the present invention in liquid form is obtained.

実施例4 Mり素            6・fWIt化カリク
ム         40170%(V/V)zl/−
k     eTSmグリセリン峰ノオレエー)   
   6170%(V/V ”)エタノ−A/にグリセ
リンそノオレエートを混合し湯浴上溶解させ、放冷後不
溶分をP*し、Fi液KW?素及び璽り化カリクムを−
加え日−Fチンキ金彫型の本発明組成物を得る。
Example 4 M 6・fWIt potassium 40170% (V/V) zl/-
k eTSm glycerinmine noolea)
6170% (V/V'') ethanol-A/ is mixed with glycerin oleate, dissolved on a hot water bath, left to cool, the insoluble matter is P*, and Fi liquid KW?
In addition, a composition of the present invention in the form of a day-F tincture and gold sculpture is obtained.

実施例6 l−((怠−クロWフェニル)ジツエニルメチル〕イミ
ダゾール     lOI消毒用エタノール     
 1000s/L−アラニン         50f
L−アラニンを消毒用エタノールに溶解して得九液Kl
−((!−クロWフェニル)ジフェニルメチルコイミダ
ゾールを添加溶解して、水車治療剤として有効tklI
L剤形ll金形発明組成物を得る。
Example 6 l-((lazy-chloroWphenyl)ditzenylmethyl)imidazole lOI disinfectant ethanol
1000s/L-alanine 50f
Nine liquid Kl obtained by dissolving L-alanine in disinfectant ethanol
-((!-ChloW phenyl)diphenylmethylcoimidazole is added and dissolved in tklI, which is effective as a water wheel treatment agent.
A L dosage form II molded inventive composition is obtained.

実施例6 1プロパツール       1001ナツカリン  
         IIエリスロシン        
o、ottメントール         o、ogy−
上記薬品を混合して口洗料形IIO本発明組成物を得る
Example 6 1 Proper Tool 1001 Natsukarin
II Erythrosine
o, ott menthol o, ogy-
The above chemicals are mixed to obtain a mouthwash form IIO composition of the present invention.

本薬剤を水にて適当に希釈してうがい41によ勤口を洗
えば虫歯のlK因である口中の微生物を殺菌し、煙草ヤ
ニによ・る−の汚染物中ニンニク類中七の他による口臭
を除くのみならず扁桃腺の腫暖を防ぐ作用がある。
If you dilute this drug appropriately with water and wash your mouth and mouth, it will kill the microorganisms in your mouth that are the cause of tooth decay, and it will kill the microorganisms in your mouth that are the cause of tooth decay. It has the effect of not only eliminating bad breath but also preventing swelling of the tonsils.

実施何丁 クロロヘキシジン          4fメントール
             !!fチ峰−ルール   
       ’LUIチョクジ油         
   1.・f桂皮油               
8f消壽用エタノール        toooIII
tポリオキシエチレングリコール   601以上を混
合して溶解し本発明の舎獣口洗剤とすゐ。これは実施例
6で得九口洸粁と同様の作用効果を奏し得る。
How many chlorohexidine and 4f menthol! ! f chi peak - rules
'LUI Chokji Oil
1.・F cinnamon oil
8f Ethanol for consumption tooIII
The animal mouth detergent of the present invention is prepared by mixing and dissolving polyoxyethylene glycol 601 or more. This can produce the same effect as in Example 6.

実施例8 消毒用エタノール         1001ポリオキ
シエチレングリコール    !lグリセリン峰ノオリ
エー)       81黴粒子無水シリカ     
    Toeデツカリン             
0.6Fハツカ油             0.61
上記O薬品を均一に混練して粘いペースト状形IIO本
発明m成物を得る。
Example 8 Ethanol for disinfection 1001 polyoxyethylene glycol! 81 mold particles anhydrous silica
Toe detsukarin
0.6F heart oil 0.61
The above O chemical is uniformly kneaded to obtain a viscous paste-like IIO composition of the present invention.

これは歯科診療Oll歯科用エンジンに取付けた回転プ
クシを浸漬し回転しクク煙草ヤニにて汚染した歯にあて
て磨けば歯に付着した煙草ヤニを除去してきれいな歯と
すると同時に*に寄生したストレプ)プツカスミエータ
ンス410微生物を殺菌して虫歯を予防しあわせて口臭
を除去すゐ効果がある。
This can be done by soaking a rotary brush attached to a dental engine in a dental clinic, rotating it, and applying it to teeth contaminated with cigarette tar to remove the cigarette tar from the teeth and make them clean. Strep) Putukasumietans 410 is effective in killing microorganisms, preventing tooth decay, and eliminating bad breath.

実施例9 消毒用エタノール        100fプロピレン
グリコール      gOf微粒子無水シリカ   
     70fサツカリン           0
.6fハツカ油            0.61実施
例7と同様にして上紀組弐のペースト状形型の本発明組
成物を得−ゐ。
Example 9 Disinfecting ethanol 100f propylene glycol gOf fine particle anhydrous silica
70f Satukarin 0
.. 6f Core oil 0.61 In the same manner as in Example 7, a composition of the present invention in the form of a paste of Jokigumi 2 was obtained.

実施例、10 99.6%(V/V) 工fルyルコール  757グ
リヤリ、             16fC,M、C
、got アラニン             mlフラクトース
           6f炭酸カルシクム     
    1001リン酸カルシクム2水和物    1
oorメントール           0.6f水 
                       !I
s/C,M、C,を予めグリセリン中に分散し、次に水
を混合して粘稠な糊状とし、これにエチルアルコールを
加え、これにアラニン、7ツクトクス、安息香酸ソー〆
を溶解し、更に炭酸カルシツム、リン酸カルレクム2水
和物を混線して均一なペースト状とし、最後Kl粁を添
加混合して練歯磨形flO本発明組成物を得る0本線歯
磨は虫歯を予防し歯の煙草ヤニによる汚染物中ニンニク
類その他による口臭を除く効果がある。
Example, 10 99.6% (V/V) 757 Griyari, 16fC, M, C
, got alanine ml fructose 6f calcium carbonate
1001 Calcicum phosphate dihydrate 1
oor menthol 0.6f water
! I
Disperse s/C, M, and C in glycerin in advance, then mix with water to make a viscous paste, add ethyl alcohol to this, and dissolve alanine, 7-tox, and benzoic acid salt. Then, calcium carbonate and calrecum phosphate dihydrate are mixed to form a uniform paste, and finally, Kl is added and mixed to obtain a toothpaste-type flO composition of the present invention. It is effective in removing bad breath caused by garlic and other contaminants caused by cigarette tar.

実施例11 消毒用エタノール         !Gotグリセ替
ンモノンモノオリエート  101ツラクトース   
        61パニク調合香料        
   51d多孔質メタケイ酸アルミン酸  1000
fマグネシクム (イノシリン) 酢酸ビニール樹脂       toooy消毒用エタ
ノール、グリセリンモノオリエート、香料をメタグイ験
アルミン駿マグネシクムと混じメタグイ駿アルミン駿マ
グネシクムの多孔質の内部に吸収飽和せしめ、これを別
に消毒用エタノールにて軟化した酢酸ビニール樹脂中に
混練し、一定の厚さに分出しせみ板状tLWM物の表裏
をポリビニールアルコールフィルム等にて被覆して消毒
用エタノールの揮散を防ぎ適宜の大きさに裁断してチュ
クインガム形急の本発明組成物を得る。
Example 11 Ethanol for disinfection! Got glycerin monomonooleate 101 turactose
61 panic blended fragrance
51d porous metasilicate aluminate 1000
f Magnesicum (Inocillin) Vinyl acetate resin Toooy Disinfectant ethanol, glycerin monooleate, and fragrance are mixed with Metagui-tested alumin-Shun magnesicum and absorbed and saturated into the porous interior of Metagui-tested alumin-Shun magnesicum, and this is separately mixed with disinfectant ethanol. The product is kneaded in softened vinyl acetate resin, distributed to a certain thickness, and the front and back of the plate-shaped tLWM product is covered with polyvinyl alcohol film, etc. to prevent the disinfectant ethanol from volatilizing and cut into appropriate sizes. A chewing gum-shaped composition of the present invention is obtained.

このチュクインガ五を噛むことによ砂虫歯を予防し煙草
ヤニによる歯の汚染物を除きニンニク類中その他による
口臭を除去することができる。
By chewing this chukuinga, you can prevent dental caries, remove tooth stains caused by tobacco tar, and remove bad breath caused by garlic and other substances.

実施例1g 消毒用エタノール        20017ツクトー
ス           101アルギン酸     
       o、gf多孔質メタグイ駿アルミン酸 
 1500Iiグネシクム(ノイシリン) メントール            0.1fM!’M
               50fI尚MPM  
とは、2−メチル−6−ビニルビリジンーメチルアクリ
レートとメタクリル酸とO共重合体(田辺製薬社製)で
ある。
Example 1g Disinfecting ethanol 20017 Tuctose 101 Alginic acid
o, gf porous metal aluminic acid
1500Ii Gnesicum (Neushilin) Menthol 0.1fM! 'M
50fI Sho MPM
is 2-methyl-6-vinylpyridine-methyl acrylate, methacrylic acid, and O copolymer (manufactured by Tanabe Seiyaku Co., Ltd.).

消毒用エタノール、7ツクトース、アルギン酸、メント
ールを混合して溶解し、均一な液とし、これに多孔質メ
タグイ駿アルミン駿マグネシクムを混合し、その多孔質
の内部に食浸せしめ、これにMPM を少量のアルコー
ルに溶解した粘稠な液を加えて混線して後、これを顆粒
ないし錠形にしエタノールの揮散を肪ぐためにポリビニ
ールアルコールにて被覆し、更にその*田をステアリン
酸カルシクムにて光沢をつけて顆粒剤又は錠剤形態の本
発明組成物を得る・ これは常に噛むことによ〉虫歯を予防し、煙草ヤニにて
P#乗し丸歯を龜れv−&にし、叉ニンニク臭等を除く
作用を有する。
Disinfecting ethanol, 7-tuctose, alginic acid, and menthol are mixed and dissolved to make a homogeneous solution, and porous metal aluminium magnesium is mixed with this, and the porous interior is soaked, and a small amount of MPM is added to this. After adding a viscous liquid dissolved in alcohol and mixing it, it is made into granules or tablets and coated with polyvinyl alcohol to prevent evaporation of ethanol, and the surface is made glossy with calcium stearate. The composition of the present invention in the form of granules or tablets is obtained by applying it. This prevents tooth decay by constantly chewing it, and it also prevents tooth decay by applying P# with tobacco tar to make the round teeth look cloudy and smell like garlic. It has the effect of eliminating.

(以上) 1、事件の表示 昭和56年 特 許 願第1!19274 号3、補正
をする者 4、代理人 大阪市東区平野町2の10平和ビル内電話06−203
−0941(代)8、補正の内容 別紙添附の通り 補正の内容 (1)  明細書中の記載を下記正課表の通シ訂正する
(Above) 1. Indication of the case 1982 Patent Application No. 1! 19274 3. Person making the amendment 4. Agent Telephone number 06-203 in Heiwa Building, 2-10 Hirano-cho, Higashi-ku, Osaka City
-0941 (generation) 8, Contents of the amendment As shown in the attached sheet, Contents of the amendment (1) The description in the specification will be corrected in the regular schedule below.

(2)明細書第16〜17頁に記載の第1表中の下記供
試組成物屋の下記添加量の項の記載を次の通シ訂正する
(2) The description of the amount added below for the following sample composition in Table 1 on pages 16 to 17 of the specification is corrected as follows.

(3)  明細書第19頁第2表の「供試組成物A16
」(4)  明細書第20頁第3表の[供試組成物A3
0Jの「供試化合物添加量(/100m#)Jの項にr
 1.67 f (飽和)」とあるをro、54F(飽
和)」と訂正すると共に「供試組成物A32」の同項に
「5f」とあるをro、49F(飽和)」と訂正する。
(3) “Test composition A16” in Table 2 on page 19 of the specification
(4) [Test composition A3 in Table 3 on page 20 of the specification]
0J, "Amount of test compound added (/100m#)"
1.67 f (saturated)'' is corrected to ``ro, 54F (saturated)'' and the ``5f'' in the same section of ``Test Composition A32'' is corrected to ``ro, 49F (saturated)''.

(以 上)(that's all)

Claims (1)

【特許請求の範囲】 ■ エタノール及び(又は)グロパノールに、食品添加
物叉#i医薬品添加物として許容される多価アルツー#
類%L、、<はその誘導体、1叉#i冨個のカルボキシ
ル基を有するアミノ酸及び資息薔駿ベンジルからなる群
かbllばれた少なくとも1種を配合し九ことを枠機と
すゐ刺歇性Oな一アルコーJ&Jl威物。 ■ #価アルコール類もしくはそowe体が水酸基を1
1個有するアルブール叉はそのエーテルもしく轄エステ
ルである特許請求の範I!第1項に記載Oag物。 ■ 多価アルコ−A/諷4しくはそO誘導体が、エチレ
ンクリプール、プロピレングリプール、l。 8−ブタンジオール、ポリオキレ1ルキレングリプール
、ポリオキシアルキレントリオール、グリセリン、ペン
タエリスリトール、ソルビトール、クルコース、マンニ
ラ)、79り)−ス、しよ着、ポリオキシエチレン令ノ
オレエート、グリセリン七ノ脂肪酸エステル、プロピレ
ングリフール脂肪酸エステル、ポリオキシエチレンソル
ビタン峰ノオレエート、シよ糖脂肪酸エステル、ポリオ
キシエチレンノニルフェノールエーテル及びトリメチロ
ールプロパン脂肪酸エステルから選択される特許請求a
SS第8項に記グリレン、アラニン、フェニルアラニン
、アルギニン、グルタミン酸、アスパラギン酸及び区ス
チジンから選択される特許請求0111111111項
に記載の組成物。 ■ 洗浄、消臭、殺菌、消毒剤である特許請求の範lI
集11[KE記載組成物。 ■ 液剤彫型、璽−ドチンキ剤yg11.含獣剤彫謙、
ペースト状形型、歯磨形態、チェーインガム形憩で用い
られる特許請求の111181項KE截O組成物。
[Scope of Claims] ■ Ethanol and/or glopanol contain polyhydric altyl which is acceptable as a food additive or pharmaceutical additive.
%L, , < is a derivative thereof, which is formulated with at least one member of the group consisting of one or more carboxyl group-containing amino acids and benzyl derivatives. Alco J & Jl is a powerhouse with a sense of humor. ■ #hydric alcohols or owe alcohols have 1 hydroxyl group
Claim I which is an ether or ester thereof having one arboul or its ether or ester! Oag product described in item 1. ■ Polyhydric alcohol A/O derivatives include ethylene glycol, propylene glycol, and l. 8-butanediol, polyoxyalkylene glycol, polyoxyalkylene triol, glycerin, pentaerythritol, sorbitol, glucose, mannilla), 79-su, salt, polyoxyethylene dioleate, glycerin heptanofatty acid ester , propylene glyfur fatty acid ester, polyoxyethylene sorbitan monooleate, sucrose fatty acid ester, polyoxyethylene nonylphenol ether, and trimethylolpropane fatty acid ester, claim a.
The composition according to claim 0111111111 selected from glylene, alanine, phenylalanine, arginine, glutamic acid, aspartic acid and sutidine as described in SS paragraph 8. ■ Claims that are cleaning, deodorizing, sterilizing, and disinfecting agents
Collection 11 [KE described composition. ■ Liquid engraving, seal-do tincture yg11. Animal agent Horiken,
111181. The KE-cut O composition of claim 111181, which is used in paste form, toothpaste form, and chain gum form.
JP56139274A 1981-09-03 1981-09-03 Alcohol composition Granted JPS5839620A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56139274A JPS5839620A (en) 1981-09-03 1981-09-03 Alcohol composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56139274A JPS5839620A (en) 1981-09-03 1981-09-03 Alcohol composition

Publications (2)

Publication Number Publication Date
JPS5839620A true JPS5839620A (en) 1983-03-08
JPH0340008B2 JPH0340008B2 (en) 1991-06-17

Family

ID=15241461

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56139274A Granted JPS5839620A (en) 1981-09-03 1981-09-03 Alcohol composition

Country Status (1)

Country Link
JP (1) JPS5839620A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5929613A (en) * 1982-08-11 1984-02-16 Lion Corp Detergent for oral cavity
JPS61289025A (en) * 1985-06-15 1986-12-19 Pijiyon Kk Washing agent for artificial tooth
WO1994017811A1 (en) * 1993-02-10 1994-08-18 Mcconn Stern Rita Wound-healing compositions containing iodine and a non-reducing sugar
JPH10203955A (en) * 1997-01-20 1998-08-04 Noevir Co Ltd Antimicrobial low-irritating cosmetic
JPH11508252A (en) * 1995-06-22 1999-07-21 ミネソタ マイニング アンド マニュファクチャリング カンパニー Stable hydroalcohol composition
JPH11508253A (en) * 1995-06-22 1999-07-21 ミネソタ マイニング アンド マニュファクチャリング カンパニー Stable hydroalcohol composition
JPWO2004028518A1 (en) * 2002-09-26 2006-02-09 独立行政法人科学技術振興機構 Mucosal tissue contractility therapeutic agent, treatment method for diseases related to mucosal tissue, syringe, and treatment tool set
JP2012171961A (en) * 2011-02-18 2012-09-10 Mcneil Ppc Inc Sedative
WO2018043677A1 (en) * 2016-09-02 2018-03-08 花王株式会社 Intraoral dental plaque dispersant

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4941280A (en) * 1972-03-17 1974-04-18
JPS5691753A (en) * 1979-12-25 1981-07-24 Toyo Shizai Kogyo Kk Prevention of hand roughness

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4941280A (en) * 1972-03-17 1974-04-18
JPS5691753A (en) * 1979-12-25 1981-07-24 Toyo Shizai Kogyo Kk Prevention of hand roughness

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5929613A (en) * 1982-08-11 1984-02-16 Lion Corp Detergent for oral cavity
JPS61289025A (en) * 1985-06-15 1986-12-19 Pijiyon Kk Washing agent for artificial tooth
JPH0450290B2 (en) * 1985-06-15 1992-08-13 Pigeon Corp
WO1994017811A1 (en) * 1993-02-10 1994-08-18 Mcconn Stern Rita Wound-healing compositions containing iodine and a non-reducing sugar
JP2009084283A (en) * 1995-06-22 2009-04-23 3M Co Stable hydroalcoholic composition
JPH11508252A (en) * 1995-06-22 1999-07-21 ミネソタ マイニング アンド マニュファクチャリング カンパニー Stable hydroalcohol composition
JPH11508253A (en) * 1995-06-22 1999-07-21 ミネソタ マイニング アンド マニュファクチャリング カンパニー Stable hydroalcohol composition
JP2010001294A (en) * 1995-06-22 2010-01-07 3M Co Stable hydroalcoholic composition
JPH10203955A (en) * 1997-01-20 1998-08-04 Noevir Co Ltd Antimicrobial low-irritating cosmetic
JPWO2004028518A1 (en) * 2002-09-26 2006-02-09 独立行政法人科学技術振興機構 Mucosal tissue contractility therapeutic agent, treatment method for diseases related to mucosal tissue, syringe, and treatment tool set
JP2012171961A (en) * 2011-02-18 2012-09-10 Mcneil Ppc Inc Sedative
WO2018043677A1 (en) * 2016-09-02 2018-03-08 花王株式会社 Intraoral dental plaque dispersant
JP2018039800A (en) * 2016-09-02 2018-03-15 花王株式会社 Intraoral dental plaque dispersant
CN109640929A (en) * 2016-09-02 2019-04-16 花王株式会社 Oral cavity internal tooth dirt dispersing agent
CN109640929B (en) * 2016-09-02 2021-11-16 花王株式会社 Oral tartar dispersion
TWI746627B (en) * 2016-09-02 2021-11-21 日商花王股份有限公司 Intraoral tartar dispersant
US11413229B2 (en) 2016-09-02 2022-08-16 Kao Corporation Oral plaque dispersion agent

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Publication number Publication date
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