JPH02286165A - Deodorant - Google Patents

Deodorant

Info

Publication number
JPH02286165A
JPH02286165A JP1108253A JP10825389A JPH02286165A JP H02286165 A JPH02286165 A JP H02286165A JP 1108253 A JP1108253 A JP 1108253A JP 10825389 A JP10825389 A JP 10825389A JP H02286165 A JPH02286165 A JP H02286165A
Authority
JP
Japan
Prior art keywords
protein
sepn
soln
solid
subjected
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.)
Pending
Application number
JP1108253A
Other languages
Japanese (ja)
Inventor
Keizo Yamaji
山地 啓三
Sakiko Murakami
村上 咲子
Kimiko Nawata
縄田 喜美子
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.)
Kanebo Ltd
Original Assignee
Kanebo Ltd
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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP1108253A priority Critical patent/JPH02286165A/en
Publication of JPH02286165A publication Critical patent/JPH02286165A/en
Pending legal-status Critical Current

Links

Landscapes

  • Cosmetics (AREA)
  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)

Abstract

PURPOSE:To obtain the deodorant applicable for intraoral use in a wide range by using the high-polymer fraction of a specific mol.wt. obtd. by protease decomposition of separated soy bean protein as the effective component. CONSTITUTION:Dry green soy beans are roughly ground and after the skin is removed therefrom, the soy beans are further ground to <=30 mesh powder. The powder is degreased by using n-hexane or a soln. mixture composed of methanol and chloroform as a solvent and is dissolved by a weakly alkaline soln. The soln. is subjected to a solid-liquid sepn. by a centrifugal sepn. or the like by which the undissolved matter is removed. The pH of the supernatant liquid thereof is controlled to weak acidity to allow the protein to settle and the protein is subjected to the solid-liquid sepn. by the centrifugal sepn. or the like. The separated solid is freeze-dried after washing with water and is separated by which the soy bean protein is obtd. This protein is sufficiently decomposed by the protease and after the oxygen is deactivated, the protein is subjected to the solid-liquid sepn. by the centrifugal sepn. or the like. The residues thereof are dissolved again in the alkaline soln. of the weak alkalinity and <100000 fractions are removed by an ultrafilter membrane of 100000mol.wt. The remaining soln. of >=100000 fractions is subjected to isoelectric point precipitation to recover the protein. After the protein is thoroughly washed with water, the protein is freeze- dried.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、親水性、疎水性、いずれの硫黄系臭気成分に
対しても良好な消臭作用を示す消臭剤に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a deodorant that exhibits a good deodorizing effect on both hydrophilic and hydrophobic sulfur-based odor components.

(従来の技術) 一般に、硫黄化合物は悪臭源としてよく知られている。(Conventional technology) Generally, sulfur compounds are well known as a source of bad odors.

例えば、クラフト製造工場、畜産業、尿尿処理場、魚腸
骨処理場等でしばしば発生する臭気がこれに該当する。
For example, this applies to the odors that often occur in craft manufacturing factories, livestock farms, urine treatment plants, fish ilium treatment plants, and the like.

また、口臭、胃内奥及びにんに(奥の主成分も硫黄化合
物であり、不快感を与える要因となっている。
In addition, sulfur compounds are also the main components of bad breath, deep in the stomach, and inside garlic, which causes discomfort.

そこで、これら硫黄系臭気成分等の悪臭物質の消臭剤と
して現在までに槌々提案がされている。
Therefore, many proposals have been made to date as deodorants for malodorous substances such as these sulfur-based odor components.

例えば、臭気成分を吸着・包接して物理的に無臭、化す
る活性炭、ゼオライト、サイクロデキストリン、化学反
応によって臭気成分を分解する酸化剤溶液、酸液、チル
カリ液等の各種試薬、あるいは強い香気成分によって官
能的に臭気を感じにくくするマスキング剤としての各種
香料等がある。
For example, activated carbon, zeolite, cyclodextrin, which adsorbs and clathrates odor components to make them physically odorless, various reagents such as oxidizer solutions, acid solutions, and chilkali solutions that decompose odor components through chemical reactions, or strong aroma components. There are various fragrances and the like that act as masking agents that make it difficult to perceive odors sensually.

ところで、口臭を除去する目的で、各間食品、歯みがき
、洗口液等に含有される消臭剤については、特に人体へ
の安全性を考慮して基準が定められているため、使用し
うる素材が限られている。
By the way, with regard to deodorants contained in foods, toothpaste, mouthwash, etc. for the purpose of removing bad breath, standards have been established with particular consideration to safety for the human body, so it is not possible to use them. Materials are limited.

口腔用消臭剤としてよ(用いられるものには、香料化合
物、サイクロデキストリン、クロロフィル、フラボノイ
ド等が挙げられる。
As an oral deodorant (useful compounds include fragrance compounds, cyclodextrin, chlorophyll, flavonoids, etc.).

しかしながら、香料化合物ぼ、香料の強い刺赦によって
官能的に嗅覚を麻痺させ、臭気を感じにくくするもので
あって、本質的な消臭ではなく、また、サイクロデキス
トリン(以下CDと記す)は、澱粉に酵素サイクロマル
トデキストリン グルカノトランスフェラーゼ(Oyc
lomaltodextringlucanotran
aferase)を作用させてつくられ、ブドウ糖がa
−1,4結合して環状となったものである。CDの種類
としては、ブドウ糖6個からなるα−(3D、7個から
なるβ−CD、8個からなるj−CD等が知られている
。これらCDは疎水性の環状構造を有し、分子内空洞に
物質をとりこんで包接するという性質があるため、臭気
成分を抑える働きがある。また、CDは殆ど無味無臭で
あるので、適用しうる食品の範囲が広い。しかしながら
、ODの空洞に侵入しうる分子の性質や、立体構造、分
子量等に制限があるため、包接できる臭気成分の種類が
限られる。また包接が充分で性であるため疎水性のCD
環内に包接されにくいが、ジアリルジスルフィドのよう
な疎水性の硫黄化合物は包接されやすい。
However, cyclodextrin (hereinafter referred to as CD) is a fragrance compound that sensually numbs the sense of smell and makes it difficult to perceive odors due to the strong sting of the fragrance, and is not an essential deodorizer. The enzyme cyclomaltodextrin glucanotransferase (Oyc) is added to starch.
lomaltodextringlucanotran
aferase), and glucose is
-1,4 bond to form a ring. As types of CD, α-(3D consisting of 6 glucose units, β-CD consisting of 7 units, j-CD consisting of 8 units, etc.) are known. These CDs have a hydrophobic cyclic structure, Since CD has the property of taking substances into the intramolecular cavity and clathrating them, it has the effect of suppressing odor components.Also, since CD is almost tasteless and odorless, it can be applied to a wide range of foods.However, if the OD cavity The types of odor components that can be included are limited because there are restrictions on the properties, three-dimensional structure, and molecular weight of the molecules that can invade.Also, since inclusion is sufficient and sexual, hydrophobic CD
Hydrophobic sulfur compounds such as diallyl disulfide are difficult to be included in the ring, but hydrophobic sulfur compounds such as diallyl disulfide are easily included.

また、クロロフィル、フラボノイドは、それ自もあり、
またサイクロデキストリンに比べ消臭効果は弱い。
In addition, chlorophyll and flavonoids also exist on their own,
Also, its deodorizing effect is weaker than that of cyclodextrin.

上記のように、従来の口腔用消臭剤は、適用しうる製品
範囲、あるいは消臭しうる臭気成分の種類のいずれかが
不適当であるのが実情であった。
As mentioned above, the reality is that conventional oral deodorants are inadequate in either the applicable product range or the types of odor components that can be deodorized.

(発明が解決しようとする課Ml) 本発明はこのような事情に鑑みなされたものであって、
その目的とするところは、親水性、疎水性、いずれの硫
黄系臭気成分に対しても消臭効果が高く、かつ消臭剤自
身は無味、無臭、無色で、安全性が高く、口腔用として
広い範囲で適用しうる消臭剤を提供するにある。
(Problem to be solved by the invention Ml) The present invention was made in view of the above circumstances, and
The purpose of this product is to have a high deodorizing effect against both hydrophilic and hydrophobic sulfur-based odor components, and the deodorant itself is tasteless, odorless, and colorless, making it highly safe and suitable for use in the oral cavity. The purpose of the present invention is to provide a deodorant that can be applied in a wide range of applications.

(課題を解決するための手段) 上記の目的は、分離大豆蛋白をプロテアーゼ分解して得
られる分子量10万以上の高分子画分を有効成分とする
消臭剤によって達成される。
(Means for Solving the Problem) The above object is achieved by a deodorant containing as an active ingredient a polymer fraction having a molecular weight of 100,000 or more obtained by decomposing isolated soybean protein with protease.

すなわち、本発明者らは、上記目的を連成するため、鋭
意検討を行った結果、大豆の分l:a蛋白をプロテアー
ゼ分解して得られた分子[10万以上の高分子画分が硫
黄系臭気成分に対して優れた消臭効果を有し、かつ殆ん
ど無味、無臭、無色で口腔用消臭剤として好適であるこ
とを見い出し、本発明を完成するに至ったものである。
That is, in order to couple the above objectives, the present inventors conducted intensive studies and found that a molecule obtained by protease decomposition of soybean fraction l:a protein [more than 100,000 polymer fractions contain sulfur] The present invention was completed based on the discovery that it has an excellent deodorizing effect on odor components, and is almost tasteless, odorless, and colorless, making it suitable as an oral deodorant.

以下、本発明につき詳しく説明する。The present invention will be explained in detail below.

本発明の消臭剤の有効成分である分離大豆蛋白分解高分
子画分は、例えば、次のようにして製造することができ
る。すなわち、まず乾燥生大豆を荒粉砕し、皮を除いた
後、さらにsOメッシA以下の粉末にする。これをn−
ヘキサン、もしくはメタノール/クロロホルム混合液を
溶剤として用いて脱脂する。得られた脱脂大豆を弱アル
カリ性のアルカリ溶液にて溶解し、遠心分離等で固液分
離し、不溶解物を除去する。こめ上澄液のpHを弱酸性
にgR節し、蛋白質を沈殿させ、遠心分離等で固液分層
し、水洗1ili[M乾燥し、分1 大豆蛋白を得る。
The isolated soybean proteolytic polymer fraction, which is the active ingredient of the deodorant of the present invention, can be produced, for example, as follows. That is, first, dry raw soybeans are roughly ground, the skins are removed, and then the powder is further made into a powder of sO Messi A or lower. This is n-
Degrease using hexane or a methanol/chloroform mixture as a solvent. The obtained defatted soybeans are dissolved in a weakly alkaline alkaline solution, solid-liquid separation is performed by centrifugation, etc., and undissolved substances are removed. Adjust the pH of the rice supernatant to slightly acidic, precipitate the protein, separate the solid-liquid layer by centrifugation, wash with water and dry for 1 minute to obtain soybean protein.

次に、仁の分離大豆蛋白をプロテアーゼで十分に分解し
、酵素を失活後遠心分離等で固液分離して残渣を得る。
Next, the separated soybean protein from the kernel is sufficiently decomposed with protease, and after the enzyme is inactivated, solid-liquid separation is performed by centrifugation or the like to obtain a residue.

この残渣を再び弱アルカリ性のアルカリ溶液に溶解し、
分子量10万の限外濾過膜で10万未満の画分を除く。
This residue was dissolved again in a slightly alkaline alkaline solution,
A fraction with a molecular weight of less than 100,000 is removed using an ultrafiltration membrane with a molecular weight of 100,000.

残った10万以上の両分の溶液を再孝等電点沈殿させ、
蛋白を回収し、よく水洗した後、凍結乾燥すれば粉末状
の分離大豆蛋白高分子画分を得ることができる。
The remaining 100,000 or more solutions were subjected to isoelectric precipitation,
If the protein is collected, thoroughly washed with water, and then freeze-dried, a powdered separated soybean protein polymer fraction can be obtained.

上記プロテアーゼとしては種々のものが使用可能である
が、アスペルギルス(Aapergillus) Rく
麹カビ〉またはバチルス・ズブチリス(Bacillu
ssubtilis) <枯草菌〉起源の微生物の産生
ずるエンド型及びエキソ型プロテアーゼを使用すること
が、風味上好ましい。
Various proteases can be used as the protease mentioned above, including Aspergillus (Aapergillus R. Aspergillus or Bacillus subtilis).
From the viewpoint of flavor, it is preferable to use endo- and exo-type proteases produced by microorganisms originating from Bacillus subtilis.

と記のようにして得られた本発明の消臭剤は、親水性、
疎水性、いずれの硫黄系臭気成分に対しても優れた消臭
効果を示す。この硫黄系臭気成分は、硫化水素、メチル
メルカプタン及びエチルメルカプタン並びに低級アルキ
ルおよびアルケニルスルフィド、ジスルフィド、トリス
ルフィド等を含み、その−例として腐敗臭の一つである
親水性のメチルメルカプタン、にんにく臭の一つである
疎水性のジアリルジスルフィド等が挙げられる。
The deodorant of the present invention obtained as described above has hydrophilicity,
It is hydrophobic and exhibits an excellent deodorizing effect against all sulfur-based odor components. These sulfur-based odor components include hydrogen sulfide, methyl mercaptan, ethyl mercaptan, lower alkyl and alkenyl sulfides, disulfides, trisulfides, etc. Examples include hydrophilic methyl mercaptan, which is a putrid odor, and garlic odor. One example is hydrophobic diallyl disulfide.

本発明の消臭剤は、色が薄く殆んど白色に近いもので、
味も臭いも殆んどなく、製品配合上で問題がない。更に
、大豆蛋白由来のものであるため、使用上の安全性も高
いものである。
The deodorant of the present invention is pale in color and almost white,
There is almost no taste or odor, and there are no problems with product formulation. Furthermore, since it is derived from soybean protein, it is highly safe to use.

また本発明の消臭剤は、水には難溶であるが、懸濁溶液
、ペースト状、粉粒状、ブロック状等の所望の形態に胸
製し得る。この場合、本発明の消臭剤は、固形状態、水
溶液状態等種々の形態において、その消臭効果が非常に
安定に持続し、種々の型で製剤化することが可能である
Although the deodorant of the present invention is sparingly soluble in water, it can be prepared into a desired form such as a suspension, paste, powder, or block. In this case, the deodorant of the present invention maintains its deodorizing effect very stably in various forms such as solid state and aqueous solution state, and can be formulated in various forms.

本発明の消臭剤は、前述したその特長から、−般食品(
例えば、ガム等の菓子)、歯磨、洗口液等に配合される
口腔用消臭剤として利用できる。
Due to the above-mentioned features, the deodorant of the present invention has - general food (
For example, it can be used as an oral deodorizer that is incorporated into confectionery such as gum), toothpaste, mouthwash, and the like.

このとき、本発明の消臭剤の配合屋は、製品全体に対し
ては、好ましくは0.001〜sO重量%(以下%と記
す)、よゆ好ましくは0.1〜10%である。更に、本
発明の消臭剤は、口腔用消臭剤に限らず生ごみ用、冷蔵
庫用、車内用、トイレ用の消臭剤及び汚水処理場、各揮
悪臭が発生する工しては十分に優れた消臭能力を発揮す
るが、アミン類、低級脂肪酸類等も含む臭気成分に対し
ても効能を発揮させるときには、β−0D1フラボノイ
ド類、クロロフィル等の他の消臭剤を併用すると好適で
ある。
At this time, the compounder of the deodorant of the present invention preferably uses 0.001 to sO weight % (hereinafter referred to as %), more preferably 0.1 to 10%, to the entire product. Furthermore, the deodorizer of the present invention is not limited to oral deodorizers, but is also suitable for garbage, refrigerators, car interiors, toilets, and sewage treatment plants, as well as works that generate volatile odors. It exhibits excellent deodorizing ability against odor components such as amines and lower fatty acids, but it is suitable to use it in combination with other deodorants such as β-0D1 flavonoids and chlorophyll. It is.

(発明の効果) 本発明の消臭剤は、分離大豆蛋白をプロテアーゼ分解し
て得られた分子量10万以上の高分子画分を有効成分と
するものである。
(Effects of the Invention) The deodorant of the present invention contains as an active ingredient a polymer fraction having a molecular weight of 100,000 or more obtained by decomposing isolated soybean protein with protease.

この高分子画分は、上述のようにメチルメルカプタンや
にんにく臭の主成分であるジアリルジスルフィド等の親
水性、疎水性いずれの硫黄系臭気成分に対しても優れた
消臭効果を発揮する。
As mentioned above, this polymer fraction exhibits an excellent deodorizing effect against both hydrophilic and hydrophobic sulfur-based odor components such as methyl mercaptan and diallyl disulfide, which is the main component of garlic odor.

更に、はぼ無味、無臭、無色の粉体ゆえ、製品配合上で
問題が少なく、かつ使用上の安全性が高いものである。
Furthermore, since it is a tasteless, odorless, and colorless powder, it poses few problems in product formulation and is highly safe to use.

したがって、口腔用消臭剤として使用可能であることは
もちろん、種々の硫黄系臭気成分の消臭剤として使用で
きる。
Therefore, it can be used not only as a deodorant for the oral cavity but also as a deodorant for various sulfur-based odor components.

以下、実施例を挙げて本発明を具体的に説明する。The present invention will be specifically described below with reference to Examples.

(実施例) まず、乾燥生大豆を荒粉砕し、皮を除いた後、さらに5
0メツシユ以下の粉末にした。これを、メタノール/ク
ロロホルム(=1/1混合溶1を溶剤として、フラスコ
内で80〜60℃で5時間還流して脱脂し脱脂大豆(陽
1)を得た。得られた脱脂大豆をpH9の水酸化ナトリ
ウム水溶液に溶解させ、遠心分離で固液分離し、不溶解
物を除去した。この上澄液を1Nの塩酸でpH4,5に
謁節し、蛋白質を沈吸させ、遠心分離で固液分離し、水
洗後、凍結乾燥し、分離大豆蛋白(N[L2)を得た。
(Example) First, dry raw soybeans are roughly crushed, the skin is removed, and then
It was made into a powder with less than 0 mesh. This was defatted by refluxing in a flask at 80 to 60°C for 5 hours using methanol/chloroform (=1/1 mixed solution 1) to obtain defatted soybeans (Yo 1).The resulting defatted soybeans had a pH of 9. The protein was dissolved in an aqueous solution of sodium hydroxide, separated into solid and liquid by centrifugation, and undissolved matter was removed. Solid-liquid separation was performed, washed with water, and freeze-dried to obtain isolated soybean protein (N[L2).

次に、このようにして得た分離大豆蛋白5o。Next, the thus obtained isolated soybean protein 5o.

gを、pH7,0のリン酸緩衝液501に分散させ、エ
ンド型及びエキソ型プロテアーゼを含むバチルス ズブ
チリス(Bacillus Suptillg)起源の
プロテアーゼ製剤10g(長瀬産業社製、ビオブラーゼ
8p−4)を添加し、40℃で10時間反応させた。反
応後、86℃で20分間加熱し、酵素を失活させた後、
溶液を遠心分離(10000rpm x10分)し、上
澄溶液と残渣とを得た。
g was dispersed in phosphate buffer 501 at pH 7.0, and 10 g of a protease preparation derived from Bacillus subtilg containing endo-type and exo-type proteases (manufactured by Nagase Sangyo Co., Ltd., Biobrase 8p-4) was added, The reaction was carried out at 40°C for 10 hours. After the reaction, heat at 86°C for 20 minutes to inactivate the enzyme,
The solution was centrifuged (10,000 rpm x 10 minutes) to obtain a supernatant solution and a residue.

この残渣をよく水洗後、凍結乾燥したところ、粉末が約
75.1得られた。この凍結乾燥粉末をpHIIの水酸
化ナトリウム水溶液に溶解し、分子ff1lO万と2万
の限界濾過膜(サルトリウス(sartorius)社
製)で10万以上、10万未満〜2万以上、2万未満に
分画した。分画量は、等電点沈殿させ、遠心分離後よく
水洗し、凍結乾燥して粉末とした。各粉末の収量はそれ
ぞれ84.81(Nhj )、o、asf(m4)、0
.12511t8)であった。また、上澄溶液は凍結乾
燥した。(隘また、上記分離大豆蛋白を用い、プロテア
ーゼとしてアスペルギルス オリザエ(Assperg
illusoryzaa)起源のプロテアーゼ(長顔産
業社製、ブナチームAP)を作用させ、上記と同様にし
て、操作を行った。分解後の遠心分離で上澄溶液と残渣
に分゛け、残渣を限外r過膜で上記と同様に10万以上
、10万未満〜2万以下、2万未満に分画し粉末を得た
。それぞれの収量は、14.3f(Nu1)、11 F
 (陽8)、0.56y(陽8)であった。上澄溶液は
凍結乾燥した。(Nllll O)上記サンプルNo1
〜N010及びβ−CD (ll&111)をヘッドス
ペース法により各々その消臭力について比較した。すな
わち、内容量20m1のバイアルびんに上記サンプルs
omyと水1mlを添加し、これにメチルメルカプタン
溶液(1μfl/met   エタノール溶液)20μ
e もしくは、ジアリルジスルフィド溶液(50μtt
/”l s  エタノール溶液)20μlを添加し、直
ちにゴム栓をして10分間激しく撹拌後、25℃で30
分間静置した。その後、ガスタイトシリンジにてバイア
ルびん中の0.4mlのヘッドスペースガスを採取し、
直ちにガスクロマトグラフ(島津14人)に注入し、サ
ンプルのピーク高さカウント(8)を測定した。サンプ
ルを添加しない場合をコントロールのピーク高さカウン
ト(のとし、下記式から消臭率を求めた。
This residue was thoroughly washed with water and then freeze-dried to obtain a powder of about 75.1%. This freeze-dried powder was dissolved in a pH II sodium hydroxide aqueous solution, and the molecular size was reduced to 100,000 or more, less than 100,000 to 20,000 or more, less than 20,000 using ultrafiltration membranes (manufactured by Sartorius) with molecular ff110,000 and 20,000. Fractionated. The fractions were subjected to isoelectric precipitation, centrifuged, thoroughly washed with water, and freeze-dried to form a powder. The yield of each powder is 84.81 (Nhj), o, asf (m4), 0, respectively.
.. 12511t8). In addition, the supernatant solution was freeze-dried. (Also, using the above isolated soybean protein, Aspergillus oryzae (Aspergillus oryzae) was used as a protease.
The same procedure as above was performed using a protease originating from A. After decomposition, centrifuge to separate the supernatant solution and residue, and use an ultrafiltration membrane to separate the residue into 100,000 or more, less than 100,000 to 20,000, and less than 20,000 in the same manner as above to obtain a powder. Ta. The respective yields are 14.3f (Nu1), 11F
(positive 8), 0.56y (positive 8). The supernatant solution was lyophilized. (Nllll O) Above sample No.1
~N010 and β-CD (11&111) were compared in terms of deodorizing power using the headspace method. That is, the above sample s is placed in a vial with an internal capacity of 20 m1.
Add omy and 1ml of water, and add 20μ of methyl mercaptan solution (1μfl/met ethanol solution) to this.
e Or diallyl disulfide solution (50 μtt
Add 20 μl of ethanol solution), immediately cover with a rubber stopper, stir vigorously for 10 minutes, and incubate at 25°C for 30 minutes.
It was left standing for a minute. After that, collect 0.4ml of headspace gas in the vial with a gastight syringe,
Immediately, the sample was injected into a gas chromatograph (14 people from Shimadzu) and the peak height count (8) of the sample was measured. The case where no sample was added was used as the peak height count (of the control), and the deodorization rate was calculated from the following formula.

C:コントロールのピーク高さカウント8:サンプルの
ピーク高さカウント 上記の操作を各サンプルについて行った。
C: Control peak height count 8: Sample peak height count The above operation was performed for each sample.

これらの結果を第1表に示す。These results are shown in Table 1.

秦)年末発明の実施例。Qin) Examples of year-end inventions.

また、上記実施例、比較例の各サンプルの官能的な消臭
効果をみるために、!g2表の様な基準により評価を行
った。すなわち、メチルメルカプタン溶液(1μI/m
e、エタノール溶液)及びジアリルジスルフィド溶液(
60μI/mLエタノール溶液)を対象臭気成分として
、これらどちらかの溶[20μeと水1 mlの入った
’lQml バイヤルびんに、上記サンプルs o o
 mp を添加し、10名のパネラ−が第2表に示す6
段階で臭気強度を官能評価し、その平均値を禅出した。
Also, in order to see the sensual deodorizing effect of each sample of the above Examples and Comparative Examples,! Evaluation was performed using criteria such as the g2 table. That is, methyl mercaptan solution (1μI/m
e, ethanol solution) and diallyl disulfide solution (
60μI/mL ethanol solution) was used as the target odor component, and the above sample s o o
mp was added, and 10 panelists added 6 as shown in Table 2.
The odor intensity was sensory evaluated in stages, and the average value was calculated.

なお、サンプルを添加しない時の臭気強度(ブランク)
を4とした。2種の臭気成分に対して各サンプルについ
て評価を行った。第5表にその結果を示す。
In addition, odor intensity when no sample is added (blank)
was set as 4. Each sample was evaluated for two types of odor components. Table 5 shows the results.

第2表 第3表 1M)年末発明の実施例 以上の如く、本発明の消臭剤有効成分は、親水性のメチ
ルメルカプタンや、疎水性のジアリルジスルフィド等硫
黄化合物に対して、消臭率、官能評価共に優れた消臭効
果を示した。特に、通常食品に消臭剤として広く利用さ
れるβ−ODと比較しても、はるかに優れた消臭力を示
した。
Table 2 Table 3 1M) Examples of year-end inventions As described above, the deodorant active ingredient of the present invention has a high deodorization rate and a high deodorization rate against sulfur compounds such as hydrophilic methyl mercaptan and hydrophobic diallyl disulfide. It showed excellent deodorizing effect in both sensory evaluations. In particular, it showed far superior deodorizing power compared to β-OD, which is widely used as a deodorizing agent in ordinary foods.

また、本発明の消臭剤は、大豆蛋白を原料とするもので
あり、殆んど無色、無味、無臭で、人体に対する危険性
がないので、種々の製品に対し、あらゆる形態で使用す
ることができる。
In addition, the deodorant of the present invention is made from soybean protein, is almost colorless, tasteless, and odorless, and poses no danger to the human body, so it can be used in various forms in various products. I can do it.

以下に、その使用例を示す。An example of its use is shown below.

〔使用例1〕 チューインガム ガムペース      20% 砂   糖          64 グルコース       6 水   m           20アツプル香料 
     Ols 計       too、o% 上記配合にて、常法に従いチューインガムを調製し、7
2 X 19 X 1.9 m/mに成型し、消臭ガム
を得た。このガムは、アップル風味を有する板ガムであ
るが、本発明の消臭剤がガムの風味、食感、色調に影響
することなく、ガム本来の品質を維持できるものであっ
た。
[Usage example 1] Chewing gum gum paste 20% sugar 64 glucose 6 water m 20 apple flavor
Ols total too, o% With the above formulation, chewing gum was prepared according to a conventional method, and 7
It was molded into a size of 2 x 19 x 1.9 m/m to obtain a deodorizing gum. This gum is a sheet gum with an apple flavor, and the deodorant of the present invention was able to maintain the original quality of the gum without affecting the flavor, texture, or color tone of the gum.

〔使用例2〕 錠菓 粉   糖          80%グルコース  
    11.5 クエン酸         2 計       10 〔使用例S〕 練歯磨 リン酸水素カルシウム  4 プロピレングリコール ソルビトール      ! カルボキシメチルセルロースナトリウムコロイド状シリ
カ ラウリル硫酸ナトリウム 0.0 % 0.0 % 2.0 1.1 !。0 1.6 モノフルオルリン酸ナトリウム  0.16水 残り 計       100.0% 〔使用例4〕 洗口剤 エタノール      20% ラウリル硫酸ナトリウム   1 香   料            1グリセリン  
   10 リン酸水素ナトリウム   0.5 水         残り 計       100.0% 以上のように、本発明の消臭剤は、それ自体が殆ど無味
、無臭、無色でしかも少量で消臭効果を発揮しつるので
、従来の製法を用いて稲々、の製品を製造することがで
き、しかも食品等種々の製品の品質に影響することがな
かった。
[Usage example 2] Tablet confectionery powder Sugar 80% glucose
11.5 Citric acid 2 Total 10 [Usage example S] Toothpaste calcium hydrogen phosphate 4 Propylene glycol sorbitol! Carboxymethyl cellulose sodium colloidal silica lauryl sulfate 0.0% 0.0% 2.0 1.1! . 0 1.6 Sodium monofluorophosphate 0.16 Water remaining 100.0% [Usage example 4] Mouth wash ethanol 20% Sodium lauryl sulfate 1 Fragrance 1 Glycerin
10 Sodium hydrogen phosphate 0.5 Water Total remaining 100.0% As mentioned above, the deodorant of the present invention itself is almost tasteless, odorless, and colorless, and exhibits a deodorizing effect in a small amount. It was possible to produce rice products using conventional production methods without affecting the quality of various products such as foods.

Claims (1)

【特許請求の範囲】[Claims] 分離大豆蛋白をプロテアーゼ分解して得られる分子量1
0万以上の高分子画分を有効成分とする消臭剤。
Molecular weight 1 obtained by decomposing isolated soybean protein with protease
A deodorant containing a polymer fraction of 0,000 or more as an active ingredient.
JP1108253A 1989-04-27 1989-04-27 Deodorant Pending JPH02286165A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1108253A JPH02286165A (en) 1989-04-27 1989-04-27 Deodorant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1108253A JPH02286165A (en) 1989-04-27 1989-04-27 Deodorant

Publications (1)

Publication Number Publication Date
JPH02286165A true JPH02286165A (en) 1990-11-26

Family

ID=14479973

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1108253A Pending JPH02286165A (en) 1989-04-27 1989-04-27 Deodorant

Country Status (1)

Country Link
JP (1) JPH02286165A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1510200A1 (en) * 2003-08-26 2005-03-02 Johnson & Johnson Consumer France SAS Stabilized antiperspirant compositions containing soy products
JP2007082680A (en) * 2005-09-21 2007-04-05 Sansho Kk Scavenger composition for airborne fine materials
US7897144B2 (en) 2001-02-28 2011-03-01 Johnson & Johnson Comsumer Companies, Inc. Compositions containing legume products

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7897144B2 (en) 2001-02-28 2011-03-01 Johnson & Johnson Comsumer Companies, Inc. Compositions containing legume products
EP1510200A1 (en) * 2003-08-26 2005-03-02 Johnson & Johnson Consumer France SAS Stabilized antiperspirant compositions containing soy products
WO2005018594A1 (en) * 2003-08-26 2005-03-03 Johnson & Johnson Consumer France S.A.S. Stabilized antiperspirant compositions containing soy products
JP2007082680A (en) * 2005-09-21 2007-04-05 Sansho Kk Scavenger composition for airborne fine materials

Similar Documents

Publication Publication Date Title
KR100637922B1 (en) Method for manufacturing and using food and deodorant composition including deodorant of removing tobacco odor
JP4947505B2 (en) Deodorants
JPH02286165A (en) Deodorant
Hashimoto Application of cyclodextrins to foods, toiletries and other products in Japan
JP3561829B2 (en) Deodorant composition
JPH03236305A (en) Cosmetic
JP3897862B2 (en) Method for producing oral bad breath deodorant
JP2003093488A (en) Deodorizing composition and deodorizing method
JPH1175771A (en) Healthy food of algae
JPH0816048B2 (en) Oral composition
JPH0533925B2 (en)
JPS6077763A (en) Deodorant
JPH0471563A (en) Deodorant
JPH10108900A (en) Barley-derived natural deodorant
JP2640824B2 (en) Deodorants
JPH05269187A (en) Composition for deodorization and food and cosmetics compounded with this composition
JP4914538B2 (en) Deodorant and its use
KR100314505B1 (en) Composition of tooth paste and the process of preparation thereof
JPH04193277A (en) Deodorant
JPH1033648A (en) Deodorant
US20210052473A1 (en) Composition for removing aldehyde-based odors and reactive oxygen species
JPH10158137A (en) Deodorant
JPS60207664A (en) Deodorizing agent for non-edible substance
JPH0339164A (en) Deodorant
JP2508061B2 (en) Liquid deodorant composition