JPS5813507A - Gelatinous aromatic composition - Google Patents

Gelatinous aromatic composition

Info

Publication number
JPS5813507A
JPS5813507A JP56108837A JP10883781A JPS5813507A JP S5813507 A JPS5813507 A JP S5813507A JP 56108837 A JP56108837 A JP 56108837A JP 10883781 A JP10883781 A JP 10883781A JP S5813507 A JPS5813507 A JP S5813507A
Authority
JP
Japan
Prior art keywords
perfume
fragrance
weight
water
composition
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
JP56108837A
Other languages
Japanese (ja)
Inventor
Yasuo Taniguchi
康雄 谷口
Hideaki Miyawaki
宮脇 英昭
Tsukasa Imura
居村 司
Yasuo Inagaki
稲垣 靖夫
Teruo Shiraishi
白石 照雄
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.)
TAIYO KORYO KK
Original Assignee
TAIYO KORYO KK
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 TAIYO KORYO KK filed Critical TAIYO KORYO KK
Priority to JP56108837A priority Critical patent/JPS5813507A/en
Publication of JPS5813507A publication Critical patent/JPS5813507A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:The titled composition, containing 3-methyl-3-methoxybutanol having a high compatibility with water and a moderate volatility as a perfume volatility adjustor, a gelling agent, a emulsifyig agent, water and a perfume in a specific proportion without changing the perfume tone, and capable of keeping the good diffusivity and lasting property. CONSTITUTION:A gelatinous aromatic composition containing 3-methyl-3-methoxybutanol as a perfume volatility adjustor in an amount of in the range of 5- 30wt% and 0.5-5wt% gelling agent selected from carrageenan, agar, locust bean gum, etc. 0.1-5wt% emulsifying agent selcted from polyoxyethylene hardened castor oil, polyoxyethylene alkyll phenyl ether, etc., 60-90wt% water and 1-20wt% perfume. The titled composition is prepared by dissolving the respective components a given proportion under heating at about 70-90 deg.C, cooling to 60 deg.C or below, allowing the solution to cool, or heating the and cooling the heated solution to a suitable temperature and adding a perfume composition thereto.

Description

【発明の詳細な説明】 本発明はゲル状芳香組成物、更に詳細には3−メチル−
3−メトキシブタノールを香料揮発調整剤として含むゲ
ル状芳香組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a gel-like aroma composition, more particularly a 3-methyl-
The present invention relates to a gel fragrance composition containing 3-methoxybutanol as a fragrance volatilization regulator.

従来、水をキャリアーにしたゲル状芳香剤に関しては公
知であシ、ゲル化剤としては例えばカラギナン、寒天、
ローカストビーンガム等があり増粘剤としては例えばカ
ルボキシメチルセルローズ。
Conventionally, gel fragrances using water as a carrier have been known, and examples of gelling agents include carrageenan, agar,
There are locust bean gums, etc., and examples of thickeners include carboxymethyl cellulose.

ヒドロキシ低級アルキルセルローズ、メチルセルローズ
、水溶性ポリエチレンオキサイド、デンプングリコール
酸塩等を特定割合で配合する拳によシ好ましい水ゲル組
成物が調製できることが開示されている(米国特許第2
,927.055号1%公昭47=36630)。しか
しながら、かような処方からなるゲル状組成物に香料を
配合した場合香調に長期間一定のバランスを保持し、拡
散性と持続性を所与することは、極めて困難である。こ
の理由としては揮発速度の速い水がキャリアーである為
、低沸点の香料成分が水と共に揮発し香料組成が変シ、
香調のバランスがくずれる為だとされている。本発明者
らはこの様な欠陥を克服すべく鋭意検討した結果、3−
メチル−3−メトキシブタノールを香料揮発調整剤とし
てゲル状組成物に配合する事により長期間、香調に一定
のバランスを保持し拡散性と持続性を所与、することを
見出した。
It has been disclosed that a water gel composition suitable for use can be prepared by blending hydroxy lower alkyl cellulose, methyl cellulose, water-soluble polyethylene oxide, starch glycolate, etc. in specific proportions (U.S. Patent No. 2).
, No. 927.055 1% Kosho 47 = 36630). However, when a fragrance is added to a gel-like composition having such a formulation, it is extremely difficult to maintain a constant balance in the fragrance tone over a long period of time and to provide it with diffusibility and sustainability. The reason for this is that water, which has a high volatilization rate, is used as a carrier, so low boiling point perfume ingredients volatilize with water, changing the perfume composition.
It is said that this is because the balance of fragrance is disrupted. As a result of intensive studies to overcome these defects, the inventors of the present invention found that 3-
It has been found that by blending methyl-3-methoxybutanol into a gel composition as a fragrance volatilization regulator, it is possible to maintain a certain balance in the fragrance tone over a long period of time, and to impart diffusibility and sustainability.

本発明のゲル状芳香組成物は3−メチル−3−メトキシ
ブタノール5〜30重量係、ゲル化剤0.5〜5重量係
、乳化剤0.1〜5重量−6水60〜90重量饅及び香
料1〜20重量係を含有する。
The gel-like aroma composition of the present invention contains 3-methyl-3-methoxybutanol 5-30% by weight, a gelling agent 0.5-5% by weight, an emulsifier 0.1-5% by weight, 6 water 60-90% by weight, and Contains 1 to 20 parts by weight of fragrance.

本発明で用いる3−メチル−3−メトキシブタノールは
有機溶剤として引火点(71℃)及び発火点(395℃
)が高く、毒性も著しく低い(LD505.838/に
#)。また、水との相溶性が大きく、適度の揮発性を有
し、且つ臭気も軽い匂いなので室内芳香剤の香料揮発調
整剤として非常に好ましい’I黴を有している。
3-Methyl-3-methoxybutanol used in the present invention has a flash point (71°C) and an ignition point (395°C) as an organic solvent.
) and extremely low toxicity (LD505.838/#). In addition, it has 'I mold, which is highly compatible with water, has appropriate volatility, and has a light odor, which makes it very suitable as a fragrance volatilization regulator for indoor air fresheners.

本発明ではゲル状芳香組成物中に3−メチル−3−メト
キシブタノール社香熟揮発調整d”hして5〜30重量
%の範囲で使用するが、5重量%未′満では香料揮発調
整剤としての効果がうすく、また30重量sl越えると
安定なゲルが得られない−ので上記の範朋にて用いる必
要がある。
In the present invention, 3-methyl-3-methoxybutanol is used in the gel aroma composition in a range of 5 to 30% by weight, but if it is less than 5% by weight, the fragrance is adjusted for volatilization. It has little effect as an agent, and if it exceeds 30 weight sl, a stable gel cannot be obtained, so it must be used within the above range.

本発明によればゲル化剤としては例えばカラギナン、寒
天、ローカストビーンガム等を用いることができ、その
配合割合は0.5〜5重量憾の範囲で使用される。ゲル
化剤が0.5重量s4満となると、芳香組成物がゲル化
しにくくなシ、一方5重量−を越えるとゲル化剤が溶解
しにくくなシ且つ芳香組成物がかたくなシすぎるので好
ましくない。
According to the present invention, for example, carrageenan, agar, locust bean gum, etc. can be used as the gelling agent, and the blending ratio thereof is in the range of 0.5 to 5% by weight. If the amount of gelling agent is less than 0.5 weight s4, the aroma composition will not gel easily, while if it exceeds 5 weight, it will be difficult to dissolve the gelling agent and the aroma composition will be too hard, which is not preferable. .

また水性媒質中に於ける香料の分散剤・とじて乳化剤が
使用される。適当な乳化剤としては例えばポリオキシエ
チレン硬化ヒマシ油、ポリオキシエチレンアルキルフェ
ニルエーテル、ポリオキシエチレンアルキルエーテル、
ポリオキシエチレンソルビタン脂肪酸エステル、ポリオ
キシエチレンステアレート、クリセロール脂肪酸エステ
ル等の非イオン界面活性剤が利用でき、その配合割合は
ゲル組成物中0.1〜1□51重量?′好適である。乳
化剤の量が0.1重量饅未満となると、芳香組成物の各
適当でない。その他、着色剤、防腐剤等は必要に応じて
任意の割合で配合することができる。
Emulsifiers are also used to disperse and bind fragrances in aqueous media. Suitable emulsifiers include, for example, polyoxyethylene hydrogenated castor oil, polyoxyethylene alkylphenyl ether, polyoxyethylene alkyl ether,
Nonionic surfactants such as polyoxyethylene sorbitan fatty acid ester, polyoxyethylene stearate, and chrycerol fatty acid ester can be used, and their proportion in the gel composition is 0.1 to 1□51% by weight? 'Suitable. If the amount of emulsifier is less than 0.1 weight, the fragrance composition will not be suitable. In addition, colorants, preservatives, etc. can be blended in any proportion as necessary.

芳香組成物に加える水の配合量は60〜900〜90重
量%水の量が60*量饅未満となると、ゲル化しにくく
なシ各成分が分離しやすくなる。
The amount of water added to the aromatic composition is 60 to 900 to 90% by weight.If the amount of water is less than 60*amount, the components that are difficult to gel are likely to separate.

また一方、他の成分の配合割合から90重量96t−越
えて水を加えること社困難である。
On the other hand, it is difficult to add water in excess of 96 tons by weight due to the proportions of other components.

香料は0.5〜20重量%の範囲で用いる。0.5重量
−未満では適度の芳香が得られなくなシ、一方20重量
−を越えて用いてもさほどの効果があがらない。
The fragrance is used in a range of 0.5 to 20% by weight. If it is less than 0.5 weight, it will not be possible to obtain a suitable fragrance, while if it is used in excess of 20 weight, the effect will not be so great.

本発明のゲル状芳香剤組成物の香料成分として好ましく
用いることのできる調合香料の処方例を挙げると次の通
シである。
Examples of formulations of blended fragrances that can be preferably used as the fragrance component of the gel fragrance composition of the present invention are as follows.

レモン系調合香料 シトラール          25・0レモングラス
オイル     15.0リナロール        
   6.0リナリールアセテー)      6.、
0シトロネ、ロール          8.0・  
 s oos ジャスミン系調合香料 ジャスミン P−9030(商品名 大洋香料−)重量
% ジャスミンペース       37.Oベンジルアル
コール       5.0アミルシンナミツクアルデ
ヒド   30.0ペンシールアセテ−)      
17・0インドール           0.2リナ
リールアセテー)       10.0メチルベンゾ
エート0.8 10G!! ローズ系調合香料 ローズ P−7893−1(商品名 大洋香料■製)重
量− ローズベース          35.0フエニルエ
チルアルコール      30.0シトロネロール 
         8.0ゲラニオール       
   5.0ネロール           14.0
ローズフエノン          5.0シトロネリ
ールフオーメート3.0 10(1 本発明のゲル状芳香組成物は前述した各成分を前述の量
比にて約70°〜95Cに加熱して十分溶解した後60
℃以下に冷却または放冷することによシ調製することが
できるが、香料が加熱によシ影響されるような場合には
加熱後適度の温度にまで降下させた後に香料成分を添加
するようにするのが望しい。
Lemon-based blended fragrance Citral 25.0 Lemongrass oil 15.0 Linalool
6.0 linaryl acetate) 6. ,
0 citronnet, roll 8.0・
soos Jasmine-based blended fragrance Jasmine P-9030 (Product name: Taiyo Kogyo-) Weight% Jasmine Pace 37. O Benzyl alcohol 5.0 Amyl cinnamic aldehyde 30.0 Pensyl acetate)
17.0 indole 0.2 linaryl acetate) 10.0 methyl benzoate 0.8 10G! ! Rose-based mixed fragrance Rose P-7893-1 (Product name: Taiyo Kogyo ■) Weight - Rose base 35.0 Phenylethyl alcohol 30.0 Citronellol
8.0 Geraniol
5.0 Nerol 14.0
Rose Phenone 5.0 Citronellyl Formate 3.0 10 (1) The gel-like aroma composition of the present invention is prepared by heating the above-mentioned components in the above-mentioned ratios at about 70° to 95°C and thoroughly dissolving them, and then
It can be prepared by cooling to below ℃ or leaving it to cool, but if the fragrance is affected by heating, add the fragrance ingredients after heating and cooling to an appropriate temperature. It is desirable to do so.

比穀例1 公知のプロピレングリコールを用いて下記の成分組成よ
シ芳香組成物を調製した。
Grain Ratio Example 1 An aromatic composition having the following ingredient composition was prepared using known propylene glycol.

(g) 1 カラギナン            2.02 プ
ロピレングリコール       2.03  水  
                      87.
94 2.6−ジターシャリ−ブチルバラクレゾール(
防腐剤)0.15  ポリオキシエチレンノルビタΔm
酸エステル      1.0(乳化剤) 6 香料 v−e ンP−981,57、0−1,2,
3,4,5を200−ビーカーに入れ、75〜80℃に
加熱し、各成分を溶解Cた後、60℃まで冷却し、香料
6を加えてよくかきまぜて放冷すると、ゲル状芳香剤が
得られた。この芳香剤を室温に放置し、香調を調%した
ところ約2週間で香調が変り木。
(g) 1 carrageenan 2.02 propylene glycol 2.03 water
87.
94 2.6-Ditertiary-butylvalacresol (
Preservative) 0.15 Polyoxyethylene Norvita Δm
Acid ester 1.0 (emulsifier) 6 Fragrance v-e N P-981,57, 0-1,2,
3, 4, and 5 are placed in a 200-cm beaker, heated to 75-80°C, each component is dissolved, and then cooled to 60°C. Fragrance 6 is added, stirred well, and left to cool, resulting in a gel-like fragrance. was gotten. When I left this air freshener at room temperature and adjusted the scent, the scent changed in about two weeks.

実施例1 (g) 】 カラギナン            2.02 3
−メチル−3−メトキシブタノール         
15.03  水                 
     74.94 2.6−ジターシャリ−、ブチ
ルバラクレゾール(防腐剤)0.15  ポリオキシエ
チレンノルビタン脂肪酸エステル     1.0(乳
化剤) 6 香料 レモyP−9815・7.0上記1.2.3
.4.5を200−ビーカーに入れ、75〜80℃に加
熱し、各成分を溶解した後、60℃まで冷却し、香料6
を加えてよくかきまぜて放冷すると、安定なゲル状芳香
剤が得られ良。この芳香剤を室温に放置し、その香調を
調査したが約1ケ月後でも香調に変化線みられなかった
Example 1 (g) Carrageenan 2.02 3
-Methyl-3-methoxybutanol
15.03 Wednesday
74.94 2.6-ditertiary, butylvalacresol (preservative) 0.15 Polyoxyethylene norbitane fatty acid ester 1.0 (emulsifier) 6 Fragrance LemoyP-9815/7.0 1.2.3 above
.. 4.5 into a 200-degree beaker and heated to 75-80°C to dissolve each component, cool to 60°C, and add fragrance 6.
If you add it, stir well and let it cool, you will get a stable gel-like fragrance. This fragrance was left at room temperature and its fragrance tone was investigated, but no change was observed in the fragrance tone even after about one month.

実施例2               (g)l 寒
天               2,02  水  
                     73.9
3 3−メチル−3−メトキシブタノール      
   15.04  ポリオキシエチレン硬化ヒマシ油
(乳化剤)     1,05 2.6−ジターシャリ
−ブチルパラクレゾール(防腐剤)0.16 香料  
ジャスミンP−90308,0上記1.2を200−ビ
ーカーに入れ、90〜95℃に加熱し、寒天を溶解した
後、60℃まで冷却し、3.4.5.6を加え、よくか
きまぜて放冷すると、安定なゲル状芳香剤が得られた。
Example 2 (g)l Agar 2.02 Water
73.9
3 3-Methyl-3-methoxybutanol
15.04 Polyoxyethylene hydrogenated castor oil (emulsifier) 1,05 2.6-ditertiary-butyl para-cresol (preservative) 0.16 Fragrance
Jasmine P-90308,0 Put the above 1.2 into a 200-degree beaker, heat it to 90-95℃, dissolve the agar, cool it to 60℃, add 3.4.5.6 and stir well. Upon cooling, a stable gel-like fragrance was obtained.

仁の芳香剤を室温に放置し、その香調を調べたところ約
1ケ月間香調は変化しなかった。
When we left a kernel fragrance at room temperature and examined its scent, the scent did not change for about a month.

実施例3                (g)l 
カラギナン            2.02  水 
                     73.9
3 3−メチル−3−メトキシブタノール      
    13.04  グリセロール脂肪酸エステル(
乳化剤)        1.05 2.6−ジターシ
ャリ−ブチルパラクレゾール(防腐剤)’0.16 香
料 o−、(P−7893−1’  10.0実施例1
と同様にしヤ上記成分よシゲル状芳香剤を調製し友。約
1ケ月間室温に放置したが、ローズの香調は変化しなか
った@
Example 3 (g)l
carrageenan 2.02 water
73.9
3 3-Methyl-3-methoxybutanol
13.04 Glycerol fatty acid ester (
Emulsifier) 1.05 2.6-Ditertiary-butyl para-cresol (preservative)'0.16 Fragrance o-, (P-7893-1' 10.0Example 1
Similarly, use the above ingredients to prepare a gelatinous fragrance. I left it at room temperature for about a month, but the rose scent did not change.

Claims (1)

【特許請求の範囲】 1)3−メチル−3−メトキシブタノール5〜30重蓋
饅、ゲル化剤0.5〜5重量饅、乳化剤0.1〜5重量
%、水60〜90重量%及び香料1〜20重量%・を含
むゲル状芳香組成物。 2)前記ゲル化剤がカラギナン、寒天、ローカストビー
ンガムからなる群より選択されることを特徴とする特許
請求の範囲第1項記載のゲル状芳香組成物。 3)前記乳化剤がポリオキシエチレン硬化ヒマシ油、ポ
リオキシエチレンアルキルフェニルエーテル、ポリオキ
シエチレンアルキルエーテル。 ポリオキシエチレンステアレート及びグリセロール脂肪
酸エステルからなる群より選択されることを特徴とする
特許請求の範囲第1項記載のゲル状芳香組成物。
[Claims] 1) 3-methyl-3-methoxybutanol 5 to 30 weight %, gelling agent 0.5 to 5 weight %, emulsifier 0.1 to 5 weight %, water 60 to 90 weight %, and A gel-like aromatic composition containing 1 to 20% by weight of a fragrance. 2) The gel-like aromatic composition according to claim 1, wherein the gelling agent is selected from the group consisting of carrageenan, agar, and locust bean gum. 3) The emulsifier is polyoxyethylene hydrogenated castor oil, polyoxyethylene alkylphenyl ether, or polyoxyethylene alkyl ether. The gel-like aroma composition according to claim 1, characterized in that it is selected from the group consisting of polyoxyethylene stearate and glycerol fatty acid ester.
JP56108837A 1981-07-14 1981-07-14 Gelatinous aromatic composition Pending JPS5813507A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56108837A JPS5813507A (en) 1981-07-14 1981-07-14 Gelatinous aromatic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56108837A JPS5813507A (en) 1981-07-14 1981-07-14 Gelatinous aromatic composition

Publications (1)

Publication Number Publication Date
JPS5813507A true JPS5813507A (en) 1983-01-26

Family

ID=14494812

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56108837A Pending JPS5813507A (en) 1981-07-14 1981-07-14 Gelatinous aromatic composition

Country Status (1)

Country Link
JP (1) JPS5813507A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0462605A2 (en) * 1990-06-20 1991-12-27 Kuraray Co., Ltd. Fragrance dispensing composition with controlled evaporation rate and air fragrance dispenser for dispensing same
EP0687460A3 (en) * 1994-06-15 1996-09-11 Shiseido Co Ltd Low-alcohol perfume compositions
WO2007037493A1 (en) * 2005-09-30 2007-04-05 Kobayashi Pharmaceutical Co., Ltd. Sol-form fragrance composition
WO2012042243A1 (en) * 2010-09-29 2012-04-05 Tristel Plc Hand sanitizer

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0462605A2 (en) * 1990-06-20 1991-12-27 Kuraray Co., Ltd. Fragrance dispensing composition with controlled evaporation rate and air fragrance dispenser for dispensing same
EP0687460A3 (en) * 1994-06-15 1996-09-11 Shiseido Co Ltd Low-alcohol perfume compositions
WO2007037493A1 (en) * 2005-09-30 2007-04-05 Kobayashi Pharmaceutical Co., Ltd. Sol-form fragrance composition
JP2007097739A (en) * 2005-09-30 2007-04-19 Kobayashi Pharmaceut Co Ltd Sol-like aromatic composition
WO2012042243A1 (en) * 2010-09-29 2012-04-05 Tristel Plc Hand sanitizer
CN103269582A (en) * 2010-09-29 2013-08-28 雀艾斯达有限公司 Hand sanitizer
US8562907B2 (en) 2010-09-29 2013-10-22 Tristel Plc Hand sanitizer
CN103269582B (en) * 2010-09-29 2014-06-11 雀艾斯达有限公司 Hand sanitizer

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