JPS62249652A - Gel like aroma composition - Google Patents

Gel like aroma composition

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Publication number
JPS62249652A
JPS62249652A JP61069473A JP6947386A JPS62249652A JP S62249652 A JPS62249652 A JP S62249652A JP 61069473 A JP61069473 A JP 61069473A JP 6947386 A JP6947386 A JP 6947386A JP S62249652 A JPS62249652 A JP S62249652A
Authority
JP
Japan
Prior art keywords
fragrance
gel
weight
present
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
JP61069473A
Other languages
Japanese (ja)
Inventor
山崎 承三
信弘 林
布施 美香子
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP61069473A priority Critical patent/JPS62249652A/en
Publication of JPS62249652A publication Critical patent/JPS62249652A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はゲル状芳香剤組成物、さらに詳しくは、特定の
パラフィン系炭化水素を香料揮散のための担体とし、ス
チレン−ブタジエン−スチレンブロック共重合体をゲル
化剤として形成した透明で美麗なゲルで、香料の揮散に
応じて、ゲルの体積が透明で美麗な状態を維持し乍ら減
少し、しかも香料の揮散が安定なゲル状芳香剤組成物に
関するものである。
Detailed Description of the Invention [Industrial Application Field] The present invention relates to a gel fragrance composition, more specifically, a gel fragrance composition using a specific paraffinic hydrocarbon as a carrier for fragrance volatilization, and a styrene-butadiene-styrene block combination. A transparent and beautiful gel formed using a polymer as a gelling agent.As the fragrance evaporates, the volume of the gel decreases while maintaining a transparent and beautiful state, and the fragrance is stable in terms of volatilization. The present invention relates to a drug composition.

〔従来の技術〕[Conventional technology]

ゲル状芳香剤組成物に使用されるゲルは、水性ゲルと油
性ゲルに大別される。
Gels used in gel fragrance compositions are broadly classified into aqueous gels and oil-based gels.

水を媒介とする水性ゲルにおいて主に使用されるゲル化
剤には、天然物としては、寒天、カラギーナン及びペク
チン等があり、また合成物としては、水不溶性の高吸収
性樹脂を用いたもの(特開昭58−138461号公報
)及び水溶性高分子(特開昭55−81655号公報)
等がある。
Gelling agents mainly used in water-based aqueous gels include natural products such as agar, carrageenan, and pectin, and synthetic products that use water-insoluble superabsorbent resins. (Japanese Unexamined Patent Publication No. 58-138461) and water-soluble polymer (Unexamined Japanese Patent Publication No. 55-81655)
etc.

しかし、この様な水性ゲルには幾つかの欠点がある。1
つは、水性ゲル中に香料を乳化分散させる場合、香料の
種類によっては安定性が著しく悪く、長期間の保存によ
り香調の変化あるいは異臭の発生を生じる問題がある。
However, such aqueous gels have several drawbacks. 1
First, when a perfume is emulsified and dispersed in an aqueous gel, the stability is extremely poor depending on the type of perfume, and there is a problem in that the fragrance tone changes or the generation of off-flavors occurs during long-term storage.

このような問題を解決するためには、水性ゲル中で不安
定な単品香料(リナリルアセテート、ベンジルアセテー
トなどのようなエステル系、あるいはシクラメンアルデ
ハイドのようなアルデハイド系)を使用しない等の方法
示考えられるが、上記香料は調合香料の基剤となるもの
で、上記香料を抜いては嗜好性の高い調合香料を得難い
、そこで、このような欠点を補うために、上記香料に安
息香酸アルカリ土属塩等のハイドロトロープ剤を添加し
たり (特開昭55−15438号)、特定の燐酸塩ま
たは炭酸塩を添加し、更にp Hを調整するなどの方法
が提案されているものの、その分ゲルの配合や製法が複
雑になることは避けられない。また、香料を担持させた
水性ゲルの他の欠点は、水は殆どの香料よりも揮散し易
いため、香料及び水の揮散量のバランスが崩れるのが速
く、安定した香調、強さを保持し難いことである。
In order to solve this problem, we have proposed methods such as not using single fragrances that are unstable in aqueous gels (ester-based fragrances such as linalyl acetate, benzyl acetate, etc., or aldehyde-based fragrances such as cyclamen aldehyde). However, the above fragrances serve as the base for mixed fragrances, and it is difficult to obtain a highly palatable prepared fragrance without the above fragrances.Therefore, in order to compensate for this drawback, alkaline earth benzoate is added to the above fragrances. Although methods have been proposed such as adding hydrotropes such as salts (Japanese Patent Application Laid-Open No. 15438/1982), adding specific phosphates or carbonates, and further adjusting the pH, It is inevitable that the formulation and manufacturing method will become complicated. Another disadvantage of aqueous gels that carry fragrances is that water evaporates more easily than most fragrances, so the balance between the amount of fragrance and water evaporates is quickly disrupted, and the fragrance maintains a stable fragrance tone and intensity. This is difficult.

また、油性ゲルは、水性ゲルの欠点を比較的カバーし易
く、ゲル状芳香剤組成物を形成するためのゲルとしては
水性ゲルに比して有利な点が多いが、香料選択上及び外
見上の問題点を有している。
In addition, oil-based gels are relatively easy to overcome the drawbacks of water-based gels, and have many advantages over water-based gels as gels for forming gel-like fragrance compositions, but they have many advantages in terms of fragrance selection and appearance. It has the following problems.

叩ち、油脂を媒介とする油性ゲルのゲル化剤としては、
ステアリン酸ナトリウム(特開昭55−141243号
)、金属石鹸(特開昭56−89261号)、ジベンジ
リデンソルビトール(特開昭60−41967号)、微
粉末シリカ(特開昭54−92630号)及びN−アシ
ルアミノ酸誘導体(特開昭51−1913.9号)等が
挙げられるが、ステアリン酸ナトリウム及び微粉末シリ
カを用いて形成される油性ゲルは、ゲル強度が充分では
な(、不透明で且つひび割れが起き易く外見上好ましく
ない。金属石鹸を用いる場合には、ゲル形成時の添加量
が201量%以上と多量になり、しかも透明ゲルを形成
し得る香料選択の巾が狭い。
As a gelling agent for oil-based gel using oil and fat as a medium,
Sodium stearate (JP 55-141243), metal soap (JP 56-89261), dibenzylidene sorbitol (JP 60-41967), fine powder silica (JP 54-92630) and N-acylamino acid derivatives (Japanese Unexamined Patent Publication No. 1913.9/1989), etc. However, the oil-based gel formed using sodium stearate and finely powdered silica does not have sufficient gel strength (it is opaque and In addition, it is easy to crack and is unfavorable in appearance.When using metal soap, the amount added during gel formation is as large as 201% by weight or more, and the selection range of fragrances that can form a transparent gel is narrow.

ジベンジリデンソルビトールを用いる場合には、担体が
SP値が約8.7未満の溶剤、例えばリモネンオイル、
パラフィンオイル等の炭化水素溶剤ではゲルを形成しな
いため、エタノール等を主な溶剤とせざるを得す、揮散
コントロールにも問題がある。N−アシルアミノ酸誘導
体を用いる場合には、透明ゲルを得られる溶剤(担体)
が炭化水素系溶剤の中ではテルペン系に限られ、パラフ
ィン系では、経日変化によりゲルの不透明化が起る。
When dibenzylidene sorbitol is used, the carrier is a solvent having an SP value of less than about 8.7, such as limonene oil,
Hydrocarbon solvents such as paraffin oil do not form gels, so ethanol or the like must be used as the main solvent, which also poses problems in volatilization control. When using N-acylamino acid derivatives, a solvent (carrier) that can obtain a transparent gel
However, among hydrocarbon solvents, this is limited to terpene solvents, and with paraffin solvents, the gel becomes opaque due to aging.

また、テルペン系の溶剤はそれ自体の臭が強いため、テ
ルペン系溶剤を用いると得られる香調が限られる欠点が
ある。
Furthermore, since terpene-based solvents themselves have a strong odor, the use of terpene-based solvents has the disadvantage that the aroma tone that can be obtained is limited.

また、熱可塑性ゴムを用いた徐放性香料組成物が特開昭
50−129755号公報に記載されており、該公報に
は上記香料組成物にSBS共重合体を用いることが記載
されているが、上記香料組成物は、SBS共重合体を熱
可塑性ゴムとして用いるもので、熱可塑性ゴムに可塑側
、安定剤、香料を混練した固形香料組成物であり、ゲル
状芳香剤でなく、香調も一定でなく、揮散とともに均一
な体積の減少を生じるものではない。
Further, a sustained release fragrance composition using thermoplastic rubber is described in JP-A-50-129755, and the publication describes the use of an SBS copolymer in the above fragrance composition. However, the above fragrance composition uses SBS copolymer as a thermoplastic rubber, and is a solid fragrance composition made by kneading a thermoplastic rubber with a plasticizer, a stabilizer, and a fragrance, and is not a gel fragrance. The volume is not constant, and the volume does not decrease uniformly with volatilization.

〔問題を解決するための手段〕[Means to solve the problem]

本発明者らは、透明で美麗なゲル伏態が香料の振散終了
時まで持続し、香料の揮散が安定で、且つ衝撃に強いゲ
ル強度を存するゲル伏芳香剤組成物を提供することを目
的として種々検討した結果、香料揮散のための担体とし
て、室温で液体且つ揮発性のパラフィン系炭化水素を特
定量用い、ゲル化剤としてスチレン−ブタジエン−スチ
レンブロック共重合体(SBS共重合体)を特定量用い
ることにより上記目的が達成されることを知見した。
The present inventors have aimed to provide a gel-forming fragrance composition that maintains a transparent and beautiful gel state until the end of perfume dispersion, has stable volatilization of perfume, and has gel strength that is resistant to impact. As a result of various studies, we found that a specific amount of paraffinic hydrocarbon, which is liquid and volatile at room temperature, was used as a carrier for perfume volatilization, and a styrene-butadiene-styrene block copolymer (SBS copolymer) was used as a gelling agent. It has been found that the above object can be achieved by using a specific amount of.

本発明は、上記知見に基づきなされたもので、室温で液
体且つ揮発性のパラフィン系炭化水素50〜90i遺%
、スチレンーブタジエンースチレンブロンク共重合体2
〜30重量%及び香料0.5〜30重量%からなるゲル
状芳香剤組成物を提供するものである。
The present invention has been made based on the above findings, and is based on the above findings.
, styrene-butadiene-styrene blank copolymer 2
The present invention provides a gel-like fragrance composition consisting of ~30% by weight and 0.5-30% by weight of fragrance.

以下に本発明のゲル伏芳香剤組成物について詳述する。The gel-forming fragrance composition of the present invention will be described in detail below.

本発明のゲル状芳香剤組成物における常温で液体且つ揮
発性のパラフィン系炭化水素は、香料の担体(分散媒)
として用いられるもので、該パラフィン系炭化水素とし
ては、炭素数8〜16程度で且つSP値が6.5〜8.
0程度のものが好ましく、25℃での蒸気圧が1〜20
mmHg程度のものが特に好ましい、このパラフィン系
炭化水素の配合量は50〜90重量%、好ましくは70
〜85重量%である。
The paraffinic hydrocarbon that is liquid and volatile at room temperature in the gel fragrance composition of the present invention is a carrier (dispersion medium) for the fragrance.
The paraffinic hydrocarbons have approximately 8 to 16 carbon atoms and an SP value of 6.5 to 8.
It is preferably about 0, with a vapor pressure of 1 to 20 at 25°C.
The paraffinic hydrocarbon is particularly preferably about mmHg, and the blending amount is 50 to 90% by weight, preferably 70% by weight.
~85% by weight.

また、本発明のゲル伏芳香剤組成物におけるSBS共重
合体は、香料を担持(分散)させた上記パラフィン系炭
化水素のゲル化剤として用いられるもので、該SBS共
重合体としては、スチレン/ブタジェン比が10/90
〜40/60程度の側鎖もしくは直鎖状の共重合体で可
塑剤を含有しないものが好ましく、特にスチレン/ブタ
ジェン比が25/75〜35/65程度の側鎖状共重合
体が好ましい。このSBS共重合体の配合量は2〜30
重量%、好ましくは8〜20重量%である。
In addition, the SBS copolymer in the gel-forming fragrance composition of the present invention is used as a gelling agent for the paraffinic hydrocarbon on which a fragrance is supported (dispersed). /butadiene ratio is 10/90
A side chain or linear copolymer with a ratio of about 40/60 to about 40/60 and containing no plasticizer is preferred, and a side chain copolymer with a styrene/butadiene ratio of about 25/75 to 35/65 is particularly preferred. The blending amount of this SBS copolymer is 2 to 30
% by weight, preferably 8-20% by weight.

5BS−#I−fi合体が2重量%未満、特に1%以下
ではゲル強度が不足し、30%超ではゲル化するものの
香料揮散の悪化、連敗残渣の増加が起こり目的とするゲ
ル状芳香剤組成物を得難くなる。
If the 5BS-#I-fi combined content is less than 2% by weight, especially less than 1%, the gel strength will be insufficient, and if it exceeds 30%, gelation will occur, but perfume volatilization will worsen and residue will increase, resulting in the desired gel-like fragrance. It becomes difficult to obtain the composition.

また、本発明のゲル状芳香剤組成物に用いられる香料は
、透明ゲルを得るためには上記パラフィン系炭化水素に
溶解する香料でなければならず、そのような香料であれ
ば、その種類には特に制限されないが、SP値10以下
の単品香料を用いた調合香料が好ましく、特に9.5以
下の単品香料を用いた調合香料が好ましい。
In addition, the fragrance used in the gel-like fragrance composition of the present invention must be a fragrance that dissolves in the above-mentioned paraffinic hydrocarbon in order to obtain a transparent gel. is not particularly limited, but a blended flavor using a single flavor with an SP value of 10 or less is preferred, and a blended flavor using a single flavor with an SP value of 9.5 or less is particularly preferred.

しかし、SP値10以上の単品香料を用いた調合香料で
も該調合香料におけるSP(*10以上の単品香料の割
合が50M量%以下、さらに好ましくは30重量%以下
であれば、系に完全に可溶化するので完全な透明ゲルが
得られるから、目的とする香調等に応じ、上記パラフィ
ン系炭化水素に溶解し得る調合香料を調製することがで
きる。上記香料の配合量は、0.5〜30重量%、好ま
しくは5〜20重量%で、0.5重量%未満では香りが
弱く、30重量%超ではゲル強度の低下をまねくため、
目的とするゲル状芳香剤組成物を得難くなる。
However, even in a blended fragrance using a single fragrance with an SP value of 10 or more, if the proportion of the single fragrance with an SP (*10 or more) in the blended fragrance is 50M% or less, more preferably 30% by weight or less, it will not completely enter the system. Since it is solubilized and a completely transparent gel is obtained, it is possible to prepare a blended fragrance that can be dissolved in the above paraffin hydrocarbon depending on the desired fragrance tone etc. The blending amount of the above fragrance is 0.5 ~30% by weight, preferably 5 to 20% by weight; less than 0.5% by weight causes a weak fragrance, and more than 30% by weight leads to a decrease in gel strength;
It becomes difficult to obtain the desired gel-like fragrance composition.

本発明のゲル状芳香剤組成物は、上述の如く、香料の担
体として上記のパラフィン系炭化水素を用い、ゲル化剤
としてSBS共重合体を用いることにより所期の目的を
達成し得るもので、パラフィン系炭化水素を配合しない
場合には、本発明のゲル状芳香剤組成物の重要な利点の
一つである香料揮散とともにゲルの体積が減少し、その
終点が目で見てはっきりわかるという特徴が失われる。
As mentioned above, the gel fragrance composition of the present invention can achieve the intended purpose by using the above paraffinic hydrocarbon as a fragrance carrier and an SBS copolymer as a gelling agent. When paraffinic hydrocarbons are not blended, the volume of the gel decreases as the fragrance evaporates, which is one of the important advantages of the gel fragrance composition of the present invention, and the end point is clearly visible. Characteristics are lost.

すなわち、例えば、香料90重量%に対しSBS共重合
体lO重量%を用いてゲル化させた場合には、粘性のあ
る液体状になってゲル化せず、逆にSBS共重合体の配
合量を増加させた場合、例えば香料20重量%、SBS
共重合体80重量%によりゲル化させた場合には固化す
るが、揮散する割合が20重量%未満迄で、体積の減少
はわずかである。また、香料の担体として上記パラフィ
ン系炭化水素以外のものを用いた場合及びゲル化剤とし
て5BSP:5合体以外の従来のゲル化剤を用いた場合
には、従来の問題点を解決できず本発明の目的を達成で
きない。
That is, for example, when 90% by weight of fragrance is gelled using 10% by weight of SBS copolymer, it becomes a viscous liquid and does not gel. For example, 20% by weight of fragrance, SBS
When gelatinized with 80% by weight of the copolymer, it solidifies, but the volatilization rate is less than 20% by weight, and the volume decreases only slightly. Furthermore, when using something other than the above-mentioned paraffinic hydrocarbons as a fragrance carrier, and when using a conventional gelling agent other than the 5BSP:5 combination as a gelling agent, the problems of the conventional methods cannot be solved, and this problem cannot be solved. The purpose of the invention cannot be achieved.

尚、本発明のゲル状芳香剤組成物において、均一な香料
の揮散が行われ、香りの強さ、香調が最後まで変化しな
い効果が奏せられるのは、香料とその担体である上記パ
ラフィン系炭化水素との相互作用も寄与しているものと
認められる。
In addition, in the gel-like fragrance composition of the present invention, the effect that the fragrance is uniformly volatilized and the strength and tone of the fragrance do not change until the end is achieved because of the fragrance and the paraffin as its carrier. It is recognized that interaction with hydrocarbons also contributes.

上述した本発明のゲル状芳香剤組成物は、次のようにし
て容易に得られる。
The above-mentioned gel fragrance composition of the present invention can be easily obtained as follows.

即ち、上記液伏パラフィン系炭化水素50〜90重量%
、SBS共重合体2〜30重量%及び香料0.5〜30
重量%の混合物を100℃以下で加熱攪拌し、5BS−
111−重合体が充分に溶解して透明になった時点で該
各液を適当な容器に移し放冷するか、種々の形状の型に
入れて放冷後、型より取り出すことにより、美麗な透明
ゲルである本発明のゲル状芳香剤組成物が得られる。尚
、上記混合液は、60℃以下に冷えれば速やかにゲル化
するので、本発明のゲル状芳香剤組成物は短時間で容易
に得られ、また、製造時に油溶性の着色料を添加するこ
とにより、着色された透明のゲル状芳香剤組成物とする
こともできる。
That is, 50 to 90% by weight of the liquid paraffinic hydrocarbon
, SBS copolymer 2-30% by weight and fragrance 0.5-30%
The mixture of % by weight was heated and stirred at 100°C or less, and 5BS-
111-When the polymer is sufficiently dissolved and becomes transparent, each liquid can be transferred to a suitable container and left to cool, or put into molds of various shapes and taken out from the mold after cooling. A gel fragrance composition of the present invention which is a transparent gel is obtained. In addition, since the above-mentioned mixed liquid quickly gels when cooled to 60° C. or lower, the gel-like fragrance composition of the present invention can be easily obtained in a short period of time. By doing so, it is also possible to obtain a colored transparent gel-like fragrance composition.

〔実施例〕〔Example〕

実施例1 香料(フローラル系調合香料)   10重量%イソパ
ラフィン系炭化水素 (炭素数12のものを80重量 %含を、IPソルヘント162 0、出光石油化学)       80重量%SBS共
重合体(スチレン/ブ タジェン比=30/70、カリ フレックスTR1184、シェ ル化学)            10重量%上記原料
を混合し、混合物を100℃で約1時間攪拌し、SBS
共重合体が完全に溶解した時点で直径6c11、高さ3
cmの円柱形のAs製透明容器に流し込み室温で放冷し
、透明で美麗なゲル状芳香剤組成物(本発明品)を得た
。このゲル状芳香剤組成物は弾性もあり、非常に衝撃に
強かった。
Example 1 Fragrance (floral mixed fragrance) 10% by weight isoparaffinic hydrocarbon (80% by weight containing 12 carbon atoms, IP Solgent 1620, Idemitsu Petrochemical) 80% by weight SBS copolymer (styrene/butadiene) Ratio = 30/70, Califlex TR1184, Shell Chemical) 10% by weight The above raw materials were mixed, the mixture was stirred at 100°C for about 1 hour, and SBS
When the copolymer is completely dissolved, the diameter is 6c11 and the height is 3.
The mixture was poured into a cylindrical transparent container made of As and left to cool at room temperature to obtain a transparent and beautiful gel-like fragrance composition (product of the present invention). This gel-like fragrance composition was also elastic and highly resistant to impact.

た以外は上記実施例と全く同様にしてゲル状芳香剤組成
物(対照品)を得た。
A gel fragrance composition (control product) was obtained in exactly the same manner as in the above example except for the above.

上記本発明品及び上記対照品について、香調、香りの強
さ及び透明性の経口変化を調べた。その結果を下記第1
表に示す。
Oral changes in aroma tone, aroma intensity, and transparency were investigated for the above-mentioned products of the present invention and the above-mentioned control products. The results are shown in the first section below.
Shown in the table.

第1表 *l :香りの強さが弱まった。Table 1 *l: The strength of the scent was weakened.

*2 :香りの強さが著しく弱まった。*2: The strength of the scent was significantly weakened.

*3 :不透明 上記表中、香調、香りの強さ及び透明性の各欄の上段は
本発明品の結果を示し、下段は対照品の結果を示す。
*3: Opaque In the above table, the upper row of each column for scent tone, scent strength, and transparency shows the results for the product of the present invention, and the lower row shows the results for the control product.

また、上記本発明及び上記対照品について、20℃下に
揮散試験を行った。その結果を第1図に示す。
Further, a volatilization test was conducted at 20° C. for the above-mentioned present invention and the above-mentioned control product. The results are shown in FIG.

上記第1表に示す結果から、本発明品は、香調、香りの
強さ及び透明性の何れにおいても経口変化が認められな
いことが判る。また、第1図に示す結果から本発明品は
香料の揮散が安定していることが判る。
From the results shown in Table 1 above, it can be seen that the products of the present invention show no oral changes in any of the fragrance tone, fragrance intensity, and transparency. Moreover, from the results shown in FIG. 1, it can be seen that the product of the present invention exhibits stable volatilization of fragrance.

更に、本発明品と対照品について香料の揮散による外観
変化(形状変化)を観察したところ、本発明品は、体積
が均一に減少していき残渣を僅がしか出さなかったが、
対照品は体積が不均一に減少し且つ途中でしわしわとな
り見苦しい外観を呈し大量の残渣を出した。
Furthermore, when we observed changes in appearance (changes in shape) due to the volatilization of perfume between the products of the present invention and the control products, we found that the products of the present invention decreased in volume uniformly and produced only a small amount of residue, but
The control product decreased in volume unevenly and wrinkled in the middle, giving an unsightly appearance and producing a large amount of residue.

また、本発明品の保存安定性について調べたところ、−
5〜50℃下に2力月間保存後において全く変化を生じ
なかった。
Furthermore, when we investigated the storage stability of the product of the present invention, we found that -
No change occurred after storage at 5-50°C for 2 months.

実施例2 上記実施例1において用いたイソパラフィン系炭化水素
をノルマルパラフィン系炭化水素(ネオチオゾールLC
,中央化成#@)に代えた以外は実施例1と全く同様に
してゲル状芳香剤組成物(本発明品)を得た。この本発
明品も、実施例1で得たものと同様な種々の性能(性状
)を有していた。
Example 2 The isoparaffinic hydrocarbon used in Example 1 above was replaced with normal paraffinic hydrocarbon (Neothiosol LC
A gel-like fragrance composition (product of the present invention) was obtained in exactly the same manner as in Example 1, except that the composition was replaced with Chuo Kasei #@). This invention product also had various performances (properties) similar to those obtained in Example 1.

〔発明の効果〕〔Effect of the invention〕

本発明のゲル状芳香剤組成物は、透明で美麗な外観を呈
し、衝撃にも強いゲルであり、揮散とともに均一に体積
が減少して残渣も僅かであり、使用し得る香料の幅が広
く、香調、香りの強さの経時変化も少ない等、芳香剤と
して種々の優れた性能(性状)を有するものである。
The gel fragrance composition of the present invention has a transparent and beautiful appearance, is a gel that is resistant to impact, and its volume decreases uniformly as it evaporates, leaving only a small amount of residue, allowing it to be used in a wide range of fragrances. It has various excellent performances (properties) as an aromatic agent, such as little change in scent tone and strength over time.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、本発明品及び対照品についての揮散試験結果
を示す、相対揮散量(%)−経日の関係グラフである。
FIG. 1 is a graph showing the relationship between the relative volatilization amount (%) and the passage of time, showing the volatilization test results for the products of the present invention and the control product.

Claims (1)

【特許請求の範囲】[Claims] 室温で液体且つ揮発性のパラフィン系炭化水素50〜9
0重量%、スチレン−ブタジエン−スチレンブロック共
重合体2〜30重量%及び香料0.5〜30重量%から
なるゲル状芳香剤組成物。
Paraffinic hydrocarbons that are liquid and volatile at room temperature 50-9
0% by weight, 2 to 30% by weight of a styrene-butadiene-styrene block copolymer, and 0.5 to 30% by weight of a fragrance.
JP61069473A 1986-03-27 1986-03-27 Gel like aroma composition Pending JPS62249652A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61069473A JPS62249652A (en) 1986-03-27 1986-03-27 Gel like aroma composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61069473A JPS62249652A (en) 1986-03-27 1986-03-27 Gel like aroma composition

Publications (1)

Publication Number Publication Date
JPS62249652A true JPS62249652A (en) 1987-10-30

Family

ID=13403680

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61069473A Pending JPS62249652A (en) 1986-03-27 1986-03-27 Gel like aroma composition

Country Status (1)

Country Link
JP (1) JPS62249652A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2372447A (en) * 2001-02-21 2002-08-28 Jeyes Group Ltd Air fresheners
JP2005218761A (en) * 2004-02-09 2005-08-18 Seed Co Ltd Perfume-including gel

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5675159A (en) * 1979-11-22 1981-06-22 Tsuginori Nada Perfume incorporating composition
JPS56115377A (en) * 1980-02-16 1981-09-10 St Kagaku Kogyo Kk Prolonged action solid volatile material
JPS6238166A (en) * 1985-08-12 1987-02-19 曽田香料株式会社 Transparent gel like aroma volatilizing body and its production

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5675159A (en) * 1979-11-22 1981-06-22 Tsuginori Nada Perfume incorporating composition
JPS56115377A (en) * 1980-02-16 1981-09-10 St Kagaku Kogyo Kk Prolonged action solid volatile material
JPS6238166A (en) * 1985-08-12 1987-02-19 曽田香料株式会社 Transparent gel like aroma volatilizing body and its production

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2372447A (en) * 2001-02-21 2002-08-28 Jeyes Group Ltd Air fresheners
JP2005218761A (en) * 2004-02-09 2005-08-18 Seed Co Ltd Perfume-including gel

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