JPS6168410A - Fragrant agent - Google Patents
Fragrant agentInfo
- Publication number
- JPS6168410A JPS6168410A JP59191369A JP19136984A JPS6168410A JP S6168410 A JPS6168410 A JP S6168410A JP 59191369 A JP59191369 A JP 59191369A JP 19136984 A JP19136984 A JP 19136984A JP S6168410 A JPS6168410 A JP S6168410A
- Authority
- JP
- Japan
- Prior art keywords
- solid
- fragrant
- hydrogenated phospholipid
- constituents
- liquid oil
- 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
Links
- 150000003904 phospholipids Chemical class 0.000 claims abstract description 22
- 239000007787 solid Substances 0.000 claims abstract description 14
- 239000007788 liquid Substances 0.000 claims abstract description 9
- 239000000843 powder Substances 0.000 claims abstract description 4
- 239000010409 thin film Substances 0.000 claims abstract 2
- 239000003205 fragrance Substances 0.000 claims description 17
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 239000000203 mixture Substances 0.000 abstract description 8
- 239000003795 chemical substances by application Substances 0.000 abstract description 7
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052740 iodine Inorganic materials 0.000 abstract description 6
- 239000011630 iodine Substances 0.000 abstract description 6
- 239000000654 additive Substances 0.000 abstract description 2
- 210000002969 egg yolk Anatomy 0.000 abstract description 2
- 239000012530 fluid Substances 0.000 abstract description 2
- 239000008247 solid mixture Chemical class 0.000 abstract description 2
- 239000000470 constituent Substances 0.000 abstract 4
- 239000012188 paraffin wax Substances 0.000 abstract 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- 239000003921 oil Substances 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- 238000009472 formulation Methods 0.000 description 4
- 239000012528 membrane Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920001083 polybutene Polymers 0.000 description 3
- 238000013268 sustained release Methods 0.000 description 3
- 239000012730 sustained-release form Substances 0.000 description 3
- 239000002386 air freshener Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 229920001748 polybutylene Polymers 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000013345 egg yolk Nutrition 0.000 description 1
- -1 fatty acid esters Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は新規な芳香剤の固形基剤に関するもので、芳香
成分を長い間とどめておくことができ、様々な形態のも
のを作ることのできる基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 novel solid base for fragrances, which is capable of retaining fragrance components for a long period of time, and is easy to manufacture into various forms. It is related to the base material that can be used.
従来、固形芳香基剤は、はとんどのものが粘土或いはゼ
ラチンなどの水溶性高分子が用いられている。Conventionally, solid aromatic bases have mostly been clay or water-soluble polymers such as gelatin.
しかし、水溶性高分子を使用した固形基剤は、芳香成分
を長い開基剤中にとどめておくことが難しいため、容器
に工夫をこらしてつかわれている。したがって芳香剤の
形態はブロック状あるいは使用する容器の内部空間にあ
わせた形態しかとることができない。However, since it is difficult to keep the aromatic components in the solid base using a water-soluble polymer for a long time, the containers must be designed in a creative way. Therefore, the fragrance can only take the form of a block or a form that matches the internal space of the container in which it is used.
このような状況において、本発明者らは、様々な商品形
態が可能であり、又、外観のきれいな、芳香成分を長い
間とどめておくような基剤を得ることを目的として研究
をかさねた結果、水素添加リン脂質或いは水素添加リン
脂質に液状油を配合した固形物中に香料をとり込ませる
ことによって目的とする組成物が得られることを見いだ
し、本発明を完成した。Under these circumstances, the inventors of the present invention have conducted extensive research with the aim of obtaining a base that can be manufactured into various product forms, has a beautiful appearance, and retains the aromatic components for a long period of time. The present invention was completed based on the discovery that the desired composition can be obtained by incorporating a fragrance into a hydrogenated phospholipid or a solid mixture of a hydrogenated phospholipid and a liquid oil.
即ち、本発明は卵黄もしくは植物に由来するリン脂質の
水素添加物からなる固形物あるいは水素添加リン脂質に
液状油を配合した固形物に香料等の芳香成分をとり込ま
せることを特徴とする芳香剤である。液状油を配合する
場合は、水素添加リン脂質に対して４重量倍以下である
必要がある。That is, the present invention provides a fragrance characterized by incorporating an aromatic component such as a fragrance into a solid material made of a hydrogenated product of phospholipid derived from egg yolk or a plant, or a solid material made by blending a hydrogenated phospholipid with a liquid oil. It is a drug. If liquid oil is blended, it needs to be at most 4 times the weight of the hydrogenated phospholipid.
水素添加リン脂質のヨウ素価は６０以下が望ましい。The iodine value of the hydrogenated phospholipid is preferably 60 or less.
本発明で使用される液状油としては、流動パラフィン、
スクワラン、α−オレフィンオリゴマー、流動ポリイソ
ブチレン、ポリブテンなどの炭化水素油および高級脂肪
酸エステルが最適であるが、その他動植物油、高級脂肪
酸、高級アルコールなど通常の液状油はどんなものでも
使用できる。The liquid oil used in the present invention includes liquid paraffin,
Hydrocarbon oils such as squalane, α-olefin oligomers, fluid polyisobutylene, and polybutene and higher fatty acid esters are most suitable, but any other ordinary liquid oils such as animal and vegetable oils, higher fatty acids, and higher alcohols can be used.
、 〔発明の効果〕
本発明の芳香剤は、外観が透明できれいであり除放性で
耐久性の良いものである。また、水素添加リン脂質のヨ
ウ素価を変えることにより、あるいは何種類かのヨウ素
価の水素添加リン脂質を使用することにより、あるいは
添加剤を加えることにより容易に香料の揮発速度をコン
トロールすることができる。[Effects of the Invention] The aromatic agent of the present invention has a transparent and clean appearance, sustained release properties, and good durability. In addition, the volatilization rate of fragrances can be easily controlled by changing the iodine value of hydrogenated phospholipids, by using hydrogenated phospholipids with several types of iodine values, or by adding additives. can.
水素添加リン脂質膜は芳香成分を容易に通過させること
ができ、かつ揮発速度をコントロールすることができる
ので、従来の芳香剤の表面にコーティングすることもで
き、形態もゲル状、ステイク状、ブロック状、膜状、粉
状などさまざまなものが可能である。Hydrogenated phospholipid membranes allow aroma components to pass through easily and control the rate of volatilization, so they can be coated on the surface of conventional fragrances, and can be applied in gel-like, stake-like, or block-like forms. It can be in various forms such as solid, film, and powder forms.
水素添加リン脂質は生体成分の一つであり、安全性が非
常に高く、室内芳香剤、食品関係芳香剤など広い範囲で
使用することができる。Hydrogenated phospholipids are one of the biological components, are extremely safe, and can be used in a wide range of applications, including indoor air fresheners and food-related air fresheners.
以下、本発明の実施例を示すが、本発明は実施例に限定
されるものではない。Examples of the present invention will be shown below, but the present invention is not limited to the examples.
実施例１
ブロック状除放性透明芳香剤
水素添加リン脂質 ４０重量部
ポリブテン ５重量部
流動パラフィン ４０重量部
香料 ２重量部
染料 ０．１重量部
７０℃で上記の配合物を混合攪拌後、型に流し込み冷却
しブロック状の除放性透明芳香剤を得た。Example 1 Block-shaped sustained release transparent fragrance Hydrogenated phospholipid 40 parts by weight Polybutene 5 parts by weight Liquid paraffin 40 parts by weight Fragrance 2 parts by weight Dye 0.1 part by weight After mixing and stirring the above formulation at 70°C, mold The mixture was poured into a container and cooled to obtain a block-shaped sustained release transparent fragrance.
実施例２
透明膜状芳香剤
水素添加リン脂質 １０重量部
ポリブテン １重量部
香料 ０．５重量部
へブタン ６６重量部
６０℃で上記の配合物を混合、溶解後、紙、樹脂等に流
し、乾燥し、透明膜状芳香剤を得た。Example 2 Transparent membrane aromatic hydrogenated phospholipid 10 parts by weight Polybutene 1 part by weight Fragrance 0.5 parts by weight Butane 66 parts by weight After mixing and dissolving the above formulation at 60°C, pour it onto paper, resin, etc. It was dried to obtain a transparent film-like fragrance.
水素添加リン脂質のヨウ素価及びポリブテンの使用量に
よって揮発速度をコントロールすることができる。The rate of volatilization can be controlled by the iodine value of the hydrogenated phospholipid and the amount of polybutene used.
実施例３
芳香成分のコーティング
水素添加リン脂質 １０重量部
ポリブテン １重量部
ヘキサン ９０重量部
上記の配合物を６０℃に加熱、溶解後、市販芳香剤を容
器から取り出し溶液中に浸した。約３０秒後に取り出し
、ヘキサンを乾燥させた。このコーティング化芳香剤は
容器により揮発速度をコントロールする必要がなく、市
販品と同等の揮発速度を得ることができた。Example 3 Coating of fragrance components Hydrogenated phospholipid 10 parts by weight Polybutene 1 part by weight Hexane 90 parts by weight After heating and dissolving the above formulation at 60° C., a commercially available fragrance was taken out of the container and immersed in the solution. It was taken out after about 30 seconds and the hexane was dried. With this coated aromatic agent, there was no need to control the volatilization rate depending on the container, and it was possible to obtain a volatilization rate equivalent to that of a commercially available product.
実施例４
粉状芳香剤
水素添加リン脂質 １０重量部
香料 ０．５重量部
ヘキサン ４０重量部
上記の配合物を６０℃に加熱、溶解後、ヘキサンを除去
し、透明膜状とした。この膜を粉砕し粉状とした。Example 4 Powdered aroma agent Hydrogenated phospholipid 10 parts by weight Perfume 0.5 parts by weight Hexane 40 parts by weight The above-mentioned formulation was heated to 60°C and dissolved, and the hexane was removed to form a transparent film. This membrane was crushed into powder.
Claims (1)
に対して液状油を４重量倍以下配合した固形物に芳香成
分を取り込ませたことを特徴とする芳香剤固形基剤 ２、薄膜状である特許請求の範囲第１項記載の芳香剤固
形基剤 ３、粉状である特許請求の範囲第１項記載の芳香剤固形
基剤 ４、ゲル状である特許請求の範囲第１項記載の芳香剤固
形基剤[Scope of Claims] 1. An aromatic solid base, characterized in that an aromatic component is incorporated into a hydrogenated phospholipid solid, or a solid containing 4 times by weight or less of a liquid oil relative to the hydrogenated phospholipid. The fragrance solid base 3 according to claim 1 is in the form of a thin film, the solid fragrance base 4 according to claim 1 is in the form of a powder, and the solid base 4 according to claim 1 is in the form of a gel. Aromatic solid base according to scope 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59191369A JPS6168410A (en) | 1984-09-12 | 1984-09-12 | Fragrant agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59191369A JPS6168410A (en) | 1984-09-12 | 1984-09-12 | Fragrant agent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6168410A true JPS6168410A (en) | 1986-04-08 |
Family
ID=16273437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59191369A Pending JPS6168410A (en) | 1984-09-12 | 1984-09-12 | Fragrant agent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6168410A (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60166368A (en) * | 1984-02-09 | 1985-08-29 | Kawaken Fine Chem Co Ltd | Thickening and gelling agent |
-
1984
- 1984-09-12 JP JP59191369A patent/JPS6168410A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60166368A (en) * | 1984-02-09 | 1985-08-29 | Kawaken Fine Chem Co Ltd | Thickening and gelling agent |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4184099A (en) | Composition for slow release of volatile ingredients at _high temperature; and article comprising same | |
| DE69735435T2 (en) | ESTER-TERMINATED POLYAMIDE GEL | |
| US5578089A (en) | Clear candle | |
| US5041421A (en) | Fragrant material | |
| MXPA04006528A (en) | Multilayered compressed candle and method for manufacture. | |
| JPS61502794A (en) | Edible preformed film barrier material | |
| US5246919A (en) | Fragrant material | |
| JPH05345127A (en) | Moisture resistant barrier and method of manufacturing the same | |
| US3000753A (en) | Emulsified wax compositions | |
| CA2107577C (en) | Insecticidal composition and insecticidal units | |
| GB2347683A (en) | Transparent candle composition | |
| JPS60500750A (en) | Device that continuously diffuses cleaning agent vapor | |
| KR100837793B1 (en) | Composite fragrance composition showing long-term uniform divergence | |
| JPS6168410A (en) | Fragrant agent | |
| US4664914A (en) | Jojoba oil compositions and methods | |
| JPS63501921A (en) | Water vapor migration resistant edible film barrier | |
| CN112368025A (en) | Solid fragrance composition and method of making | |
| US4904639A (en) | Air fresheners | |
| EP0994177A2 (en) | Multifunctional and/or multi-aroma imparting, multisectional, multiwick candles; kits for preparing same; processes for preparing same and processes for using same | |
| US2892732A (en) | Aerated solid wax composition and process of making it | |
| JPH0439441B2 (en) | ||
| KR101020805B1 (en) | Deodorizing and fragrance-containing composition containing phytoncide and preparation method thereof | |
| CA2256622C (en) | Method for the encapsulation of liquids | |
| GB2372450A (en) | Air fresheners | |
| JP2000159661A (en) | Aqueous composition containing sustained release microcapsules |