JPS582990B2 - Aerosol saves - Google Patents
Aerosol savesInfo
- Publication number
- JPS582990B2 JPS582990B2 JP50040847A JP4084775A JPS582990B2 JP S582990 B2 JPS582990 B2 JP S582990B2 JP 50040847 A JP50040847 A JP 50040847A JP 4084775 A JP4084775 A JP 4084775A JP S582990 B2 JPS582990 B2 JP S582990B2
- Authority
- JP
- Japan
- Prior art keywords
- stock solution
- aerosol
- propellant
- alcohol
- ethylene oxide
- 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.)
- Expired
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/046—Aerosols; Foams
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/26—Aluminium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/925—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of animal origin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/12—Aerosols; Foams
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/30—Materials not provided for elsewhere for aerosols
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Dispersion Chemistry (AREA)
- Birds (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Surface Treatment Of Glass (AREA)
- Colloid Chemistry (AREA)
Description
【発明の詳細な説明】 本発明はエアゾール組成物に関するものである。[Detailed description of the invention] The present invention relates to aerosol compositions.
更に詳しくは、乳化安定性の非常に優れた水一アルコー
ルベースのエアゾール組成物に関するものである。More specifically, the present invention relates to a water-alcohol-based aerosol composition that has excellent emulsion stability.
従来から、ガラスクリーナー、家具クリーナー等の種々
のクリーナー、消臭剤、殺虫剤、化粧品等多くの商品が
エアゾール製品として使われている。Conventionally, many products such as various cleaners such as glass cleaners and furniture cleaners, deodorants, insecticides, and cosmetics have been used as aerosol products.
このようなエアゾール製品では噴射剤との相溶性を良く
するために低級アルコール等の溶剤をベースとし、これ
に有効成分あるいは薬効成分を溶解、分散させる方法が
一般的であるが、このような溶剤ベースのエアゾールは
それ自体が可燃性で危険性があり、噴射剤も高価なフロ
ンガス等の不燃性のガスを使用しなげればならず、また
その用途によっては有効成分としてエタノール等の溶剤
に不溶のものを使う必要のある場合もある。In order to improve compatibility with the propellant, such aerosol products generally use a solvent such as lower alcohol as a base, and the active ingredient or medicinal ingredient is dissolved and dispersed in this solvent. The base aerosol itself is flammable and dangerous, and the propellant must be an expensive non-flammable gas such as chlorofluorocarbon gas, and depending on its use, the active ingredient is insoluble in solvents such as ethanol. Sometimes it is necessary to use one.
従って最近では安全であり、しかも可燃性ではあるが安
価な低級炭化水素を噴射剤として使用することのできる
経済的な水ベースのあるいは水一アルコールベースのエ
アゾール製品が注目されている。Therefore, attention has recently been focused on safe and economical water-based or water-alcohol-based aerosol products that can use flammable but inexpensive lower hydrocarbons as propellants.
しかしながら、水と噴射剤とは互に不溶性でありかつ比
重が相違するため、そのエアゾール化は非常に困難であ
る。However, since water and propellant are mutually insoluble and have different specific gravities, it is very difficult to make them into an aerosol.
即ち、水ベースの原液と噴射剤との組合せより成るエア
ゾール製品においては原液と噴射剤との均一な混合が極
めて困難であり、原液と噴射剤が二層に分離し易い。That is, in aerosol products made of a combination of a water-based stock solution and a propellant, it is extremely difficult to mix the stock solution and the propellant uniformly, and the stock solution and the propellant tend to separate into two layers.
かゝる欠点を改善する目的で例えばポリオキシエチレン
アルキルエーテル系あるいは多価アルコール脂肪族エス
テル系等の各種の界面活性剤を乳化剤として用いて、原
液と噴射剤との乳化状態を改善する方法が提案されてい
るが、必ずしも満足しうる結果が得られていない。In order to improve this drawback, there is a method of improving the emulsification state between the stock solution and the propellant by using various surfactants such as polyoxyethylene alkyl ether type or polyhydric alcohol aliphatic ester type as an emulsifier. Although it has been proposed, satisfactory results have not always been obtained.
さらには、有効成分、薬効成分中には種々の水不溶性の
物質を含みこのようなものを安定に分散させるためには
、水ベースの原液よりも、水に例えばメタノール、エタ
ノール、インプロパノール等の低級アルコールを添加し
た水一アルコールベースの原液がより一層好ましい。Furthermore, active ingredients and medicinal ingredients include various water-insoluble substances, and in order to stably disperse such substances, it is better to use methanol, ethanol, impropanol, etc. in water than to prepare a water-based stock solution. A water-alcohol based stock solution to which a lower alcohol has been added is even more preferred.
しかしながらこのような水一アルコールベースのエアゾ
ール組成物では水のみの場合よりも噴射剤と原液との乳
化状態の崩壊が早く、特にアルコール分を20〜80重
量%含む水一アルコールベースのエアゾール組成物では
原液と噴射剤との乳化性能の優れた界面活性剤は皆無で
あった。However, in such water-alcohol-based aerosol compositions, the emulsified state of the propellant and stock solution breaks down more quickly than in the case of only water, especially in water-alcohol-based aerosol compositions containing 20 to 80% by weight of alcohol. However, there were no surfactants that had excellent emulsifying performance between the stock solution and the propellant.
本発明者らはこれらの欠点を解決し、噴射剤に対して優
れた乳化安定性を有する水−アルコールベースのエアゾ
ール組成物を得るべく研究した結果、本発明を完成した
。The present inventors completed the present invention as a result of research aimed at solving these drawbacks and obtaining a water-alcohol-based aerosol composition having excellent emulsion stability against propellants.
即ち、本発明は有効成分乃至薬効成分を含む原液と噴射
剤とからなり、原液と噴射剤との混合割合が重量比で9
5/5〜20/80で、原液がアルコール分を20〜8
0重量%含む炭素原子数3以下のアルコールの水溶液に
有効成分及び/又は薬効成分を溶解又は分散させた液か
らなるエアゾール組成物において、原液に対し酸化エチ
レンの平均付加モル数25〜150のヒマシ油又は水素
添加ヒマシ油の酸化エチレン付加物が乳化剤として配合
されてなることを特徴とするエアゾール組成物である。That is, the present invention consists of a stock solution containing an active ingredient or medicinal ingredient and a propellant, and the mixing ratio of the stock solution and the propellant is 9 by weight.
5/5 to 20/80, the alcohol content of the stock solution is 20 to 8
In an aerosol composition consisting of a liquid in which an active ingredient and/or a medicinal ingredient is dissolved or dispersed in an aqueous solution of an alcohol having 3 or less carbon atoms containing 0% by weight, an average number of moles of ethylene oxide added to the stock solution is 25 to 150 castor. This is an aerosol composition characterized by containing an ethylene oxide adduct of oil or hydrogenated castor oil as an emulsifier.
本発明において、水一アルコールベースのエアゾール組
成物とはメタノール、エタノール、イソプロパノール等
の炭素原子数3以下の低級アルコール水溶液にその用途
に応じた薬効成分その他の必要成分を溶解または分散さ
せた原液と噴射剤とからなるものであり、薬効成分その
他の必要成分の種類及びその添加量に応じてアルコール
水溶液の濃度を20〜80%の範囲で適宜選択できる。In the present invention, a water-alcohol-based aerosol composition is a stock solution in which medicinal ingredients and other necessary ingredients are dissolved or dispersed in an aqueous solution of a lower alcohol having 3 or less carbon atoms, such as methanol, ethanol, or isopropanol. The concentration of the alcohol aqueous solution can be appropriately selected in the range of 20 to 80% depending on the types of medicinal ingredients and other necessary ingredients and their added amounts.
20%以下では有効成分乃至薬効成分を溶解、分散させ
るのに一般に不充分であり、又80%以上では乳化剤を
用いても満足すべき乳化状態が得難い。If it is less than 20%, it is generally insufficient to dissolve and disperse the active ingredients or medicinal ingredients, and if it is more than 80%, it is difficult to obtain a satisfactory emulsified state even if an emulsifier is used.
また、本発明において使用する噴射剤としては特に限定
されるものではなく、ジクロロジフルオ口メタン、トリ
クロロモノフルオロメタン等のフロンガスのほかに、従
来の溶剤ベースのエアゾール組成物では使用できなかっ
た可燃性の低級炭化水素ガス例えばプロパン、ブタン、
液化石油ガス(以下LPGと略記する。In addition, the propellant used in the present invention is not particularly limited, and in addition to fluorocarbon gases such as dichlorodifluoromethane and trichloromonofluoromethane, flammable propellants that cannot be used in conventional solvent-based aerosol compositions may also be used. lower hydrocarbon gases such as propane, butane,
Liquefied petroleum gas (hereinafter abbreviated as LPG).
)等フロンガスに比べて廉価なものが使用でき経済的に
有利である。) It is economically advantageous because it can be used at a lower cost than chlorofluorocarbon gases.
本発明のエアゾール組成物に於ける上記原液と噴射剤と
の混合割合は重量比で95/5〜20/80であり、こ
の範囲より噴射剤の割合が少ないとエアゾールとしての
性能が低下し、又この範囲より多いと原液の割合が少な
すぎて不経済である本発明のエアゾール組成物において
は、上記の原液及び噴射剤とともに、その乳化剤として
酸化エチレンの平均付加モル数が25〜150のヒマシ
油又は水素添加(硬化)ヒマシ油の酸化エチレン付加物
を用いる。The mixing ratio of the above-mentioned stock solution and propellant in the aerosol composition of the present invention is 95/5 to 20/80 by weight, and if the proportion of the propellant is less than this range, the performance as an aerosol will deteriorate; In addition, in the aerosol composition of the present invention, where the proportion of the stock solution is too small and uneconomical if it exceeds this range, in addition to the above-mentioned stock solution and propellant, castor powder having an average added mole number of ethylene oxide of 25 to 150 is used as an emulsifier. Using ethylene oxide adducts of oil or hydrogenated (hardened) castor oil.
この配合割合は原液に対して0.05〜1.0重量%で
あれば良好なかつ安定な乳化状態のエアゾール組成物が
得られる。If the blending ratio is 0.05 to 1.0% by weight based on the stock solution, an aerosol composition in a good and stable emulsified state can be obtained.
上記本発明に係わるヒマシ油又は水素添加ヒマシ油の酸
化エチレン付加物は公知方法で得ることが出来る(例え
ば工業化学雑誌53巻(1950年)431頁参照)。The castor oil or the ethylene oxide adduct of hydrogenated castor oil according to the present invention can be obtained by a known method (see, for example, Industrial Chemistry Magazine Vol. 53 (1950), p. 431).
一般に酸又はアルカリ触媒の存在下に加熱加圧下(10
0〜200℃、1〜5kg/cm2)でヒマシ油又は水
素添加ヒマシ油に酸化エチレンを付加することにより得
られる。Generally, in the presence of an acid or alkali catalyst under heat and pressure (10
It is obtained by adding ethylene oxide to castor oil or hydrogenated castor oil at 0 to 200°C and 1 to 5 kg/cm2).
酸化エチレンの平均付加モル数はリシノレイン酸トリグ
リセライドのみから成るとして計算されたヒマシ油1モ
ルに対しアルカリ触媒の存在下で酸化エチレンガスを導
入した時吸収された酸化エチレンのモル数である。The average number of moles of ethylene oxide added is the number of moles of ethylene oxide absorbed when ethylene oxide gas is introduced in the presence of an alkali catalyst to one mole of castor oil calculated as consisting only of ricinoleic acid triglyceride.
本発明では平均付加モル数が25〜150の酸化エチレ
ン付加物を乳化剤として上記原液に配合することにより
、実験例及び実施例に示す如き優れた乳化安定性が得ら
れる。In the present invention, by blending an ethylene oxide adduct having an average addition mole number of 25 to 150 as an emulsifier in the above stock solution, excellent emulsion stability as shown in the experimental examples and examples can be obtained.
水ベースのエアゾール組成物においては、従来もポリオ
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等の非イオン界面活性剤が乳化
剤として使用されていたが、これらの界面活性剤では水
一アルコールベースのエアゾール組成物の場合には安定
な乳化状態を得ることは全く不可能であったが、前記本
発明のエアゾール組成物では良好なかつ安定な乳化状態
が得られる。In water-based aerosol compositions, nonionic surfactants such as polyoxyethylene alkyl ether and polyoxyethylene sorbitan fatty acid ester have traditionally been used as emulsifiers; In the case of an aerosol composition, it was completely impossible to obtain a stable emulsified state, but with the aerosol composition of the present invention, a good and stable emulsified state can be obtained.
これらの本発明特徴を次に実験例をもって示す。These features of the present invention will be illustrated below using experimental examples.
実験例
原液(エタノール/水−50/50) 60重量%噴
射剤 40乳化剤として次
表に示す各種界面活性剤を上記原液に対して0.5重量
%添加し、これを透明容器に上記の割合となるように噴
射剤とともに充填してエアゾール組成物を作り、その乳
化安定性を調べた。Experimental example stock solution (ethanol/water - 50/50) 60% by weight propellant 40 Add 0.5% by weight of various surfactants shown in the following table as emulsifiers to the above stock solution, and add this to the above ratio in a transparent container. An aerosol composition was prepared by filling together with a propellant so that the emulsion stability was investigated.
試験方法は上記組成物を15秒間振盪した後室温に放置
し、乳化状態が破壊されて二層に分離するまでの時間を
測定した。The test method was to shake the above composition for 15 seconds, then leave it at room temperature, and measure the time until the emulsified state was broken and the composition separated into two layers.
噴射剤としてはLPG及びジクロロジフルオロメタン(
F−12)を用いた。Propellants include LPG and dichlorodifluoromethane (
F-12) was used.
この結果を次表に示す。×:振盪直後〜5分で分離
Δ:振盪後5分〜30分で分離
○:振盪後30分〜60分で分離
◎:振盪後60分以上して分離
本発明のエアゾール組成物は、従来エアゾールタイプで
使用されている種々の用途に、その用途に応じた薬効成
分あるいは有効成分を添加して使用することができ、例
えば殺虫剤、各種クリーナー、ヘアースプレー、塗料、
消臭剤、制汗剤、エアーフレッシュナー、化粧品等が挙
げられる。The results are shown in the table below. ×: Separated 5 minutes after shaking Δ: Separated 5 minutes to 30 minutes after shaking ○: Separated 30 minutes to 60 minutes after shaking ◎: Separated 60 minutes or more after shaking Aerosol types can be used for various purposes by adding medicinal or active ingredients depending on the purpose, such as insecticides, various cleaners, hair sprays, paints, etc.
Examples include deodorants, antiperspirants, air fresheners, and cosmetics.
次に本発明の代表的な実施例を示す。Next, typical examples of the present invention will be shown.
実施例中%は重量%を、部は重量部を示す。In the examples, % indicates weight %, and parts indicate parts by weight.
実施例1
エアー・フレッシュナー
原液
香料 1.0%
トリエチレングリコール 4.0%エタ
ノール 50.0水素添加ヒ
マシ油酸化エチレン付加 0.3物(P≒25)
イオン交換水 バランス100
.0
香料としてはゲラニオール、シトロネロール、リナロー
ル、リナリルアセテート、フエニルエチルアルコールの
混合物を使用した。Example 1 Air freshener stock fragrance 1.0% Triethylene glycol 4.0% Ethanol 50.0 Hydrogenated castor oil Ethylene oxide addition 0.3 (P≒25) Ion exchange water Balance 100
.. 0 A mixture of geraniol, citronellol, linalool, linalyl acetate, and phenylethyl alcohol was used as the fragrance.
又トリエチレングリコールは塵や煙草の煙をとりかこん
でおとす役目をする空気清浄剤である。Triethylene glycol is also an air purifier that traps dust and cigarette smoke.
本実施例及び上記実験例で用いた水素添加ヒマシ油酸化
エチレン付加物の沃素価は0.9である。The iodine value of the hydrogenated castor oil oxidized ethylene adduct used in this example and the above experimental examples is 0.9.
原液65部に対し噴射剤としてLPG35部の割合でエ
アゾール罐に充填しエアーフレッシュナーを得た。An air freshener was obtained by filling an aerosol can with 65 parts of the stock solution and 35 parts of LPG as a propellant.
実施例2
ガラス・クリーナーエアゾール
原液 %ホリオキシ
エチレンノニルフエニル 0.1エーテル(P≒9
)
ポリオキシエチレンソルビタンオレ 0.1エート
(P≒20)
エチルアルコール 30.0ヒマ
シ油酸化エチレン付加物(P≒ o.1100)
イオン交換水 バランス100.
0
ポリオギシエチレンノニルフエニルエーテル及びポリオ
キシエチレンソルビタンオレートは洗浄剤(洗浄成分)
である。Example 2 Glass cleaner aerosol stock solution % pholyoxyethylene nonyl phenyl 0.1 ether (P≒9
) Polyoxyethylene sorbitan oleate 0.1 ate (P≒20) Ethyl alcohol 30.0 Castor oil oxidized ethylene adduct (P≒ o.1100) Ion exchange water Balance 100.
0 Polyoxyethylene nonyl phenyl ether and polyoxyethylene sorbitan oleate are cleaning agents (cleaning ingredients)
It is.
原液85部に対して噴射剤としてLPG15部で同様に
してガラスクリーナーエアゾールを得た。A glass cleaner aerosol was obtained in the same manner using 15 parts of LPG as a propellant to 85 parts of the stock solution.
実施例1及び実施例2のエアゾール組成物について乳化
状態を調べたところ何れも良好なかつ安定な乳化状態を
得ることができた。When the emulsification state of the aerosol compositions of Examples 1 and 2 was examined, good and stable emulsification states could be obtained in both cases.
即ちこれらのエアゾール組成物を50℃で貯蔵試験した
が、20日後も分離しなかった。That is, when these aerosol compositions were subjected to a storage test at 50° C., they did not separate even after 20 days.
Claims (1)
り、原液と噴射剤との混合割合が重量比で95/5〜2
0/80で、原液がアルコール分を20〜80重量%含
む炭素原子数3以下のアルコールの水溶液に有効成分及
び/又は薬効成分を溶解又は分散させた液からなるエア
ゾール組成物において、原液に対し酸化エチレンの平均
付加モル数25〜150のヒマシ油又は水素添加ヒマシ
油の酸化エチレン付加物が乳化剤として配合されてなる
ことを特徴とするエアゾール組成物。1 Consists of a stock solution containing an active ingredient or medicinal ingredient and a propellant, and the mixing ratio of the stock solution and propellant is 95/5 to 2 by weight.
0/80, the stock solution is an aerosol composition consisting of a liquid in which an active ingredient and/or a medicinal ingredient is dissolved or dispersed in an aqueous solution of an alcohol having 3 or less carbon atoms and containing 20 to 80% by weight of alcohol, compared to the stock solution. An aerosol composition characterized in that castor oil or an ethylene oxide adduct of hydrogenated castor oil having an average added mole number of ethylene oxide of 25 to 150 is blended as an emulsifier.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50040847A JPS582990B2 (en) | 1975-04-04 | 1975-04-04 | Aerosol saves |
| PH18276A PH12659A (en) | 1975-04-04 | 1976-03-30 | Aerosol composition |
| GB12793/76A GB1498935A (en) | 1975-04-04 | 1976-03-30 | Aerosol compositions |
| US05/751,163 US4083954A (en) | 1975-04-04 | 1976-12-16 | Aerosol composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50040847A JPS582990B2 (en) | 1975-04-04 | 1975-04-04 | Aerosol saves |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS51116185A JPS51116185A (en) | 1976-10-13 |
| JPS582990B2 true JPS582990B2 (en) | 1983-01-19 |
Family
ID=12591965
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50040847A Expired JPS582990B2 (en) | 1975-04-04 | 1975-04-04 | Aerosol saves |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JPS582990B2 (en) |
| GB (1) | GB1498935A (en) |
| PH (1) | PH12659A (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54106082A (en) * | 1978-02-07 | 1979-08-20 | Toyo Eazooru Kougiyou Kk | Threeephasic aerosol product |
| JPS578280A (en) * | 1980-06-20 | 1982-01-16 | Toyo Aerosol Kogyo Kk | Aerosol suspension |
| JPS62187664U (en) * | 1986-05-19 | 1987-11-28 | ||
| JP4719501B2 (en) * | 2005-05-11 | 2011-07-06 | 株式会社アサヒテックコーポレーション | Spoon straw packaging apparatus and packaging method |
| US8465728B2 (en) | 2005-06-28 | 2013-06-18 | S.C. Johnson & Son, Inc. | Composition and aerosol spray dispenser for eliminating odors in air |
| TW200806342A (en) * | 2006-06-28 | 2008-02-01 | S C Johnson & Amp Son Inc | Composition and aerosol spray dispenser for eliminating odors in air |
| US9078947B2 (en) | 2013-03-15 | 2015-07-14 | Kimberly-Clark Worldwide, Inc. | Composition for forming a porous absorbent structure |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1121563A (en) * | 1966-06-07 | 1968-07-31 | Yardley And Company Ltd | Self-propelled homogeneous liquid compositions |
| ZA722756B (en) * | 1971-05-07 | 1973-12-19 | Colgate Palmolive Co | Improved spray starch formulation |
| DE2243281B2 (en) * | 1972-09-02 | 1980-12-04 | Henkel Kgaa, 4000 Duesseldorf | Skin care products |
| US3781212A (en) * | 1972-10-27 | 1973-12-25 | Townsend & Townsend | Aerosol enzyme detergents stabilized with carbon dioxide |
-
1975
- 1975-04-04 JP JP50040847A patent/JPS582990B2/en not_active Expired
-
1976
- 1976-03-30 PH PH18276A patent/PH12659A/en unknown
- 1976-03-30 GB GB12793/76A patent/GB1498935A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB1498935A (en) | 1978-01-25 |
| PH12659A (en) | 1979-07-11 |
| JPS51116185A (en) | 1976-10-13 |
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