JPH04332786A - Propellant composition for aerosol - Google Patents
Propellant composition for aerosolInfo
- Publication number
- JPH04332786A JPH04332786A JP13191691A JP13191691A JPH04332786A JP H04332786 A JPH04332786 A JP H04332786A JP 13191691 A JP13191691 A JP 13191691A JP 13191691 A JP13191691 A JP 13191691A JP H04332786 A JPH04332786 A JP H04332786A
- Authority
- JP
- Japan
- Prior art keywords
- aerosol
- propellant composition
- heptafluoropropane
- hydrocarbons
- ethers
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 19
- 239000003380 propellant Substances 0.000 title claims abstract description 19
- 239000000443 aerosol Substances 0.000 title claims abstract description 9
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims abstract description 16
- 150000008282 halocarbons Chemical class 0.000 claims abstract description 9
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 9
- 150000002170 ethers Chemical class 0.000 claims abstract description 8
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 claims abstract description 6
- UKACHOXRXFQJFN-UHFFFAOYSA-N heptafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)F UKACHOXRXFQJFN-UHFFFAOYSA-N 0.000 claims abstract description 5
- ATEBGNALLCMSGS-UHFFFAOYSA-N 2-chloro-1,1-difluoroethane Chemical compound FC(F)CCl ATEBGNALLCMSGS-UHFFFAOYSA-N 0.000 claims abstract description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 5
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 claims description 3
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 claims description 3
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims description 3
- 239000004338 Dichlorodifluoromethane Substances 0.000 claims description 3
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 3
- 235000019404 dichlorodifluoromethane Nutrition 0.000 claims description 3
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 claims description 3
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 3
- 229940029284 trichlorofluoromethane Drugs 0.000 claims description 3
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims description 2
- FRCHKSNAZZFGCA-UHFFFAOYSA-N 1,1-dichloro-1-fluoroethane Chemical compound CC(F)(Cl)Cl FRCHKSNAZZFGCA-UHFFFAOYSA-N 0.000 claims description 2
- BOUGCJDAQLKBQH-UHFFFAOYSA-N 1-chloro-1,2,2,2-tetrafluoroethane Chemical compound FC(Cl)C(F)(F)F BOUGCJDAQLKBQH-UHFFFAOYSA-N 0.000 claims description 2
- BKWAVXQSZLEURV-UHFFFAOYSA-N 2-chloro-1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)C(Cl)C(F)(F)F BKWAVXQSZLEURV-UHFFFAOYSA-N 0.000 claims description 2
- COAUHYBSXMIJDK-UHFFFAOYSA-N 3,3-dichloro-1,1,1,2,2-pentafluoropropane Chemical compound FC(F)(F)C(F)(F)C(Cl)Cl COAUHYBSXMIJDK-UHFFFAOYSA-N 0.000 claims description 2
- 239000004341 Octafluorocyclobutane Substances 0.000 claims description 2
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 claims description 2
- 235000019407 octafluorocyclobutane Nutrition 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 230000006378 damage Effects 0.000 abstract 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000003915 liquefied petroleum gas Substances 0.000 description 6
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 239000005436 troposphere Substances 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 230000001166 anti-perspirative effect Effects 0.000 description 2
- 239000003213 antiperspirant Substances 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- -1 chlorine radicals Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- BHNZEZWIUMJCGF-UHFFFAOYSA-N 1-chloro-1,1-difluoroethane Chemical compound CC(F)(F)Cl BHNZEZWIUMJCGF-UHFFFAOYSA-N 0.000 description 1
- NVJUHMXYKCUMQA-UHFFFAOYSA-N 1-ethoxypropane Chemical compound CCCOCC NVJUHMXYKCUMQA-UHFFFAOYSA-N 0.000 description 1
- CXBDYQVECUFKRK-UHFFFAOYSA-N 1-methoxybutane Chemical compound CCCCOC CXBDYQVECUFKRK-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical class F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008266 hair spray Substances 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- VNKYTQGIUYNRMY-UHFFFAOYSA-N methoxypropane Chemical compound CCCOC VNKYTQGIUYNRMY-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000005437 stratosphere Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- BWMISRWJRUSYEX-SZKNIZGXSA-N terbinafine hydrochloride Chemical compound Cl.C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 BWMISRWJRUSYEX-SZKNIZGXSA-N 0.000 description 1
- 201000004647 tinea pedis Diseases 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明はエアゾール用噴射剤組成
物に関するものである。FIELD OF THE INVENTION This invention relates to propellant compositions for aerosols.
【0002】0002
【従来の技術】エアゾール用噴射剤に要求される特性と
して、適当な溶解力、適当な蒸気圧、無毒、化学的安定
性、容器等に対する腐蝕性のないこと、無臭、さらに不
燃であること等が挙げられる。従来、これらの要求を満
足するものとして、トリクロロモノフルオロメタン、ジ
クロロジフルオロメタン、トリクロロトリフルオロエタ
ン、ジクロロテトラフルオロエタン等のクロロフルオロ
カーボン系化合物(以下CFCという)があり、これら
のガスを単独又は混合して使用されてきた。[Prior Art] Properties required for aerosol propellants include appropriate dissolving power, appropriate vapor pressure, non-toxicity, chemical stability, non-corrosion to containers, etc., odorless, and nonflammability. can be mentioned. Conventionally, there are chlorofluorocarbon compounds (hereinafter referred to as CFCs) such as trichloromonofluoromethane, dichlorodifluoromethane, trichlorotrifluoroethane, and dichlorotetrafluoroethane that satisfy these requirements, and these gases can be used alone or in combination. It has been used as
【0003】液化石油ガス(LPG)、DME(ジメチ
ルエーテル)等も用いられるが、可燃性ガスであるため
に、エアゾール製品の燃焼性が高く、使用、貯蔵時の火
災の危険性がある。Liquefied petroleum gas (LPG), DME (dimethyl ether), etc. are also used, but since they are flammable gases, aerosol products are highly combustible and pose a risk of fire during use and storage.
【0004】0004
【発明が解決しようとする課題】前述のCFCは、噴射
剤として理想的な性状を有しているが、化学的に極めて
安定なため、対流圏内での寿命が長く、拡散して成層圏
に達し、ここで太陽光線により分解して発生する塩素ラ
ジカルがオゾンと連鎖反応を起こし、オゾン層を破壊す
るとのことから、その使用規制が実施されることとなっ
た。このため、従来のCFCに替わり、オゾン層を破壊
しにくい代替噴射剤の探索が活発に行なわれている。[Problems to be Solved by the Invention] The above-mentioned CFC has ideal properties as a propellant, but because it is chemically extremely stable, it has a long life in the troposphere and diffuses into the stratosphere. The use of chlorine radicals, which are decomposed by sunlight and generated here, causes a chain reaction with ozone and destroys the ozone layer, so the use of chlorine radicals has been regulated. For this reason, in place of conventional CFCs, there is active search for alternative propellants that are less likely to destroy the ozone layer.
【0005】代替噴射剤として、前述のLPG、DME
の他に、クロロジフルオロメタン、クロロジフルオロエ
タン、ジクロロトリフルオロエタン等のハイドロクロロ
フルオロカーボン系化合物(以下HCFCという)等が
検討されているが、LPG,DMEは製品の燃焼性が高
く、事故の増加が予想され、特に人体へ直接使用するエ
アゾール製品に使用することは望ましくない。また、H
CFCは、CFCに比べれば水素を含有するので対流圏
での寿命が短く、オゾン層への影響は極めて小さいが零
ではなく、さらに環境への影響の少ない噴射剤の開発が
必要である。[0005] As alternative propellants, the above-mentioned LPG, DME
In addition, hydrochlorofluorocarbon compounds (hereinafter referred to as HCFCs) such as chlorodifluoromethane, chlorodifluoroethane, and dichlorotrifluoroethane are being considered, but LPG and DME are highly flammable products and are likely to cause an increase in accidents. Therefore, it is not desirable to use it in aerosol products that are intended to be used directly on the human body. Also, H
Compared to CFC, CFC contains hydrogen, so it has a short life in the troposphere, and its impact on the ozone layer is extremely small, but not zero, and there is a need to develop propellants that have even less impact on the environment.
【0006】本発明は、従来のCFCが有している優れ
た特性を満足しながら環境への影響の極めて少ない代替
噴射剤として使用できる新規な噴射剤組成物を提供する
ことを目的とするものである。The object of the present invention is to provide a novel propellant composition that can be used as an alternative propellant that has extremely little impact on the environment while satisfying the excellent properties of conventional CFC. It is.
【0007】[0007]
【課題を解決するための手段】本発明は、前述の問題点
を解決すべくなされたものであり、1,1,1,2,2
,3,3−ヘプタフルオロプロパン(以下R227cと
いう)を主成分とするエアゾール用噴射剤組成物および
炭化水素類、エーテル類およびハロゲン化炭化水素類か
ら選ばれる少なくとも1種とR227cを含むエアゾー
ル用噴射剤組成物を提供するものである。[Means for Solving the Problems] The present invention has been made to solve the above-mentioned problems.
, 3,3-heptafluoropropane (hereinafter referred to as R227c) as a main component, and an aerosol propellant composition containing R227c and at least one selected from hydrocarbons, ethers, and halogenated hydrocarbons. The present invention provides a drug composition.
【0008】本発明において、炭化水素類としては、エ
タン、プロパン,n−ブタン、イソブタン、ブチレン、
シクロペンタン,n−ペンタン、イソペンタン等あるい
は液化プロパン(プロパン/プロピレン)、液化ブタン
(ブタン/ブチレン)等のLPGが挙げられ、好ましく
は炭素数2〜5の炭化水素類である。これらは単独でま
た2種以上の混合物として使用でき、好ましくはLPG
である。In the present invention, hydrocarbons include ethane, propane, n-butane, isobutane, butylene,
Examples include LPG such as cyclopentane, n-pentane, isopentane, liquefied propane (propane/propylene), and liquefied butane (butane/butylene), and preferably hydrocarbons having 2 to 5 carbon atoms. These can be used alone or as a mixture of two or more, preferably LPG
It is.
【0009】また、エーテル類としては、ジメチルエー
テル、メチルエチルエーテル、メチルプロピルエーテル
、メチルブチルエーテル、ジエチルエーテル、エチルプ
ロピルエーテル等の炭素数2〜5のエーテル類が好まし
く、特に毒性が低いことからジメチルエーテルが好適で
ある。これらは、単独または2種以上の混合物として使
用できる。[0009] As the ethers, ethers having 2 to 5 carbon atoms such as dimethyl ether, methyl ethyl ether, methyl propyl ether, methyl butyl ether, diethyl ether, and ethyl propyl ether are preferable, and dimethyl ether is particularly preferred because of its low toxicity. suitable. These can be used alone or as a mixture of two or more.
【0010】ハロゲン化炭化水素類としては、トリクロ
ロモノフルオロメタン、ジクロロジフルオロメタン、ク
ロロジフルオロメタン、トリクロロトリフルオロエタン
、ジクロロテトラフルオロエタン、ジクロロトリフルオ
ロエタン、クロロテトラフルオロエタン、テトラフルオ
ロエタン、ジクロロフルオロエタン、クロロジフルオロ
エタン、ジクロロペンタフルオロプロパン、クロロヘキ
サフルオロプロパン、オクタフルオロシクロブタン等R
227c以外のハロゲン化炭化水素であり、これらは単
独または2種以上の混合物として使用できる。Examples of halogenated hydrocarbons include trichloromonofluoromethane, dichlorodifluoromethane, chlorodifluoromethane, trichlorotrifluoroethane, dichlorotetrafluoroethane, dichlorotrifluoroethane, chlorotetrafluoroethane, tetrafluoroethane, and dichlorofluoroethane. Ethane, chlorodifluoroethane, dichloropentafluoropropane, chlorohexafluoropropane, octafluorocyclobutane, etc. R
It is a halogenated hydrocarbon other than 227c, and these can be used alone or in a mixture of two or more.
【0011】さらにこれらの炭化水素類、エーテル類お
よびハロゲン化炭化水素類を2種以上混合して使用する
こともできる。Furthermore, two or more of these hydrocarbons, ethers and halogenated hydrocarbons may be used in combination.
【0012】炭化水素類、エーテル類およびハロゲン化
炭化水素類から選ばれる少なくとも1種とR227cか
らなる混合物の混合割合は、R227cが50〜90w
t%、炭化水素類が0〜50wt%、好ましくは5〜5
0wt%、エーテル類が0〜50wt%、好ましくは5
〜50wt%、ハロゲン化炭化水素類が0〜50wt%
、好ましくは5〜50wt%である。[0012] The mixing ratio of the mixture consisting of at least one selected from hydrocarbons, ethers and halogenated hydrocarbons and R227c is such that R227c is 50 to 90w.
t%, hydrocarbons from 0 to 50 wt%, preferably from 5 to 5
0 wt%, ethers 0 to 50 wt%, preferably 5
~50wt%, 0 to 50wt% of halogenated hydrocarbons
, preferably 5 to 50 wt%.
【0013】本発明の組成物には、皮膚薬、制汗剤、水
虫薬、消臭剤等の各種薬剤、エタノール、イソプロピル
アルコール等のアルコール系溶媒、タルク、カオリン、
セライト、ベンガラ等の疎水性粉末あるいはニトロメタ
ン、エピクロルヒドリン等の防蝕剤等を配合しエアゾー
ル組成物とすることができる。The composition of the present invention includes various drugs such as skin medicines, antiperspirants, athlete's foot medicines, and deodorants, alcoholic solvents such as ethanol and isopropyl alcohol, talc, kaolin,
An aerosol composition can be prepared by blending hydrophobic powders such as celite and red iron or anticorrosive agents such as nitromethane and epichlorohydrin.
【0014】[0014]
【実施例】以下に本発明の実施例を示す。
[実施例1〜12]制汗剤として使用した例を表1に、
虫よけ剤として使用した例を表2に、ヘアスプレーとし
て使用した例を表3に示す。なお、数字の単位は重量部
である。また、2,2−ジクロロ−1,1,1− トリ
フルオロエタンはR123、1−クロロ−1,1−ジフ
ルオロエタンはR142bと称する。[Examples] Examples of the present invention are shown below. [Examples 1 to 12] Examples of use as antiperspirants are shown in Table 1.
Examples of use as an insect repellent are shown in Table 2, and examples of use as a hair spray are shown in Table 3. Note that the units of numbers are parts by weight. Further, 2,2-dichloro-1,1,1-trifluoroethane is referred to as R123, and 1-chloro-1,1-difluoroethane is referred to as R142b.
【0015】[0015]
【表1】[Table 1]
【0016】[0016]
【表2】[Table 2]
【0017】[0017]
【表3】[Table 3]
【0018】[0018]
【発明の効果】本発明の1,1,1,2,2,3,3−
ヘプタフルオロプロパンは、水素原子を含むので対流圏
での寿命が短く、さらに塩素原子を含まないのでオゾン
層を全く破壊しない。さらに、1,1,1,2,2,3
,3−ヘプタフルオロプロパンは、不燃性であり火災の
危険性がない。したがって、本発明のエアゾール用噴射
剤は環境への影響が極めて小さく、かつ実施例に示した
ように火災の危険性が極めて少なく優れたものである。Effect of the invention: 1,1,1,2,2,3,3- of the present invention
Since heptafluoropropane contains hydrogen atoms, it has a short lifetime in the troposphere, and since it does not contain chlorine atoms, it does not destroy the ozone layer at all. Furthermore, 1, 1, 1, 2, 2, 3
,3-heptafluoropropane is nonflammable and poses no fire hazard. Therefore, the aerosol propellant of the present invention has an extremely small impact on the environment, and as shown in the Examples, has an extremely low risk of fire and is therefore excellent.
Claims (5)
オロプロパンを主成分とするエアゾール用噴射剤組成物
。Claims: 1. An aerosol propellant composition containing 1,1,1,2,2,3,3-heptafluoropropane as a main component.
炭化水素類から選ばれる少なくとも1種と1,1,1,
2,2,3,3−ヘプタフルオロプロパンを含むエアゾ
ール用噴射剤組成物。2. At least one selected from hydrocarbons, ethers and halogenated hydrocarbons and 1,1,1,
An aerosol propellant composition comprising 2,2,3,3-heptafluoropropane.
ゾール用噴射剤組成物。3. The aerosol propellant composition according to claim 2, wherein the hydrocarbon is LPG.
項2のエアゾール用噴射剤組成物。4. The aerosol propellant composition according to claim 2, wherein the ether is dimethyl ether.
ルオロメタン、ジクロロジフルオロメタン、クロロジフ
ルオロメタン、トリクロロトリフルオロエタン、ジクロ
ロテトラフルオロエタン、ジクロロトリフルオロエタン
、クロロテトラフルオロエタン、テトラフルオロエタン
、ジクロロフルオロエタン、クロロジフルオロエタン、
ジクロロペンタフルオロプロパン、クロロヘキサフルオ
ロプロパン、およびオクタフルオロシクロブタンから選
ばれる少なくとも1種である請求項2のエアゾール用噴
射剤組成物。5. The halogenated hydrocarbons are trichloromonofluoromethane, dichlorodifluoromethane, chlorodifluoromethane, trichlorotrifluoroethane, dichlorotetrafluoroethane, dichlorotrifluoroethane, chlorotetrafluoroethane, tetrafluoroethane, dichlorofluoro ethane, chlorodifluoroethane,
The propellant composition for aerosol according to claim 2, which is at least one selected from dichloropentafluoropropane, chlorohexafluoropropane, and octafluorocyclobutane.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13191691A JPH04332786A (en) | 1991-05-08 | 1991-05-08 | Propellant composition for aerosol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13191691A JPH04332786A (en) | 1991-05-08 | 1991-05-08 | Propellant composition for aerosol |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04332786A true JPH04332786A (en) | 1992-11-19 |
Family
ID=15069191
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13191691A Withdrawn JPH04332786A (en) | 1991-05-08 | 1991-05-08 | Propellant composition for aerosol |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04332786A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996033913A1 (en) | 1995-04-28 | 1996-10-31 | Great Lakes Chemical Corporation | Novel uses of heptafluoropropane |
US5672293A (en) * | 1994-03-11 | 1997-09-30 | E. I. Du Pont De Nemours And Company | Hydrofluorocarbon compositions |
US5681501A (en) * | 1995-10-11 | 1997-10-28 | E. I. Du Pont De Nemours And Company | Compositions including a hydrofluoropropane |
US6531441B1 (en) | 1994-03-11 | 2003-03-11 | E. I. Du Pont De Nemours And Company | Hydrofluorocarbon compositions |
-
1991
- 1991-05-08 JP JP13191691A patent/JPH04332786A/en not_active Withdrawn
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5672293A (en) * | 1994-03-11 | 1997-09-30 | E. I. Du Pont De Nemours And Company | Hydrofluorocarbon compositions |
US5785883A (en) * | 1994-03-11 | 1998-07-28 | E. I. Du Pont De Nemours And Company | Hydrofluorocarbon compositions with tetrafluoroethane and cyclopropane |
US6531441B1 (en) | 1994-03-11 | 2003-03-11 | E. I. Du Pont De Nemours And Company | Hydrofluorocarbon compositions |
US6846792B2 (en) | 1994-03-11 | 2005-01-25 | E. I. Du Pont De Nemours And Company | Hydrofluorocarbon compositions |
WO1996033913A1 (en) | 1995-04-28 | 1996-10-31 | Great Lakes Chemical Corporation | Novel uses of heptafluoropropane |
US5681501A (en) * | 1995-10-11 | 1997-10-28 | E. I. Du Pont De Nemours And Company | Compositions including a hydrofluoropropane |
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