JPS606659B2 - solid fragrance deodorant - Google Patents
solid fragrance deodorantInfo
- Publication number
- JPS606659B2 JPS606659B2 JP56054960A JP5496081A JPS606659B2 JP S606659 B2 JPS606659 B2 JP S606659B2 JP 56054960 A JP56054960 A JP 56054960A JP 5496081 A JP5496081 A JP 5496081A JP S606659 B2 JPS606659 B2 JP S606659B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- surfactant
- carbon atoms
- water
- fragrance
- 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
- 239000003205 fragrance Substances 0.000 title claims description 11
- 239000007787 solid Substances 0.000 title claims description 5
- 239000002781 deodorant agent Substances 0.000 title description 4
- 239000000203 mixture Substances 0.000 claims description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 10
- 150000005846 sugar alcohols Polymers 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 238000005886 esterification reaction Methods 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 230000032050 esterification Effects 0.000 claims description 4
- 239000003349 gelling agent Substances 0.000 claims description 4
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 2
- 230000005484 gravity Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 3
- 239000002386 air freshener Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- -1 Bentaerytrit Chemical compound 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 239000002184 metal Chemical class 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- JJOJFIHJIRWASH-UHFFFAOYSA-N icosanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCCCC(O)=O JJOJFIHJIRWASH-UHFFFAOYSA-N 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Description
【発明の詳細な説明】
本発明は、比重1以上を有するワックス状組成物を用い
てなる固型芳香消臭剤に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a solid aromatic deodorant using a waxy composition having a specific gravity of 1 or more.
近年、香料、界面活性剤、ゲル化剤等を混合、固化した
固型芳香消臭剤を水中で機能させるタイプの製品が、市
販されている。BACKGROUND ART In recent years, products of a type in which a solid aromatic deodorant containing a fragrance, a surfactant, a gelling agent, etc. are mixed and solidified and function in water have been commercially available.
これらの製品は、水洗トイレの貯水タンクに投入し、芳
香、消臭及び洗浄などの役割を果すものである。水中投
下型固型芳香消臭剤は、その中に含まれる界面活性剤を
、一定濃度で、かつ長期間港出させることが重要である
から、貯水タンクに沈降させなければならず、その方法
がいくつか実施されている。These products are placed in the water tank of a flush toilet and serve as fragrance, deodorizer, and cleaning. Since it is important for underwater drop type solid air freshener deodorizers to leave the surfactant contained therein at a constant concentration and for a long period of time, it must be allowed to settle in a water storage tank. Some have been implemented.
即ち従来、このタイプの芳香剤は、次のような方法で水
中に沈降させていた。‘11重い容器に入れて使用する
。■比重の重い活性剤を使用する。‘3ー樹脂中に香料
や活性剤を添加する。しかし、mの方法では容器がかさ
ばるうえに、香料や活性剤が綾出した後も容器が残存す
る。■の方法では、活性剤の中への溶出速度が遠すぎて
、長期間の使用に問題がある。{3}の方法では、溶出
速度が遅すぎて充分にその機能を果せない。そのうえ樹
脂が残存するといった欠点があった。また、比重の重い
ブロム化物や金属塩を用いるといった方法も考えられる
が、排水後の生分解性や安全性の点で問題が生じる。本
発明者らは、上記問題点を解決するため、種々の研究を
重ねた結果、以下に示す多価アルコール、二塩基酸、脂
肪酸からなる団体状ェステル化生成物が有効であること
を見し、出し、本発明に達した。That is, conventionally, this type of fragrance has been precipitated in water by the following method. '11 Use in a heavy container. ■Use an activator with a heavy specific gravity. '3- Adding fragrances and activators to the resin. However, in method M, the container is bulky, and the container remains even after the fragrance and active agent have been released. In method (2), the rate of elution into the active agent is too slow and there is a problem in long-term use. In the method {3}, the elution rate is too slow to perform its function satisfactorily. Furthermore, there was a drawback that resin remained. Another possible method is to use a brominated compound or metal salt with a heavy specific gravity, but this poses problems in terms of biodegradability and safety after drainage. In order to solve the above problems, the present inventors have conducted various studies and found that the following collective esterification products consisting of polyhydric alcohols, dibasic acids, and fatty acids are effective. , and arrived at the present invention.
即ち本発明は、3価以上の多価アルコール1、炭素数4
〜20の直鎖飽和脂肪族二塩基酸2及び炭素数12〜2
2の直鏡飽和脂肪酸3のェステル化生成物であって、‘
111モルに対い2)0.5〜1モルを用い、かつ‘1
’,(2’を反応させて得られるヱステルの残存水酸基
の2/3以下を脚でェステル化してなるワックス状組成
物をゲル化剤乃至固化剤として用いることを特徴とする
、水中に投下して使用するための園型芳香消臭剤である
。以下、本発明の構成について説明する。That is, the present invention uses 1 polyhydric alcohol having a valence of 3 or more and 4 carbon atoms.
-20 linear saturated aliphatic dibasic acids and 12 to 2 carbon atoms
An esterification product of the direct mirror saturated fatty acid 3 of 2,
2) using 0.5 to 1 mol for 111 mol, and '1
A waxy composition obtained by esterifying 2/3 or less of the residual hydroxyl groups of the ester obtained by reacting ', (2') with the legs is used as a gelling agent or solidifying agent, This is a garden-type aromatic deodorant for use in the garden.The structure of the present invention will be explained below.
本発明で用いる多価アルコールとしては、グリセリン、
ベンタヱリトリツト、ソルビトール、及びそれらの縮合
物、並びに前記多価アルコールにエチレンオキサイド及
び(又は)プロピレンオキサィドを水酸基あたり1〜3
モル付加したポリエーテルポリオールなどであり、二塩
基酸としては、コハク酸、アジピン酸、セパシン酸、1
−、18−、オクタデカメチレンジカルボン酸などの炭
素数4以上20以下の直鎖飽和脂肪族二塩基酸が使用で
きる。The polyhydric alcohol used in the present invention includes glycerin,
Bentaerytrit, sorbitol, and condensates thereof, and the polyhydric alcohol containing 1 to 3 ethylene oxides and/or propylene oxides per hydroxyl group.
Polyether polyols with molar addition, etc., and dibasic acids include succinic acid, adipic acid, sepacic acid,
A linear saturated aliphatic dibasic acid having 4 to 20 carbon atoms such as -, 18-, and octadecamethylene dicarboxylic acid can be used.
脂肪酸としては、ラウリン酸、ミリスチン酸「バルミチ
ン酸、ステアリン酸、アラキン酸、べへン酸などの炭素
数12〜22の直鏡飽和脂肪酸が使用できる。これら3
成分を、多価アルコール1モルに対して、二塩基酸が0
.5〜1モルの比で、かつ多価アルコールと二塩基酸か
らなる縮合物の残存水酸基の2/3以下を脂肪酸でェス
テル化することにより、比重1以上のワックス状組成物
が得られる。As fatty acids, direct mirror saturated fatty acids having 12 to 22 carbon atoms such as lauric acid, myristic acid, valmitic acid, stearic acid, arachidic acid, and behenic acid can be used.
The ingredients are 0 dibasic acid per mol of polyhydric alcohol.
.. A waxy composition having a specific gravity of 1 or more can be obtained by esterifying 2/3 or less of the remaining hydroxyl groups of the condensate of a polyhydric alcohol and a dibasic acid with a fatty acid at a ratio of 5 to 1 mole.
上記組成比は、反応位込時のものであり、生成物はこの
組成比を中心とした各種縮合混合物となる。ェステル化
反応は、常圧もしくは減圧下、無触媒あるいは酸、アル
カリ、金属塩等のェステル化触媒を用いた通常の反応で
得られる。The above composition ratio is the one at the time of reaction implantation, and the products are various condensation mixtures centered on this composition ratio. The esterification reaction is carried out under normal pressure or reduced pressure without a catalyst or by a normal reaction using an esterification catalyst such as an acid, an alkali, or a metal salt.
得られたワックス状組成物は香料や界面活性剤との相溶
性が良く、成型物が水中で型くずれしない成型性の良い
ワックスである。The resulting waxy composition has good compatibility with perfumes and surfactants, and is a moldable wax that does not lose its shape in water.
したがって、香料や界面活性剤の水への渡世速度は、ワ
ックスに対する香料や界面活性剤の比率を変えることに
よって自由に調整できる利点を有している。また、本ワ
ックス状組成物は、適度に水に分散する為、香料や界面
活性剤が溶出した後もワックスが残存することはない。
さらに、このものは、多価アルコ−ル、直鎖飽和二塩脂
肪酸、直鎖飽和脂肪酸からなるため、安全性が高く、生
分解性が良く、環境汚梁の問題もない。そして本ワック
ス状組成物はそれ自体の比重が1以上であり、香料や界
面活性剤の比重も通常1以上であるから、これからなる
成型物の比重は1以上となり水中に容易に沈降する。Therefore, it has the advantage that the rate at which the fragrance or surfactant passes into water can be freely adjusted by changing the ratio of the fragrance or surfactant to the wax. Furthermore, since the present waxy composition is appropriately dispersed in water, no wax remains even after the fragrance and surfactant are eluted.
Furthermore, since this product is composed of polyhydric alcohol, linear saturated di-salt fatty acid, and linear saturated fatty acid, it is highly safe, has good biodegradability, and does not cause environmental pollution problems. Since the present wax-like composition itself has a specific gravity of 1 or more, and the specific gravity of the fragrance and surfactant is also usually 1 or more, a molded product made from it has a specific gravity of 1 or more and easily settles in water.
以上の点から本ワックス状組成物をゲル化剤乃至固化剤
として用いれば、従来の欠点を払拭した優れた品質の水
中投下型団型芳香消臭剤を製造することができる。From the above points, if the present waxy composition is used as a gelling agent or solidifying agent, it is possible to produce an excellent quality drop-in-water group-type aromatic deodorizer that eliminates the drawbacks of conventional products.
上記の効果は、前述した炭素数、モル比、残存水酸基に
関する限定によって初めてもたらされるものである。The above effects are first brought about by the aforementioned limitations regarding the number of carbon atoms, molar ratio, and residual hydroxyl groups.
次に、実施例を示す。Next, examples will be shown.
実施例 1
ワックス状組成物の調整とそれらの性状
1‐1 合成例
縄梓機、温度計、窒素ガス吸込管、水分離器を備えた1
その4ツロフラスコに、グリセリン184夕、無水コハ
ク酸100夕、ステアリン酸244.5夕を仕込み、触
媒として、塩化スズを全仕込み量の0.3%、還流溶剤
として、キシロールを全仕込み量の5%加え、160〜
230qoで、5時間反応を行なった。Example 1 Preparation of waxy compositions and their properties 1-1 Synthesis example 1 equipped with a rope scaler, thermometer, nitrogen gas suction pipe, and water separator
Into the four flasks, 184 g of glycerin, 100 g of succinic anhydride, and 244.5 g of stearic acid were charged, tin chloride was used as a catalyst at 0.3% of the total amount charged, and xylol was added as a refluxing solvent at 5% of the total amount charged. % added, 160~
The reaction was carried out at 230qo for 5 hours.
反応終了後、溶剤を留去し、触媒を炉別することにより
、目的のワックス状組成物を得た。以下同様にして、表
−1の実験No.1〜10のワックス状組成物を調整し
た。1‐2 物性
ワックス状組成物の組成比および一般性状を表一1に示
す。After the reaction was completed, the solvent was distilled off and the catalyst was separated in a furnace to obtain the desired waxy composition. Similarly, experiment No. 1 in Table 1 was used. Waxy compositions 1 to 10 were prepared. 1-2 Physical Properties The composition ratio and general properties of the waxy composition are shown in Table 1.
表 − 1 組成比および一般性状
※ 組成比(iii)の中の()内は、(i)と(ii
)のェステル化物の理論残存水酸基に対する(ili)
の量を示す次にワックス状組成物について、界面活性剤
の相溶性および成型性を調べた。Table-1 Composition ratio and general properties* The numbers in parentheses in composition ratio (iii) are (i) and (ii).
) for the theoretical residual hydroxyl group of the esterified product (ili)
Next, the compatibility of the surfactant and the moldability of the waxy composition were investigated.
結果を表−2に示す。相溶性試験は、ワックス状組成物
:界面活性剤(ポリオキシエチレンーオレイルエーテル
)=1:1(重量比)を、加熱溶解後、混合し、溶液の
状態を調べた。The results are shown in Table-2. In the compatibility test, the waxy composition: surfactant (polyoxyethylene-oleyl ether) = 1:1 (weight ratio) was heated and dissolved, then mixed, and the state of the solution was examined.
成型性については、相潟性試験で用いたワックス状組成
物と界面活性剤の混合液を型に入れて、室温まで冷却し
、こうして得られた固型物を、水の入ったビーカー中に
吊るし、マグネチツク・スターラ−にて3時間縄拝する
ことにより、型くずれの有無を調べた。Regarding moldability, the mixture of the waxy composition and surfactant used in the compatibility test was placed in a mold, cooled to room temperature, and the solid material thus obtained was placed in a beaker containing water. The sample was hung and stirred for 3 hours using a magnetic stirrer to check for deformation.
表 − 2 相溶性および成型」 △ やン型くずれのあったもの。Table 2 “Compatibility and molding” △ Yarn shape has deteriorated.
○ 型くずれのろかったもの。○ Things that are slow to lose their shape.
表−2の結果より相溶性、成型性いずれも良好な性能を
示した。From the results in Table 2, both compatibility and moldability showed good performance.
実施例 2 個型芳香消臭剤の調整
固化剤としてワックス状組成物を配合した水洗トイレ用
タンク投下型芳香消臭剤の次の配合例のように調製した
が、いずれも良好な性能であつた。Example 2 Adjustment of individual air freshener deodorizer A tank-type air freshener deodorizer for flushing toilets containing a waxy composition as a solidifying agent was prepared as shown in the following formulation example, but all had good performance. Ta.
配合例 1
ワックス状組成物(実験則o.6) 35%
(重量。Formulation example 1 Waxy composition (experimental rule o.6) 35%
(weight.
Claims (1)
鎖飽和脂肪族二塩基酸2及び炭素数12〜22の直鎖飽
和脂肪酸3のエステル化生成物であって、(1)1モル
に対し(2)0.5〜1モルを用い、かつ(1),(2
)を反応させて得られるエステルの残存水酸基の2/3
以下を(3)でエステル化してなるワツクス状組成物を
ゲル化剤乃至固化剤として用い、界面活性剤と香料を酸
合することを特徴とする。 水中に投下して使用するための固型芳香消臭剤。[Scope of Claims] 1. An esterification product of 1 a trihydric or higher polyhydric alcohol, 2 a linear saturated aliphatic dibasic acid having 4 to 20 carbon atoms, and 3 a linear saturated fatty acid having 12 to 22 carbon atoms. (2) 0.5 to 1 mol per 1 mol of (1), and (1), (2
) of the remaining hydroxyl groups of the ester obtained by reacting
It is characterized in that a wax-like composition obtained by esterifying the following with (3) is used as a gelling agent or solidifying agent, and a surfactant and a fragrance are acidified. A solid aromatic deodorizer that can be dropped into water.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56054960A JPS606659B2 (en) | 1981-04-14 | 1981-04-14 | solid fragrance deodorant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56054960A JPS606659B2 (en) | 1981-04-14 | 1981-04-14 | solid fragrance deodorant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57170259A JPS57170259A (en) | 1982-10-20 |
| JPS606659B2 true JPS606659B2 (en) | 1985-02-19 |
Family
ID=12985231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56054960A Expired JPS606659B2 (en) | 1981-04-14 | 1981-04-14 | solid fragrance deodorant |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS606659B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61122147U (en) * | 1985-01-20 | 1986-08-01 | ||
| JPS62238150A (en) * | 1986-04-07 | 1987-10-19 | Nissan Motor Co Ltd | Wiper control device |
| JPS62238151A (en) * | 1986-04-07 | 1987-10-19 | Nissan Motor Co Ltd | Device for controlling intermittent drive of wiper |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6337179A (en) * | 1986-07-31 | 1988-02-17 | Taiyo Koryo Kk | Transparent gelatinous aromatic composition |
| US7722894B2 (en) | 2001-10-22 | 2010-05-25 | Massachusetts Institute Of Technology | Biodegradable polymer |
| JP2009523864A (en) | 2006-01-12 | 2009-06-25 | マサチューセッツ インスティテュート オブ テクノロジー | Biodegradable elastomer |
| WO2008144514A2 (en) | 2007-05-17 | 2008-11-27 | Massachusetts Institute Of Technology | Polyol-based polymers |
-
1981
- 1981-04-14 JP JP56054960A patent/JPS606659B2/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61122147U (en) * | 1985-01-20 | 1986-08-01 | ||
| JPS62238150A (en) * | 1986-04-07 | 1987-10-19 | Nissan Motor Co Ltd | Wiper control device |
| JPS62238151A (en) * | 1986-04-07 | 1987-10-19 | Nissan Motor Co Ltd | Device for controlling intermittent drive of wiper |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57170259A (en) | 1982-10-20 |
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