JPWO2009013991A1 - 固形化した洗浄剤組成物およびその製造方法 - Google Patents
固形化した洗浄剤組成物およびその製造方法 Download PDFInfo
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- JPWO2009013991A1 JPWO2009013991A1 JP2009524438A JP2009524438A JPWO2009013991A1 JP WO2009013991 A1 JPWO2009013991 A1 JP WO2009013991A1 JP 2009524438 A JP2009524438 A JP 2009524438A JP 2009524438 A JP2009524438 A JP 2009524438A JP WO2009013991 A1 JPWO2009013991 A1 JP WO2009013991A1
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- chloride
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- same
- surfactant
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- 125000000217 alkyl group Chemical group 0.000 claims abstract description 25
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 19
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 17
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- -1 halogen ion Chemical group 0.000 claims description 49
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- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 claims description 4
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- HXWGXXDEYMNGCT-UHFFFAOYSA-M decyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)C HXWGXXDEYMNGCT-UHFFFAOYSA-M 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- FGEMVHCDHVPYQX-UHFFFAOYSA-M triethyl(tetradecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](CC)(CC)CC FGEMVHCDHVPYQX-UHFFFAOYSA-M 0.000 claims description 3
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- KTYABYYUGJUQOW-UHFFFAOYSA-M [Cl-].C(CCCCCCCCCCCCCCCCC)[N+](CC[Si](C)(C)C)(C)C Chemical compound [Cl-].C(CCCCCCCCCCCCCCCCC)[N+](CC[Si](C)(C)C)(C)C KTYABYYUGJUQOW-UHFFFAOYSA-M 0.000 claims description 2
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- PDDAPIMCOTWLRX-UHFFFAOYSA-M diethyl-octadecyl-(3-trimethoxysilylpropyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](CC)(CC)CCC[Si](OC)(OC)OC PDDAPIMCOTWLRX-UHFFFAOYSA-M 0.000 claims description 2
- HRBYCVPFYWTROV-UHFFFAOYSA-M dimethyl-octadecyl-(3-triethoxysilylpropyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCC[Si](OCC)(OCC)OCC HRBYCVPFYWTROV-UHFFFAOYSA-M 0.000 claims description 2
- IELHBSJGCUPYDX-UHFFFAOYSA-M dimethyl-octadecyl-[3-tri(propan-2-yloxy)silylpropyl]azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCC[Si](OC(C)C)(OC(C)C)OC(C)C IELHBSJGCUPYDX-UHFFFAOYSA-M 0.000 claims description 2
- OIYJQMZNRJJLJX-UHFFFAOYSA-M dodecyl(trimethyl)azanium;acetate Chemical compound CC([O-])=O.CCCCCCCCCCCC[N+](C)(C)C OIYJQMZNRJJLJX-UHFFFAOYSA-M 0.000 claims description 2
- XLGBLPNKBBGIQB-UHFFFAOYSA-M dodecyl-tri(propan-2-yl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C(C)C)(C(C)C)C(C)C XLGBLPNKBBGIQB-UHFFFAOYSA-M 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 2
- YXIONSMVVATJSX-UHFFFAOYSA-M heptadecyl-di(propan-2-yl)-(2-triethoxysilylethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCC[N+](C(C)C)(C(C)C)CC[Si](OCC)(OCC)OCC YXIONSMVVATJSX-UHFFFAOYSA-M 0.000 claims description 2
- FVOCUSGXQAQFAK-UHFFFAOYSA-M hexadecyl-dimethyl-(3-trimethoxysilylpropyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CCC[Si](OC)(OC)OC FVOCUSGXQAQFAK-UHFFFAOYSA-M 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 229940035429 isobutyl alcohol Drugs 0.000 claims description 2
- MWPGECNOSCRMII-UHFFFAOYSA-M octadecyl(tripropyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](CCC)(CCC)CCC MWPGECNOSCRMII-UHFFFAOYSA-M 0.000 claims description 2
- VQHINEGBLTYXBJ-UHFFFAOYSA-M octadecyl-dipropyl-(4-trimethoxysilylbutyl)azanium;acetate Chemical compound CC([O-])=O.CCCCCCCCCCCCCCCCCC[N+](CCC)(CCC)CCCC[Si](OC)(OC)OC VQHINEGBLTYXBJ-UHFFFAOYSA-M 0.000 claims description 2
- ZTXVWEKBRXHTRO-UHFFFAOYSA-M pentadecyl(tripropyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCC[N+](CCC)(CCC)CCC ZTXVWEKBRXHTRO-UHFFFAOYSA-M 0.000 claims description 2
- DGMKFQYCZXERLX-UHFFFAOYSA-N proglumide Chemical compound CCCN(CCC)C(=O)C(CCC(O)=O)NC(=O)C1=CC=CC=C1 DGMKFQYCZXERLX-UHFFFAOYSA-N 0.000 claims description 2
- 229960003857 proglumide Drugs 0.000 claims description 2
- WPPGURUIRLDHAB-UHFFFAOYSA-M triethyl(hexadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](CC)(CC)CC WPPGURUIRLDHAB-UHFFFAOYSA-M 0.000 claims description 2
- OWGHQYPQNSZTFQ-UHFFFAOYSA-M triethyl(octadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](CC)(CC)CC OWGHQYPQNSZTFQ-UHFFFAOYSA-M 0.000 claims description 2
- OPOYIRZGOYMLBV-UHFFFAOYSA-M triethyl(pentadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCC[N+](CC)(CC)CC OPOYIRZGOYMLBV-UHFFFAOYSA-M 0.000 claims description 2
- PGNGVFSZMOYXEM-UHFFFAOYSA-N triethyl(tridecyl)azanium Chemical compound CCCCCCCCCCCCC[N+](CC)(CC)CC PGNGVFSZMOYXEM-UHFFFAOYSA-N 0.000 claims description 2
- OHCYZUDVCRJREC-UHFFFAOYSA-M trimethyl(pentadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCC[N+](C)(C)C OHCYZUDVCRJREC-UHFFFAOYSA-M 0.000 claims description 2
- YCXLTTZJNXCOML-UHFFFAOYSA-N 3-triethoxysilylpropan-1-amine;hydrochloride Chemical compound Cl.CCO[Si](OCC)(OCC)CCCN YCXLTTZJNXCOML-UHFFFAOYSA-N 0.000 claims 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 claims 1
- 239000005695 Ammonium acetate Substances 0.000 claims 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 claims 1
- YXGARHNOYWRRRO-UHFFFAOYSA-M [Cl-].C(CCCCCCCCCCCCCCCCC)[N+](CCC[SiH2][Si](C(C)C)(C(C)C)C(C)C)(C)C Chemical compound [Cl-].C(CCCCCCCCCCCCCCCCC)[N+](CCC[SiH2][Si](C(C)C)(C(C)C)C(C)C)(C)C YXGARHNOYWRRRO-UHFFFAOYSA-M 0.000 claims 1
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- UZNSSUOXQKJMPY-UHFFFAOYSA-M heptadecyl-dimethyl-(3-trimethoxysilylpropyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCC[N+](C)(C)CCC[Si](OC)(OC)OC UZNSSUOXQKJMPY-UHFFFAOYSA-M 0.000 claims 1
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- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- SLYCYWCVSGPDFR-UHFFFAOYSA-N octadecyltrimethoxysilane Chemical compound CCCCCCCCCCCCCCCCCC[Si](OC)(OC)OC SLYCYWCVSGPDFR-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940072223 pentasa Drugs 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229950006451 sorbitan laurate Drugs 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 235000011067 sorbitan monolaureate Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- CEYYIKYYFSTQRU-UHFFFAOYSA-M trimethyl(tetradecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)C CEYYIKYYFSTQRU-UHFFFAOYSA-M 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- CWOBBUOEWRRVPD-UHFFFAOYSA-M tripropyl(tetradecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](CCC)(CCC)CCC CWOBBUOEWRRVPD-UHFFFAOYSA-M 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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Abstract
Description
前記ケイ素含有化合物に、(b)陽イオン界面活性剤(ただし、上記ケイ素化合物を除く)(b1)および非イオン界面活性剤(b2)からなる群から選ばれた少なくとも1種の界面活性剤を添加した溶液を調製する工程、および該溶液を減圧乾燥する工程を有することを特徴とする、前記ケイ素含有化合物のゲル化を防止する方法も提供する。
前記ケイ素化合物の溶液を減圧乾燥する工程、および上記工程で得られた減圧乾燥物に(b)陽イオン界面活性剤(ただし、上記ケイ素化合物を除く)(b1)および非イオン界面活性剤(b2)からなる群から選ばれた少なくとも1種の界面活性剤を添加する工程を有することを特徴とする、前記ケイ素含有化合物のゲル化を防止する方法も提供する。
抗菌性洗浄剤であるオクタデシルジメチル(3−トリメトキシシリルプロピル)アンモニウムクロライド(以下QAS)の原液(メタノール溶液)に、陽イオン界面活性剤であるヘキサデシルトリメチルアンモニウム(以下HD)を添加し、さらに共沸させるためにアセトンまたはエタノールを添加した試料溶液を作製し,70℃で共沸させたが,固形化には至らなかった。得られたゲル化物に水道水を5mL添加したが、多くの試料でゲル化が高度に進み、数分〜1時間の間に固形化し、実用化には適しなかった(表1)。
QAS原液を固形化し、そのまま、あるいは界面活性剤を添加して再溶解したサンプルの抗菌性について評価した。すなわち、QAS原液1mLを凍結乾燥した後に固形化し、そのこの固形化物を(1)そのまま(QASのみ)、(2)QAS固形化物にPO 1mLを添加したもの、(3)QAS固形化物にHD 0.1mgを添加したもの、の上記(1)〜(3)を10mLの蒸留水(MQ)で再度溶解した。なおこの時点で10倍希釈となっている。各々の再溶解液を10倍ずつ段階希釈したサンプル900μLに、1×106cells/mLに調整したC. albicans IFO1385株の菌液を40μL加え、さらに1mLのサブロー培地を添加し,37℃で72時間培養し,抗菌性を検討した。
(1)QAS原液1mL、(2)QAS原液1mL+PO 1mL、(3)QAS原液+HD 0.1mgの各サンプルを凍結乾燥して固形化し、10mLの蒸留水(MQ)に再度溶解した。この時点で×10希釈となる。
Claims (26)
- (a)一般式(1)
- 前記減圧乾燥を−30℃〜―60℃で行うことを特徴とする、請求項1または2記載の固形化した洗浄剤組成物。
- 上記一般式(1)で表されるケイ素含有化合物(a)のR1は炭素原子数10〜25のアルキル基を示し、R2およびR3は同一または異なっていてもよい炭素原子数1ないし6の低級アルキル基を示し、R4は炭素原子数1ないし6の低級アルキレン基を示し、R5、R6およびR7は同一または異なっていてもよい炭素原子数1ないし6の低級アルキル基またはアルコシ基を示し、Xはハロゲンイオンまたは有機カルボキニルオキシイオンであることを特徴とする請求項1ないし3のいずれか1項に記載の固形化した洗浄剤組成物。
- 上記一般式(1)で表されるケイ素含有化合物(a)が、オクタデシルジメチル(3−トリメトキシシリルプロピル)アンモニムクロライド、オクタデシルジエチル(3−トリメトキシシリルプロピル)アンモニウムクロライド、オクタデシルジメチル(2−トリメチルシリルエチル)アンモニウムクロライド、オクタデシルジプロピル(4−トリメトキシシリルブチル)アンモニムアセテート、オクタデシルジメチル(3−トリエトキシシリルプロビル)アンモニウムクロライド、オクタデシルジメチル(3−トリイソプロポキシシリルプロビル)アンモニウムクロライド、オクタデシルジメチル(3−トリエチルシシリルプロビル)アンモニウムクロライド、オクタデシルジメチル(3−トリイソプロピルシシリルプロビル)アンモニウムクロライド、ヘプタデシルジメチル(3−トリメトキシシリルプロピル)アンモニウムクロライド、ヘプタデシルジイソプロピル(2−トリエトキシシリルエチル)アンモニウムクロライド、ヘキサデシルジメチル(3−トリメトキシシリルプロピル)アンモニムクロライド、ヘキサデシルジメチル(3−トリメトキシシリルプロピル)アンモニムアセテートおよびペンタサデシルジメチル(3−トリエトキシシリルプロピル)アンモニムクロライドからなる群から選ばれた少なくとも1種のケイ素含有化合物であることを特徴とする請求項1ないし4のいずれか1項に記載の固形化した洗浄剤組成物。
- 上記一般式(1)で表されるケイ素含有化合物(a)が、オクタデシルジメチル(3−トリメトキシシリルプロピル)アンモニウムクロライドである請求項1ないし5のいずれか1項に記載の固形化した洗浄剤組成物。
- 上記一般式(2)で表される上記陽イオン界面活性剤(b11)のR11は炭素原子数10〜25のアルキル基を示し、R12、R13およびR14は同一または異なっていてもよい炭素原子数1ないし6の低級アルキル基を示し、Yがハロゲンイオンまたは有機カルボニルオキシイオンであることを特徴とする請求項7に記載の固形化した洗浄剤組成物。
- 上記陽イオン界面活性剤(b11)がデシルトリメチルアンモニウムクロライド、デシルトリエチルアンモニウムアセテート、ドデシルトリメチルアンモニウムアセテート、ドデシルトリイソプロピルアンモニウムブロマイド、トリデシルトリエチルアンモニウムプロマイド、テトラデシルトリメチルアンモニウムクロライド、テトラデシルトリエチルアンモニウムクロライド、テトラデシルトリ−n−プロピルアンモニウムクロライド、ペンタデシルトリメチルアンモニウムクロライド、ペンタデシルトリエチルアンモニウムクロライド、ペンタデシルトリ−n−プロピルアンモニウムクロライド、ヘキサデシルトリメチルアンモニウムクロライド、ヘキサデシルトリエチルアンモニウムクロライド、ヘキサデシルトリ−n−プロピルアンモニウムクロライド、オクタデシルトリメチルアンモニウムクロライドおよびオクタデシルトリエチルアンモニウムクロライドおよびオクタデシルトリ−n−プロピルアンモニウムクロライドからなる群から選ばれた少なくとも1種であることを特徴とする請求項7または8に記載の固形化した洗浄剤組成物。
- 上記陽イオン界面活性剤(b1)が、ヘキサデシルトリメチルアンモニウムクロライドであることを特徴とする請求項1ないし9のいずれか1項に記載の固形化した洗浄剤組成物。
- 上記非イオン界面活性剤(b2)が、ポリオキシエチレン単位および/またはポリオキシプロピレン単位を含有するポリオキシアルキレングリコールのアルキルエーテルまたは脂肪酸エステル、ソルビタン脂肪酸エステルおよび脂肪酸モノグリセライドからなる群から選ばれた少なくとも1種の非イオン系界面活性剤であることを特徴とする請求項1ないし6のいずれか1項に記載の固形化した洗浄剤組成物。
- 上記非イオン界面活性剤(b2)は、ポリオキシエチレンソルビタンモノラウレートであることを特徴とする請求項1ないし6、11のいずれか1項に記載の固形化した洗浄剤組成物。
- 上記ケイ素含有化合物(a)としてオクタデシルジメチル(3−トリメトキシシリルプロピル)アンモニウムクロライド、および上記陽イオン界面活性剤(b1)としてヘキサデシルトリメチルアンモニウムクロライドを含有することを特徴とする請求項1ないし10のいずれか1項に記載の固形化した洗浄剤組成物。
- 上記ケイ素含有化合物(a)としてオクタデシルジメチル(3−トリメトキシシリルプロピル)アンモニウムクロライド、および上記非イオン界面活性剤(b2)としてポリオキシエチレンソルビタンモノラウレートを含有することを特徴とする請求項1ないし6、11ないし12のいずれか1項に記載の固形化した洗浄剤組成物。
- 必要に応じて更に炭素数10以下の低級アルコールを含有することを特徴とする請求項1ないし14のいずれか1項に記載の固形化した洗浄剤組成物。
- 前記低級アルコールが炭素数5以下のアルコールであることを特徴とする請求項15に記載の固形化した洗浄剤組成物。
- 前記低級アルコールがエタノール、t−ブチルアルコール、プロピルアルコール、n-ブチルアルコール、イソブチルアルコール、sec-ブチルアルコール、tert-ブチルアルコールおよびペンチルアルコールからなる群から選ばれたものであることを特徴とする請求項15または16に記載の固形化した洗浄剤組成物。
- 水道水に再溶解可能であることを特徴とする請求項1ないし17のいずれか1項に記載の固形化した洗浄剤組成物。
- (a)一般式(1)
該溶液を減圧乾燥する工程を有することを特徴とする、固形化した洗浄剤組成物の製造方法。 - (a)一般式(1)
上記工程で得られた減圧乾燥物に(b)陽イオン界面活性剤(ただし、上記ケイ素化合物を除く)(b1)および非イオン界面活性剤(b2)からなる群から選ばれた少なくとも1種の界面活性剤を添加する工程を有することを特徴とする、固形化した洗浄剤組成物の製造方法。 - 前記減圧乾燥を、−30℃〜―60℃で行うことを特徴とする、請求項19または20に記載の方法。
- 必要に応じて前記溶液に更に炭素数10以下の低級アルコールを添加する工程を有することを特徴とする、請求項19〜21のいずれか1項に記載の方法。
- (a)一般式(1)
前記ケイ素含有化合物に、(b)陽イオン界面活性剤(ただし、上記ケイ素化合物を除く)(b1)および非イオン界面活性剤(b2)からなる群から選ばれた少なくとも1種の界面活性剤を添加した溶液を調製する工程、および
該溶液を減圧乾燥する工程を有することを特徴とする、前記ケイ素含有化合物のゲル化を防止する方法。 - (a)一般式(1)
前記ケイ素化合物の溶液を減圧乾燥する工程、および
上記工程で得られた減圧乾燥物に(b)陽イオン界面活性剤(ただし、上記ケイ素化合物を除く)(b1)および非イオン界面活性剤(b2)からなる群から選ばれた少なくとも1種の界面活性剤を添加する工程を有することを特徴とする、前記ケイ素含有化合物のゲル化を防止する方法。 - 前記減圧乾燥を、−30℃〜―60℃で行うことを特徴とする、請求項23または24に記載の方法。
- 必要に応じて前記溶液に更に炭素数10以下の低級アルコールを添加する工程を有することを特徴とする、請求項23〜25のいずれか1項に記載の方法。
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EP (1) | EP2186873A4 (ja) |
JP (1) | JP5424482B2 (ja) |
KR (1) | KR20100051672A (ja) |
CN (1) | CN101809137B (ja) |
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CN1117395C (zh) | 1994-03-18 | 2003-08-06 | 日立化成工业株式会社 | 半导体组件的制造方法及半导体组件 |
US9278107B2 (en) | 2008-12-25 | 2016-03-08 | Hiroshima University | Antibacterial agent composition and antiviral agent composition comprising silicon-containing compound; antibacterializing method, cleaning/mouth rinsing method; method for fixing antibacterial agent and antiviral agent |
CN103535372B (zh) * | 2013-10-09 | 2017-02-15 | 江苏惠兴康科技有限公司 | 可固化复合季铵盐、制备方法及其消毒抗菌灭菌应用 |
KR20160129449A (ko) | 2015-04-30 | 2016-11-09 | 주식회사 아오스 | 의치 세정제 |
JP2021070672A (ja) * | 2019-11-01 | 2021-05-06 | ジェクス株式会社 | 害虫忌避剤 |
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US4005028A (en) * | 1975-04-22 | 1977-01-25 | The Procter & Gamble Company | Organosilane-containing detergent composition |
JPH0788280B2 (ja) | 1987-02-09 | 1995-09-27 | 大塚化学株式会社 | 抗菌性ウイスカ− |
US5411585A (en) * | 1991-02-15 | 1995-05-02 | S. C. Johnson & Son, Inc. | Production of stable hydrolyzable organosilane solutions |
JPH05295002A (ja) | 1992-04-23 | 1993-11-09 | Nichiden Kagaku Kk | 抗菌性澱粉、水溶性多糖類及びその製造方法 |
US6740626B2 (en) * | 1996-04-02 | 2004-05-25 | S.C. Johnson & Son, Inc. | Acidic cleaning formulation containing a surface modification agent and method of applying the same |
US5959014A (en) * | 1996-05-07 | 1999-09-28 | Emory University | Water-stabilized organosilane compounds and methods for using the same |
US6632805B1 (en) | 1996-05-07 | 2003-10-14 | Emory University | Methods for using water-stabilized organosilanes |
WO1999056714A1 (fr) | 1998-04-30 | 1999-11-11 | Kyowa Limited | Bactericide pour detergent |
JP4570196B2 (ja) | 2000-03-31 | 2010-10-27 | 小林製薬株式会社 | 義歯洗浄剤 |
US6528472B2 (en) * | 2000-11-17 | 2003-03-04 | S.C. Johnson & Son, Inc. | Antimicrobial compositions containing quaternary ammonium compounds, silanes and other disinfectants with furanones |
GB0207850D0 (en) | 2002-04-04 | 2002-05-15 | Unilever Plc | Fabric treatment compositions |
JP3834655B2 (ja) | 2002-12-16 | 2006-10-18 | 国立大学法人広島大学 | 抗菌性材料、及びその製造方法 |
GB2407581A (en) * | 2003-11-01 | 2005-05-04 | Reckitt Benckiser Inc | Hard surface cleaning and disinfecting compositions |
US8999363B2 (en) * | 2005-02-07 | 2015-04-07 | Sishield Technologies, Inc. | Methods and compositions for antimicrobial surfaces |
WO2006086271A2 (en) * | 2005-02-07 | 2006-08-17 | Jacques Elfersy | Methods and compositions for biocidal treatments |
US7704313B2 (en) | 2005-07-06 | 2010-04-27 | Resource Development L.L.C. | Surfactant-free cleansing and multifunctional liquid coating composition containing nonreactive abrasive solid particles and an organosilane quaternary compound and methods of using |
US7754004B2 (en) * | 2005-07-06 | 2010-07-13 | Resource Development, L.L.C. | Thickened surfactant-free cleansing and multifunctional liquid coating compositions containing nonreactive abrasive solid particles and an organosilane quaternary compound and methods of using |
JP4810150B2 (ja) * | 2005-07-22 | 2011-11-09 | 国立大学法人広島大学 | 抗菌剤水溶液及びその保存方法 |
JP4972743B2 (ja) * | 2005-11-04 | 2012-07-11 | 国立大学法人広島大学 | 洗浄剤組成物および洗浄方法 |
CN1314320C (zh) * | 2005-11-30 | 2007-05-09 | 山东大学 | 一种有机硅季铵盐杀菌剂的制备方法 |
CN101394747B (zh) * | 2006-03-02 | 2013-04-24 | 威泰克专业化学有限公司 | 水稳定的抗菌有机硅烷产物、组合物及其使用方法 |
US8367595B2 (en) * | 2006-06-20 | 2013-02-05 | Reckitt Benckiser Llc | Solid treatment blocks for sanitary appliances |
ATE426654T1 (de) * | 2006-07-31 | 2009-04-15 | Reckitt Benckiser Uk Ltd | Verbesserte reinigungsmittel fur feste oberflachen |
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US8304379B2 (en) | 2012-11-06 |
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AU2008278417B2 (en) | 2013-07-25 |
CN101809137B (zh) | 2012-02-29 |
EP2186873A1 (en) | 2010-05-19 |
AU2008278417A1 (en) | 2009-01-29 |
WO2009013991A1 (ja) | 2009-01-29 |
EP2186873A4 (en) | 2012-06-27 |
CN101809137A (zh) | 2010-08-18 |
US20100190683A1 (en) | 2010-07-29 |
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