JP5148998B2 - 恒温槽用清浄剤 - Google Patents
恒温槽用清浄剤 Download PDFInfo
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- JP5148998B2 JP5148998B2 JP2007506010A JP2007506010A JP5148998B2 JP 5148998 B2 JP5148998 B2 JP 5148998B2 JP 2007506010 A JP2007506010 A JP 2007506010A JP 2007506010 A JP2007506010 A JP 2007506010A JP 5148998 B2 JP5148998 B2 JP 5148998B2
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- group
- acid
- detergent
- aminopropyl
- surfactant
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- 239000003599 detergent Substances 0.000 title claims description 104
- -1 polyoxyethylene Polymers 0.000 claims description 229
- 239000002253 acid Substances 0.000 claims description 39
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 29
- 125000004432 carbon atom Chemical group C* 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 239000003755 preservative agent Substances 0.000 claims description 23
- 239000004094 surface-active agent Substances 0.000 claims description 22
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 21
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims description 20
- 230000000694 effects Effects 0.000 claims description 19
- JGFDZZLUDWMUQH-UHFFFAOYSA-N Didecyldimethylammonium Chemical group CCCCCCCCCC[N+](C)(C)CCCCCCCCCC JGFDZZLUDWMUQH-UHFFFAOYSA-N 0.000 claims description 18
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 18
- 239000003153 chemical reaction reagent Substances 0.000 claims description 18
- 229940078672 didecyldimethylammonium Drugs 0.000 claims description 18
- 229910052708 sodium Inorganic materials 0.000 claims description 18
- 239000011734 sodium Substances 0.000 claims description 18
- 230000002335 preservative effect Effects 0.000 claims description 17
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- 150000005215 alkyl ethers Chemical class 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 12
- BACYUWVYYTXETD-UHFFFAOYSA-N N-Lauroylsarcosine Chemical compound CCCCCCCCCCCC(=O)N(C)CC(O)=O BACYUWVYYTXETD-UHFFFAOYSA-N 0.000 claims description 11
- 108700004121 sarkosyl Proteins 0.000 claims description 11
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- 239000002280 amphoteric surfactant Substances 0.000 claims description 6
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical group OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 5
- ZIDSRMWDSUOESX-UHFFFAOYSA-N 4-methylheptadecane-1,5,5-triamine Chemical compound CCCCCCCCCCCCC(N)(N)C(C)CCCN ZIDSRMWDSUOESX-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
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- 229910052799 carbon Inorganic materials 0.000 claims description 4
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- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 claims 1
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- 125000001931 aliphatic group Chemical group 0.000 description 11
- 125000001183 hydrocarbyl group Chemical group 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- 229960000686 benzalkonium chloride Drugs 0.000 description 10
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 10
- 210000002966 serum Anatomy 0.000 description 10
- 125000001424 substituent group Chemical group 0.000 description 10
- 229920001817 Agar Polymers 0.000 description 9
- 102000004190 Enzymes Human genes 0.000 description 9
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- 239000008272 agar Substances 0.000 description 9
- 239000012153 distilled water Substances 0.000 description 9
- 230000005484 gravity Effects 0.000 description 9
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- 102000004169 proteins and genes Human genes 0.000 description 9
- 108090000623 proteins and genes Proteins 0.000 description 9
- 239000011550 stock solution Substances 0.000 description 9
- 235000014469 Bacillus subtilis Nutrition 0.000 description 8
- 101710098398 Probable alanine aminotransferase, mitochondrial Proteins 0.000 description 8
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 238000002835 absorbance Methods 0.000 description 7
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- 238000003860 storage Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
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- 238000010521 absorption reaction Methods 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
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- 125000004122 cyclic group Chemical group 0.000 description 5
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- 238000013112 stability test Methods 0.000 description 5
- 230000001954 sterilising effect Effects 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000005639 Lauric acid Substances 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 4
- 238000011481 absorbance measurement Methods 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 235000001014 amino acid Nutrition 0.000 description 4
- 229940024606 amino acid Drugs 0.000 description 4
- 230000002421 anti-septic effect Effects 0.000 description 4
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 4
- 239000002504 physiological saline solution Substances 0.000 description 4
- 229910052697 platinum Inorganic materials 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 4
- YQUVCSBJEUQKSH-UHFFFAOYSA-N 3,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 229920001214 Polysorbate 60 Polymers 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 229960003237 betaine Drugs 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 239000003093 cationic surfactant Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
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- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
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- 229910052700 potassium Inorganic materials 0.000 description 3
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- KSAVQLQVUXSOCR-UHFFFAOYSA-N sodium;2-[dodecanoyl(methyl)amino]acetic acid Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC(O)=O KSAVQLQVUXSOCR-UHFFFAOYSA-N 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
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- PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
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- QDSWHSQBAUPQGK-UHFFFAOYSA-K trisodium;dodecyl hydrogen phosphate;dodecyl phosphate Chemical compound [Na+].[Na+].[Na+].CCCCCCCCCCCCOP(O)([O-])=O.CCCCCCCCCCCCOP([O-])([O-])=O QDSWHSQBAUPQGK-UHFFFAOYSA-K 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic with cationic compounds
-
- C—CHEMISTRY; METALLURGY
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Description
又は/及び両性界面活性能を有する防腐剤と、界面活性剤を含む恒温槽用清浄剤。
(2)上記(1)記載の清浄剤を恒温槽に添加することを特徴とする、恒温槽の清浄方法。
の構造を持つN−ビス(3−アミノプロピル)ドデシルアミン、3−アミノプロピル−ドデシルプロパンジアミン、1,3−プロパンジアミン−3−アミノプロピル−N−ドデシルが、特にN-ビス(3−アミノプロピル)ドデシルアミンが好ましい。
以下に実施例を挙げて、本発明を更に詳細に説明するが、本発明は、これにより何等限定されるものではない。
(1)薬剤及び試験菌
1)薬剤
ジデシルジメチルアンモニウムアジペート(DDAA)、N-ビス(3-アミノプロピル)ドデシルアミン(TAA)及び塩化ベンザルコニウム(BC)を用いた。
2)試験菌
Bacillus subtilis(枯草菌、NBRC13719)、Escherichia coli(大腸菌、NBRC3972)、Pseudonas aeruginosa(緑膿菌、NBRC12689)、Staphylococcus aureus(黄色ブドウ球菌、NBRC12732)、Aspergillus niger(黒コウジカビ、NBRC6341)、Chaetomium globosum(クロカワカビ、NBRC6347)、Cladosporium cladosporioides(NBRC6348)、Penicillium citrinum(青カビ属、NBRC6352)及びTrichoderma viride(ツチアオカビ属、NBRC31831)を用いた。
直径90mmの滅菌シャーレに、各薬剤を蒸留水で希釈した水溶液を、全量20mLに調製した場合の薬剤濃度が所定の濃度となるように取り、次いで、シャーレに滅菌水を、滅菌水と薬剤水溶液の合計が2mLとなるように入れた。更に、シャーレに、高圧蒸気滅菌して50℃±2℃に保存しておいた普通寒天培地を18mL入れ、固化させて、寒天平板培地を得た。
(3)抗菌力評価方法
予めブイヨン培地で1×108個/mLになるまで培養した各種試験菌を、滅菌生理食塩水で100倍に希釈した(1×106個/mL)。次いで白金耳を用いて、調製した試験菌溶液を(2)の寒天平板培地表面に塗抹し、35℃±2℃で24時間培養した。
培養後、培地表面における菌の生育の有無を確認し、菌の生育が認められない最小の薬剤濃度を、その薬剤の最小発育阻止濃度(MIC、μg/mL)とした。
結果を表1に示す。
また、表1に示した各菌体の略称は、夫々下記の通りである。
B.s=Bacillus subtilis=枯草菌(NBRC13719)
E.c=Escherichia coli=大腸菌(NBRC3972)
P.a=Pseudonas aeruginosa=緑膿菌(NBRC12689)
S.a=Staphylococcus aureus=黄色ブドウ球菌(NBRC12732)
A.n=Aspergillus niger=黒コウジカビ(NBRC6341)
C.g=Chaetomium globosum=クロカワカビ(NBRC6347)
Cl.cl=Cladosporium cladosporioides(NBRC6348)
P.c=Penicillium citrinum=青カビ属(NBRC6352)
T.v=Trichoderma viride=ツチアオカビ属(NBRC31831)
(1)薬剤及び試験菌
1)薬剤
ジデシルジメチルアンモニウムアジペート(DDAA)、N-ビス(3-アミノプロピル)ドデシルアミン(TAA)及び塩化ベンザルコニウム(BC)を用いた。
2)試薬溶液
・GOT(グルタミン酸オキサロ酢酸トランスアミナーゼ)溶液:LタイプワコーGOT ・J2キット(和光純薬工業(株)製)のGOT基質酵素液及びGOT・L2α-KG溶液を、蒸留水で0.2w/w%水溶液になるように調製した。
・GPT(グルタミン酸ピルビン酸トランスアミナーゼ)溶液:LタイプワコーGPT ・J2キット(和光純薬工業(株)製)のGPT基質酵素液及びGPT・L2α-KG溶液を、蒸留水で0.2w/w%水溶液になるように調製した。
・血清:コントロール血清IIワコー(和光純薬工業(株)製)を蒸留水で0.2w/w%水溶液になるように調製した。
3)試験菌
Bacillus subtilis(枯草菌、NBRC13719)、Escherichia coli(大腸菌、NBRC3972)、Pseudonas aeruginosa(緑膿菌、NBRC12689)及びStaphylococcus aureus(黄色ブドウ球菌、NBRC12732)を用いた。
直径90mmの滅菌シャーレに、各薬剤を蒸留水で希釈した水溶液を、全量20mLに調製した場合の薬剤濃度が所定の濃度となるように、また試薬中の各成分(GOT、GPT、血清)の終濃度が、全量20mLに調製した場合に100μg/mLとなるように、薬剤水溶液と試薬溶液を夫々シャーレに取り、次いで、シャーレに滅菌水を、滅菌水と薬剤水溶液と試薬溶液との合計が2mLとなるように入れた。更に、シャーレに、高圧蒸気滅菌して50℃±2℃に保存しておいた普通寒天培地を18mL入れ、固化させて、寒天平板培地を得た。また、対照として薬剤溶液の代わりに純水を入れた寒天平板培地も調製した。
(3)抗菌力評価方法
予めブイヨン培地で1×108個/mLになるまで培養した各種試験菌を、滅菌生理食塩水で100倍に希釈した(1×106個/mL)。次いで白金耳を用いて、調製した試験菌溶液を(2)の寒天平板培地表面に塗抹し、35℃±2℃で24時間培養した。
培養後、培地表面における菌の生育の有無を確認し、菌の生育が認められない最小の薬剤濃度を、その薬剤の最小発育阻止濃度(MIC、μg/mL)とした。
結果を表2に示す。
また、表2に示した各菌体の略称は、夫々下記の通りである。
B.s=Bacillus subtilis=枯草菌(NBRC13719)
E.c=Escherichia coli=大腸菌(NBRC3972)
P.a=Pseudonas aeruginosa=緑膿菌(NBRC12689)
S.a=Staphylococcus aureus=黄色ブドウ球菌(NBRC12732)
一方、BCは、蛋白質が共存すると抗菌力が低下し、恒温槽用清浄剤に用いるのには好ましいものとはいえないことが判った。
(1)薬剤及び試験菌等
1)薬剤
ジデシルジメチルアンモニウムアジペート(DDAA)、N-ビス(3-アミノプロピル)ドデシルアミン(TAA)及び塩化ベンザルコニウム(BC)を、夫々蒸留水で1w/w%となるように調製した。
2)試薬溶液
・GOT溶液:LタイプワコーGOT ・J2キット(和光純薬工業(株)製)のGOT基質酵素液及びGOT・L2α-KG溶液を、蒸留水で0.1w/w%水溶液になるように調製した。
・GPT溶液:LタイプワコーGPT ・J2キット(和光純薬工業(株)製)のGPT基質酵素液及びGPT・L2α-KG溶液を、蒸留水で0.1w/w%水溶液になるように調製した。
・血清:コントロール血清IIワコー(和光純薬工業(株)製)を蒸留水で0.1w/w%水溶液になるように調製した。
3)試験菌
Bacillus subtilis(枯草菌、NBRC13719)、Escherichia coli(大腸菌、NBRC3972)、Pseudonas aeruginosa(緑膿菌、NBRC12689)及びStaphylococcus aureus(黄色ブドウ球菌、NBRC12732)を用いた。
i)予めブイヨン培地で1×108個/mLになるまで培養した各種試験菌を、滅菌生理食塩水で100倍に希釈して試験菌溶液とした(1×106個/mL)。
ii)予め乾熱滅菌しておいた20mLのガラス製試験管に、薬剤水溶液、試薬溶液、及び上記i)で調製した試験菌溶液を、全量10mLに調製した場合に、薬剤の終濃度が50μg/mLに、試薬の終濃度が100μg/mLに、試験菌が1×105個/mLになるように入れ、十分に攪拌した。
iii)一定時間(5分、10分、15分)経過後、上記ii)で得られた溶液を、予め調製しておいた普通寒天平板培地表面に、白金耳を用いて塗抹し、35℃±2℃で24時間培養した。
iv)培養後、培地表面における菌の生育の有無を確認した。
結果を表3に示す。
表3に於いて、培地表面に菌の生育が認められた場合を+、培地表面に菌の生育が認められなかった場合を−で夫々示す。
表3に示した各菌体の略称は、実験例2で記載した通りである。
実験例1〜3の結果より、ジデシルジメチルアンモニウムアジペート及びN-ビス(3-アミノプロピル)ドデシルアミンが抗菌力、殺菌力共に優れていることが判ったので、これを含有する本発明の恒温槽用清浄剤を調製した。そして、本発明の恒温槽用清浄剤と、従来の恒温槽用清浄剤について、各種菌に対する殺菌力の比較を行った。
ジデシルジメチルアンモニウムアジペート 5.6w/w%、N-ビス(3-アミノプロピル)ドデシルアミン 2.4w/w%、EDTA4Na 0.02w/w%、ポリオキシエチレンアルキルエーテル 4.5w/w%、ラウロイルサルコシンナトリウム 0.5w/w%となるように純水に溶解し、水酸化ナトリウム水溶液でpH11.4に調製し、本発明の恒温槽用清浄剤とした。
(2)従来の恒温槽用清浄剤の調製
ポリオキシエチレンノニルフェニルエーテル:モノエテノールアミン:蒸留水=20:5:5:70の重量比となるように混合したものを調製し、従来の恒温槽用清浄剤とした。
(3)試験菌
Bacillus subtilis(枯草菌、NBRC13719)、Escherichia coli(大腸菌、NBRC3972)、Pseudonas aeruginosa(緑膿菌、NBRC12689)、Staphylococcus aureus(黄色ブドウ球菌、NBRC12732)を用いた。
i)予めブイヨン培地で1×108個/mLになるまで培養した各種試験菌を、滅菌生理食塩水で100倍に希釈して試験菌溶液とした(1×106個/mL)。
ii)予め乾熱滅菌しておいた20mLのガラス製試験管に、本発明の恒温槽用清浄剤又は従来の恒温槽用清浄剤を、全量10mLに調製した場合の濃度が所定の濃度(0.05w/w%、0.1w/w%、0.2w/w%)となるように入れた。次いで該試験管に、上記i)で得られた試験菌溶液を、恒温槽用清浄剤と試験菌溶液の合計が10μlとなるように入れた。
iii) 一定時間(5分、10分、15分)経過後、上記ii)で得られた試験菌溶液を、予め調製しておいた普通寒天平板培地表面に、白金耳を用いて塗抹し、35℃±2℃で24時間培養した。
iv)培養後、培地表面における菌の生育の有無を確認し、菌の生育が認められない最小の恒温槽用清浄剤の濃度を求めた。
結果を表4示す。
表4に於いて、培地表面に菌の発育が認められた場合を+、培地表面に菌の発育が認められなかった場合を−で夫々示す。
表4に示した各菌体の略称は、実験例2で記載した通りである。
尚、表4に於いて、各濃度の本発明の恒温槽用清浄剤中の、各成分の終濃度は夫々以下の通りである。
恒温槽用清浄剤の濃度が0.1w/w%の場合、ジデシルジメチルアンモニウムアジペートは0.0056w/w%、N-ビス(3-アミノプロピル)ドデシルアミンは0.0024w/w%、EDTA4Naは0.00002w/w%、ポリオキシエチレンアルキルエーテルは0.0045w/w%、ラウロイルサルコシンナトリウムは0.0005w/w%である。
恒温槽用清浄剤の濃度が0.2w/w%の場合、ジデシルジメチルアンモニウムアジペートは0.0112w/w%、N-ビス(3-アミノプロピル)ドデシルアミンは0.0048w/w%、EDTA4Naは0.00004w/w%、ポリオキシエチレンアルキルエーテルは0.009w/w%、ラウロイルサルコシンナトリウムは0.001w/w%である。
(1)本発明の恒温槽用清浄剤の調製
ジデシルジメチルアンモニウムアジペート 5.6w/w%、EDTA4Na 0.02w/w%、ポリオキシエチレンアルキルエーテル 4.5w/w%、ラウロイルサルコシンナトリウム 0.5w/w%となるように純水に溶解し、水酸化ナトリウム水溶液でpH11.4に調製し、本発明の恒温槽用清浄剤とした。
上記(1)で調製した本発明の清浄剤の原液またはこれを純水で0.2w/w%に希釈したものを、室温又は40℃の恒温水槽に入れ、上部を透明フィルムで覆った後、放置した。所定期間放置後、恒温水槽の水の、外観、比重(20℃)、粘度(mm 2 /s, 25℃)、pH、及び800〜400nm,340nm,300nmでの吸光度を測定した。また、実験例1と同様の方法で抗菌力を、実施例1と同様の方法で5分間処理に於ける殺菌力を試験した。室温で保存した場合の結果を表5に、40℃で保存した場合の結果を表6に夫々示す。
また、各表に示した各菌体の略称は、実験例2で記載した通りである。
以上のことから、本発明の恒温槽用清浄剤は、長期間の保存安定性に優れていることが判った。
(1)本発明の恒温槽用清浄剤の調製
N-ビス(3-アミノプロピル)ドデシルアミン 2.4w/w%、EDTA4Na 0.02w/w%、ポリオキシエチレンアルキルエーテル 4.5w/w%、ラウロイルサルコシンナトリウム 0.5w/w%となるように純水に溶解し、水酸化ナトリウム水溶液でpH11.4に調製し、本発明の恒温槽用清浄剤とした。
上記(1)で調製した本発明の清浄剤の原液またはこれを純水で0.2w/w%に希釈したものを、室温又は40℃の恒温水槽に入れ、上部を透明フィルムで覆った後、放置した。所定期間放置後、恒温水槽の水の、外観、比重(20℃)、粘度(mm 2 /s, 25℃)、pH、及び800〜400nm,340nm,300nmでの吸光度を測定した。また、実験例1と同様の方法で抗菌力を、実施例1と同様の方法で5分間処理に於ける殺菌力を試験した。室温で保存した場合の結果を表7に、40℃で保存した場合の結果を表8に夫々示す。
また、各表に示した各菌体の略称は、実験例2で記載した通りである。
以上のことから、本発明の恒温槽用清浄剤は、長期間の保存安定性に優れていることが判った。
実施例1で調製した本発明の清浄剤の原液またはこれを純水で0.2w/w%に希釈したものを、室温又は40℃の恒温水槽に入れ、上部を透明フィルムで覆った後、放置した。所定期間放置後、恒温水槽の水の、外観、比重(20℃)、粘度(mm 2 /s, 25℃)、pH、及び800〜400nm,340nm,300nmでの吸光度を測定した。また、実験例1と同様の方法で抗菌力を、実施例1と同様の方法で5分間処理に於ける殺菌力を試験した。室温で保存した場合の結果を表9に、40℃で保存した場合の結果を表10に夫々示す。
また、各表に示した各菌体の略称は、実験例2で記載した通りである。
以上のことから、本発明の恒温槽用清浄剤は、長期間の保存安定性に優れていることが判った。
Claims (14)
- (1)下記一般式[I]で示される第4級アンモニウム塩
(式中、R1〜R4はそれぞれ独立してアルキル基を示す。但し、R1〜R4のうち、少なくとも一つは炭素数8〜18のアルキル基であり、且つ少なくとも一つは炭素数1〜3の低級アルキル基である。X―は炭素数2以上のカルボン酸由来のアニオンを示す。)又は/及び
(2)N−ビス(3−アミノプロピル)ドデシルアミン、3−アミノプロピル−ドデシルプロパンジアミン、1,3−プロパンジアミン−N−3−アミノプロピル―N−ドデシル、アルキルアミノグリシン、アルキルジアミノエチルグリシン塩酸塩、アルキルアミノエチルアミノエチルグリシン、アルキルアミノプロピルアミノ酢酸、及びアルキルポリアミノエチルグリシンから選択される両性界面活性能を有する防腐剤と、
(3)界面活性剤(但し、上記(1)及び(2)に含まれるものを除く。)
を含む恒温槽用清浄剤。 - 一般式[I]で示される第4級アンモニウム塩がジアルキルジメチルアンモニウムアジペート又はジアルキルジメチルアンモニウムプロピオネートである、請求項1に記載の清浄剤。
- 第4級アンモニウム塩がジデシルジメチルアンモニウムアジペートである、請求項1に記載の清浄剤。
- 両性界面活性能を有する防腐剤がN−ビス(3−アミノプロピル)ドデシルアミンである、請求項1〜3の何れかに記載の清浄剤。
- 界面活性剤が非イオン性界面活性剤又は陰イオン性界面活性剤である、請求項1〜4の何れかに記載の清浄剤。
- 界面活性剤がポリオキシエチレンアルキルエーテル又は/及びラウロイルサルコシンナトリウムである、請求項1〜5の何れかに記載の清浄剤。
- (1)一般式[I]で示される第4級アンモニウム塩と、(2)N−ビス(3−アミノプロピル)ドデシルアミン、3−アミノプロピル−ドデシルプロパンジアミン、1,3−プロパンジアミン−N−3−アミノプロピル―N−ドデシル、アルキルアミノグリシン、アルキルジアミノエチルグリシン塩酸塩、アルキルアミノエチルアミノエチルグリシン、アルキルアミノプロピルアミノ酢酸、及びアルキルポリアミノエチルグリシンから選択される両性界面活性能を有する防腐剤と、(3)界面活性剤(但し、上記(1)及び(2)に含まれるものを除く。)を含む、請求項1に記載の恒温槽用清浄剤。
- 一般式[I]で示される第4級アンモニウム塩がジデシルジメチルアンモニウムアジペートで、両性界面活性能を有する防腐剤がN−ビス(3−アミノプロピル)ドデシルアミンで、界面活性剤がポリオキシエチレンアルキルエーテル又は/及びラウロイルサルコシンナトリウムである請求項7に記載の清浄剤。
- 更に、キレート剤を含有する請求項1〜8の何れかに記載の清浄剤。
- キレート剤がエチレンジアミン四酢酸塩である、請求項9記載の清浄剤。
- 更に、液性をアルカリ性にする試薬を含有する、請求項1〜10の何れかに記載の清浄剤。
- 液性をアルカリ性にする試薬が水酸化ナトリウムである、請求項11に記載の清浄剤。
- 液性がpH10〜12のアルカリ性である、請求項1〜12の何れかに記載の清浄剤。
- 請求項1に記載の清浄剤を恒温槽に添加することを特徴とする、恒温槽の清浄方法。
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JP5384981B2 (ja) * | 2009-03-26 | 2014-01-08 | アクアス株式会社 | 水系中でアメーバと共存しているレジオネラ属菌の除菌方法 |
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JP5830359B2 (ja) * | 2011-11-10 | 2015-12-09 | ライオン株式会社 | 液体洗浄剤 |
JP6188236B2 (ja) * | 2014-05-15 | 2017-08-30 | ライオン株式会社 | 液体洗浄剤及びその製造方法 |
JP6654353B2 (ja) * | 2015-03-26 | 2020-02-26 | 株式会社Adeka | 硬質表面洗浄剤組成物及び硬質表面の洗浄方法 |
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