JPH0759482B2 - Disinfectant - Google Patents
DisinfectantInfo
- Publication number
- JPH0759482B2 JPH0759482B2 JP61162548A JP16254886A JPH0759482B2 JP H0759482 B2 JPH0759482 B2 JP H0759482B2 JP 61162548 A JP61162548 A JP 61162548A JP 16254886 A JP16254886 A JP 16254886A JP H0759482 B2 JPH0759482 B2 JP H0759482B2
- Authority
- JP
- Japan
- Prior art keywords
- bzk
- solution
- weight
- sterilization
- agent
- 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 - Lifetime
Links
- 239000000645 desinfectant Substances 0.000 title description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 45
- -1 alkyl dimethyl benzyl ammonium Chemical compound 0.000 claims description 23
- 150000003839 salts Chemical class 0.000 claims description 16
- 239000002736 nonionic surfactant Substances 0.000 claims description 11
- 239000002280 amphoteric surfactant Substances 0.000 claims description 10
- 239000002738 chelating agent Substances 0.000 claims description 10
- CYDRXTMLKJDRQH-UHFFFAOYSA-N benzododecinium Chemical compound CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 CYDRXTMLKJDRQH-UHFFFAOYSA-N 0.000 claims description 7
- 239000003206 sterilizing agent Substances 0.000 claims description 5
- 239000000243 solution Substances 0.000 description 68
- 238000004659 sterilization and disinfection Methods 0.000 description 41
- 230000001954 sterilising effect Effects 0.000 description 40
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 39
- 229910052799 carbon Inorganic materials 0.000 description 27
- 235000019441 ethanol Nutrition 0.000 description 27
- 239000007864 aqueous solution Substances 0.000 description 21
- 239000003795 chemical substances by application Substances 0.000 description 17
- 230000000844 anti-bacterial effect Effects 0.000 description 16
- 230000000249 desinfective effect Effects 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 14
- 239000007788 liquid Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 12
- 241000894006 Bacteria Species 0.000 description 9
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- 229960000686 benzalkonium chloride Drugs 0.000 description 9
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- 230000002070 germicidal effect Effects 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 238000005201 scrubbing Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 235000019864 coconut oil Nutrition 0.000 description 6
- 239000003240 coconut oil Substances 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 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 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000008399 tap water Substances 0.000 description 5
- 235000020679 tap water Nutrition 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 230000035764 nutrition Effects 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZFKJMWUAXIBRKM-UHFFFAOYSA-N 2-[2-aminoethyl(dodecyl)amino]acetic acid;hydrochloride Chemical compound Cl.CCCCCCCCCCCCN(CCN)CC(O)=O ZFKJMWUAXIBRKM-UHFFFAOYSA-N 0.000 description 3
- 241000590020 Achromobacter Species 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003899 bactericide agent Substances 0.000 description 3
- UWLPCYBIJSLGQO-UHFFFAOYSA-N dodecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCC(O)=O UWLPCYBIJSLGQO-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- HLERILKGMXJNBU-UHFFFAOYSA-N norvaline betaine Chemical compound CCCC(C([O-])=O)[N+](C)(C)C HLERILKGMXJNBU-UHFFFAOYSA-N 0.000 description 3
- 235000016709 nutrition Nutrition 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 3
- 239000012085 test solution Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 238000005554 pickling Methods 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- SHHOXQWCXVHCLT-UHFFFAOYSA-N 2-(2,2-diaminoethylamino)acetic acid;hydrochloride Chemical compound Cl.NC(N)CNCC(O)=O SHHOXQWCXVHCLT-UHFFFAOYSA-N 0.000 description 1
- IYVVKFYDGRJWTR-UHFFFAOYSA-N 2-decanoylglycerol Chemical compound CCCCCCCCCC(=O)OC(CO)CO IYVVKFYDGRJWTR-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000588986 Alcaligenes Species 0.000 description 1
- 241000588813 Alcaligenes faecalis Species 0.000 description 1
- 241000589513 Burkholderia cepacia Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000607715 Serratia marcescens Species 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- VYTBPJNGNGMRFH-UHFFFAOYSA-N acetic acid;azane Chemical compound N.N.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O VYTBPJNGNGMRFH-UHFFFAOYSA-N 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 229940005347 alcaligenes faecalis Drugs 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- HFNQLYDPNAZRCH-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O.OC(O)=O HFNQLYDPNAZRCH-UHFFFAOYSA-N 0.000 description 1
- 230000002301 combined effect Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229960001269 glycine hydrochloride Drugs 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- ZPIRTVJRHUMMOI-UHFFFAOYSA-N octoxybenzene Chemical compound CCCCCCCCOC1=CC=CC=C1 ZPIRTVJRHUMMOI-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- OQZCJRJRGMMSGK-UHFFFAOYSA-M potassium metaphosphate Chemical compound [K+].[O-]P(=O)=O OQZCJRJRGMMSGK-UHFFFAOYSA-M 0.000 description 1
- 235000019828 potassium polyphosphate Nutrition 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- XTUSEBKMEQERQV-UHFFFAOYSA-N propan-2-ol;hydrate Chemical compound O.CC(C)O XTUSEBKMEQERQV-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 239000003009 skin protective agent Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 235000019830 sodium polyphosphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明はドデシル・ジメチル・ベンジルアンモニウムま
たはその塩を約80重量%以上を含有するアルキル・ジメ
チル・ベンジルアンモニウムまたはその塩を利用する殺
菌消毒剤に関する。TECHNICAL FIELD The present invention relates to a germicidal disinfectant using alkyl dimethyl benzyl ammonium or its salt containing about 80% by weight or more of dodecyl dimethyl benzyl ammonium or its salt.
従来の技術 アルキル・ジメチル・ベンジルアンモニウム、たとえば
その塩化物はベンザルコニウムクロライド(以後ベンザ
ルコニウムクロライドをBZKと略称することがある)ま
たは逆性石けんと称され、無色、無臭の水溶性殺菌消毒
剤として、医療用等をはじめとして広く用いられてい
る。BACKGROUND ART Alkyl dimethyl benzyl ammonium, for example, its chloride is called benzalkonium chloride (hereinafter benzalkonium chloride is sometimes abbreviated as BZK) or reverse soap, and it is a colorless and odorless water-soluble germicidal disinfection. It is widely used as an agent for medical purposes.
ところで、第10改正日本薬局方によればBZK液中のBZKの
側鎖アルキル基はC8H17,C10H21,C12H25,C14H29,C16H33,
C18H37の混合物であり、主としてC12H25およびC14H29か
らなるとされ、両者の割合について特に規定されていな
い。一方、市販BZK液の種々の試料について、各側鎖を
有するBZKの含量について高速液体クロマトグラフィー
法[アール・シー・メイヤー:ジャーナル・オブ・ファ
ーマシュウティカル・サイエンス(R.C.Meyer:J.Pharm.
Sci..)69,1148−1150,1980]により測定するとC12H25B
ZK 59−63%,C14H29BZK 29−34%,C16H33BZK 6〜8%で
あった。By the way, according to the 10th revised Japanese Pharmacopoeia, the side chain alkyl group of BZK in the BZK solution is C 8 H 17 , C 10 H 21 , C 12 H 25 , C 14 H 29 , C 16 H 33 ,
It is a mixture of C 18 H 37 and is said to consist mainly of C 12 H 25 and C 14 H 29 , and the ratio of the both is not specified. On the other hand, for various samples of commercially available BZK liquid, the content of BZK having each side chain is analyzed by a high performance liquid chromatography method [RC Meyer: Journal of Pharmaceutical Sciences (RCMeyer: J. Pharm.
Sci ..) 69, C 12 as measured by 1148-1150,1980] H 25 B
ZK 59-63%, C 14 H 29 BZK 29-34%, was C 16 H 33 BZK 6~8%.
殺菌消毒剤の一般的性質として有機物、たとえば血液な
どの有機物の混入により殺菌力の低下が起こる。BZKも
この例外でなく、10%の高濃度の馬血清がBZK液中に存
在すると殺菌力が1/2〜1/4に低下すると報告されている
[ハイネマン・ピー・ジー:ジャーナル・オブ・アメリ
カン・ファーマシュウティカル・アソシエーション(He
ineman,P.G:J.Amer.Pharm.,Assoc.)26,711,1937]。As a general property of sterilizing agents, organic substances, for example, organic substances such as blood are mixed to reduce the sterilizing power. BZK is no exception to this rule, and it has been reported that the bactericidal activity is reduced to 1/2 to 1/4 when 10% high-concentration horse serum is present in the BZK solution [Heinemann P. G: Journal of. American Pharmaceutical Association (He
ineman, PG:.. J.Amer.Pharm, Assoc) 26, 711,1937].
殺菌消毒剤の場合、抗生物質と異なり、短時間で殺菌力
を発揮するため、耐性菌の出現は容易ではない。殊にBZ
Kの場合、殺菌に要する時間が非常に短時間であるた
め、他殺菌剤に比し耐性菌の出現はほとんど認められな
い。しかし、現在市販BZKを主成分とする製品の場合、
製造工程などが不備の場合、まれにアルカリゲネス(Al
caligenes),アクロモバクター(Achromobacter)属な
どの微生物がその溶液中に発育し、汚染される可能性が
ある(日本細菌学雑誌,15,1271,1960)。In the case of a bactericidal disinfectant, unlike antibiotics, bactericidal power is exerted in a short time, so that emergence of resistant bacteria is not easy. Especially BZ
In the case of K, the time required for sterilization is extremely short, so that the appearance of resistant bacteria is hardly observed compared to other bactericides. However, in the case of products currently based on commercial BZK,
If the manufacturing process is inadequate, rarely
There is a possibility that microorganisms such as caligenes) and the genus Achromobacter may grow in the solution and be contaminated (Japanese Journal of Bacteriology, 15 , 1271, 1960).
発明が解決しようとする問題点 BZKは、現在、広く用いられている殺菌消毒剤ではある
が、従来の組成品には前述の知見にもみられるようにさ
らに改良すべき点がある。Problems to be Solved by the Invention Although BZK is a sterilizing and disinfecting agent that is widely used at present, conventional compositions have further points to be improved as seen in the above findings.
その一つは、従来の組成品は有機物の混入により殺菌力
が低下することから、医療用や手指の殺菌消毒のように
使用頻度が高く蛋白質等の有機物で汚染される機会の多
い使用目的では殺菌力が低下し、殺菌剤として実用上こ
の点が問題である。また、従来組成品はアルカリゲネス
属、アクロモバクター属などの微生物が時によって発育
することがあり、これまで以上に広範な微生物に対しよ
り効果的に殺菌力を示すよう改良することも実用上極め
て重要なことである。One of them is that conventional compositions have a low bactericidal activity due to the inclusion of organic substances, so they are often used for medical purposes and sterilization of fingers, and are often used for organic purposes such as proteins. This is a problem in practical use as a bactericide because the bactericidal power decreases. Further, in the conventional composition, microorganisms such as Alcaligenes spp. And Achromobacter spp. May sometimes grow, and it is extremely practically possible to improve so as to show more effective bactericidal activity against a wider range of microorganisms than ever. It's important.
問題点を解決するための手段 本発明者らは、上記の様な状況に鑑み、市販BZKは種々
の側鎖アルキル基を有することに着目し、種々検討の結
果、ドデシル・ジメチル・ベンジルアンモニウムまたは
その塩を特定量以上含有せしめることにより、従来のBZ
K組成品が有する欠点が解消できることを見出した(特
願昭59−197072)。本発明者らはさらに検討を重ね、上
記殺菌消毒剤とともにエチルアルコール,イソプロピル
アルコール,エチレン・ジアミン四酢酸ナトリウムまた
はアルキル・ジアミノエチルグリシン塩酸塩の適量を含
有させることにより、より一層の殺菌効果があることを
見出し、さらに検討して本発明を完成した。Means for Solving the Problems In view of the situation as described above, the present inventors have focused on that commercially available BZK has various side chain alkyl groups, and as a result of various studies, dodecyl dimethyl benzyl ammonium or By containing a certain amount or more of that salt, conventional BZ
It was found that the drawbacks of the K composition product can be eliminated (Japanese Patent Application No. 59-197072). The inventors of the present invention have made further studies, and by adding an appropriate amount of ethyl alcohol, isopropyl alcohol, sodium ethylenediaminetetraacetate or alkyldiaminoethylglycine hydrochloride together with the above-mentioned germicidal disinfectant, a further germicidal effect can be obtained. The present invention has been completed and further studies have been made to complete the present invention.
すなわち、本発明は(1)ドデシル・ジメチル・ベンジ
ルアンモニウムまたはその塩を約80重量%以上含有する
アルキル・ジメチル・ベンジルアンモニウムまたはその
塩(以下、単に「本ADBAC剤」と略称することがある)
と、低級アルコール類、キレート剤および両性または非
イオン性界面活性剤の1種または2種以上とを含有して
なる殺菌消毒剤 本ADBAC剤において、ドデシル・ジメチル・ベンジルア
ンモニウムまたはその塩は常法で得たものが用いられ、
特にドデシル・ジメチル・ベンジルアンモニウムクロラ
イドが有利に使用できる。本剤の特徴はアルキル・ジメ
チル・ベンジルアンモニウムまたはその塩としてドデシ
ル・ジメチル・ベンジルアンモニウムまたはその塩の含
量を約80重量%以上にする点にあるが、約83重量%以上
含有せしめることによりさらに好ましい効果が発揮さ
れ、またその上限の含量は特に限定はないが一般に95重
量%までである。ドデシル体以外のアルキル・ジメチル
・ベンジルアンモニウムまたはその塩としては、その側
鎖アルキル基がC8H17,C10C21,C14H29,C16H33あるいはC
18H37のものがあげられ、これらは1種または2種以上
が含有されていてもよい。That is, the present invention provides (1) alkyl dimethyl benzyl ammonium or a salt thereof containing about 80% by weight or more of dodecyl dimethyl benzyl ammonium or a salt thereof (hereinafter, may be simply referred to as "the present ADBAC agent").
And a lower alcohol, a chelating agent, and one or more of amphoteric or nonionic surfactants. In this ADBAC agent, dodecyl dimethyl benzyl ammonium or its salt is a conventional method. The one obtained in
Especially, dodecyl dimethyl benzyl ammonium chloride can be advantageously used. The characteristic of this agent is that the content of dodecyl dimethyl benzylammonium or its salt as alkyl dimethyl benzylammonium or its salt is about 80% by weight or more, but it is more preferable to contain about 83% by weight or more. The effect is exhibited, and the upper limit content is not particularly limited, but is generally up to 95% by weight. As alkyl dimethyl benzyl ammonium other than dodecyl body or its salt, the side chain alkyl group is C 8 H 17 , C 10 C 21 , C 14 H 29 , C 16 H 33 or C
18 H 37 , and these may contain one kind or two or more kinds.
次に、低級アルコールとしては、一般に炭素数が1〜3
のものが用いられ、特にエチルアルコール,イソプロピ
ルアルコールが有利に用いられる。キレート剤として
は、一般にアルカリ性のものが好ましく、例ばエチレン
ジアミン四酢酸ナトリウムあるいは重合リン酸塩(例、
ポリリン酸ナトリウム,ポリリン酸カリウム)などが挙
げられる。また両性または非イオン性界面活性剤として
は、例えば、アルキル・ジアミノエチルグリシン塩酸塩
(例、ドデシル・アミノエチル・グリシン塩酸塩、テト
ラデシル・アミノエチル・グリシン塩酸塩)、グリセリ
ン脂肪酸エステル(例、グリセリンモノラウレート、グ
リセリンモノカプレート)などが挙げられる。Next, the lower alcohol generally has 1 to 3 carbon atoms.
Those of ethyl alcohol and isopropyl alcohol are particularly advantageously used. As the chelating agent, an alkaline one is generally preferable, for example, sodium ethylenediaminetetraacetate or a polymerized phosphate (eg,
Sodium polyphosphate, potassium polyphosphate) and the like. Examples of amphoteric or nonionic surfactants include alkyl diaminoethylglycine hydrochloride (eg, dodecyl aminoethyl glycine hydrochloride, tetradecyl aminoethyl glycine hydrochloride), glycerin fatty acid ester (eg, glycerin Monolaurate, glycerin monocaprate) and the like.
次に、本発明の殺菌消毒剤における本ADBAC剤と上記の
各併用成分との量比は、たとえば本ADBAC剤100重量部に
対し、低級アルコール類は約100〜100万重量部、好まし
くは約800〜80万重量部、また手指,器具などの消毒に
際し更に好ましくは約3.000〜3万重量部、キレート剤
は約0.02〜1000重量部、好ましくは約0.2〜500重量部、
また器具,室内消毒などに際し更に好ましくは約10〜20
0重量部、また両性または非イオン性界面活性剤は約0.2
〜1000重量部、好ましくは約0.5〜200重量部また手指な
どの消毒に際し更に好ましくは約10〜100重量部の割合
とするのがよい。Next, the amount ratio of the present ADBAC agent and each of the above-mentioned combined components in the sterilizing agent of the present invention is, for example, 100 parts by weight of the present ADBAC agent, lower alcohols are about 100 to 1,000,000 parts by weight, and preferably about 1 part by weight. 800 to 800,000 parts by weight, more preferably about 3.000 to 30,000 parts by weight when disinfecting fingers, instruments, etc., chelating agent about 0.02 to 1000 parts by weight, preferably about 0.2 to 500 parts by weight,
Further, when disinfecting equipment, indoors, etc., more preferably about 10 to 20
0 parts by weight, and about 0.2% amphoteric or nonionic surfactant.
˜1000 parts by weight, preferably about 0.5 to 200 parts by weight, and more preferably about 10 to 100 parts by weight when disinfecting fingers and the like.
本殺菌消毒剤の剤型は、各併用成分の形状により粉剤、
液剤等に調製され、その調製法自体は公知手段を用いる
ことができる。The dosage form of this germicidal disinfectant depends on the shape of each combined ingredient,
It is prepared as a liquid agent or the like, and a known method can be used for the preparation method itself.
本殺菌消毒剤を使用するに際しては、本ADBAC剤と各併
用成分とを前記量比で含有する製剤を、本ADBAC剤の濃
度として約0.01〜5%、好ましくは約0.02〜3%、更に
好ましくは約0.05〜2%(重量/容量)となるように必
要に応じ適宜の溶媒、例えば水で希釈して殺菌消毒の対
象物に接触せしめる。一般に、低級アルコール類は約7
〜90%、好ましくは約15〜80%、更に好ましくは15〜30
%(容量/容量)で、キレート剤は約0.001〜0.1%、好
ましくは約0.005〜0.1%、更に好ましくは0.05〜0.1
(重量/容量)で、また両性または非イオン性界面活性
剤は約0.01〜0.1%、好ましくは約0.02〜0.1、更に好ま
しくは約0.05〜0.1%(重量/容量)の各濃度で併用さ
れる。When using the present germicidal disinfectant, a formulation containing the present ADBAC agent and each combination component in the above-mentioned quantitative ratio is used as the concentration of the present ADBAC agent of about 0.01 to 5%, preferably about 0.02 to 3%, and further preferably Is diluted with an appropriate solvent, such as water, if necessary so as to be about 0.05 to 2% (weight / volume) and brought into contact with an object to be sterilized. Generally, lower alcohols are about 7
~ 90%, preferably about 15-80%, more preferably 15-30
% (Volume / volume), the chelating agent is about 0.001 to 0.1%, preferably about 0.005 to 0.1%, more preferably 0.05 to 0.1%.
(Weight / volume), and the amphoteric or nonionic surfactant is used at a concentration of about 0.01-0.1%, preferably about 0.02-0.1%, more preferably about 0.05-0.1% (weight / volume). .
本殺菌消毒法は一般にpHが約6.5〜8.5、好ましくは7〜
8.5で実施されるが、殺菌消毒の対象物の種類によって
は、例えば医療器具・施設、工場等に適用する場合に
は、pHを約9〜11、好ましくは10〜11付近まで高めて実
施することが効果上好ましい。この場合のpHの調整剤と
しては、適宜のアルカリ剤を使用でき、例えば水酸化ア
ルカリ(例、水酸化ナトリウム、水酸化カリウム)、炭
酸アルカリ塩(例、炭酸ナトリウム、炭酸カリウム、炭
酸水素ナトリウム、炭酸水素カリウム)などが挙げられ
る。This sterilization method generally has a pH of about 6.5-8.5, preferably 7-8.5.
It is carried out in 8.5, but depending on the type of the object of sterilization, when it is applied to medical equipment / facility, factory, etc., the pH is raised to about 9-11, preferably 10-11. Is preferable in terms of effect. As the pH adjuster in this case, an appropriate alkali agent can be used, and examples thereof include alkali hydroxide (eg, sodium hydroxide, potassium hydroxide), carbonate carbonate (eg, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, (Potassium hydrogen carbonate) and the like.
また殺菌消毒に際して洗浄作用を付与することにより除
菌効果を向上させることが出来るので洗浄または起泡力
を有する薬剤などを併用することにより殺菌消毒効果を
より促進することができる。重合リン酸塩あるいは界面
活性剤は、このような目的においても併用することがで
き、この場合にはこれら薬剤を一般に約0.1〜30重量%
の濃度で併用するのが好ましい。このときの界面活性剤
としては、具体的にはポリオキシエチレン・ポリオキシ
プロピレン・グリコール・エーテル,ポリオキシエチレ
ンノニルフェノール・エーテル,ポリオキシエチレン・
オクチルフエニルエーテル,ヤシ油脂肪酸アミド・プロ
ピルベタイン,ヤシ油脂肪酸ジエタノールアミド,高級
アルコールポリエチレングリコール型非イオン性界面活
性剤およびN−ココイル−L−アルギニンエチルエステ
ル−DL−ピロリドンカルボン酸などの非イオン性界面活
性剤が挙げられる。これら界面活性剤の一種または2種
以上添加することにより、除菌効果とともに手荒れ防止
にも有用となる。更に詳しくはヤシ油脂肪酸アミドプロ
ピルベタイン約10〜30%,またはポリオキシエチレンポ
リオキシプロピレングリコールエーテル約10〜30%およ
びヤシ油脂肪酸ジエタノールアミド約3〜10%の混液に
エタノールを約10〜30%添加することにより殺菌消毒力
の有効性が増加する。さらに、殺菌消毒剤による手指消
毒を頻繁に実施する場合、手荒れ防止のため皮膜形成
剤,保湿剤等の皮膚保護剤を加えることにより有用性が
向上する。皮膚保護剤としてはラノリン,ポリオール,
トリ−2−エチルヘキシル酸グリセリンなどを製剤中に
約0.1〜5重量%添加して用いることもできる。更には
器具消毒には防錆剤としてよく知られている亜硝酸ナト
リウムを0.01〜2重量%程度添加することにより有用性
が向上する。In addition, since a bactericidal effect can be improved by imparting a cleaning action during sterilization and disinfection, the sterilization and disinfection effect can be further promoted by using a chemical having a cleaning or foaming ability in combination. Polymerized phosphates or surfactants can also be used together for such purpose, and in this case, these agents are generally contained in an amount of about 0.1 to 30% by weight.
It is preferable to use them together at a concentration of. Specific examples of the surfactant at this time include polyoxyethylene / polyoxypropylene / glycol ether, polyoxyethylene / nonylphenol / ether, and polyoxyethylene /
Octyl phenyl ether, coconut oil fatty acid amide / propyl betaine, coconut oil fatty acid diethanolamide, higher alcohol polyethylene glycol type nonionic surfactant and nonionic such as N-cocoyl-L-arginine ethyl ester-DL-pyrrolidone carboxylic acid And a surface active agent. Addition of one or more of these surfactants will be effective in disinfecting as well as preventing hand roughness. More specifically, about 10 to 30% of coconut oil fatty acid amide propyl betaine, or about 10 to 30% of polyoxyethylene polyoxypropylene glycol ether and about 3 to 10% of coconut oil fatty acid diethanolamide, and about 10 to 30% of ethanol. Addition increases the effectiveness of the disinfecting power. Furthermore, when hand disinfection with a germicidal disinfectant is frequently performed, the usefulness is improved by adding a skin protective agent such as a film-forming agent or a moisturizer to prevent rough hands. As skin protectant, lanolin, polyol,
Glycerin tri-2-ethylhexylate or the like can be added to the preparation in an amount of about 0.1 to 5% by weight and used. Further, the usefulness is improved by adding 0.01 to 2% by weight of sodium nitrite, which is well known as a rust preventive, for disinfecting equipment.
殺菌消毒対象物への接触方法は、従来公知の方法を採用
することができ、たとえば浸漬,スプレー,ふりかけ,
洗浄などにより実施すればよい。また、手指などの殺菌
消毒については上記溶液の3〜10mlを手掌にとり手指を
よくもみ洗いすることにより手指の汚染菌を殺菌するこ
とができる。接触時間は殺菌対象物あるいは殺菌消毒剤
の使用濃度等を考慮して選択されるが、通常約10秒以
上,好ましくは1分以上である。As a method for contacting the object to be sterilized and disinfected, a conventionally known method can be adopted, for example, dipping, spraying, sprinkling,
It may be carried out by washing or the like. For sterilization of fingers and the like, contaminated bacteria on the fingers can be sterilized by taking 3 to 10 ml of the above solution on the palm and thoroughly rubbing the fingers. The contact time is selected in consideration of the sterilization target or the concentration of the disinfectant used, but is usually about 10 seconds or more, preferably 1 minute or more.
本殺菌消毒剤は、微生物の汚染を排除する目的で各種用
途に幅広く適用できる。たとえば、人体、動物の患部あ
るいは各種医療器具・施設などの医療用、手指の消毒、
理容・美容院、学校等の公共施設、家屋、乗物、食器、
食品製造工場あるいはその製造設備等の殺菌消毒に用い
ることができる。本剤は後述の実験例に示されていると
おり、有機物の混入下であっても充分に殺菌消毒力を示
す。従って、消毒液を医療用などのように頻繁に用いる
場合、あるいは蛋白質等有機物による汚染の著しい手指
などの消毒により好ましく適用できる。本殺菌消毒法の
好ましい実施態様は、例えば次のとおりである。本ADBA
C剤の約0.1〜0.5%(重量/容量)と両性または非イオ
ン性界面活性剤(例、アルキル,ジアミノエチルグリシ
ン塩酸塩または/およびグリセリン脂肪酸エステル)の
約0.05〜0.1%(重量/容量)を含む水溶液は、医師・
看護婦等が手術前の手洗用殺菌消毒剤として好ましく用
いられる。一般の手指の殺菌消毒の場合は、本ADBAC剤
の約0.1〜0.5(重量/容量)と、低級アルコール類
(例、エチルアルコールまたは/およびイソプロピルア
ルコール)の約15〜30%(容量/容量)または/および
両性または非イオン性界面活性剤(例、アルキル・ジア
ミノエチルグリシン塩酸塩または/およびグリセリン脂
肪酸エステル)の約0.05〜0.1%(重量/容量)を含む
水溶液を手掌にとり約10秒以上、好ましくは約30〜60秒
以上、もみ洗いすることにより、皮膚あれを起こすこと
なく殺菌消毒できる。医療用器具(例、ハサミ,メスな
ど)の場合は、本ADBAC剤の約0.05〜0.2%(重量/容
量)と、低級アルコール類(例、エチルアルコールまた
は/およびイソプロピルアルコール)の約15〜30%(容
量/容量)または/およびキレート剤(例、エチレンジ
アミン四酢酸ナトリウムまたは/および重合リン酸塩)
の約0.05〜0.1%(重量/重量)を含む水溶液に、一般
に約10分以上浸漬することにより殺菌消毒の目的が達せ
される。また、室内あるいは乗物等の殺菌消毒には本AD
BAC剤の約0.05〜0.2%(重量/容量)とキレート剤
(例、エチレンジアミ四酢酸ナトリウムまたは/および
重合リン酸塩)の約0.05〜0.1(重量/重量)を含む水
溶液を常法によりスプレーすることにより好ましく実施
できる。The disinfectant can be widely applied to various uses for the purpose of eliminating microbial contamination. For example, medical treatment of affected areas of human bodies and animals or various medical instruments and facilities, disinfection of fingers,
Barber / beauty salon, public facilities such as schools, houses, vehicles, tableware,
It can be used for sterilizing and disinfecting food manufacturing factories or their manufacturing facilities. As shown in the experimental examples described below, this agent exhibits sufficient sterilizing and disinfecting power even when mixed with organic substances. Therefore, it can be preferably applied when the disinfectant solution is frequently used for medical purposes, or by disinfecting a finger or the like which is significantly contaminated with organic substances such as proteins. A preferred embodiment of this sterilization method is as follows, for example. Book ADBA
About 0.1 to 0.5% (weight / volume) of agent C and about 0.05 to 0.1% (weight / volume) of amphoteric or nonionic surfactant (eg, alkyl, diaminoethylglycine hydrochloride or / and glycerin fatty acid ester) Aqueous solution containing
A nurse or the like is preferably used as a sterilizing agent for hand washing before surgery. In the case of general hand sterilization, about 0.1 to 0.5 (weight / volume) of this ADBAC agent and about 15 to 30% (volume / volume) of lower alcohols (eg, ethyl alcohol or / and isopropyl alcohol) Or / and an aqueous solution containing about 0.05 to 0.1% (weight / volume) of an amphoteric or nonionic surfactant (eg, alkyl diaminoethylglycine hydrochloride or / and glycerin fatty acid ester) is palmed for about 10 seconds or more, It is possible to sterilize and disinfect without causing skin irritation by washing with rice for preferably about 30 to 60 seconds or more. In the case of medical equipment (eg, scissors, scalpel, etc.), about 0.05 to 0.2% (weight / volume) of this ADBAC agent and about 15 to 30 of lower alcohols (eg, ethyl alcohol or / and isopropyl alcohol) % (Volume / volume) or / and chelating agent (eg sodium ethylenediaminetetraacetate or / and polymerized phosphate)
The purpose of sterilization is generally achieved by immersing in an aqueous solution containing about 0.05 to 0.1% (weight / weight) of about 10 minutes or more. In addition, this AD is used for sterilization of indoors or vehicles.
An aqueous solution containing about 0.05 to 0.2% (weight / volume) of the BAC agent and about 0.05 to 0.1 (weight / weight) of the chelating agent (eg sodium ethylenediamitetraacetate or / and polymerized phosphate) is sprayed by a conventional method. This can be preferably carried out.
実施例 以下に、実験例および実施例をあげて本発明をさらに具
体的に説明する。EXAMPLES Hereinafter, the present invention will be described more specifically with reference to experimental examples and examples.
なお、以下の記載において「95%C12BZK」とはアルキル
側鎖がC12H25のもの95%、C14H29のもの3%,C16H33の
もの1%,その他のアルキル側鎖のもの1%を含むBZK
をいい、また「83%C12BZK」とはアルキル側鎖がC12H25
のもの83%,C14H29のもの13%,C16H33のもの2%,その
他のアルキル側鎖のもの1%を含むBZKをいうものとす
る。また対照として用いた市販塩化ベンザルコニウム
(商品名:オスバン )はC12H25BZKを約60%、C14H29B
ZKを約30%、C16H33BZKを約8%、その他のBZKを約1%
を含むものである。In addition, "95% C12BZK is an alkyl
Side chain is C12Htwenty five95% of things, C14H293%, C16H33of
BZK containing 1% of those containing 1% of other alkyl side chains
See you again, "83% C12"BZK" means that the alkyl side chain is C12Htwenty five
Of 83%, C14H29Of 13%, C16H332% of that
BZK containing 1% of other alkyl side chains
It Commercial benzalkonium chloride used as a control
(Product name: Osvan ) Is C12Htwenty fiveBZK about 60%, C14H29B
ZK about 30%, C16H33About 8% of BZK and about 1% of other BZK
Is included.
実験例1 試験菌としてアクロモバクター・グッタチスA−39およ
びアルカリゲネス・フェカリス572を使用した。それぞ
れの試験菌の1白金耳をSCD培地(大五栄養化学KK)を1
/50に稀釈した培地(以後1/50SCDと略す)に接種して30
℃,3日間培養した。市販塩化ベンザルコニウム(オスバ
ン ),95%C12BZKおよび83%C12BZKのものについて以
下の方法で殺菌力を測定した。Experimental Example 1 As a test bacterium, Achromobacter guttatis A-39 and
And Alcaligenes faecalis 572 were used. That's it
1 platinum loop of each of these test bacteria was added to SCD medium (Daigo Nutrition Chemistry KK)
Inoculate the medium diluted to 50/50 (hereinafter abbreviated as 1/50 SCD) to 30
Cultivated at ℃ for 3 days. Commercially available benzalkonium chloride (Osba
The ), 95% C12BZK and 83% C12About BZK
The bactericidal power was measured by the following method.
すなわち、1/50SCD液単独7%,15%または30%エチルア
ルコールをそれぞれ含む1/50SCD液中に上記殺菌剤をそ
れぞれ50μg/mlから10mg/mlの各濃度の溶液を調製し
た。これらの各試験液に、前記培養の各試験菌の生菌数
が106CFU/mlになる様に接種して、25℃に1分間あるい
は10分間接触させた。接触時間後、直ちにこれらの各液
500μを採取して、10mlのSCDLP培地(大五栄養化学KK)
に移した。これらの各培養液はSCDLP寒天平板上で生菌
数を測定するとともに35℃,72時間培養して、試験菌の
発育の有無を観察し、生菌の存在が認められない濃度を
殺菌濃度とした。That is, 1/50 SCD solutions alone were prepared into 1/50 SCD solutions containing 7%, 15% or 30% ethyl alcohol, respectively, to prepare solutions of the above bactericide at respective concentrations of 50 μg / ml to 10 mg / ml. Each of these test solutions was inoculated so that the viable cell count of each test bacterium in the culture was 10 6 CFU / ml, and contacted at 25 ° C for 1 minute or 10 minutes. Immediately after the contact time, each of these solutions
Collect 500μ, 10ml of SCDLP medium (Daigo Nutrition Chemistry KK)
Moved to. For each of these cultures, the number of viable cells was measured on SCDLP agar plates and incubated at 35 ° C for 72 hours, and the presence or absence of growth of the test cells was observed. did.
本実験結果を第1表(1)および(2)に示す。この結
果から明らかなように、95%C12BZKおよび83%C12BZKは
市販塩化ベンザルコニウムに比して、エチルアルコール
との併用による殺菌効果が極めて高いことが認められ
た。The results of this experiment are shown in Table 1 (1) and (2). As is clear from these results, it was confirmed that 95% C 12 BZK and 83% C 12 BZK had extremely high bactericidal effect when used in combination with ethyl alcohol, as compared with commercial benzalkonium chloride.
実験例2 グローブ・ジュース法による手指消毒効果を検した。す
なわち、神木の方法(神木照雄:外科診療25巻,第2
号,256頁−261頁,昭和58年)に準じて5人の被検者を
対象にして、消毒前の手指菌数(ベースライン値)を測
定し、つぎに市販塩化ベンザルコニウム,95%C12BZK,83
%C12BZKをそれぞれ0.1%含有する50%エチルアルコー
ル水溶液ならびに対照として50%エチルアルコール単独
水溶液の消毒効果を調べた。これらの液5mlを手掌にと
り、手指全体にすりつけ、乾燥するまでマッサージす
る。この操作を3回くり返す。消毒した手指については
上記の方法に準じて菌数を測定した。消毒後に検出され
た菌数をベースライン値で除した値の百分率値を100か
ら差し引いた値を減菌率とした。その結果を第2表に示
す。 Experimental Example 2 The hand disinfection effect by the glove juice method was examined. That is, the method of the sacred tree (Teruo sacred tree: Surgical practice 25 volumes, 2nd
No., pp. 256-261, 1983), the number of hand bacteria before sterilization (baseline value) was measured for 5 subjects, and then commercially available benzalkonium chloride, 95 % C 12 BZK, 83
The disinfecting effect of 50% ethyl alcohol aqueous solution containing 0.1% of each% C 12 BZK and 50% ethyl alcohol alone aqueous solution as a control was examined. Take 5 ml of these liquids on your palm, rub them over your fingers, and massage until dry. Repeat this operation 3 times. For the disinfected fingers, the number of bacteria was measured according to the above method. The sterilization rate was defined as the value obtained by subtracting 100 from the percentage value of the number of bacteria detected after disinfection divided by the baseline value. The results are shown in Table 2.
減菌率は5回の測定の平均値を示し、エチルアルコール
との併用において市販塩化ベンザルコニウムに比し、95
%C12BZKまたは83%C12BZKとの併用区による減菌率が相
乗的に効果が高められることが示された。The sterilization rate shows the average value of 5 measurements, and when used in combination with ethyl alcohol, it is 95% higher than that of commercially available benzalkonium chloride.
It was shown that the sterilization rate was synergistically enhanced by the combined use with% C 12 BZK or 83% C 12 BZK.
実験例3 実験例1と同様な試験菌およびBZKを用いて1/50SCD液お
よび15%または30%イソプロピルアルコールを含む1/50
SCD液中における殺菌力を検した。方法は実験例1と同
様である。 Experimental Example 3 1/50 containing 1/50 SCD solution and 15% or 30% isopropyl alcohol using the same test strain and BZK as in Experimental Example 1
The bactericidal activity in the SCD solution was examined. The method is the same as in Experimental Example 1.
第3表に示す結果から明らかなように95%C12BZKまたは
83%C12BZKはそれぞれ15%または30%イソプロピルアル
コールが共存すると、市販塩化ベンザルコニウムに比較
して、相乗的に殺菌力が増強することが認められた。As can be seen from the results shown in Table 3, 95% C 12 BZK or
It was found that 83% C 12 BZK synergistically enhances the bactericidal activity as compared with commercial benzalkonium chloride when 15% or 30% isopropyl alcohol coexists.
実験例4 シュードモナス・セパシア TN1943およびセラチア・マ
ルセスセンス82−2−52をそれぞれの斜面培養から1白
金耳をとり、SCD培地(大五栄養化学KK)に接種して35
℃,20時間培養した。1/50SCD液中に市販塩化ベンザルコ
ニウム,95%C12BZK,83%C12BZKのそれぞれにエチレン・
ジアミン四酢酸・4ナトリウム,アルキル・ジアミノエ
チル・グリシン塩酸塩を添加したものについて殺菌力を
測定した。すなわち、各濃度の試験液に対し、前記培養
液をほぼ105CFU/mlになる様に接種した。接種後、15秒
および5分間接触した後、これらの液をSCDLP培地(大
五栄養化学KK)で20倍稀釈して、各殺菌剤を不活性化し
た。これらの液中の生菌数を測定して各試験液の殺菌力
を検した。その結果を第4表に示す。 Experimental Example 4 One platinum loop was taken from each slope culture of Pseudomonas cepacia TN1943 and Serratia marcescens 82-2-52 and inoculated on SCD medium (Daigo Nutrition Chemistry KK).
Incubated at ℃ for 20 hours. Commercially available benzalkonium chloride, 95% C 12 BZK, 83% C 12 BZK containing ethylene /
The bactericidal activity was measured for those to which diaminetetraacetic acid / 4 sodium and alkyl diaminoethyl glycine hydrochloride were added. That is, the test solution at each concentration was inoculated with the culture solution at about 10 5 CFU / ml. After contacting for 15 seconds and 5 minutes after inoculation, these liquids were diluted 20 times with SCDLP medium (Daigo Nutrition Co., Ltd. KK) to inactivate each fungicide. The viable cell count in these solutions was measured and the bactericidal activity of each test solution was examined. The results are shown in Table 4.
実施例1 95%C12BZKの50%(w/v)水溶液に95%エチルアルコー
ルと水を注入して稀釈して、エチルアルコールとして15
%と、BZKとしてそれぞれ2%w/v液,1%w/v液,0.5%w/v
液,0.2%w/v液および0.1%w/v液を調製した。それぞれ
の調製液を5ml当り手掌にとり、3回よくもみ洗いした
後、減菌率を調べると50%以上であった。 Example 1 95% ethyl alcohol and water were poured into a 50% (w / v) 50% aqueous solution of 95% C 12 BZK to dilute it to obtain ethyl alcohol as 15%.
%, BZK as 2% w / v solution, 1% w / v solution, 0.5% w / v
Solution, 0.2% w / v solution and 0.1% w / v solution were prepared. After taking 5 ml of each preparation solution in the palm and thoroughly scrubbing 3 times, the sterilization rate was 50% or more.
実施例2 95%C12BZKの50%(w/v)水溶液に95%エチルアルコー
ル水を注入して稀釈し、エチルアルコールとして30%
と、BZKとしてそれぞれ2%w/v液,1%w/v液,0.5%w/v
液,0.2%w/v液および0.1%w/v液を調製した。それぞれ
の調製液を5ml当り手掌にとり、3回よくもみ洗いした
後、減菌率を調べると50%以上であった。Example 2 95% C 12 BZK was diluted with 50% (w / v) aqueous solution by injecting 95% ethyl alcohol water to obtain 30% ethyl alcohol.
And BZK as 2% w / v solution, 1% w / v solution, 0.5% w / v
Solution, 0.2% w / v solution and 0.1% w / v solution were prepared. After taking 5 ml of each preparation solution in the palm and thoroughly scrubbing 3 times, the sterilization rate was 50% or more.
実施例3 83%C12BZKの50%(w/v)水溶液に95%エチルアルコー
ルと水を注入して稀釈して、エチルアルコールとして20
%,BZKとして2%w/v液,1%w/v液,0.5%w/v液,0.2%w/v
および0.1%w/v液を調製した。それぞれの調製液を5ml
当り手掌にとり、3回よくもみ洗いした後、減菌率を調
べると50%以上であった。Example 3 95% ethyl alcohol and water were poured into a 50% (w / v) aqueous solution of 83% C 12 BZK to dilute it to obtain 20% ethyl alcohol.
%, BZK as 2% w / v solution, 1% w / v solution, 0.5% w / v solution, 0.2% w / v
And 0.1% w / v solution were prepared. 5 ml of each preparation
The sterilization rate was 50% or more when the sterilization rate was examined after picking it up on the palm of the hand and thoroughly rubbing it 3 times.
実施例4 83%C12BZKの50%(w/v)水溶液に95%イソプロピルア
ルコールと水を注入して稀釈し、イソプロピルアルコー
ルとして20%と、BZKとしてそれぞれ2%w/v液,1%w/v
液,0.5%w/v液,0.2%w/v液および0.1%w/v液を調製し
た。それぞれの調製液を5ml当り手掌にとり、3回よく
もみ洗いした後、減菌率を調べると50%以上であった。Example 4 95% isopropyl alcohol and water were poured into a 50% (w / v) aqueous solution of 83% C 12 BZK to dilute it, and 20% as isopropyl alcohol and 2% w / v solution as BZK, 1% respectively. w / v
Solution, 0.5% w / v solution, 0.2% w / v solution and 0.1% w / v solution were prepared. After taking 5 ml of each preparation solution in the palm and thoroughly scrubbing 3 times, the sterilization rate was 50% or more.
実施例5 95%C12BZKの50%(w/v)水溶液に95%エチルアルコー
ルと水を注入して稀釈して、エチルアルコールとして15
%とし、更にエチレンジアミン四酢酸・4ナトリウムを
溶解して、エチレンジアミン四酢酸ナトリウムとして0.
05%,BZKとしてそれぞれ1%,0.5%,0.2%および0.1%w
/v液を調製した。それぞれの調製液を5ml当り手掌にと
り、3回よくもみ洗いした後、減菌率を調べると50%以
上であった。Example 5 95% ethyl alcohol and water were added to a 50% (w / v) aqueous solution of 95% C 12 BZK to dilute it to obtain ethyl alcohol as 15%.
%, And further dissolve ethylenediaminetetraacetic acid.4 sodium to give sodium ethylenediaminetetraacetate of 0.
05%, BZK 1%, 0.5%, 0.2% and 0.1% w respectively
A / v solution was prepared. After taking 5 ml of each preparation solution in the palm and thoroughly scrubbing 3 times, the sterilization rate was 50% or more.
実施例6 83%C12BZKの50%(w/v)水溶液に95%イソプロピルア
ルコールと水を注入して稀釈し、イソプロピルアルコー
ルとして15%とし、更に30%アルキルジエチルアミノエ
チルグリシン塩酸塩(商品名:テゴー51:ドデシル・ア
ミノエチルグリシン塩酸塩18%およびテトラデシル・ア
ミノエチルグリシン塩酸塩12%を含む。)を溶解して、
アルキルジエチルアミノエチルグリシン塩酸塩として0.
05%,BZKとしてそれぞれ1%,0.5%,0.2%および0.1%w
/v液を調製した。それぞれの調製液を5ml当り手掌にと
り、3回よくもみ洗いした後、減菌率を調べると50%以
上であった。Example 6 95% isopropyl alcohol and water were poured into a 50% (w / v) aqueous solution of 83% C 12 BZK to dilute it to 15% as isopropyl alcohol, and 30% alkyldiethylaminoethylglycine hydrochloride (trade name). : Tego 51: containing 18% of dodecyl aminoethylglycine hydrochloride and 12% of tetradecyl aminoethylglycine hydrochloride.),
Alkyldiethylaminoethylglycine hydrochloride as 0.
05%, BZK 1%, 0.5%, 0.2% and 0.1% w respectively
A / v solution was prepared. After taking 5 ml of each preparation solution in the palm and thoroughly scrubbing 3 times, the sterilization rate was 50% or more.
実施例7 83%C12BZKの50%(w/v)水溶液にエチレン・ジアミン
四酢酸ナトリウムを溶解して、エチレン・ジアミン四酢
酸ナトリウムとして0.1%,BZKとしてそれぞれ2%w/v
液,1%w/v液,0.5%w/v液,0.2%w/v液および0.1%w/v液
を調製した。それぞれの調製液をスプレーにより室内に
散布し、10分後、減菌率を調べると90%以上であった。Example 7 Sodium ethylenediaminetetraacetate was dissolved in a 50% (w / v) aqueous solution of 83% C 12 BZK to obtain 0.1% sodium ethylenediaminetetraacetate and 2% w / v as BZK respectively.
Solutions, 1% w / v solution, 0.5% w / v solution, 0.2% w / v solution and 0.1% w / v solution were prepared. Each preparation solution was sprayed indoors, and after 10 minutes, the sterilization rate was 90% or more.
実施例8 95%C12BZKの50%(w/v)水溶液に30%アルキルジエチ
ルアミノエチルグリシン塩酸塩を溶解して、アルキルジ
エチルアミノエチルグリシン塩酸塩として0.05%,BZKと
してそれぞれ2%w/v液,1%w/v液,0.5%w/v液,0.2%w/v
液および0.1%w/v液を調製した。それぞれの調製液を5m
l当り手掌にとり、3回よくもみ洗いした後、減菌率を
調べると50%以上であった。Example 8 30% alkyldiethylaminoethylglycine hydrochloride was dissolved in a 50% (w / v) aqueous solution of 95% C 12 BZK to obtain 0.05% alkyldiethylaminoethylglycine hydrochloride and 2% w / v solutions as BZK. , 1% w / v solution, 0.5% w / v solution, 0.2% w / v
Solution and 0.1% w / v solution were prepared. 5m of each preparation
It was 50% or more when the sterilization rate was examined after pickling on the palm and thoroughly rubbing 3 times.
実施例9 83%C12BZKの50%(W/V)水溶液に水道水を入れて希釈
するとともにトリポリ燐酸ナトリウムを溶解して、トリ
ポリ燐酸ナトリウムとして0.1%(W/V)とBZK1%,0.5%
0.2%および0.1%(W/V)をそれぞれ含む液を調整し
た。それぞれの調整液2をステンレス容器に入れ、ハ
サミ,メスなどの医療用器具を侵漬した。侵漬10分後滅
菌率を調べると90%以上であった。Example 9 83% C 12 BZK 50% (W / V) aqueous solution was diluted by adding tap water and sodium tripolyphosphate was dissolved to obtain 0.1% (W / V) sodium tripolyphosphate and BZK 1%, 0.5. %
Liquids containing 0.2% and 0.1% (W / V) were prepared. Each adjusting liquid 2 was put into a stainless steel container, and medical instruments such as scissors and a scalpel were immersed. The sterilization rate was 90% or more after 10 minutes of immersion.
実施例10 83%C12BZKの50%(W/V)水溶液に90%イソプロピルア
ルコールと水を注入して希釈し、イソプロピルアルコー
ルとして15%(W/V)とし、更にエチレン・ジアミン四
酢酸・4ナトリウムを溶解して、エチレン・ジアミン四
酢酸・4ナトリウムとして0.05%(W/V),BZKとしてそ
れぞれ1%,0.5%,0.2%(W/V)液を調整した。それぞ
れの調整液2を合成樹脂製容器に入れ、ハサミ,メス
など医療用器具を侵漬した。侵漬10分後の滅菌率は90%
以上であった。Example 10 Injecting 90% isopropyl alcohol and water into a 50% (W / V) aqueous solution of 83% C 12 BZK to dilute it to 15% (W / V) as isopropyl alcohol, and further add ethylenediaminetetraacetic acid. By dissolving 4 sodium, 0.05% (W / V) of ethylenediaminetetraacetic acid / 4 sodium and 1%, 0.5%, 0.2% (W / V) of BZK were prepared. Each of the adjustment liquids 2 was placed in a synthetic resin container, and medical instruments such as scissors and a scalpel were immersed. Sterilization rate after 90 minutes of immersion is 90%
That was all.
実施例11 95%C12BZKの50%(W/V)水溶液にグリセリンモノラウ
レートを溶解して、グリセリンモノラウレートとして0.
005%,BZKとしてそれぞれ2%W/V液,1%W/V液,0.5%W/V
液,0.2%W/V液および0.1%W/V液を調製した。それぞれ
の調製液を5ml当り手掌にとり、3回よくもみ洗いした
後、滅菌率を調べると50%以上であった。Example 11 Glycerin monolaurate was dissolved in a 50% (W / V) 50% aqueous solution of 95% C 12 BZK to prepare a glycerin monolaurate of 0.1%.
005%, 2% W / V liquid as BZK, 1% W / V liquid, 0.5% W / V
Solution, 0.2% W / V solution and 0.1% W / V solution were prepared. 5 ml of each of the prepared liquids was picked up on the palm and thoroughly scrubbed 3 times, and the sterilization rate was 50% or more.
実施例12 83%C12BZKの50%(w/v)水溶液に95%エチルアルコー
ルと水を注入して稀釈し、エチルアルコールとして50
%,BZKとして2%w/v液,1%w/v液,0.5%w/v液,0.2%w/v
および0.1%w/v液を調製した。それぞれの調製液を5ml
当り手掌にとり、3回よくもみ洗いした後、減菌率を調
べると50%以上であった。Example 12 A 50% (w / v) aqueous solution of 83% C 12 BZK was diluted by injecting 95% ethyl alcohol and water to obtain 50% ethyl alcohol.
%, BZK as 2% w / v solution, 1% w / v solution, 0.5% w / v solution, 0.2% w / v
And 0.1% w / v solution were prepared. 5 ml of each preparation
The sterilization rate was 50% or more when the sterilization rate was examined after picking it up on the palm of the hand and thoroughly rubbing it 3 times.
実施例13 83%C12BZKの50%(w/v)水溶液に95%イソプロピルア
ルコール水を注入して稀釈し、イソプロピルアルコール
として40%とし、更に30%アルキルジエチルアミノエチ
ルグリシン塩酸塩(商品名テゴー51:ドデシル・アミノ
エチルグリシン塩酸塩18%およびテトラデシル・アミノ
エチルグリシン塩酸塩12%を含む。)を溶解して、アル
キルジエチルアミノエチルグリシン塩酸塩として0.02
%,BZKとしてそれぞれ1%,0.2%および0.1%w/v液を調
製した。それぞれの調製液を5ml当り手掌にとり、3回
よくもみ洗いした後、減菌率を調べると50%以上であっ
た。Example 13 95% isopropyl alcohol water was poured into a 50% (w / v) aqueous solution of 83% C 12 BZK to dilute it to 40% as isopropyl alcohol, and 30% alkyldiethylaminoethylglycine hydrochloride (trade name: Tego 51: Dodecyl-aminoethylglycine hydrochloride 18% and tetradecyl-aminoethylglycine hydrochloride 12% are dissolved) to give 0.02 as alkyldiethylaminoethylglycine hydrochloride.
%, BZK were prepared as 1%, 0.2% and 0.1% w / v solutions, respectively. After taking 5 ml of each preparation solution in the palm and thoroughly scrubbing 3 times, the sterilization rate was 50% or more.
実施例14 95%C12BZKの50%(w/v)水溶液に30%アルキルジエチ
ルアミノエチルグリシン塩酸塩を溶解して、アルキルジ
エチルアミノエチルグリシン塩酸塩として0.1%,BZKと
してそれぞれ2%w/v液,1%w/v液,0.5%w/v液,0.2%w/v
液および0.1%w/v液を調製した。それぞれの調製液を5m
l当り手掌にとり、3回よくもみ洗いした後、減菌率を
調べると50%以上であった。Example 14 30% Alkyldiethylaminoethylglycine hydrochloride was dissolved in 50% (w / v) aqueous solution of 95% C 12 BZK to prepare 0.1% of alkyldiethylaminoethylglycine hydrochloride and 2% w / v of BZK respectively. , 1% w / v solution, 0.5% w / v solution, 0.2% w / v
Solution and 0.1% w / v solution were prepared. 5m of each preparation
It was 50% or more when the sterilization rate was examined after pickling on the palm and thoroughly rubbing 3 times.
実施例15 界面活性剤ポリオキシ・エチレン・ポリオキシプロピレ
ングリコールエーテル250gを殺菌水道水500mlに溶解
し、これに更にヤシ油脂肪酸ジエタノールアミド50gを
溶解した。この溶液に83%C12BZK40%(W/V)水溶液を
3.75ml、25ml、50mlまたは125ml注入した。つぎに、こ
れらの各液に95%エチルアルコールを200ml加えた後、
殺菌水道水を加え全量を各1,000mlとし、全BZKとしてそ
れぞれ0.15%、1%、2%および5%(W/V)液を調製
した。それぞれの調製液を約5ml手掌にとり、よくもみ
洗いした後、滅菌率を調べると95%以上であった。Example 15 250 g of the surfactant polyoxyethylene polyoxypropylene glycol ether was dissolved in 500 ml of sterilized tap water, and 50 g of coconut oil fatty acid diethanolamide was further dissolved therein. Add 83% C 12 BZK 40% (W / V) solution to this solution.
3.75 ml, 25 ml, 50 ml or 125 ml was injected. Next, after adding 200 ml of 95% ethyl alcohol to each of these liquids,
Sterilized tap water was added to adjust the total amount to 1,000 ml, and 0.15%, 1%, 2% and 5% (W / V) solutions were prepared as total BZK, respectively. Approximately 5 ml of each preparation was placed on the palm of the hand, thoroughly washed with rubbing, and the sterilization rate was 95% or more.
実施例16 界面活性剤ヤシ油脂肪酸アミドプロピルベタイン100gを
殺菌水道水500mlに溶解し、これに更にポリオキシエチ
レンポリオキシプロピレングリコールエーテル100gを溶
解した。この溶液に83%C12BZK40%(W/V)水溶液を3.7
5ml、25ml、50mlまたは125ml注入した。つぎに、これら
の各液に95%エチルアルコールを200ml加えた後、殺菌
水道水を加え全量を各1,000mlとし、全BZKとしてそれぞ
れ0.15%、1%、2%および5%(W/V)液を調製し
た。それぞれの調製液を約5ml手掌にとり、よくもみ洗
いした後、滅菌率をを調べると95%以上出あった。Example 16 Surfactant 100 g of coconut oil fatty acid amide propyl betaine was dissolved in 500 ml of sterilized tap water, and further 100 g of polyoxyethylene polyoxypropylene glycol ether was dissolved therein. Add 83% C 12 BZK 40% (W / V) aqueous solution to this solution.
5 ml, 25 ml, 50 ml or 125 ml was injected. Next, after adding 200 ml of 95% ethyl alcohol to each of these liquids, sterilized tap water was added to make the total amount 1,000 ml each, and the total BZK was 0.15%, 1%, 2% and 5% (W / V), respectively. A liquid was prepared. Approximately 5 ml of each prepared solution was found on the palm, and after thoroughly scrubbing, the sterilization rate was 95% or more.
発明の効果 本発明はドデシル・ジメチル・ベンジルアンモニウムま
たはその塩を約80重量%以上含有するアルキル・ジメチ
ル・ベンジルアンモニウムまたはその塩と、低級アルコ
ール類,キレート剤および両性または非イオン性界面活
性剤の1種または2種以上を併用することに特徴があ
る。この併用によると、低級アルコール類、キレート
剤、または両性または非イオン性界面活性剤が通常、単
独では殺菌消毒効果を顕著に示さない程度の使用量で
も、上記アルキル・ジメチル・ベンジルアンモニウムま
たはその塩の殺菌消毒力が著しく増強される。また、低
級アルコール類、キレート剤、または両性または非イオ
ン性界面活性剤の単独使用で殺菌消毒力が認められる濃
度の場合には、上記アルキル・ジメチル・ベンジルアン
モニウムまたはその塩との併用によって相乗的に殺菌消
毒力が増強されるものである。このような併用効果は、
従来組成のアルキル・ジメチル・ベンジルアンモニウム
またはその塩の場合に比して、極めて顕著に認められ
る。EFFECTS OF THE INVENTION The present invention comprises an alkyl dimethyl benzyl ammonium or a salt thereof containing about 80% by weight or more of dodecyl dimethyl benzyl ammonium or a salt thereof, a lower alcohol, a chelating agent and an amphoteric or nonionic surfactant. It is characterized by using one kind or two or more kinds in combination. According to this combination, the lower alcohol, the chelating agent, or the amphoteric or nonionic surfactant is usually used in an amount such that the sterilizing and disinfecting effect is not significantly exhibited by itself, but the alkyl dimethyl benzyl ammonium or the salt thereof is used. The sterilizing and disinfecting power of is significantly enhanced. In addition, when the concentration is such that the disinfecting power can be recognized by using lower alcohols, chelating agents, or amphoteric or nonionic surfactants alone, synergistic effects can be obtained by using them together with the above alkyl dimethyl benzyl ammonium or a salt thereof. The sterilizing and disinfecting power is enhanced. Such combined effect is
Compared with the case of alkyl dimethyl benzyl ammonium having a conventional composition or a salt thereof, it is extremely remarkably observed.
この結果、本発明の殺菌消毒法は各種の対象物に幅広く
有効に適用することができ、とりわけ対象物中に有機物
が存在していても殺菌消毒力の低下が少ないという点で
実用的に有用である。As a result, the sterilization method of the present invention can be widely and effectively applied to various kinds of objects, and in particular, it is practically useful in that the sterilization and disinfection power is less likely to decrease even if organic substances are present in the objects. Is.
Claims (1)
ムまたはその塩を約80重量%以上含有するアルキル・ジ
メチル・ベンジルアンモニウムまたはその塩と、低級ア
ルコール類,キレート剤および両性または非イオン性界
面活性剤の1種または2種以上とを含有してなる殺菌消
毒剤。1. An alkyl dimethyl benzyl ammonium or a salt thereof containing dodecyl dimethyl benzyl ammonium or a salt thereof in an amount of about 80% by weight or more, and a lower alcohol, a chelating agent and an amphoteric or nonionic surfactant. A sterilizing agent containing one or more species.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61162548A JPH0759482B2 (en) | 1985-07-10 | 1986-07-09 | Disinfectant |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15323985 | 1985-07-10 | ||
| JP60-153239 | 1985-08-19 | ||
| JP60-182656 | 1985-08-19 | ||
| JP18265685 | 1985-08-19 | ||
| JP61162548A JPH0759482B2 (en) | 1985-07-10 | 1986-07-09 | Disinfectant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62129202A JPS62129202A (en) | 1987-06-11 |
| JPH0759482B2 true JPH0759482B2 (en) | 1995-06-28 |
Family
ID=27320430
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61162548A Expired - Lifetime JPH0759482B2 (en) | 1985-07-10 | 1986-07-09 | Disinfectant |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0759482B2 (en) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2557242B2 (en) * | 1987-12-23 | 1996-11-27 | 株式会社ジーシーデンタルプロダクツ | Cleaning and disinfecting solution for dental treatment instruments |
| EP0629347B1 (en) * | 1992-01-23 | 1997-07-02 | Morinaga Milk Industry Co., Ltd. | Antibacterial agent and treatment of article therewith |
| GB9323270D0 (en) * | 1993-11-12 | 1994-01-05 | Green Bruce P | Disinfectant composition |
| JP3636611B2 (en) * | 1999-03-19 | 2005-04-06 | 日華化学株式会社 | Disinfectant composition |
| GB9910251D0 (en) * | 1999-05-05 | 1999-06-30 | Ciba Geigy Ag | Process for the preparation of pigment compositions |
| JP2002193706A (en) * | 2000-12-25 | 2002-07-10 | Kenei Pharmaceutical Co Ltd | Antibacterial disinfectant for external use |
| JP4632676B2 (en) * | 2004-02-23 | 2011-02-16 | 小林製薬株式会社 | Spatial disinfection composition and spatial disinfection method |
| JP4632675B2 (en) * | 2004-02-23 | 2011-02-16 | 小林製薬株式会社 | Spatial disinfection composition and spatial disinfection method |
| JP2006069919A (en) * | 2004-08-31 | 2006-03-16 | Asahi Kasei Chemicals Corp | Disinfectant |
| JP5567264B2 (en) * | 2008-11-27 | 2014-08-06 | ユニ・チャーム株式会社 | Chemical solution for alcohol sanitization sheet and alcohol sanitization sheet containing the same |
| JP5784920B2 (en) * | 2011-02-10 | 2015-09-24 | 花王株式会社 | Anti-residential fungi |
| JP2020128354A (en) * | 2019-02-08 | 2020-08-27 | 吉田製薬株式会社 | Disinfection agent |
| JP7345886B2 (en) * | 2020-05-25 | 2023-09-19 | 株式会社東洋新薬 | Alcohol-containing composition |
| JP2022092900A (en) * | 2020-12-11 | 2022-06-23 | サンスター株式会社 | Oral composition |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS529684B2 (en) * | 1971-12-29 | 1977-03-17 | ||
| JPS50132126A (en) * | 1974-04-13 | 1975-10-20 | ||
| JPS5330786A (en) * | 1976-09-03 | 1978-03-23 | Oki Electric Cable | Shield core of flexible cord |
| JPS5379029A (en) * | 1976-12-24 | 1978-07-13 | Nippon Oil & Fats Co Ltd | Preventives against putrefaction and mold growing of artificial feed for sericulture |
| PL110343B1 (en) * | 1977-11-16 | 1980-07-31 | Inst Przemyslu Organiczego | Parasite killing agent for detrimental microbes control |
-
1986
- 1986-07-09 JP JP61162548A patent/JPH0759482B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62129202A (en) | 1987-06-11 |
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