JP6527856B2 - ブロノポール、ダゾメット、または4−(2−ニトロブチル)モルホリンと4,4’−(2−エチル−2−ニトロトリメチレン)ジモルホリンとの混合物を含む殺微生物性組成物 - Google Patents
ブロノポール、ダゾメット、または4−(2−ニトロブチル)モルホリンと4,4’−(2−エチル−2−ニトロトリメチレン)ジモルホリンとの混合物を含む殺微生物性組成物 Download PDFInfo
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- 239000000203 mixture Substances 0.000 title claims description 47
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 title claims description 26
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 title claims description 18
- GQHVWDKJTDUZRP-UHFFFAOYSA-N 4-(2-nitrobutyl)morpholine Chemical compound CCC([N+]([O-])=O)CN1CCOCC1 GQHVWDKJTDUZRP-UHFFFAOYSA-N 0.000 title claims description 6
- 239000005644 Dazomet Substances 0.000 title description 14
- 230000003115 biocidal effect Effects 0.000 title description 6
- XPGDDCOXMUFUCB-UHFFFAOYSA-N 4,4'-(ethyl-2-nitropropane-1,3-diyl)bismorpholine Chemical compound C1COCCN1CC([N+]([O-])=O)(CC)CN1CCOCC1 XPGDDCOXMUFUCB-UHFFFAOYSA-N 0.000 title description 5
- 229960003168 bronopol Drugs 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 239000002736 nonionic surfactant Substances 0.000 claims description 27
- 230000003641 microbiacidal effect Effects 0.000 claims description 15
- 230000002195 synergetic effect Effects 0.000 claims description 11
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 6
- -1 2-ethyl-2-nitro-trimethylene Chemical group 0.000 claims description 5
- 241000894006 Bacteria Species 0.000 claims description 4
- 241000233866 Fungi Species 0.000 claims description 3
- 241000192125 Firmicutes Species 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 description 24
- RFUIWOPDUBEIOE-UHFFFAOYSA-N 4-[2-(morpholin-4-ylmethyl)-2-nitrobutyl]morpholine;4-(2-nitrobutyl)morpholine Chemical compound CCC([N+]([O-])=O)CN1CCOCC1.C1COCCN1CC([N+]([O-])=O)(CC)CN1CCOCC1 RFUIWOPDUBEIOE-UHFFFAOYSA-N 0.000 description 12
- 239000003139 biocide Substances 0.000 description 10
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- 244000005700 microbiome Species 0.000 description 7
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- 230000001070 adhesive effect Effects 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000002401 inhibitory effect Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229940126062 Compound A Drugs 0.000 description 4
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 4
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 229940124561 microbicide Drugs 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 238000005555 metalworking Methods 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- PUSPAPGHKSLKKH-UHFFFAOYSA-N 2-methyl-1,2-thiazolidin-3-one Chemical compound CN1SCCC1=O PUSPAPGHKSLKKH-UHFFFAOYSA-N 0.000 description 2
- 101100288310 Arabidopsis thaliana KTI2 gene Proteins 0.000 description 2
- 241000222122 Candida albicans Species 0.000 description 2
- 229940095731 candida albicans Drugs 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- WSDISUOETYTPRL-UHFFFAOYSA-N dmdm hydantoin Chemical compound CC1(C)N(CO)C(=O)N(CO)C1=O WSDISUOETYTPRL-UHFFFAOYSA-N 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
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- 239000002609 medium Substances 0.000 description 2
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- 229920003023 plastic Polymers 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- OLQJQHSAWMFDJE-UHFFFAOYSA-N 2-(hydroxymethyl)-2-nitropropane-1,3-diol Chemical group OCC(CO)(CO)[N+]([O-])=O OLQJQHSAWMFDJE-UHFFFAOYSA-N 0.000 description 1
- 241000228245 Aspergillus niger Species 0.000 description 1
- 244000276440 Betula nigra Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000199914 Dinophyceae Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000237852 Mollusca Species 0.000 description 1
- 240000005428 Pistacia lentiscus Species 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 241000295644 Staphylococcaceae Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241001061127 Thione Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000003619 algicide Substances 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
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- 239000011093 chipboard Substances 0.000 description 1
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- 239000002537 cosmetic Substances 0.000 description 1
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- 239000003599 detergent Substances 0.000 description 1
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- 230000000694 effects Effects 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000002828 fuel tank Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000002855 microbicide agent Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 239000001965 potato dextrose agar Substances 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- AKUNSPZHHSNFFX-UHFFFAOYSA-M tributyl(tetradecyl)phosphanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC AKUNSPZHHSNFFX-UHFFFAOYSA-M 0.000 description 1
- 239000001974 tryptic soy broth Substances 0.000 description 1
- 108010050327 trypticase-soy broth Proteins 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
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- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は、(a)構造、
R2O(CH2CH(CH3)O)3(CH2CH2O)5H
を有し、式中、R2が、C8−C14直鎖アルキル基の混合物である、非イオン性界面活性剤と、(b)2−ブロモ−2−ニトロプロパン−1,3−ジオールと、を含み、該非イオン性界面活性剤と2−ブロモ−2−ニトロプロパン−1,3−ジオールとの重量比が、1:0.08〜1:0.12または1:0.2〜1:1.8286である、相乗的な殺微生物性組成物を対象とする。
R2O(CH2CH(CH3)O)3(CH2CH2O)5H
を有し、式中、R2が、C8−C14直鎖アルキル基の混合物である、非イオン性界面活性剤と、(b)テトラヒドロ−3,5−ジメチル−2H−1,3,5−チアジアジン−2−チオンと、を含み、該非イオン性界面活性剤とテトラヒドロ−3,5−ジメチル−2H−1,3,5−チアジアジン−2−チオンとの重量比が、1:0.0024〜1:0.4571である、相乗的な殺微生物性組成物を対象とする。
R1O(CH2CH(CH3)O)5(CH2CH2O)9H
を有し、式中、R1がC8アルキル基である、非イオン性界面活性剤と、(b)81:5の重量比での4−(2−ニトロブチル)モルホリンと4,4’−(2−エチル−2−ニトロトリメチレン)ジモルホリンとの混合物と、を含み、該非イオン性界面活性剤と該混合物との重量比が、1:0.0006〜1:0.2743である、相乗的な殺微生物性組成物を対象とする。
R2O(CH2CH(CH3)O)3(CH2CH2O)5H
を有し、式中、R2が、C8−C14直鎖アルキル基の混合物である、非イオン性界面活性剤と、BNPDとの重量比は、1:0.2286〜1:1.18286である。
R2O(CH2CH(CH3)O)3(CH2CH2O)5H
を有し、式中、R2が、C8−C14直鎖アルキル基の混合物である、非イオン性界面活性剤と、(b)BNPDと、を添加することによって、水性培地中のかび、好ましくはカンジダ・アルビカンスの増殖を阻害するための方法を対象とし、該非イオン性界面活性剤とBNPDとの重量比は、1:0.08〜1:0.12または1:0.2〜1:1.8286、好ましくは1:0.2286〜1:1.18286である。
R2O(CH2CH(CH3)O)3(CH2CH2O)5H
を有し、式中、R2が、C8−C14直鎖アルキル基の混合物である、非イオン性界面活性剤と、ダゾメットとの重量比は、1:0.0114〜1:0.4571である。
R2O(CH2CH(CH3)O)3(CH2CH2O)5H
を有し、式中、R2が、C8−C14直鎖アルキル基の混合物である、非イオン性界面活性剤と、(b)ダゾメットと、を添加することによって、水性培地中の黄色ブドウ球菌の増殖を阻害するための方法を対象とし、該非イオン性界面活性剤とダゾメットとの重量比は、1:0.0114〜1:0.4571である。
R1O(CH2CH(CH3)O)5(CH2CH2O)9H
を有し、式中、R1が、C8アルキル基である、非イオン性界面活性剤と、BIOBAN P−1487との重量比は、1:0.0160〜1:0.2743である。
R1O(CH2CH(CH3)O)5(CH2CH2O)9H
を有し、式中、R1が、C8アルキル基である、非イオン性界面活性剤をBIOBAN P−1487に添加することによって、水性培地中の真菌、好ましくはクロコウジカビの増殖を阻害するための方法を対象とし、1:0.0160〜1:0.2743である。
界面活性剤D R2O(CH2CH(CH3)O)3(CH2CH2O)5H
界面活性剤E R2O(CH2CH(CH3)O)3(CH2CH2O)7H
界面活性剤D及び界面活性剤Eにおいて、R2は、C8−C14直鎖アルキル基の混合物(70%のC8−C10直鎖アルキル及び30%のC12−C14直鎖アルキル)である。
Ca/CA+Cb/CB=相乗作用指数(「SI」)
式中、
CA=エンドポイントをもたらした、単独で作用しているppm単位での化合物Aの濃度(化合物AのMIC)。
Ca=エンドポイントをもたらした、混合物中のppm単位での化合物Aの濃度。
CB=エンドポイントをもたらした、単独で作用しているppm単位での化合物Bの濃度(化合物BのMIC)。
Cb=エンドポイントをもたらした、混合物中のppm単位での化合物Bの濃度。
Ca/CAとCb/CBとの合計が1よりも大きい場合、拮抗作用が示される。合計が1に等しい場合、相加作用が示され、1未満の場合、相乗作用が実証される。
界面活性剤A
安息香酸ナトリウム、トリスニトロ
界面活性剤E
DMDMH
界面活性剤D
CS−1246、OPP、DMDMH
界面活性剤A
DIDAC、IPBC
界面活性剤E
CMIT/MIT、IPBC、OIT、TTPC、WSCP
界面活性剤D
CMIT/MIT、OIT、DIDAC
(MBIT、IPBC、WSCPは、1つのデータ点を除いて、1:0.05でのみ相乗的であったか、それよりも劣っていた)
Claims (6)
- (a)構造、
R2O(CH2CH(CH3)O)3(CH2CH2O)5H
を有し、式中、R2が、C8−C14直鎖アルキル基の混合物である、非イオン性界面活性剤と、(b)2−ブロモ−2−ニトロプロパン−1,3−ジオールと、を含み、前記非イオン性界面活性剤の2−ブロモ−2−ニトロプロパン−1,3−ジオールに対する重量比が、1:0.08〜1:0.12または1:0.2〜1:1.8286である、かび及び酵母に対して相乗的な殺微生物性組成物。 - 前記C8−C14直鎖アルキル基の混合物が、60〜75重量%のC8−C10直鎖アルキル基及び25〜40重量%のC12−C14直鎖アルキル基を含む、請求項1に記載の相乗的な殺微生物性組成物。
- (a)構造、
R2O(CH2CH(CH3)O)3(CH2CH2O)5H
を有し、式中、R2が、C8−C14直鎖アルキル基の混合物である、非イオン性界面活性剤と、(b)テトラヒドロ−3,5−ジメチル−2H−1,3,5−チアジアジン−2−チオンと、を含み、前記非イオン性界面活性剤のテトラヒドロ−3,5−ジメチル−2H−1,3,5−チアジアジン−2−チオンに対する重量比が、1:0.012〜1:0.4571である、かび、酵母、及びグラム陽性細菌に対して相乗的な殺微生物性組成物。 - 前記C8−C14直鎖アルキル基の混合物が、60〜75重量%のC8−C10直鎖アルキル基及び25〜40重量%のC12−C14直鎖アルキル基を含む、請求項3に記載の前記相乗的な殺微生物性組成物。
- (a)構造、
R1O(CH2CH(CH3)O)5(CH2CH2O)9H
を有し、式中、R1がC8アルキル基である、非イオン性界面活性剤と、(b)81:5の重量比での4−(2−ニトロブチル)モルホリンと4,4’−(2−エチル−2−ニトロトリメチレン)ジモルホリンとの混合物と、を含み、前記非イオン性界面活性剤の前記混合物に対する重量比が、1:0.0006〜1:0.002または1:0.0032〜1:0.2743である、かび、酵母、及びグラム陰性細菌に対して相乗的な殺微生物性組成物。 - R1が、2−エチルヘキシルである、請求項5に記載の相乗的な殺微生物性組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361886344P | 2013-10-03 | 2013-10-03 | |
US61/886,344 | 2013-10-03 | ||
PCT/US2014/058954 WO2015051205A1 (en) | 2013-10-03 | 2014-10-03 | Microbicidal composition comprising bronopol, dazomet or a mixture of 4-(2-nitrobutyl)morpholine and 4,4'-(2-ethyl-2-nitrotrimethylene)dimorpholine |
Publications (2)
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JP6527856B2 true JP6527856B2 (ja) | 2019-06-05 |
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JP2016517400A Expired - Fee Related JP6527856B2 (ja) | 2013-10-03 | 2014-10-03 | ブロノポール、ダゾメット、または4−(2−ニトロブチル)モルホリンと4,4’−(2−エチル−2−ニトロトリメチレン)ジモルホリンとの混合物を含む殺微生物性組成物 |
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EP (1) | EP3027024B1 (ja) |
JP (1) | JP6527856B2 (ja) |
CN (1) | CN105578881B (ja) |
AU (1) | AU2014329443B2 (ja) |
BR (1) | BR112016006598B1 (ja) |
CA (1) | CA2926623A1 (ja) |
RU (1) | RU2653763C2 (ja) |
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AR105031A1 (es) * | 2015-06-25 | 2017-08-30 | Dow Global Technologies Llc | Composición microbicida |
US11071301B2 (en) | 2016-10-21 | 2021-07-27 | Ecolab Usa Inc. | Anti-microbial agent to control biomass accumulation in SO2 scrubbers |
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US3054749A (en) * | 1960-06-10 | 1962-09-18 | Commercial Solvents Corp | Process for the control of bacteria in water flooding operations in secondary oil recovery |
US3647703A (en) * | 1970-01-02 | 1972-03-07 | Betz Laboratories | Synergistic composition and its use |
US3664821A (en) * | 1970-01-02 | 1972-05-23 | Betz Laboratories | Slimicidal composition and its use |
US3759828A (en) * | 1971-07-12 | 1973-09-18 | Texaco Inc | Soluble oil compositions |
US4295932A (en) | 1980-07-14 | 1981-10-20 | Naloc Chemical Company | Synergistic blend of biocides |
GB2138798A (en) | 1983-04-25 | 1984-10-31 | Dearborn Chemicals Ltd | Biocide |
US4607036A (en) * | 1983-12-15 | 1986-08-19 | Lever Brothers Company | Preservative compositions employing anti-microbial morpholine derivatives |
GB8830266D0 (en) | 1988-12-24 | 1989-02-22 | Laporte Industries Ltd | Absorbent material |
US6241898B1 (en) | 1996-04-19 | 2001-06-05 | Betzdearborn Inc. | Method for inhibiting microbial adhesion on surfaces |
US6039965A (en) | 1996-09-27 | 2000-03-21 | Calgon Corporation | Surfanctants for reducing bacterial adhesion onto surfaces |
GB2354771A (en) * | 1999-10-01 | 2001-04-04 | Mcbride Ltd Robert | Bactericide combinations in detergents |
JP4815070B2 (ja) * | 2001-06-20 | 2011-11-16 | 株式会社パーマケム・アジア | トイレット用水の処理剤 |
US6562773B1 (en) * | 2002-08-26 | 2003-05-13 | Colgate-Palmolive Company | Light duty liquid cleaning compositions having improved preservative system |
DE10309425B4 (de) * | 2003-03-05 | 2010-12-30 | Bk Giulini Gmbh | Mikrobizid zur Desinfektion von industriellen Wasserkreisläufen |
JP2006036674A (ja) * | 2004-07-26 | 2006-02-09 | Permachem Asia Ltd | カップ式自動販売機用防腐・消臭剤 |
JP2006061684A (ja) * | 2004-07-28 | 2006-03-09 | Nippon Soda Co Ltd | し尿用防臭組成物 |
EP2046936A4 (en) | 2006-08-04 | 2010-01-06 | Stepan Co | BIOCIDAL COMPOSITIONS AND METHODS |
WO2008031087A1 (en) | 2006-09-08 | 2008-03-13 | Delaval Holdings Ab | Compositions comprising a c2-c14 carboxylic acid and a surfactant for treating hoof diseases |
BRPI0720328B1 (pt) * | 2007-01-11 | 2018-06-12 | Dow Global Technologies Inc. | Composição tensoativa e detergente ou limpador. |
BRPI0720337A2 (pt) * | 2007-01-12 | 2015-09-29 | Angus Chemical | "composição biocida, método para inibir o crescimento de microorganismo em um sistema base aquosa, composição na qual o crescimento microbiano está inibido e composto" |
JP2011524940A (ja) * | 2008-06-18 | 2011-09-08 | ダウ グローバル テクノロジーズ エルエルシー | ミッドレンジ・アルコキシレートを含む洗浄用組成物 |
JP5295710B2 (ja) * | 2008-10-10 | 2013-09-18 | 住化エンビロサイエンス株式会社 | 工業用抗菌組成物 |
WO2011150224A1 (en) * | 2010-05-28 | 2011-12-01 | Isp Investments Inc. | A phosphate-free highly concentrated aqueous dispersion composition of biocides and process for preparing the same |
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2014
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- 2014-10-03 CA CA2926623A patent/CA2926623A1/en not_active Abandoned
- 2014-10-03 AU AU2014329443A patent/AU2014329443B2/en not_active Ceased
- 2014-10-03 RU RU2016117115A patent/RU2653763C2/ru not_active IP Right Cessation
- 2014-10-03 EP EP14790421.3A patent/EP3027024B1/en active Active
- 2014-10-03 JP JP2016517400A patent/JP6527856B2/ja not_active Expired - Fee Related
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2017
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US20170325449A1 (en) | 2017-11-16 |
US20170325450A1 (en) | 2017-11-16 |
WO2015051205A1 (en) | 2015-04-09 |
BR112016006598A2 (pt) | 2017-08-01 |
RU2016117115A (ru) | 2017-11-10 |
RU2653763C2 (ru) | 2018-05-14 |
US9775343B2 (en) | 2017-10-03 |
AU2014329443B2 (en) | 2017-12-21 |
EP3027024A1 (en) | 2016-06-08 |
JP2016532636A (ja) | 2016-10-20 |
CN105578881B (zh) | 2018-03-27 |
CA2926623A1 (en) | 2015-04-09 |
US20160227769A1 (en) | 2016-08-11 |
US9832992B1 (en) | 2017-12-05 |
AU2014329443A1 (en) | 2016-05-05 |
BR112016006598B1 (pt) | 2020-09-15 |
RU2016117115A3 (ja) | 2018-02-28 |
EP3027024B1 (en) | 2017-07-26 |
CN105578881A (zh) | 2016-05-11 |
US9808001B1 (en) | 2017-11-07 |
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