FI105524B - Desinfiointiseokset - Google Patents

Desinfiointiseokset Download PDF

Info

Publication number: FI105524B
Authority: FI; Finland
Prior art keywords: acid; mixture; weight; disinfectant; water
Prior art date: 1992-04-16

Application number

FI931700A

Other languages

English (en)

Finnish (fi)

Swedish (sv)

Other versions

FI931700A0 (fi

FI931700L (fi

Inventor

Peter Benjamins

Boer Robbert De

Original Assignee

Unilever Nv

Priority date (The priority date 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 date listed.)

1992-04-16

Filing date

1993-04-15

Publication date

2000-09-15

1993-04-15 Application filed by Unilever Nv filed Critical Unilever Nv

1993-04-15 Publication of FI931700A0 publication Critical patent/FI931700A0/fi

1993-10-17 Publication of FI931700L publication Critical patent/FI931700L/fi

2000-09-15 Application granted granted Critical

2000-09-15 Publication of FI105524B publication Critical patent/FI105524B/fi

Links

239000000203 mixture Substances 0.000 title claims description 83
238000004659 sterilization and disinfection Methods 0.000 title claims description 5
239000000645 desinfectant Substances 0.000 claims abstract description 38
150000007524 organic acids Chemical class 0.000 claims abstract description 23
239000007787 solid Substances 0.000 claims abstract description 6
238000007865 diluting Methods 0.000 claims abstract description 3
239000000725 suspension Substances 0.000 claims abstract description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 27
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 21
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 14
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid group Chemical group C(CCC(=O)O)(=O)O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 13
235000019260 propionic acid Nutrition 0.000 claims description 7
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 7
-1 peroxy compound Chemical class 0.000 claims description 6
239000003352 sequestering agent Substances 0.000 claims description 6
238000000034 method Methods 0.000 claims description 5
239000004094 surface-active agent Substances 0.000 claims description 5
150000001412 amines Chemical class 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 claims description 2
239000003945 anionic surfactant Substances 0.000 claims description 2
230000000249 desinfective effect Effects 0.000 claims description 2
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims description 2
239000002736 nonionic surfactant Substances 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims 1
150000002894 organic compounds Chemical class 0.000 claims 1
235000011007 phosphoric acid Nutrition 0.000 claims 1
150000003016 phosphoric acids Chemical class 0.000 claims 1
229920000768 polyamine Polymers 0.000 claims 1
150000004967 organic peroxy acids Chemical class 0.000 abstract description 6
239000012141 concentrate Substances 0.000 abstract description 4
125000000864 peroxy group Chemical group O(O*)* 0.000 abstract description 2
230000003641 microbiacidal effect Effects 0.000 description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
150000004965 peroxy acids Chemical class 0.000 description 16
239000002253 acid Substances 0.000 description 12
238000009472 formulation Methods 0.000 description 12
239000012895 dilution Substances 0.000 description 11
238000010790 dilution Methods 0.000 description 11
108091003079 Bovine Serum Albumin Proteins 0.000 description 9
229940098773 bovine serum albumin Drugs 0.000 description 8
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
239000001384 succinic acid Substances 0.000 description 6
241000589516 Pseudomonas Species 0.000 description 5
235000005985 organic acids Nutrition 0.000 description 5
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
230000000694 effects Effects 0.000 description 4
241000894006 Bacteria Species 0.000 description 3
241000589517 Pseudomonas aeruginosa Species 0.000 description 3
239000007900 aqueous suspension Substances 0.000 description 3
230000003115 biocidal effect Effects 0.000 description 3
229910052938 sodium sulfate Inorganic materials 0.000 description 3
235000011152 sodium sulphate Nutrition 0.000 description 3
LMYSNFBROWBKMB-UHFFFAOYSA-N 4-[2-(dipropylamino)ethyl]benzene-1,2-diol Chemical compound CCCN(CCC)CCC1=CC=C(O)C(O)=C1 LMYSNFBROWBKMB-UHFFFAOYSA-N 0.000 description 2
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 2
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
230000015556 catabolic process Effects 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
230000007423 decrease Effects 0.000 description 2
238000006731 degradation reaction Methods 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
230000003442 weekly effect Effects 0.000 description 2
125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
FZIPCQLKPTZZIM-UHFFFAOYSA-N 2-oxidanylpropane-1,2,3-tricarboxylic acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O.OC(=O)CC(O)(C(O)=O)CC(O)=O FZIPCQLKPTZZIM-UHFFFAOYSA-N 0.000 description 1
229910014033 C-OH Inorganic materials 0.000 description 1
229910014570 C—OH Inorganic materials 0.000 description 1
241000588724 Escherichia coli Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000004594 Masterbatch (MB) Substances 0.000 description 1
241000108056 Monas Species 0.000 description 1
MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
241000588770 Proteus mirabilis Species 0.000 description 1
240000004808 Saccharomyces cerevisiae Species 0.000 description 1
241000191967 Staphylococcus aureus Species 0.000 description 1
241000194017 Streptococcus Species 0.000 description 1
244000269722 Thea sinensis Species 0.000 description 1
241000700605 Viruses Species 0.000 description 1
ZQOMKIOQTCAGCM-UHFFFAOYSA-L [Na+].[Na+].OS(O)(=O)=O.[O-]S([O-])(=O)=O Chemical compound [Na+].[Na+].OS(O)(=O)=O.[O-]S([O-])(=O)=O ZQOMKIOQTCAGCM-UHFFFAOYSA-L 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
241001148470 aerobic bacillus Species 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
208000022506 anaerobic bacteria infectious disease Diseases 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
235000013361 beverage Nutrition 0.000 description 1
239000003139 biocide Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
DUYCTCQXNHFCSJ-UHFFFAOYSA-N dtpmp Chemical compound OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)(O)=O DUYCTCQXNHFCSJ-UHFFFAOYSA-N 0.000 description 1
NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
235000013305 food Nutrition 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910017053 inorganic salt Inorganic materials 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
ZDGGJQMSELMHLK-UHFFFAOYSA-N m-Trifluoromethylhippuric acid Chemical compound OC(=O)CNC(=O)C1=CC=CC(C(F)(F)F)=C1 ZDGGJQMSELMHLK-UHFFFAOYSA-N 0.000 description 1
238000005259 measurement Methods 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
230000002906 microbiologic effect Effects 0.000 description 1
244000005700 microbiome Species 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
210000000214 mouth Anatomy 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000008194 pharmaceutical composition Substances 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
239000000126 substance Substances 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group; Thio analogues thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Food Preservation Except Freezing, Refrigeration, And Drying (AREA)

FI931700A 1992-04-16 1993-04-15 Desinfiointiseokset FI105524B (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP92201093		1992-04-16
EP92201093		1992-04-16

Publications (3)

Publication Number	Publication Date
FI931700A0 FI931700A0 (fi)	1993-04-15
FI931700L FI931700L (fi)	1993-10-17
FI105524B true FI105524B (fi)	2000-09-15

Family

ID=8210554

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI931700A FI105524B (fi)	1992-04-16	1993-04-15	Desinfiointiseokset

Country Status (8)

Country	Link
EP (1)	EP0569066B1 (fr)
AU (1)	AU667085B2 (fr)
BR (1)	BR9301552A (fr)
CA (1)	CA2093888A1 (fr)
DE (1)	DE69300694T2 (fr)
ES (1)	ES2079940T3 (fr)
FI (1)	FI105524B (fr)
ZA (1)	ZA932689B (fr)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5437868A (en) *	1991-07-23	1995-08-01	Ecolab Inc.	Peroxyacid antimicrobial composition
GB2277028B (en) *	1993-12-24	1996-01-03	Gw Chemicals Ltd	Cleaning beer dispense lines using peracetic acid
US6010729A (en)	1998-08-20	2000-01-04	Ecolab Inc.	Treatment of animal carcasses
GB2341553A (en) *	1998-09-15	2000-03-22	Procter & Gamble	Peroxyacid treatment
US6844305B1 (en)	1999-08-27	2005-01-18	The Proctor & Gamble Company	Aqueous liquid detergent compositions comprising a polymeric stabilization system
WO2001082694A1 (fr)	2000-04-28	2001-11-08	Ecolab Inc.	Composition antimicrobienne
US7150884B1 (en)	2000-07-12	2006-12-19	Ecolab Inc.	Composition for inhibition of microbial growth
US6479454B1 (en)	2000-10-05	2002-11-12	Ecolab Inc.	Antimicrobial compositions and methods containing hydrogen peroxide and octyl amine oxide
US6514556B2 (en)	2000-12-15	2003-02-04	Ecolab Inc.	Method and composition for washing poultry during processing
US7316824B2 (en)	2000-12-15	2008-01-08	Ecolab Inc.	Method and composition for washing poultry during processing
US6964787B2 (en)	2001-02-01	2005-11-15	Ecolab Inc.	Method and system for reducing microbial burden on a food product
US6627593B2 (en)	2001-07-13	2003-09-30	Ecolab Inc.	High concentration monoester peroxy dicarboxylic acid compositions, use solutions, and methods employing them
US7060301B2 (en)	2001-07-13	2006-06-13	Ecolab Inc.	In situ mono-or diester dicarboxylate compositions
US7622606B2 (en)	2003-01-17	2009-11-24	Ecolab Inc.	Peroxycarboxylic acid compositions with reduced odor
US8999175B2 (en)	2004-01-09	2015-04-07	Ecolab Usa Inc.	Methods for washing and processing fruits, vegetables, and other produce with medium chain peroxycarboxylic acid compositions
US7771737B2 (en)	2004-01-09	2010-08-10	Ecolab Inc.	Medium chain peroxycarboxylic acid compositions
US7507429B2 (en)	2004-01-09	2009-03-24	Ecolab Inc.	Methods for washing carcasses, meat, or meat products with medium chain peroxycarboxylic acid compositions
US7887641B2 (en)	2004-01-09	2011-02-15	Ecolab Usa Inc.	Neutral or alkaline medium chain peroxycarboxylic acid compositions and methods employing them
US7504123B2 (en)	2004-01-09	2009-03-17	Ecolab Inc.	Methods for washing poultry during processing with medium chain peroxycarboxylic acid compositions
BRPI0506713A (pt)	2004-01-09	2007-05-02	Ecolab Inc	composições de ácido peroxicarboxìlico de cadeia média
US7754670B2 (en)	2005-07-06	2010-07-13	Ecolab Inc.	Surfactant peroxycarboxylic acid compositions
US8075857B2 (en)	2006-10-18	2011-12-13	Ecolab Usa Inc.	Apparatus and method for making a peroxycarboxylic acid
US7547421B2 (en)	2006-10-18	2009-06-16	Ecolab Inc.	Apparatus and method for making a peroxycarboxylic acid
JP2011525539A (ja)	2008-06-24	2011-09-22	フレッシュ・エクスプレス・インコーポレイテッド	過酸および２−ヒドロキシ有機酸組成物および農産物を処理する方法
JP7334174B2 (ja)	2018-02-14	2023-08-28	エコラボユーエスエーインコーポレイティド	膜からバイオフィルムおよび胞子を低減するための組成物および方法
EP4474452A3 (fr)	2019-06-17	2025-03-05	Ecolab USA Inc.	Blanchiment et désinfection de textiles à l'aide d'une composition mixte d'acides peroxycarboxyliques hydrophiles et hydrophobes

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4147720A (en) *	1977-12-30	1979-04-03	Fmc Corporation	Process for preparing aliphatic diperoxydicarboxylic acids
GB8724899D0 (en) *	1987-10-23	1987-11-25	Unilever Plc	Detergent bleach compositions
DE3929335A1 (de) *	1989-09-04	1991-03-07	Henkel Kgaa	Verfahren zur desinfektion von textilien in waschstrassen
EP0461700A1 (fr) *	1990-06-12	1991-12-18	Akzo Nobel N.V.	Compositions désinfectantes aqueuses, et concentrées pour leur préparation
US5200189A (en) *	1991-07-23	1993-04-06	Ecolab Inc.	Peroxyacid antimicrobial composition

1993
- 1993-04-02 ES ES93200974T patent/ES2079940T3/es not_active Expired - Lifetime
- 1993-04-02 EP EP93200974A patent/EP0569066B1/fr not_active Expired - Lifetime
- 1993-04-02 DE DE69300694T patent/DE69300694T2/de not_active Expired - Lifetime
- 1993-04-13 CA CA002093888A patent/CA2093888A1/fr not_active Abandoned
- 1993-04-13 AU AU36842/93A patent/AU667085B2/en not_active Ceased
- 1993-04-15 FI FI931700A patent/FI105524B/fi not_active IP Right Cessation
- 1993-04-15 BR BR9301552A patent/BR9301552A/pt not_active IP Right Cessation
- 1993-04-16 ZA ZA932689A patent/ZA932689B/xx unknown

Also Published As

Publication number	Publication date
FI931700A0 (fi)	1993-04-15
ES2079940T3 (es)	1996-01-16
ZA932689B (en)	1994-10-16
FI931700L (fi)	1993-10-17
AU667085B2 (en)	1996-03-07
BR9301552A (pt)	1993-10-19
CA2093888A1 (fr)	1993-10-17
AU3684293A (en)	1993-10-21
EP0569066B1 (fr)	1995-10-25
EP0569066A1 (fr)	1993-11-10
DE69300694T2 (de)	1996-03-21
DE69300694D1 (de)	1995-11-30

Publication	Publication Date	Title
FI105524B (fi)	2000-09-15	Desinfiointiseokset
US4917815A (en)	1990-04-17	Stable aqueous aromatic percarboxylic acid solution
CA2108177C (fr)	2000-08-08	Composition antimicrobienne a base de peroxyacide
AU676902B2 (en)	1997-03-27	Peroxyacid antimicrobial composition
US6803057B2 (en)	2004-10-12	Hydrogen peroxide disinfectant with increased activity
AU714438B2 (en)	2000-01-06	Disinfectant compositions
AU680831B2 (en)	1997-08-14	Microbicidal compositions and methods
US5462714A (en)	1995-10-31	Antimicrobial composition and methods of use
JPH06501913A (ja)	1994-03-03	防食性殺菌剤
US7144846B2 (en)	2006-12-05	Acidic phenolic disinfectant compositions
JP2010526816A (ja)	2010-08-05	抗菌性組成物並びにそれを製造及び使用する方法
WO2005014057A1 (fr)	2005-02-17	Compositions desinfectantes et leurs procedes de fabrication et d'utilisation
EP0461700A1 (fr)	1991-12-18	Compositions désinfectantes aqueuses, et concentrées pour leur préparation
JP3098541B2 (ja)	2000-10-16	衛生剤組成物
CN111296476A (zh)	2020-06-19	一种含有过硫酸氢钾的长效消毒剂及其制备方法
CA2375936C (fr)	2008-11-18	Desinfectants a base de n1n-bis(3-aminopropyl) octylamine
JPH0327304A (ja)	1991-02-05	消毒剤濃厚液
JPH045206A (ja)	1992-01-09	殺菌消毒剤組成物
GB2205748A (en)	1988-12-21	Disinfectant compositions
US10588313B1 (en)	2020-03-17	Compounds of fatty acids and ammonium fatty acid salts
AU2006269517B2 (en)	2010-08-26	Enhanced tuburculocidal activity and decreased fumes from glutaraldehyde disinfectant using acetate salts and alcohol
PL246301B1 (pl)	2024-12-30	Płynny preparat dezynfekujący i sposób jego wytwarzania
JP2022539263A (ja)	2022-09-07	すぐに使用可能な消毒剤
EP1922302A2 (fr)	2008-05-21	Composes organiques actifs de sulfamide aromatique et utilisation de ces derniers en tant que biocides
HU210139B (en)	1995-02-28	Anticorrosive microbicide

Legal Events

Date	Code	Title	Description
2006-10-31	MA	Patent expired