FI60099C - Bestaendig loesning innehaollande perkarbonsyra - Google Patents

Bestaendig loesning innehaollande perkarbonsyra Download PDF

Info

Publication number: FI60099C
Authority: FI; Finland
Prior art keywords: acid; solutions; perglutaric; anhydride; peracid
Prior art date: 1976-11-30

Application number

FI773245A

Other languages

English (en)

Finnish (fi)

Other versions

FI773245A7 (fi

FI60099B (fi

Inventor

Heinz Eggensperger

Wolfgang Beilfuss

Original Assignee

Schuelke & Mayr Gmbh

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.)

1976-11-30

Filing date

1977-10-31

Publication date

1981-12-10

1977-10-31 Application filed by Schuelke & Mayr Gmbh filed Critical Schuelke & Mayr Gmbh

1978-05-31 Publication of FI773245A7 publication Critical patent/FI773245A7/fi

1981-08-31 Application granted granted Critical

1981-08-31 Publication of FI60099B publication Critical patent/FI60099B/fi

1981-12-10 Publication of FI60099C publication Critical patent/FI60099C/fi

Links

239000000243 solution Substances 0.000 description 44
239000002253 acid Substances 0.000 description 41
150000004965 peroxy acids Chemical class 0.000 description 20
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid group Chemical group C(CCC(=O)O)(=O)O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 12
239000003381 stabilizer Substances 0.000 description 9
VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 description 7
WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 description 6
239000000203 mixture Substances 0.000 description 6
230000009965 odorless effect Effects 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 5
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 5
230000006378 damage Effects 0.000 description 5
239000001384 succinic acid Substances 0.000 description 5
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 4
238000002425 crystallisation Methods 0.000 description 4
230000008025 crystallization Effects 0.000 description 4
239000000725 suspension Substances 0.000 description 4
DZKRDHLYQRTDBU-UPHRSURJSA-N (z)-but-2-enediperoxoic acid Chemical compound OOC(=O)\C=C/C(=O)OO DZKRDHLYQRTDBU-UPHRSURJSA-N 0.000 description 3
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
241000588748 Klebsiella Species 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
241000588769 Proteus <enterobacteria> Species 0.000 description 3
241000589516 Pseudomonas Species 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
229940014800 succinic anhydride Drugs 0.000 description 3
PIYNUZCGMLCXKJ-UHFFFAOYSA-N 1,4-dioxane-2,6-dione Chemical compound O=C1COCC(=O)O1 PIYNUZCGMLCXKJ-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
241000228212 Aspergillus Species 0.000 description 2
241000894006 Bacteria Species 0.000 description 2
241000222120 Candida <Saccharomycetales> Species 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
YZGQDNOIGFBYKF-UHFFFAOYSA-N Ethoxyacetic acid Chemical compound CCOCC(O)=O YZGQDNOIGFBYKF-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
241000191940 Staphylococcus Species 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
241000223238 Trichophyton Species 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
150000008065 acid anhydrides Chemical class 0.000 description 2
230000000721 bacterilogical effect Effects 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
239000000645 desinfectant Substances 0.000 description 2
230000000249 desinfective effect Effects 0.000 description 2
XPBOFLGWLULIJL-UHFFFAOYSA-N dioxepane-3,7-dione Chemical compound O=C1CCCC(=O)OO1 XPBOFLGWLULIJL-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
238000000034 method Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
230000001590 oxidative effect Effects 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
GJAWHXHKYYXBSV-UHFFFAOYSA-N quinolinic acid Chemical compound OC(=O)C1=CC=CN=C1C(O)=O GJAWHXHKYYXBSV-UHFFFAOYSA-N 0.000 description 2
210000002966 serum Anatomy 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
SIDULKZCBGMXJL-UHFFFAOYSA-N 1-dimethylphosphoryldodecane Chemical compound CCCCCCCCCCCCP(C)(C)=O SIDULKZCBGMXJL-UHFFFAOYSA-N 0.000 description 1
JPSKCQCQZUGWNM-UHFFFAOYSA-N 2,7-Oxepanedione Chemical compound O=C1CCCCC(=O)O1 JPSKCQCQZUGWNM-UHFFFAOYSA-N 0.000 description 1
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
VXRUADVCBZMFSV-UHFFFAOYSA-N 2-acetyloxypropane-1,2,3-tricarboxylic acid Chemical compound CC(=O)OC(CC(O)=O)(CC(O)=O)C(O)=O VXRUADVCBZMFSV-UHFFFAOYSA-N 0.000 description 1
244000063299 Bacillus subtilis Species 0.000 description 1
235000014469 Bacillus subtilis Nutrition 0.000 description 1
KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
241000233866 Fungi Species 0.000 description 1
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
241000282412 Homo Species 0.000 description 1
IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 description 1
241000219991 Lythraceae Species 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
101150024570 Mlip gene Proteins 0.000 description 1
241000187480 Mycobacterium smegmatis Species 0.000 description 1
KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 1
235000014360 Punica granatum Nutrition 0.000 description 1
PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 description 1
239000013543 active substance Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
229960003237 betaine Drugs 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000007423 decrease Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
235000011180 diphosphates Nutrition 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
238000005187 foaming Methods 0.000 description 1
235000013305 food Nutrition 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
RMIODHQZRUFFFF-UHFFFAOYSA-N methoxyacetic acid Chemical compound COCC(O)=O RMIODHQZRUFFFF-UHFFFAOYSA-N 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
150000004967 organic peroxy acids Chemical class 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
239000002304 perfume Substances 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
239000000467 phytic acid Substances 0.000 description 1
235000002949 phytic acid Nutrition 0.000 description 1
229940068041 phytic acid Drugs 0.000 description 1
239000010970 precious metal Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
CZPZWMPYEINMCF-UHFFFAOYSA-N propaneperoxoic acid Chemical compound CCC(=O)OO CZPZWMPYEINMCF-UHFFFAOYSA-N 0.000 description 1
ILVXOBCQQYKLDS-UHFFFAOYSA-N pyridine N-oxide Chemical compound [O-][N+]1=CC=CC=C1 ILVXOBCQQYKLDS-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
229940075582 sorbic acid Drugs 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 1
238000004448 titration Methods 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
201000008827 tuberculosis Diseases 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
- 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
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
- C07C407/003—Separation; Purification; Stabilisation; Use of additives
- C07C407/006—Stabilisation; Use of additives
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
- D06L4/12—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen combined with specific additives

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Dentistry (AREA)
Inorganic Chemistry (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Zoology (AREA)
General Health & Medical Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Chemical Kinetics & Catalysis (AREA)
Textile Engineering (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Detergent Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

FI773245A 1976-11-30 1977-10-31 Bestaendig loesning innehaollande perkarbonsyra FI60099C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE2654164A DE2654164C2 (de)	1976-11-30	1976-11-30	Wäßrige Perglutarsäurelösung und deren Verwendung
DE2654164		1976-11-30

Publications (3)

Publication Number	Publication Date
FI773245A7 FI773245A7 (fi)	1978-05-31
FI60099B FI60099B (fi)	1981-08-31
FI60099C true FI60099C (fi)	1981-12-10

Family

ID=5994249

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI773245A FI60099C (fi)	1976-11-30	1977-10-31	Bestaendig loesning innehaollande perkarbonsyra

Country Status (20)

Country	Link
US (1)	US4129517A (de)
JP (1)	JPS5381619A (de)
AR (1)	AR215277A1 (de)
AT (1)	AT356289B (de)
BE (1)	BE860976A (de)
BR (1)	BR7707882A (de)
CA (1)	CA1081079A (de)
CH (1)	CH635576A5 (de)
DE (1)	DE2654164C2 (de)
DK (1)	DK531777A (de)
FI (1)	FI60099C (de)
FR (1)	FR2371930B1 (de)
GB (1)	GB1560525A (de)
IE (1)	IE46265B1 (de)
IT (1)	IT1090943B (de)
LU (1)	LU78560A1 (de)
NL (1)	NL188641C (de)
NO (1)	NO140346C (de)
SE (1)	SE440848B (de)
ZA (1)	ZA777072B (de)

Families Citing this family (69)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4238192A (en) *	1979-01-22	1980-12-09	S. C. Johnson & Son, Inc.	Hydrogen peroxide bleach composition
NO150445C (no) *	1979-04-06	1984-10-17	Unilever Nv	Bleke- og vaskepreparat
DE3003875A1 (de) *	1980-02-02	1981-08-13	Norddeutsche Affinerie, 2000 Hamburg	Bodenbehandlungsmittel
GB8334249D0 (en) *	1983-12-22	1984-02-01	Tenneco Organics Ltd	Disinfectants
GB8500116D0 (en) *	1985-01-03	1985-02-13	Unilever Plc	Liquid bleaching compositions
DE3543500A1 (de) *	1985-12-10	1987-06-11	Schuelke & Mayr Gmbh	Waessrige loesung aromatischer percarbonsaeuren und deren verwendung
DE3702983A1 (de) *	1986-06-09	1987-12-10	Henkel Kgaa	Desinfektionsmittel und ihre verwendung zur haut- und schleimhautdesinfektion
US4802994A (en) *	1986-07-17	1989-02-07	Nalco Chemical Company	Biocide treatment to control sulfate-reducing bacteria in industrial process waste waters
FI880221A7 (fi) *	1988-01-19	1989-07-20	Oy Santasalo Sohlberg Ab	Menetelmä ja laite esineiden steriloimiseksi tai desinfioimiseksi.
US4895721A (en) *	1988-01-22	1990-01-23	Carter-Wallace Inc.	Peroxide gel dentifrice compositions
US4917815A (en) *	1988-06-10	1990-04-17	Sterling Drug Inc.	Stable aqueous aromatic percarboxylic acid solution
DE3914827C2 (de) *	1989-05-05	1995-06-14	Schuelke & Mayr Gmbh	Flüssiges Desinfektionsmittelkonzentrat
US5437868A (en) *	1991-07-23	1995-08-01	Ecolab Inc.	Peroxyacid antimicrobial composition
WO1993002973A1 (de) *	1991-08-05	1993-02-18	Trawöger, Werner	Mittel gegen beläge an benetzten oberflächen
GB9210526D0 (en) *	1992-05-16	1992-07-01	Laporte Esd Ltd	Compositions
DE4317420C1 (de) *	1993-05-26	1994-11-03	Degussa	Stabilisierte Percarbonsäurelösungen und Verfahren zu deren Herstellung
US5472619A (en) *	1993-09-03	1995-12-05	Birko Corporation	Waste water treatment with peracetic acid compositions
US5435808A (en) *	1993-09-03	1995-07-25	Birko Corporation	Hide raceway treatment and improved method of curing hides
US5647997A (en) *	1993-09-03	1997-07-15	Birko Corporation	Waste water treatment with peracid compositions
US5879584A (en) *	1994-09-10	1999-03-09	The Procter & Gamble Company	Process for manufacturing aqueous compositions comprising peracids
DE19512588A1 (de) *	1995-04-04	1996-10-10	Bode Chemie Gmbh & Co	Mittel zur Instrumentendesinfektion
US5827542A (en) *	1996-02-12	1998-10-27	Healthpoint, Ltd.	Quick acting chemical sterilant
US6010729A (en)	1998-08-20	2000-01-04	Ecolab Inc.	Treatment of animal carcasses
DE60114174T2 (de)	2000-04-28	2006-07-20	Ecolab Inc., St. Paul	Antimikrobielle zusammensetzung
US7150884B1 (en)	2000-07-12	2006-12-19	Ecolab Inc.	Composition for inhibition of microbial growth
US6468953B1 (en)	2000-08-03	2002-10-22	Lynntech, Inc.	Methods of preparing antimicrobial compositions comprising ozone
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1976
- 1976-11-30 DE DE2654164A patent/DE2654164C2/de not_active Expired
1977
- 1977-09-27 CH CH1178077A patent/CH635576A5/de not_active IP Right Cessation
- 1977-10-05 AT AT711577A patent/AT356289B/de not_active IP Right Cessation
- 1977-10-31 FI FI773245A patent/FI60099C/fi not_active IP Right Cessation
- 1977-11-15 NL NLAANVRAGE7712569,A patent/NL188641C/xx not_active IP Right Cessation
- 1977-11-17 SE SE7712986A patent/SE440848B/sv not_active IP Right Cessation
- 1977-11-18 BE BE182746A patent/BE860976A/xx not_active IP Right Cessation
- 1977-11-21 LU LU78560A patent/LU78560A1/xx unknown
- 1977-11-23 FR FR7735167A patent/FR2371930B1/fr not_active Expired
- 1977-11-28 US US05/855,461 patent/US4129517A/en not_active Expired - Lifetime
- 1977-11-28 NO NO774063A patent/NO140346C/no unknown
- 1977-11-28 BR BR7707882A patent/BR7707882A/pt unknown
- 1977-11-28 ZA ZA00777072A patent/ZA777072B/xx unknown
- 1977-11-29 IE IE2421/77A patent/IE46265B1/en not_active IP Right Cessation
- 1977-11-29 IT IT51999/77A patent/IT1090943B/it active
- 1977-11-29 GB GB49589/77A patent/GB1560525A/en not_active Expired
- 1977-11-29 CA CA292,034A patent/CA1081079A/en not_active Expired
- 1977-11-30 AR AR270184A patent/AR215277A1/es active
- 1977-11-30 JP JP14382477A patent/JPS5381619A/ja active Pending
- 1977-11-30 DK DK531777A patent/DK531777A/da not_active Application Discontinuation

Also Published As

Publication number	Publication date
FR2371930A1 (de)	1978-06-23
SE440848B (sv)	1985-08-26
NL7712569A (nl)	1978-06-01
IE46265L (en)	1978-05-30
NL188641C (nl)	1992-08-17
NL188641B (nl)	1992-03-16
FR2371930B1 (de)	1980-08-22
FI773245A7 (fi)	1978-05-31
JPS5381619A (en)	1978-07-19
CA1081079A (en)	1980-07-08
CH635576A5 (de)	1983-04-15
BR7707882A (pt)	1978-07-11
BE860976A (fr)	1978-03-16
ZA777072B (en)	1978-09-27
DE2654164C2 (de)	1978-08-10
US4129517A (en)	1978-12-12
IE46265B1 (en)	1983-04-20
NO140346B (no)	1979-05-07
SE7712986L (sv)	1978-05-31
NO774063L (no)	1978-05-31
GB1560525A (en)	1980-02-06
DK531777A (da)	1978-05-31
FI60099B (fi)	1981-08-31
AT356289B (de)	1980-04-25
AR215277A1 (es)	1979-09-28
ATA711577A (de)	1979-09-15
DE2654164B1 (de)	1977-12-22
IT1090943B (it)	1985-06-26
LU78560A1 (de)	1978-04-13
NO140346C (no)	1979-08-15

Legal Events

Date	Code	Title	Description
1994-05-13	MM	Patent lapsed
2004-08-31	MM	Patent lapsed	Owner name: SCHUELKE & MAYR GMBH

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KR100597092B1 (ko)	2006-07-04	과초산 수용액 및 그 제조방법
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JP7475424B2 (ja)	2024-04-26	すぐに使用可能な消毒剤
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RU2745120C2 (ru)	2021-03-22	Дезинфицирующий агент
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