IE43097B1 - Disinfectant quaternary imidazoline compounds - Google Patents
Disinfectant quaternary imidazoline compoundsInfo
- Publication number
- IE43097B1 IE43097B1 IE857/76A IE85776A IE43097B1 IE 43097 B1 IE43097 B1 IE 43097B1 IE 857/76 A IE857/76 A IE 857/76A IE 85776 A IE85776 A IE 85776A IE 43097 B1 IE43097 B1 IE 43097B1
- Authority
- IE
- Ireland
- Prior art keywords
- compound
- condensation
- range
- disinfectant
- hours
- Prior art date
Links
- 239000000645 desinfectant Substances 0.000 title claims description 35
- 125000002636 imidazolinyl group Chemical group 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 36
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 claims abstract description 9
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000460 chlorine Substances 0.000 claims abstract description 5
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims abstract description 3
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 16
- -1 cycloalkyl radical Chemical group 0.000 claims description 12
- 238000009833 condensation Methods 0.000 claims description 11
- 230000005494 condensation Effects 0.000 claims description 11
- 241000195493 Cryptophyta Species 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 9
- 241000894006 Bacteria Species 0.000 claims description 7
- 239000000839 emulsion Substances 0.000 claims description 5
- 238000005555 metalworking Methods 0.000 claims description 5
- 239000002480 mineral oil Substances 0.000 claims description 5
- 230000009182 swimming Effects 0.000 claims description 5
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 claims description 3
- 229940073608 benzyl chloride Drugs 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- 239000000498 cooling water Substances 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 235000010446 mineral oil Nutrition 0.000 claims description 3
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical group [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 238000004378 air conditioning Methods 0.000 claims description 2
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- 239000012530 fluid Substances 0.000 claims 2
- 208000015181 infectious disease Diseases 0.000 claims 1
- 230000002353 algacidal effect Effects 0.000 abstract description 11
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical class C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 abstract description 7
- 230000000844 anti-bacterial effect Effects 0.000 abstract description 6
- 230000000855 fungicidal effect Effects 0.000 abstract description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-M ethyl sulfate Chemical compound CCOS([O-])(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-M 0.000 abstract 1
- 239000006260 foam Substances 0.000 description 12
- 238000005187 foaming Methods 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 10
- 125000002091 cationic group Chemical group 0.000 description 8
- 239000003599 detergent Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 4
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000003254 anti-foaming effect Effects 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 230000003385 bacteriostatic effect Effects 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000000249 desinfective effect Effects 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- 150000002462 imidazolines Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 125000005608 naphthenic acid group Chemical group 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 description 1
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- XKXHCNPAFAXVRZ-UHFFFAOYSA-N benzylazanium;chloride Chemical compound [Cl-].[NH3+]CC1=CC=CC=C1 XKXHCNPAFAXVRZ-UHFFFAOYSA-N 0.000 description 1
- 239000012496 blank sample Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- 150000001934 cyclohexanes Chemical class 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 238000012994 industrial processing Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/06—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C07D233/08—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms
- C07D233/12—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D233/14—Radicals substituted by oxygen atoms
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752518125 DE2518125A1 (de) | 1975-04-24 | 1975-04-24 | Desinfektionsmittel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE43097L IE43097L (en) | 1976-10-24 |
| IE43097B1 true IE43097B1 (en) | 1980-12-17 |
Family
ID=5944834
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE857/76A IE43097B1 (en) | 1975-04-24 | 1976-04-23 | Disinfectant quaternary imidazoline compounds |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS51139612A (cg-RX-API-DMAC10.html) |
| AR (1) | AR208431A1 (cg-RX-API-DMAC10.html) |
| BE (1) | BE841122A (cg-RX-API-DMAC10.html) |
| BR (1) | BR7602482A (cg-RX-API-DMAC10.html) |
| DE (1) | DE2518125A1 (cg-RX-API-DMAC10.html) |
| DK (1) | DK184076A (cg-RX-API-DMAC10.html) |
| ES (1) | ES447131A1 (cg-RX-API-DMAC10.html) |
| FR (1) | FR2308625A1 (cg-RX-API-DMAC10.html) |
| GB (1) | GB1493093A (cg-RX-API-DMAC10.html) |
| IE (1) | IE43097B1 (cg-RX-API-DMAC10.html) |
| LU (1) | LU74818A1 (cg-RX-API-DMAC10.html) |
| NL (1) | NL7604050A (cg-RX-API-DMAC10.html) |
| SE (1) | SE7604649L (cg-RX-API-DMAC10.html) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2930849A1 (de) * | 1979-07-30 | 1981-02-26 | Henkel Kgaa | Neue n-hydroxyalkylimidazolinderivate, deren herstellung und verwendung |
| CA1154024A (en) * | 1980-04-17 | 1983-09-20 | Werner Schafer | Transdermal carrier materials |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL273981A (cg-RX-API-DMAC10.html) * | 1961-01-25 | |||
| US3408361A (en) * | 1967-04-05 | 1968-10-29 | Hans S. Mannheimer | Methods for producing imidazolines and derivatives thereof |
| DE2210087B2 (de) * | 1972-03-02 | 1980-11-27 | Hoechst Ag, 6000 Frankfurt | Imidazoliniumsalze und diese enthaltende Textüweichmachungsmittel |
-
1975
- 1975-04-24 DE DE19752518125 patent/DE2518125A1/de active Pending
-
1976
- 1976-01-01 AR AR262991A patent/AR208431A1/es active
- 1976-04-15 NL NL7604050A patent/NL7604050A/xx not_active Application Discontinuation
- 1976-04-19 ES ES447131A patent/ES447131A1/es not_active Expired
- 1976-04-22 LU LU74818A patent/LU74818A1/xx unknown
- 1976-04-22 SE SE7604649A patent/SE7604649L/xx unknown
- 1976-04-23 IE IE857/76A patent/IE43097B1/en unknown
- 1976-04-23 BR BR2482/76A patent/BR7602482A/pt unknown
- 1976-04-23 DK DK184076A patent/DK184076A/da not_active Application Discontinuation
- 1976-04-23 JP JP51045643A patent/JPS51139612A/ja active Pending
- 1976-04-26 BE BE166458A patent/BE841122A/xx unknown
- 1976-04-26 FR FR7612239A patent/FR2308625A1/fr not_active Withdrawn
- 1976-04-26 GB GB16784/76A patent/GB1493093A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BR7602482A (pt) | 1976-10-19 |
| DE2518125A1 (de) | 1976-11-04 |
| NL7604050A (nl) | 1976-10-26 |
| AR208431A1 (es) | 1976-12-27 |
| JPS51139612A (en) | 1976-12-02 |
| BE841122A (fr) | 1976-10-26 |
| DK184076A (da) | 1976-10-25 |
| ES447131A1 (es) | 1977-06-16 |
| IE43097L (en) | 1976-10-24 |
| GB1493093A (en) | 1977-11-23 |
| SE7604649L (sv) | 1976-10-25 |
| LU74818A1 (cg-RX-API-DMAC10.html) | 1977-02-07 |
| FR2308625A1 (fr) | 1976-11-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1245126A (en) | Biocidal water treatment | |
| US4923619A (en) | Disinfectant compositions and disinfection process applicable to infected liquids or surfaces | |
| US4874526A (en) | Treatment of water | |
| CA1294287C (en) | N,n'-dihalo-2-imidazolidinones | |
| CA2206586C (en) | Disinfecting use of quaternary ammonium carbonates | |
| US4976874A (en) | Control of biofouling in aqueous systems by non-polymeric quaternary ammonium polyhalides | |
| US5668084A (en) | Polyhexamethylene biguanide and surfactant composition and method for preventing waterline residue | |
| US5284844A (en) | Biocides for protecting industrial materials and water systems | |
| EP1258472B1 (en) | Quaternary ammonium salts having a tertiary alkyl group | |
| CA1324942C (en) | Method for the control of biofouling in recirculating water systems | |
| US4084950A (en) | Use of polyquaternary ammonium methylene phosphonates as microbiocides | |
| US4018592A (en) | Method of controlling the growth of algae | |
| EP0283509B1 (en) | The control of biofouling in aqueous systems by non-polymeric quaternary ammonium polyhalides | |
| IE43097B1 (en) | Disinfectant quaternary imidazoline compounds | |
| US4035480A (en) | Microbiocidal mixtures of polymeric quaternary ammonium compounds | |
| CN104478101B (zh) | 一种水处理咪唑啉双胍硫酸盐杀菌剂及其制备方法 | |
| EP0594329B1 (en) | Antimicrobial agents comprising polyquaternary ammonium compounds | |
| US4489098A (en) | 2,2,3-Trihalopropionaldehydes as antimicrobial agents | |
| NO142782B (no) | Polyaminforbindelser for anvendelse som antimikrobielt middel og/eller algeinhibitor | |
| JP2004168678A (ja) | 殺微生物剤組成物 | |
| JPH0550481B2 (cg-RX-API-DMAC10.html) | ||
| US3753677A (en) | Tetracyanodithiadiene and its salts as bactericides and algicides | |
| JP3550424B2 (ja) | 殺菌殺藻剤 | |
| US4339459A (en) | Guanidinium compounds and their use as microbiocidal agents | |
| DE2355026A1 (de) | Neue omega-amino-carbonsaeureamide, deren herstellung, sowie verwendung als antimikrobielle mittel |