DE2525695C2 - Komplexbildner, der mit Kationen lipidlösliche Komplexe bildet und dessen Verwendung - Google Patents
Komplexbildner, der mit Kationen lipidlösliche Komplexe bildet und dessen VerwendungInfo
- Publication number
- DE2525695C2 DE2525695C2 DE19752525695 DE2525695A DE2525695C2 DE 2525695 C2 DE2525695 C2 DE 2525695C2 DE 19752525695 DE19752525695 DE 19752525695 DE 2525695 A DE2525695 A DE 2525695A DE 2525695 C2 DE2525695 C2 DE 2525695C2
- Authority
- DE
- Germany
- Prior art keywords
- radicals
- formula
- cations
- independently
- radical
- 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
Links
- 239000008139 complexing agent Substances 0.000 title claims description 47
- 150000001768 cations Chemical class 0.000 title claims description 35
- 150000003254 radicals Chemical class 0.000 claims description 49
- -1 substituted alkyl radicals Chemical class 0.000 claims description 33
- 150000001875 compounds Chemical class 0.000 claims description 28
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
- 150000002500 ions Chemical class 0.000 claims description 10
- 125000003368 amide group Chemical group 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000004122 cyclic group Chemical group 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 8
- 239000012528 membrane Substances 0.000 claims description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 150000005840 aryl radicals Chemical class 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 150000001470 diamides Chemical class 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 12
- 125000004434 sulfur atom Chemical group 0.000 description 5
- 230000003115 biocidal effect Effects 0.000 description 4
- 150000002632 lipids Chemical class 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 150000003463 sulfur Chemical class 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 3
- 230000000536 complexating effect Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 230000000035 biogenic effect Effects 0.000 description 2
- 230000009918 complex formation Effects 0.000 description 2
- 229910001431 copper ion Inorganic materials 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
- 238000010669 acid-base reaction Methods 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 229910001422 barium ion Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000013375 chromatographic separation Methods 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 125000004956 cyclohexylene group Chemical group 0.000 description 1
- 238000000909 electrodialysis Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 230000037427 ion transport Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004460 liquid liquid chromatography Methods 0.000 description 1
- 239000003120 macrolide antibiotic agent Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 125000003375 sulfoxide group Chemical group 0.000 description 1
- 125000004354 sulfur functional group Chemical group 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- FCFNRCROJUBPLU-DNDCDFAISA-N valinomycin Chemical group CC(C)[C@@H]1NC(=O)[C@H](C)OC(=O)[C@@H](C(C)C)NC(=O)[C@@H](C(C)C)OC(=O)[C@H](C(C)C)NC(=O)[C@H](C)OC(=O)[C@@H](C(C)C)NC(=O)[C@@H](C(C)C)OC(=O)[C@H](C(C)C)NC(=O)[C@H](C)OC(=O)[C@@H](C(C)C)NC(=O)[C@@H](C(C)C)OC1=O FCFNRCROJUBPLU-DNDCDFAISA-N 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH831374A CH605661A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-06-18 | 1974-06-18 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2525695A1 DE2525695A1 (de) | 1976-01-15 |
| DE2525695C2 true DE2525695C2 (de) | 1985-12-19 |
Family
ID=4338402
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19752525695 Expired DE2525695C2 (de) | 1974-06-18 | 1975-06-10 | Komplexbildner, der mit Kationen lipidlösliche Komplexe bildet und dessen Verwendung |
Country Status (7)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0056283B1 (en) * | 1981-01-14 | 1985-07-31 | Terumo Corporation | Ion sensor |
| EP0074198A1 (en) * | 1981-08-21 | 1983-03-16 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Hydrogen ion-selective membranes and electrodes containing same |
| US4563263A (en) * | 1982-01-15 | 1986-01-07 | Terumo Corporation | Selectively permeable film and ion sensor |
| US9691240B2 (en) | 2015-01-22 | 2017-06-27 | Interface, Inc. | Floor covering system with sensors |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT987080B (it) * | 1972-04-24 | 1975-02-20 | Moeller Glasblaeserei | Procedimento per la preparazione di complessi solubili in lipidi di cationi impiego del procedi mento e impieco dei complessi |
-
1974
- 1974-06-18 CH CH831374A patent/CH605661A5/xx not_active IP Right Cessation
-
1975
- 1975-06-10 DE DE19752525695 patent/DE2525695C2/de not_active Expired
- 1975-06-11 GB GB2503175A patent/GB1515025A/en not_active Expired
- 1975-06-12 NL NL7507026A patent/NL7507026A/xx not_active Application Discontinuation
- 1975-06-16 JP JP7301775A patent/JPS5113718A/ja active Pending
- 1975-06-18 IT IT2451475A patent/IT1060379B/it active
- 1975-06-18 FR FR7519114A patent/FR2278676A2/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| IT1060379B (it) | 1982-07-10 |
| CH605661A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1978-10-13 |
| DE2525695A1 (de) | 1976-01-15 |
| FR2278676A2 (fr) | 1976-02-13 |
| NL7507026A (nl) | 1975-12-22 |
| FR2278676B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1981-01-02 |
| GB1515025A (en) | 1978-06-21 |
| JPS5113718A (ja) | 1976-02-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OD | Request for examination | ||
| 8162 | Independent application | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition |