DE2345802C2 - Organozinncarboxylate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Mikroorganismen - Google Patents
Organozinncarboxylate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von MikroorganismenInfo
- Publication number
- DE2345802C2 DE2345802C2 DE2345802A DE2345802A DE2345802C2 DE 2345802 C2 DE2345802 C2 DE 2345802C2 DE 2345802 A DE2345802 A DE 2345802A DE 2345802 A DE2345802 A DE 2345802A DE 2345802 C2 DE2345802 C2 DE 2345802C2
- Authority
- DE
- Germany
- Prior art keywords
- thiophene
- organotin
- carboxylates
- culture
- preparation
- 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
- 150000007942 carboxylates Chemical class 0.000 title claims description 15
- 238000000034 method Methods 0.000 title claims description 8
- 238000002360 preparation method Methods 0.000 title claims description 4
- 244000005700 microbiome Species 0.000 title description 7
- 150000001875 compounds Chemical class 0.000 claims description 21
- 239000011541 reaction mixture Substances 0.000 claims description 7
- -1 alkyl radical Chemical class 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 claims 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 10
- 241000191967 Staphylococcus aureus Species 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 8
- QERYCTSHXKAMIS-UHFFFAOYSA-N thiophene-2-carboxylic acid Chemical class OC(=O)C1=CC=CS1 QERYCTSHXKAMIS-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 230000005764 inhibitory process Effects 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 235000015097 nutrients Nutrition 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000011534 incubation Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229910052718 tin Inorganic materials 0.000 description 5
- SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 5
- 241000894006 Bacteria Species 0.000 description 4
- 241001515917 Chaetomium globosum Species 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- CDCBAEYBXUGGAS-UHFFFAOYSA-M trimethylstannyl thiophene-2-carboxylate Chemical compound C[Sn+](C)C.[O-]C(=O)C1=CC=CS1 CDCBAEYBXUGGAS-UHFFFAOYSA-M 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 241000192125 Firmicutes Species 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 241000233866 Fungi Species 0.000 description 3
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 3
- 241000191940 Staphylococcus Species 0.000 description 3
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- YCGAZNXXGKTASZ-UHFFFAOYSA-L thiophene-2,5-dicarboxylate Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)S1 YCGAZNXXGKTASZ-UHFFFAOYSA-L 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- CUEFBEFOUGWPBI-UHFFFAOYSA-L S1C(=CC=C1C(=O)[O-])C(=O)[O-].C(CCC)[Sn+](CCCC)CCCC.C(CCC)[Sn+](CCCC)CCCC Chemical compound S1C(=CC=C1C(=O)[O-])C(=O)[O-].C(CCC)[Sn+](CCCC)CCCC.C(CCC)[Sn+](CCCC)CCCC CUEFBEFOUGWPBI-UHFFFAOYSA-L 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000006916 nutrient agar Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- VRGCFUHQABRHGP-UHFFFAOYSA-M tributylstannyl thiophene-2-carboxylate Chemical compound [O-]C(=O)C1=CC=CS1.CCCC[Sn+](CCCC)CCCC VRGCFUHQABRHGP-UHFFFAOYSA-M 0.000 description 2
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 240000003085 Quassia amara Species 0.000 description 1
- IWAINNBZWMDHNI-UHFFFAOYSA-L S1C(=CC=C1C(=O)[O-])C(=O)[O-].C(CCC)[Sn+](CCCC)CCCC.C1(=CC=CC=C1)[Sn+](C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound S1C(=CC=C1C(=O)[O-])C(=O)[O-].C(CCC)[Sn+](CCCC)CCCC.C1(=CC=CC=C1)[Sn+](C1=CC=CC=C1)C1=CC=CC=C1 IWAINNBZWMDHNI-UHFFFAOYSA-L 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000008365 aqueous carrier Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- FTVYNGMOXYLXRT-UHFFFAOYSA-L bis(triphenylstannyl) thiophene-2,5-dicarboxylate Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)S1.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 FTVYNGMOXYLXRT-UHFFFAOYSA-L 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 230000009189 diving Effects 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- FIBARIGPBPUBHC-UHFFFAOYSA-N octyl 8-(3-octyloxiran-2-yl)octanoate Chemical compound CCCCCCCCOC(=O)CCCCCCCC1OC1CCCCCCCC FIBARIGPBPUBHC-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- YCGAZNXXGKTASZ-UHFFFAOYSA-N thiophene-2,5-dicarboxylic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)S1 YCGAZNXXGKTASZ-UHFFFAOYSA-N 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- REDSKZBUUUQMSK-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC.CCCC[Sn](CCCC)CCCC REDSKZBUUUQMSK-UHFFFAOYSA-N 0.000 description 1
- MUHFQLVFMFDJOK-UHFFFAOYSA-N triphenyl(triphenylstannyloxy)stannane Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)O[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 MUHFQLVFMFDJOK-UHFFFAOYSA-N 0.000 description 1
- PSJGBEGGTXXJRQ-UHFFFAOYSA-M triphenylstannyl thiophene-2-carboxylate Chemical class C=1C=CSC=1C(=O)O[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 PSJGBEGGTXXJRQ-UHFFFAOYSA-M 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
- C08K5/57—Organo-tin compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28790872A | 1972-09-11 | 1972-09-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2345802A1 DE2345802A1 (de) | 1974-03-21 |
| DE2345802C2 true DE2345802C2 (de) | 1982-12-23 |
Family
ID=23104886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2345802A Expired DE2345802C2 (de) | 1972-09-11 | 1973-09-11 | Organozinncarboxylate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Mikroorganismen |
Country Status (11)
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1499737A (fr) * | 1966-08-11 | 1967-10-27 | United States Borax Chem | Composés organo-stanniques, leur préparation et leurs applications |
-
1973
- 1973-07-31 ZA ZA735203A patent/ZA735203B/xx unknown
- 1973-09-06 CA CA180,426A patent/CA1016950A/en not_active Expired
- 1973-09-07 NL NL7312329A patent/NL7312329A/xx not_active Application Discontinuation
- 1973-09-10 IT IT09613/73A patent/IT1056215B/it active
- 1973-09-10 SE SE7312283A patent/SE401924B/xx unknown
- 1973-09-10 BE BE135474A patent/BE804644A/xx not_active IP Right Cessation
- 1973-09-11 AT AT788773A patent/AT320670B/de not_active IP Right Cessation
- 1973-09-11 DE DE2345802A patent/DE2345802C2/de not_active Expired
- 1973-09-11 GB GB4259873A patent/GB1399204A/en not_active Expired
- 1973-09-11 FR FR7332669A patent/FR2198950B1/fr not_active Expired
- 1973-09-11 CH CH1298473A patent/CH591507A5/xx not_active IP Right Cessation
Non-Patent Citations (1)
| Title |
|---|
| NICHTS-ERMITTELT |
Also Published As
| Publication number | Publication date |
|---|---|
| BE804644A (nl) | 1974-01-02 |
| DE2345802A1 (de) | 1974-03-21 |
| NL7312329A (US07902200-20110308-C00004.png) | 1974-03-13 |
| IT1056215B (it) | 1982-01-30 |
| CH591507A5 (US07902200-20110308-C00004.png) | 1977-09-30 |
| FR2198950B1 (US07902200-20110308-C00004.png) | 1978-03-10 |
| SE401924B (sv) | 1978-06-05 |
| GB1399204A (en) | 1975-06-25 |
| CA1016950A (en) | 1977-09-06 |
| ZA735203B (en) | 1974-07-31 |
| AT320670B (de) | 1975-02-25 |
| FR2198950A1 (US07902200-20110308-C00004.png) | 1974-04-05 |
| AU5969873A (en) | 1975-03-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE68904862T2 (de) | Carbaminsaeureester, verwendbar als mikrobicid und konservierungsmittel. | |
| DE2550507C2 (de) | Organozinnverbindungen und ihre Verwendung zur Stabilisierung von chlorhaltigen Polymeren | |
| US3214453A (en) | Bis-tributyltin carbonate and a method for the preparation thereof | |
| DE3642371A1 (de) | Gegenstaende mit fungiziden und bakteriziden eigenschaften | |
| EP0049367B1 (de) | Biocide Wirkstoffkombination und ihre Verwendung in Formmassen aus Kunststoff | |
| DE2656749A1 (de) | Neue biocide | |
| DE2705440C2 (de) | Verfahren zur Herstellung von biologisch aktiven Polymeren | |
| DE2345802C2 (de) | Organozinncarboxylate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Mikroorganismen | |
| US2745832A (en) | Metal quinolinolates and methods of making the same | |
| DE1266449B (de) | Verfahren zur Hemmung bzw. Verhinderung des Wachstums von Bakterien und Pilzen | |
| US3287210A (en) | Antimony compounds and compositions and method for protecting against microorganisms | |
| DE2845408C3 (de) | N-(2-Methyl-1 -naphthyD-maleinimid, Verfahren zu dessen Herstellung und seine Verwendung | |
| US3833543A (en) | Triorganotin salts of thiophene carboxylic acids | |
| DE2166953C3 (de) | Antimikrobielles Mittel auf der Basis von Jodoniumsalzen | |
| DE1909662A1 (de) | Verfahren zur Herstellung von Peroxycarbonylestergruppen enthaltenden Verbindungen | |
| DE2439946A1 (de) | Dreiwertiger antimonkatalysator | |
| DE849903C (de) | Verfahren zur Herstellung von Kunstharzen | |
| DE3106877C2 (US07902200-20110308-C00004.png) | ||
| AT330466B (de) | Verfahren zum schutzen von gegenstanden gegen die einwirkung von mikroorganismen | |
| CH620573A5 (US07902200-20110308-C00004.png) | ||
| WO1990001033A1 (de) | Diorganozinn-verbindungen und diese enthaltende mittel mit bakterizider und fungizider wirkung | |
| DE1815168C3 (de) | Verfahren zur Herstellung von Organozinn-mercaptocarbonsäureestersulfiden und Stabilisierungsmittel für Vinylchloridpolymerisate, welche diese enthalten | |
| DE1920543A1 (de) | Nickelalkoxyd | |
| DE1019285B (de) | Verfahren zur Herstellung von polymeren organischen Zirkon- und/oder Titansaeureesterderivaten | |
| DE2902646C2 (de) | Bis-trialkylstannylderivate chlorierter polycyclischer Dicarbonsäuren, Verfahren zu ihrer Herstellung und Mittel für Aufwuchsverhütungsüberzüge |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OGA | New person/name/address of the applicant | ||
| OD | Request for examination | ||
| D2 | Grant after examination | ||
| 8339 | Ceased/non-payment of the annual fee |