NO840653L - Triorganotinnacetylsalicylater, og biocide midler inneholdende disse - Google Patents

Triorganotinnacetylsalicylater, og biocide midler inneholdende disse

Info

Publication number: NO840653L
Authority: NO; Norway
Prior art keywords: acetylsalicylate; tri; carbon atoms; triorganotin; weight
Prior art date: 1983-02-22

Application number

NO840653A

Other languages

English (en)

Norwegian (no)

Inventor

Horst Landsiedel

Hans Plum

Original Assignee

Schering Ag

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.)

1983-02-22

Filing date

1984-02-21

Publication date

1984-08-23

1984-02-21 Application filed by Schering Ag filed Critical Schering Ag

1984-08-23 Publication of NO840653L publication Critical patent/NO840653L/no

Links

239000003139 biocide Substances 0.000 title claims description 6
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims abstract description 19
239000002023 wood Substances 0.000 claims abstract description 10
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 9
125000000217 alkyl group Chemical group 0.000 claims abstract description 7
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
241000233866 Fungi Species 0.000 claims description 10
ZUWWEGWEUMHGLQ-UHFFFAOYSA-M tributylstannyl 2-acetyloxybenzoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C1=CC=CC=C1OC(C)=O ZUWWEGWEUMHGLQ-UHFFFAOYSA-M 0.000 claims description 8
239000004480 active ingredient Substances 0.000 claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 5
241000894006 Bacteria Species 0.000 claims description 4
241000195493 Cryptophyta Species 0.000 claims description 3
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
230000003115 biocidal effect Effects 0.000 abstract description 14
238000000034 method Methods 0.000 abstract description 3
239000000758 substrate Substances 0.000 abstract 2
238000009877 rendering Methods 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
239000008096 xylene Substances 0.000 description 12
238000002360 preparation method Methods 0.000 description 11
239000000047 product Substances 0.000 description 11
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 10
238000003756 stirring Methods 0.000 description 10
BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 9
LHHPEAQVCCPLBC-UHFFFAOYSA-N tributyltin;hydrate Chemical compound O.CCCC[Sn](CCCC)CCCC LHHPEAQVCCPLBC-UHFFFAOYSA-N 0.000 description 8
239000000203 mixture Substances 0.000 description 7
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
229960001138 acetylsalicylic acid Drugs 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical class CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 6
238000001035 drying Methods 0.000 description 5
239000003973 paint Substances 0.000 description 5
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
239000007787 solid Substances 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
239000013543 active substance Substances 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 4
239000000498 cooling water Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
JUEAPPHORMOWPK-UHFFFAOYSA-M tributylstannyl benzoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C1=CC=CC=C1 JUEAPPHORMOWPK-UHFFFAOYSA-M 0.000 description 4
230000004580 weight loss Effects 0.000 description 4
KUFHDYFDMGIOHI-UHFFFAOYSA-M 2-acetyloxybenzoate;tricyclohexylstannanylium Chemical compound CC(=O)OC1=CC=CC=C1C([O-])=O.C1CCCCC1[Sn+](C1CCCCC1)C1CCCCC1 KUFHDYFDMGIOHI-UHFFFAOYSA-M 0.000 description 3
NGWGOJMXTMXFKM-UHFFFAOYSA-M 2-acetyloxybenzoate;trioctylstannanylium Chemical compound CC(=O)OC1=CC=CC=C1C([O-])=O.CCCCCCCC[Sn+](CCCCCCCC)CCCCCCCC NGWGOJMXTMXFKM-UHFFFAOYSA-M 0.000 description 3
CSHNILFEAUTCQT-UHFFFAOYSA-M 2-acetyloxybenzoate;triphenylstannanylium Chemical compound CC(=O)OC1=CC=CC=C1C([O-])=O.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 CSHNILFEAUTCQT-UHFFFAOYSA-M 0.000 description 3
241001626940 Coniophora cerebella Species 0.000 description 3
229940068372 acetyl salicylate Drugs 0.000 description 3
125000000129 anionic group Chemical group 0.000 description 3
230000001580 bacterial effect Effects 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
239000000123 paper Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
-1 tri-n-butyltin compound Chemical class 0.000 description 3
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 2
MFYSUUPKMDJYPF-UHFFFAOYSA-N 2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxo-n-phenylbutanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC1=CC=C(C)C=C1[N+]([O-])=O MFYSUUPKMDJYPF-UHFFFAOYSA-N 0.000 description 2
MLAMTPQTUDIBSY-UHFFFAOYSA-M 2-acetyloxybenzoate;tripropylstannanylium Chemical compound CCC[Sn+](CCC)CCC.CC(=O)OC1=CC=CC=C1C([O-])=O MLAMTPQTUDIBSY-UHFFFAOYSA-M 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
244000162269 Lentinus lepideus Species 0.000 description 2
235000017066 Lentinus lepideus Nutrition 0.000 description 2
235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
235000011613 Pinus brutia Nutrition 0.000 description 2
241000018646 Pinus brutia Species 0.000 description 2
241001619461 Poria <basidiomycete fungus> Species 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
239000004566 building material Substances 0.000 description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
150000001805 chlorine compounds Chemical class 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
239000000463 material Substances 0.000 description 2
244000005700 microbiome Species 0.000 description 2
239000012875 nonionic emulsifier Substances 0.000 description 2
239000002985 plastic film Substances 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
229920001522 polyglycol ester Polymers 0.000 description 2
239000004753 textile Substances 0.000 description 2
SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical class C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 2
NSPWVJAKNXJHEP-UHFFFAOYSA-N tripropyltin Chemical group CCC[Sn](CCC)CCC NSPWVJAKNXJHEP-UHFFFAOYSA-N 0.000 description 2
SFDCESVOFOYWTJ-YLLHCXABSA-M (9z,12z)-octadeca-9,12-dienoate;tributylstannanylium Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)O[Sn](CCCC)(CCCC)CCCC SFDCESVOFOYWTJ-YLLHCXABSA-M 0.000 description 1
125000005273 2-acetoxybenzoic acid group Chemical class 0.000 description 1
240000005020 Acaciella glauca Species 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
QTDRLOKFLJJHTG-UHFFFAOYSA-N Furmecyclox Chemical compound C1=C(C)OC(C)=C1C(=O)N(OC)C1CCCCC1 QTDRLOKFLJJHTG-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004264 Petrolatum Substances 0.000 description 1
241000218657 Picea Species 0.000 description 1
235000008582 Pinus sylvestris Nutrition 0.000 description 1
241000131858 Siboglinidae Species 0.000 description 1
206010041662 Splinter Diseases 0.000 description 1
GCTFWCDSFPMHHS-UHFFFAOYSA-M Tributyltin chloride Chemical compound CCCC[Sn](Cl)(CCCC)CCCC GCTFWCDSFPMHHS-UHFFFAOYSA-M 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000008272 agar Substances 0.000 description 1
229920000180 alkyd Polymers 0.000 description 1
230000003373 anti-fouling effect Effects 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000031018 biological processes and functions Effects 0.000 description 1
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
239000011449 brick Substances 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
239000011111 cardboard Substances 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
238000004040 coloring Methods 0.000 description 1
WCMMILVIRZAPLE-UHFFFAOYSA-M cyhexatin Chemical compound C1CCCCC1[Sn](C1CCCCC1)(O)C1CCCCC1 WCMMILVIRZAPLE-UHFFFAOYSA-M 0.000 description 1
230000007123 defense Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
238000005553 drilling Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000004519 grease Substances 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
238000011534 incubation Methods 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
238000010409 ironing Methods 0.000 description 1
235000021388 linseed oil Nutrition 0.000 description 1
239000000944 linseed oil Substances 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
239000002609 medium Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
AKBZLSDTRZFLRP-UHFFFAOYSA-N n-cyclohexylnitrous amide Chemical class O=NNC1CCCCC1 AKBZLSDTRZFLRP-UHFFFAOYSA-N 0.000 description 1
239000006916 nutrient agar Substances 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
229940066842 petrolatum Drugs 0.000 description 1
235000019271 petrolatum Nutrition 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
239000001839 pinus sylvestris Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000012262 resinous product Substances 0.000 description 1
229960001860 salicylate Drugs 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000002641 tar oil Substances 0.000 description 1
RIECPYZYOLVSJK-UHFFFAOYSA-N tert-butyl 2-dimethylsilyl-5-methylindole-1-carboxylate Chemical compound C[SiH](C)c1cc2cc(C)ccc2n1C(=O)OC(C)(C)C RIECPYZYOLVSJK-UHFFFAOYSA-N 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
DFNPRTKVCGZMMC-UHFFFAOYSA-M tributyl(fluoro)stannane Chemical compound CCCC[Sn](F)(CCCC)CCCC DFNPRTKVCGZMMC-UHFFFAOYSA-M 0.000 description 1
NRHFWOJROOQKBK-UHFFFAOYSA-N triphenyltin;hydrate Chemical compound O.C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 NRHFWOJROOQKBK-UHFFFAOYSA-N 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Cosmetics (AREA)
Chemical And Physical Treatments For Wood And The Like (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)

NO840653A 1983-02-22 1984-02-21 Triorganotinnacetylsalicylater, og biocide midler inneholdende disse NO840653L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3306036		1983-02-22

Publications (1)

Publication Number	Publication Date
NO840653L true NO840653L (no)	1984-08-23

Family

ID=6191453

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO840653A NO840653L (no)	1983-02-22	1984-02-21	Triorganotinnacetylsalicylater, og biocide midler inneholdende disse

Country Status (10)

Country	Link
US (1)	US4514225A (da)
EP (1)	EP0119419B1 (da)
JP (1)	JPS59157090A (da)
AT (1)	ATE28876T1 (da)
CA (1)	CA1223600A (da)
DE (1)	DE3465310D1 (da)
DK (1)	DK157814C (da)
ES (1)	ES529838A0 (da)
FI (1)	FI73693C (da)
NO (1)	NO840653L (da)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5648084A (en) *	1990-02-28	1997-07-15	Guttag; Alvin	Multiple dosage medicine drop bottle
DE69107080T2 (de) *	1991-10-22	1995-06-22	Pharmachemie Bv	Organozinnverbindungen mit Antitumoraktivität und Zusammensetzungen mit Antitumorwirkung.

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1386350A (fr) *	1963-11-28	1965-01-22	Micro Biolog Lab	Composés antimicrobiens, leur procédé de préparation et leurs applications
NL128116C (da) *	1965-03-25	1900-01-01
US3534077A (en) *	1968-12-24	1970-10-13	Perry B Hudson	Bis(tri - n - butyl tin)sulfosalicylate and tributyltin salts of ethylene diamine tetracetic acid
JPS4856655A (da) *	1971-11-24	1973-08-09
GB1541055A (en) *	1976-03-26	1979-02-21	Research Corp	Organotin compounds
NL7700738A (nl) *	1976-03-31	1977-10-04	Schering Ag	Opslagstabiele, hardbare, biocide bevattende, onverzadigde polyesterharsen, alsmede werkwijze voor het bereiden daarvan.
JPS55154905A (en) *	1979-05-22	1980-12-02	Yoshitomi Pharmaceut Ind Ltd	Wood preservative
JPS5927566B2 (ja) *	1980-07-02	1984-07-06	日本光電工業株式会社	電磁血流計

1984
- 1984-01-02 FI FI840005A patent/FI73693C/fi not_active IP Right Cessation
- 1984-02-02 EP EP84101050A patent/EP0119419B1/de not_active Expired
- 1984-02-02 AT AT84101050T patent/ATE28876T1/de active
- 1984-02-02 DK DK047584A patent/DK157814C/da not_active IP Right Cessation
- 1984-02-02 DE DE8484101050T patent/DE3465310D1/de not_active Expired
- 1984-02-06 CA CA000446852A patent/CA1223600A/en not_active Expired
- 1984-02-17 ES ES529838A patent/ES529838A0/es active Granted
- 1984-02-20 JP JP59028845A patent/JPS59157090A/ja active Pending
- 1984-02-21 US US06/581,652 patent/US4514225A/en not_active Expired - Fee Related
- 1984-02-21 NO NO840653A patent/NO840653L/no unknown

Also Published As

Publication number	Publication date
ATE28876T1 (de)	1987-08-15
JPS59157090A (ja)	1984-09-06
CA1223600A (en)	1987-06-30
US4514225A (en)	1985-04-30
FI840005A0 (fi)	1984-01-02
EP0119419A1 (de)	1984-09-26
DK47584A (da)	1984-08-23
FI73693B (fi)	1987-07-31
ES8501408A1 (es)	1984-12-01
DE3465310D1 (en)	1987-09-17
DK157814B (da)	1990-02-19
ES529838A0 (es)	1984-12-01
FI840005L (fi)	1984-08-23
FI73693C (fi)	1987-11-09
DK47584D0 (da)	1984-02-02
EP0119419B1 (de)	1987-08-12
DK157814C (da)	1990-07-16

Publication	Publication Date	Title
JPH09501688A (ja)	1997-02-18	抗細菌性および抗汚れ性オキサチアジン類およびそれらの酸化物
AU619257B2 (en)	1992-01-23	Improvments in or relating to biocidal quaternary salts of tertrafluoroborate and hexafluorophosphate
KR0139083B1 (ko)	1998-04-30	공업재료 및 급수시스템 보호를 위한 살균제
MX2011013607A (es)	2012-06-21	Combinacion sinergica de un compuesto de glifosato e ipbc.
NO840653L (no)	1984-08-23	Triorganotinnacetylsalicylater, og biocide midler inneholdende disse
DK157473B (da)	1990-01-15	Vandigt koncentrat med baktericid og fungicid virkning og anvendelse af dette til traebeskyttelse
EP0549006A2 (en)	1993-06-30	Ammonium and phosphonium salts and their use as biocides
Shiryaev et al.	2012	Application of organotin compounds for protecting wood and other materials and in nonfouling paints
JPH0548763B2 (da)	1993-07-22
CA1336427C (en)	1995-07-25	Diorganotin compounds and agents containing them having bactericidal and fungicidal activity
PL80654B1 (da)	1975-08-30
JPS6344121B2 (da)	1988-09-02
DK166249B (da)	1993-03-29	Baktericide og fungicide midler samt anvendelse heraf
EP0108039B1 (de)	1989-01-25	Neue Ammonium-Stannate-(IV)
DE2847400A1 (de)	1980-05-08	Salzartige aminoorganosilanester- phenol-addukte und verfahren zu deren herstellung
KR20120071354A (ko)	2012-07-02	글리포세이트 화합물과 ｔｂｚ의 상승적 배합물
NO861830L (no)	1986-11-10	Biocide tributyltinn-forbindelser.
SE430061B (sv)	1983-10-17	N-(2-metyl-1-naftyl)maleimid, forfarande for dess framstellning och dess anvendning som biocid
US10442758B2 (en)	2019-10-15	Zinc or Copper (II) salt and use thereof as a biocide
EP0177789B1 (de)	1988-10-26	Tris-(triorganozinn)ester der trimeren Fettsäure
DK158537B (da)	1990-06-05	Baktericidt og fungicidt middel indeholdende en blanding af trialkyltinforbindelser og 2,5-dimethyl-n-cyklohexyl-n-methoxy-3-furancarbonsyreamid
DE2237961C3 (da)	1981-02-05
KR20120071353A (ko)	2012-07-02	글리포세이트 화합물과 ｄｍｉｔｓ의 상승적 배합물
DE1817344C3 (de)	1978-07-13	Trialkylzinnsalze der Oxobenzothiazinessigsaure, deren Herstellung und Verwendung
NO177593B (no)	1995-07-10	Omsetningsproduktet av en dialkyltinnforbindelse med N-cyklo-hexyl-N'-hydroxy-diazeniumoxyd, midler med baktericid og fungicid virkning og trebeskyttelsesmiddel som inneholder disse forbindelser samt anvendelse av nevnte midler