JPS632419B2 - - Google Patents

Info

Publication number: JPS632419B2
Authority: JP; Japan
Prior art keywords: triiodo; parts; atom; test; compound
Prior art date: 1981-01-09
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

Application number

JP56001748A

Other languages

English (en)

Japanese (ja)

Other versions

JPS57116023A (en

Inventor

Yasuhiro Morisawa

Mitsuru Kataoka

Seiji Konishi

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Sankyo Co Ltd

Original Assignee

Sankyo Co Ltd

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.)

1981-01-09

Filing date

1981-01-09

Publication date

1988-01-19

1981-01-09 Application filed by Sankyo Co Ltd filed Critical Sankyo Co Ltd

1981-01-09 Priority to JP174881A priority Critical patent/JPS57116023A/ja

1982-07-19 Publication of JPS57116023A publication Critical patent/JPS57116023A/ja

1988-01-19 Publication of JPS632419B2 publication Critical patent/JPS632419B2/ja

Status Granted legal-status Critical Current

Links

239000003755 preservative agent Substances 0.000 claims description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
230000002335 preservative effect Effects 0.000 claims description 8
229910052740 iodine Inorganic materials 0.000 claims description 7
125000001424 substituent group Chemical group 0.000 claims description 6
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
125000003545 alkoxy group Chemical group 0.000 claims description 5
239000004480 active ingredient Substances 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
125000001309 chloro group Chemical group Cl* 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
238000012360 testing method Methods 0.000 description 27
-1 3,5-dichlorophenyl Chemical group 0.000 description 23
150000001875 compounds Chemical class 0.000 description 22
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
239000000203 mixture Substances 0.000 description 11
239000002023 wood Substances 0.000 description 10
238000009472 formulation Methods 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
239000002424 termiticide Substances 0.000 description 5
241000894006 Bacteria Species 0.000 description 4
239000000443 aerosol Substances 0.000 description 4
230000000843 anti-fungal effect Effects 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
239000000417 fungicide Substances 0.000 description 4
239000003973 paint Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000002994 raw material Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
241000233866 Fungi Species 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
239000000853 adhesive Substances 0.000 description 3
230000001070 adhesive effect Effects 0.000 description 3
229940121375 antifungal agent Drugs 0.000 description 3
239000004927 clay Substances 0.000 description 3
239000007789 gas Substances 0.000 description 3
239000011630 iodine Substances 0.000 description 3
238000002372 labelling Methods 0.000 description 3
239000000463 material Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
239000011120 plywood Substances 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000008096 xylene Substances 0.000 description 3
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
241000233732 Fusarium verticillioides Species 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
241000223261 Trichoderma viride Species 0.000 description 2
239000002671 adjuvant Substances 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
238000007598 dipping method Methods 0.000 description 2
230000000855 fungicidal effect Effects 0.000 description 2
239000003350 kerosene Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000002156 mixing Methods 0.000 description 2
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
239000002245 particle Substances 0.000 description 2
IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000005507 spraying Methods 0.000 description 2
230000001954 sterilising effect Effects 0.000 description 2
238000004659 sterilization and disinfection Methods 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
239000003171 wood protecting agent Substances 0.000 description 2
MKNJWAXSYGAMGJ-UHFFFAOYSA-N (2,3,4,5,6-pentachlorophenyl) dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl MKNJWAXSYGAMGJ-UHFFFAOYSA-N 0.000 description 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
HSQFVBWFPBKHEB-UHFFFAOYSA-N 2,3,4-trichlorophenol Chemical compound OC1=CC=C(Cl)C(Cl)=C1Cl HSQFVBWFPBKHEB-UHFFFAOYSA-N 0.000 description 1
BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 description 1
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
QGUPBYVADAJUNT-UHFFFAOYSA-N 6-morpholin-4-ium-4-yl-4,4-diphenylheptan-3-one;chloride Chemical compound Cl.C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)CC)CC(C)N1CCOCC1 QGUPBYVADAJUNT-UHFFFAOYSA-N 0.000 description 1
235000007173 Abies balsamea Nutrition 0.000 description 1
244000283070 Abies balsamea Species 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241000228245 Aspergillus niger Species 0.000 description 1
241000223678 Aureobasidium pullulans Species 0.000 description 1
241000218645 Cedrus Species 0.000 description 1
241000221955 Chaetomium Species 0.000 description 1
241000222290 Cladosporium Species 0.000 description 1
241000222356 Coriolus Species 0.000 description 1
235000010099 Fagus sylvatica Nutrition 0.000 description 1
240000000731 Fagus sylvatica Species 0.000 description 1
241001105467 Fomitopsis palustris Species 0.000 description 1
241000223218 Fusarium Species 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
241000257303 Hymenoptera Species 0.000 description 1
241000256602 Isoptera Species 0.000 description 1
241000228143 Penicillium Species 0.000 description 1
235000003570 Phyllostachys pubescens Nutrition 0.000 description 1
244000302661 Phyllostachys pubescens Species 0.000 description 1
235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
235000011613 Pinus brutia Nutrition 0.000 description 1
241000018646 Pinus brutia Species 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
241000235527 Rhizopus Species 0.000 description 1
241000223259 Trichoderma Species 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
239000008272 agar Substances 0.000 description 1
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
230000002421 anti-septic effect Effects 0.000 description 1
239000004599 antimicrobial Substances 0.000 description 1
239000012752 auxiliary agent Substances 0.000 description 1
ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical class C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 description 1
MCUIEDCAVHLHPG-UHFFFAOYSA-L bis(tributylstannyl) benzene-1,2-dicarboxylate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C1=CC=CC=C1C(=O)O[Sn](CCCC)(CCCC)CCCC MCUIEDCAVHLHPG-UHFFFAOYSA-L 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
JYWJULGYGOLCGW-UHFFFAOYSA-N chloromethyl chloroformate Chemical compound ClCOC(Cl)=O JYWJULGYGOLCGW-UHFFFAOYSA-N 0.000 description 1
238000004440 column chromatography Methods 0.000 description 1
238000011109 contamination Methods 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
125000005805 dimethoxy phenyl group Chemical group 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
OJLOUXPPKZRTHK-UHFFFAOYSA-N dodecan-1-ol;sodium Chemical compound [Na].CCCCCCCCCCCCO OJLOUXPPKZRTHK-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
239000003480 eluent Substances 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 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
239000000835 fiber Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
239000008103 glucose Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
230000000887 hydrating effect Effects 0.000 description 1
239000000750 industrial fungicide Substances 0.000 description 1
239000000077 insect repellent Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000010985 leather Substances 0.000 description 1
239000003915 liquefied petroleum gas Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
239000000178 monomer Substances 0.000 description 1
AKBZLSDTRZFLRP-UHFFFAOYSA-N n-cyclohexylnitrous amide Chemical compound O=NNC1CCCCC1 AKBZLSDTRZFLRP-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
150000004045 organic chlorine compounds Chemical class 0.000 description 1
150000002903 organophosphorus compounds Chemical class 0.000 description 1
239000006072 paste Substances 0.000 description 1
RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
229960000490 permethrin Drugs 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 description 1
229950001664 phoxim Drugs 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
239000002728 pyrethroid Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
238000002791 soaking Methods 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
229940005550 sodium alginate Drugs 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
239000007787 solid Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
238000010998 test method Methods 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

JP174881A 1981-01-09 1981-01-09 Trihaloallyl derivative and termite-controlling agent and antimold and antiseptic agent containing said derivative as active component Granted JPS57116023A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP174881A JPS57116023A (en)	1981-01-09	1981-01-09	Trihaloallyl derivative and termite-controlling agent and antimold and antiseptic agent containing said derivative as active component

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP174881A JPS57116023A (en)	1981-01-09	1981-01-09	Trihaloallyl derivative and termite-controlling agent and antimold and antiseptic agent containing said derivative as active component

Publications (2)

Publication Number	Publication Date
JPS57116023A JPS57116023A (en)	1982-07-19
JPS632419B2 true JPS632419B2 (de)	1988-01-19

Family

ID=11510181

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP174881A Granted JPS57116023A (en)	1981-01-09	1981-01-09	Trihaloallyl derivative and termite-controlling agent and antimold and antiseptic agent containing said derivative as active component

Country Status (1)

Country	Link
JP (1)	JPS57116023A (de)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS508359U (de) *	1973-05-10	1975-01-28
JPS51135262U (de) *	1975-04-23	1976-11-01

1981
- 1981-01-09 JP JP174881A patent/JPS57116023A/ja active Granted

Also Published As

Publication number	Publication date
JPS57116023A (en)	1982-07-19

Publication	Publication Date	Title
JPH11503376A (ja)	1999-03-26	銅化合物を含む木材保護剤
US20080175913A1 (en)	2008-07-24	Wood preservative compositions comprising isothiazolone-pyrethroids
TW521993B (en)	2003-03-01	Pesticidal compositions
JPS632419B2 (de)	1988-01-19
JPH0637369B2 (ja)	1994-05-18	殺微生物組成物
PL80654B1 (de)	1975-08-30
JPS6340402B2 (de)	1988-08-11
AU759694B2 (en)	2003-04-17	Agents and method for the protective treatment of wood
US4487781A (en)	1984-12-11	Trihaloallyl derivatives having anti-fungal activities
JPH0112747B2 (de)	1989-03-02
JPS62881B2 (de)	1987-01-10
JPS6364415B2 (de)	1988-12-12
JPS6366820B2 (de)	1988-12-22
JPS623828B2 (de)	1987-01-27
JPS6215054B2 (de)	1987-04-06
JPS6250460B2 (de)	1987-10-24
JPH0617284B2 (ja)	1994-03-09	殺微生物剤
JP3195081B2 (ja)	2001-08-06	工業用防腐防カビ組成物
JPH04500504A (ja)	1992-01-30	ジオルガノスズ化合物およびこれを含有し殺菌性および殺真菌性作用を有する薬剤
JP4783981B2 (ja)	2011-09-28	木材の保護処理用組成物および方法
US2573862A (en)	1951-11-06	Pesticidal composition comprising a zinc salt of petroleum sulphonic acids
NO861830L (no)	1986-11-10	Biocide tributyltinn-forbindelser.
JPS6310922B2 (de)	1988-03-10
CA1159604A (en)	1984-01-03	Aqueous slurry or pasty fungicidal composition
SU346834A1 (de)