SU1419504A3 - Нематоцидна композици (ее варианты) - Google Patents
Нематоцидна композици (ее варианты) Download PDFInfo
- Publication number
- SU1419504A3 SU1419504A3 SU813348255A SU3348255A SU1419504A3 SU 1419504 A3 SU1419504 A3 SU 1419504A3 SU 813348255 A SU813348255 A SU 813348255A SU 3348255 A SU3348255 A SU 3348255A SU 1419504 A3 SU1419504 A3 SU 1419504A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- composition
- compound
- general formula
- methyl
- alkylthiocarbamate
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 33
- 150000001875 compounds Chemical class 0.000 claims abstract description 21
- 239000008187 granular material Substances 0.000 claims abstract description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000004480 active ingredient Substances 0.000 claims abstract 6
- 230000001069 nematicidal effect Effects 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 229910000278 bentonite Inorganic materials 0.000 claims description 5
- 239000000440 bentonite Substances 0.000 claims description 5
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 5
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- YUGDYIWBYHTUFR-UHFFFAOYSA-N 10-methylundecyl benzenesulfonate Chemical compound CC(C)CCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YUGDYIWBYHTUFR-UHFFFAOYSA-N 0.000 claims description 4
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical group CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 claims description 4
- JYIBXUUINYLWLR-UHFFFAOYSA-N aluminum;calcium;potassium;silicon;sodium;trihydrate Chemical compound O.O.O.[Na].[Al].[Si].[K].[Ca] JYIBXUUINYLWLR-UHFFFAOYSA-N 0.000 claims description 4
- 229910001603 clinoptilolite Inorganic materials 0.000 claims description 4
- 239000004359 castor oil Substances 0.000 claims description 3
- 235000019438 castor oil Nutrition 0.000 claims description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 3
- 239000008096 xylene Chemical group 0.000 claims description 3
- IBSQPLPBRSHTTG-UHFFFAOYSA-N 1-chloro-2-methylbenzene Chemical compound CC1=CC=CC=C1Cl IBSQPLPBRSHTTG-UHFFFAOYSA-N 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims 4
- 239000000654 additive Substances 0.000 claims 2
- 230000000996 additive effect Effects 0.000 claims 2
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims 2
- 239000003995 emulsifying agent Substances 0.000 claims 2
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 claims 2
- 239000005909 Kieselgur Substances 0.000 claims 1
- 241000322338 Loeseliastrum Species 0.000 claims 1
- 230000006378 damage Effects 0.000 abstract description 6
- 235000007688 Lycopersicon esculentum Nutrition 0.000 abstract description 4
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 abstract description 4
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 abstract description 3
- 241000243786 Meloidogyne incognita Species 0.000 abstract description 3
- 229940050176 methyl chloride Drugs 0.000 abstract description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 2
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 230000001276 controlling effect Effects 0.000 abstract 2
- 241000193977 Pratylenchus musicola Species 0.000 abstract 1
- 240000003768 Solanum lycopersicum Species 0.000 abstract 1
- 208000027418 Wounds and injury Diseases 0.000 abstract 1
- 238000010521 absorption reaction Methods 0.000 abstract 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 abstract 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000010419 fine particle Substances 0.000 abstract 1
- 208000014674 injury Diseases 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 3
- 241000227653 Lycopersicon Species 0.000 description 3
- -1 polyoxyethylene Polymers 0.000 description 3
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 231100000674 Phytotoxicity Toxicity 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 244000017020 Ipomoea batatas Species 0.000 description 1
- 235000002678 Ipomoea batatas Nutrition 0.000 description 1
- 241001143352 Meloidogyne Species 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- MBABOKRGFJTBAE-UHFFFAOYSA-N methyl methanesulfonate Chemical compound COS(C)(=O)=O MBABOKRGFJTBAE-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 230000002786 root growth Effects 0.000 description 1
- YPSUCTSXOROPBS-UHFFFAOYSA-N s-methyl chloromethanethioate Chemical compound CSC(Cl)=O YPSUCTSXOROPBS-UHFFFAOYSA-N 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14636180A JPS5770805A (en) | 1980-10-21 | 1980-10-21 | Controlling agent against harmful nematode |
Publications (1)
Publication Number | Publication Date |
---|---|
SU1419504A3 true SU1419504A3 (ru) | 1988-08-23 |
Family
ID=15405973
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU813348255A SU1419504A3 (ru) | 1980-10-21 | 1981-10-19 | Нематоцидна композици (ее варианты) |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPS5770805A (enrdf_load_html_response) |
SU (1) | SU1419504A3 (enrdf_load_html_response) |
-
1980
- 1980-10-21 JP JP14636180A patent/JPS5770805A/ja active Granted
-
1981
- 1981-10-19 SU SU813348255A patent/SU1419504A3/ru active
Non-Patent Citations (1)
Title |
---|
Патент DE № 2651807, кл. А 01 N 9/20, выкл. 1977. Патент US № 3886282, кл. 424-300, опублик. 1975. * |
Also Published As
Publication number | Publication date |
---|---|
JPS6345365B2 (enrdf_load_html_response) | 1988-09-09 |
JPS5770805A (en) | 1982-05-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR960012202B1 (ko) | 살균 조성물 | |
KR20120052382A (ko) | 항식물 바이러스제 | |
SK282306B6 (sk) | Fenylhydrazínové deriváty, pesticídny prostriedok obsahujúci tieto zlúčeniny a spôsob kontrolovania nežiaduceho hmyzu | |
CS221820B2 (en) | Herbicide means | |
SU1419504A3 (ru) | Нематоцидна композици (ее варианты) | |
CS253710B2 (en) | Insecticide and nematocide | |
JPH04297455A (ja) | 4−複素環−3−(置換フェニル)酪酸誘導体および除草剤 | |
PL144332B1 (en) | Fungicide | |
US2885278A (en) | Herbicidal compositions containing esters of 1-ethynylcyclohexanol | |
JP5189642B2 (ja) | 殺有害生物用ジアゼンオキシドカルボキシレート | |
US3046104A (en) | Method for the control of weeds | |
SU1181518A3 (ru) | Способ борьбы с сорн ками | |
FR2520195A1 (fr) | Procede perfectionne pour combattre les mycetes et combinaisons fongicides utilisables dans ce procede | |
SU727107A3 (ru) | Фунгицидное средство | |
SU727108A3 (ru) | Фунгицидное средство | |
US4696947A (en) | Nematocide | |
SU656464A3 (ru) | Гербицидное средство | |
JPH0122241B2 (enrdf_load_html_response) | ||
CN117042608A (zh) | 杀螨的活性成分组合物及其用途 | |
US4265657A (en) | Herbicidal compositions containing α-halo acetanilides and substituted bicyclo(3.3.1)non-2-ene compounds as safening agents | |
JPH0139401B2 (enrdf_load_html_response) | ||
JPS62175409A (ja) | 殺ダニ剤 | |
GB2025409A (en) | Dialkyl dithiocarbamates their preparation and nematocidal compositions containing them | |
SU1181517A3 (ru) | Способ борьбы с сорн ками | |
SU799628A3 (ru) | Гербицидный состав |