DE1184147B - Mittel zur Bekaempfung von Nematoden - Google Patents
Mittel zur Bekaempfung von NematodenInfo
- Publication number
- DE1184147B DE1184147B DES73880A DES0073880A DE1184147B DE 1184147 B DE1184147 B DE 1184147B DE S73880 A DES73880 A DE S73880A DE S0073880 A DES0073880 A DE S0073880A DE 1184147 B DE1184147 B DE 1184147B
- Authority
- DE
- Germany
- Prior art keywords
- plants
- nematodes
- diacetate
- roots
- group
- 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.)
- Pending
Links
- 241000244206 Nematoda Species 0.000 title claims description 26
- 238000002360 preparation method Methods 0.000 title description 12
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000002689 soil Substances 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 150000002898 organic sulfur compounds Chemical class 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 150000007970 thio esters Chemical class 0.000 claims description 2
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 30
- 239000007788 liquid Substances 0.000 description 14
- 238000012360 testing method Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- -1 dithiol compounds Chemical class 0.000 description 5
- ZRKMQKLGEQPLNS-UHFFFAOYSA-N 1-Pentanethiol Chemical compound CCCCCS ZRKMQKLGEQPLNS-UHFFFAOYSA-N 0.000 description 4
- ULIKDJVNUXNQHS-UHFFFAOYSA-N 2-Propene-1-thiol Chemical compound SCC=C ULIKDJVNUXNQHS-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 150000004662 dithiols Chemical class 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- 241000243786 Meloidogyne incognita Species 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- 230000001069 nematicidal effect Effects 0.000 description 3
- 239000005645 nematicide Substances 0.000 description 3
- CFIOOCBLOLNSED-UHFFFAOYSA-N s-(6-acetylsulfanylhexyl) ethanethioate Chemical compound CC(=O)SCCCCCCSC(C)=O CFIOOCBLOLNSED-UHFFFAOYSA-N 0.000 description 3
- SRZXCOWFGPICGA-UHFFFAOYSA-N 1,6-Hexanedithiol Chemical compound SCCCCCCS SRZXCOWFGPICGA-UHFFFAOYSA-N 0.000 description 2
- PMBXCGGQNSVESQ-UHFFFAOYSA-N 1-Hexanethiol Chemical compound CCCCCCS PMBXCGGQNSVESQ-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 240000009088 Fragaria x ananassa Species 0.000 description 2
- 244000111489 Gardenia augusta Species 0.000 description 2
- 244000278530 Philodendron bipinnatifidum Species 0.000 description 2
- 235000018976 Philodendron bipinnatifidum Nutrition 0.000 description 2
- 241001092459 Rubus Species 0.000 description 2
- 240000003768 Solanum lycopersicum Species 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 241000218636 Thuja Species 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 235000021028 berry Nutrition 0.000 description 2
- SMTOKHQOVJRXLK-UHFFFAOYSA-N butane-1,4-dithiol Chemical compound SCCCCS SMTOKHQOVJRXLK-UHFFFAOYSA-N 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 231100000636 lethal dose Toxicity 0.000 description 2
- IXBUFAUQDFHNGI-UHFFFAOYSA-N methylsulfanylmethanethiol Chemical compound CSCS IXBUFAUQDFHNGI-UHFFFAOYSA-N 0.000 description 2
- KMTUBAIXCBHPIZ-UHFFFAOYSA-N pentane-1,5-dithiol Chemical compound SCCCCCS KMTUBAIXCBHPIZ-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- XCZMKVSTLKAKNT-UHFFFAOYSA-N s-but-2-enyl ethanethioate Chemical compound CC=CCSC(C)=O XCZMKVSTLKAKNT-UHFFFAOYSA-N 0.000 description 2
- KXXZPIFZTPWOJJ-UHFFFAOYSA-N s-butyl benzenecarbothioate Chemical compound CCCCSC(=O)C1=CC=CC=C1 KXXZPIFZTPWOJJ-UHFFFAOYSA-N 0.000 description 2
- UYZVABQVIWVBOC-UHFFFAOYSA-N s-prop-2-ynyl ethanethioate Chemical compound CC(=O)SCC#C UYZVABQVIWVBOC-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 235000021012 strawberries Nutrition 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 150000003464 sulfur compounds Chemical class 0.000 description 2
- 150000003573 thiols Chemical class 0.000 description 2
- XMEPRJBZFCWFKN-UHFFFAOYSA-N 1,3-Butanedithiol Chemical compound CC(S)CCS XMEPRJBZFCWFKN-UHFFFAOYSA-N 0.000 description 1
- GJRCLMJHPWCJEI-UHFFFAOYSA-N 1,9-Nonanedithiol Chemical compound SCCCCCCCCCS GJRCLMJHPWCJEI-UHFFFAOYSA-N 0.000 description 1
- VURHLXXBWDIITE-UHFFFAOYSA-N 2,5-dimethylhexane-1,6-dithiol Chemical compound SCC(C)CCC(C)CS VURHLXXBWDIITE-UHFFFAOYSA-N 0.000 description 1
- 241000580217 Belonolaimus Species 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- FAABFOQEIWPSKJ-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)O.C(C1=CC=CC=C1)(=O)O.C(CCCCCS)S Chemical compound C(C1=CC=CC=C1)(=O)O.C(C1=CC=CC=C1)(=O)O.C(CCCCCS)S FAABFOQEIWPSKJ-UHFFFAOYSA-N 0.000 description 1
- 206010011732 Cyst Diseases 0.000 description 1
- 241000399934 Ditylenchus Species 0.000 description 1
- 241001480224 Heterodera Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241001143352 Meloidogyne Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000201433 Nacobbus Species 0.000 description 1
- 241000193943 Pratylenchus Species 0.000 description 1
- SBWFWBJCYMBZEY-UHFFFAOYSA-N S-Propyl thioacetate Chemical compound CCCSC(C)=O SBWFWBJCYMBZEY-UHFFFAOYSA-N 0.000 description 1
- 241001267618 Tylenchulus Species 0.000 description 1
- 241001267621 Tylenchulus semipenetrans Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 125000005569 butenylene group Chemical group 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- CMKBCTPCXZNQKX-UHFFFAOYSA-N cyclohexanethiol Chemical compound SC1CCCCC1 CMKBCTPCXZNQKX-UHFFFAOYSA-N 0.000 description 1
- 208000031513 cyst Diseases 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- ZJLMKPKYJBQJNH-UHFFFAOYSA-N propane-1,3-dithiol Chemical compound SCCCS ZJLMKPKYJBQJNH-UHFFFAOYSA-N 0.000 description 1
- 125000006410 propenylene group Chemical group 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- MEQLOUCDKZRWAO-UHFFFAOYSA-N s-(4-acetylsulfanylbutyl) ethanethioate Chemical compound CC(=O)SCCCCSC(C)=O MEQLOUCDKZRWAO-UHFFFAOYSA-N 0.000 description 1
- XQLIUJWBXPIGCB-UHFFFAOYSA-N s-benzyl ethanethioate Chemical compound CC(=O)SCC1=CC=CC=C1 XQLIUJWBXPIGCB-UHFFFAOYSA-N 0.000 description 1
- JSEGXJBSYHWMMY-UHFFFAOYSA-N s-cyclohexyl ethanethioate Chemical compound CC(=O)SC1CCCCC1 JSEGXJBSYHWMMY-UHFFFAOYSA-N 0.000 description 1
- UVOBMCVOACVTNV-UHFFFAOYSA-N s-hexyl ethanethioate Chemical compound CCCCCCSC(C)=O UVOBMCVOACVTNV-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/02—Acyclic compounds
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/06—Unsaturated carboxylic acids or thio analogues thereof; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing carboxylic groups or thio analogues thereof, directly attached by the carbon atom to a cycloaliphatic ring; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US27515A US3137615A (en) | 1960-05-09 | 1960-05-09 | Method for protecting plants employing alkanedithiols |
| US5008960A | 1960-08-17 | 1960-08-17 | |
| US6670260A | 1960-11-02 | 1960-11-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1184147B true DE1184147B (de) | 1964-12-23 |
Family
ID=27363029
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DES73880A Pending DE1184147B (de) | 1960-05-09 | 1961-05-08 | Mittel zur Bekaempfung von Nematoden |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US3137615A (en, 2012) |
| BE (1) | BE603541A (en, 2012) |
| CH (1) | CH423348A (en, 2012) |
| DE (1) | DE1184147B (en, 2012) |
| ES (1) | ES267225A1 (en, 2012) |
| FR (1) | FR1288659A (en, 2012) |
| GB (1) | GB944960A (en, 2012) |
| NL (1) | NL264490A (en, 2012) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL250399A (en, 2012) * | 1960-04-11 | |||
| US3318936A (en) * | 1961-06-27 | 1967-05-09 | Takeda Chemical Industries Ltd | Dithiocyanato amino alkanes |
| US3255075A (en) * | 1963-03-29 | 1966-06-07 | Du Pont | Methane-thiol containing nematocides |
| GB1501501A (en) * | 1975-01-02 | 1978-02-15 | Realisations Scient Soc Et | Acaricidal and ovicidal compositions |
| JPS5234922A (en) * | 1975-09-12 | 1977-03-17 | Kao Corp | Novel antimicrobial agent for non-medical use |
| US4914135A (en) * | 1979-08-30 | 1990-04-03 | Herschler R J | Use of Methylsulfonylmethane to treat parasitic infections |
| LU83725A1 (fr) * | 1981-10-29 | 1983-06-07 | Seresci | Composes organiques sulfures et leur utilisation comme acaricides,insecticides et/ou fongicides |
| US4744948A (en) * | 1987-06-04 | 1988-05-17 | Texaco Inc. | Thiol ester corrosion inhibition system |
| RU2207753C1 (ru) * | 2002-02-11 | 2003-07-10 | Северо-Кавказский научно-исследовательский институт горного и предгорного сельского хозяйства | Способ защиты плодовых насаждений от болезней |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2045925A (en) * | 1932-10-15 | 1936-06-30 | Texas Co | Insecticide and fungicide |
| US2701224A (en) * | 1952-01-02 | 1955-02-01 | Phillips Petroleum Co | Nematocidal dicarbothioic acid ester composition and method of applying same |
| GB783546A (en) * | 1954-01-20 | 1957-09-25 | Exxon Research Engineering Co | Bis-mercaptomethyl aromatic compounds, their preparation and use |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2795525A (en) * | 1952-11-20 | 1957-06-11 | Phillips Petroleum Co | Method of eradicating nematodes by applying thereto sulfenyl xanthates |
| US2770638A (en) * | 1953-07-03 | 1956-11-13 | Stauffer Chemical Co | Xanthyl and trithiocarbonyl sulfones as novel compositions of matter |
| US2852426A (en) * | 1953-12-14 | 1958-09-16 | Phillips Petroleum Co | Nematocides containing carboxylic acids and their esters and method |
| US2719170A (en) * | 1954-07-28 | 1955-09-27 | Du Pont | Alkyl omega-carboxyalkyl disulfides and their lower alkyl esters |
| US2917429A (en) * | 1956-08-17 | 1959-12-15 | Collier Carbon & Chemical Co | Method of destroying nematodes employing dimethyl polysulfides |
| US3004885A (en) * | 1956-10-16 | 1961-10-17 | Monsanto Chemicals | Salts of alkanethiols |
| US2882197A (en) * | 1956-12-03 | 1959-04-14 | Collier Carbon & Chemical Co | Sulfurized alkyl thioformal fungicidal compositions |
| US2864738A (en) * | 1957-04-22 | 1958-12-16 | Collier Carbon & Chemical Co | Fungicidal compositions comprising sulfurized mercaptols |
| US2864739A (en) * | 1957-05-13 | 1958-12-16 | Collier Carbon & Chemical Co | Pesticidal compositions comprising sulfurized mercaptals |
| US2877153A (en) * | 1957-08-05 | 1959-03-10 | Collier Carbon & Chemical Co | Fungicidal compositions |
| US2998346A (en) * | 1957-11-26 | 1961-08-29 | Collier Carbon & Chemical Co | Pest control |
-
0
- BE BE603541D patent/BE603541A/xx unknown
- NL NL264490D patent/NL264490A/xx unknown
- US US3103464D patent/US3103464A/en not_active Expired - Lifetime
-
1960
- 1960-05-09 US US27515A patent/US3137615A/en not_active Expired - Lifetime
-
1961
- 1961-05-08 CH CH535861A patent/CH423348A/de unknown
- 1961-05-08 GB GB16620/61A patent/GB944960A/en not_active Expired
- 1961-05-08 DE DES73880A patent/DE1184147B/de active Pending
- 1961-05-08 ES ES0267225A patent/ES267225A1/es not_active Expired
- 1961-05-08 FR FR861112A patent/FR1288659A/fr not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2045925A (en) * | 1932-10-15 | 1936-06-30 | Texas Co | Insecticide and fungicide |
| US2701224A (en) * | 1952-01-02 | 1955-02-01 | Phillips Petroleum Co | Nematocidal dicarbothioic acid ester composition and method of applying same |
| GB783546A (en) * | 1954-01-20 | 1957-09-25 | Exxon Research Engineering Co | Bis-mercaptomethyl aromatic compounds, their preparation and use |
Also Published As
| Publication number | Publication date |
|---|---|
| US3103464A (en) | 1963-09-10 |
| BE603541A (en, 2012) | |
| NL264490A (en, 2012) | |
| CH423348A (de) | 1966-10-31 |
| FR1288659A (fr) | 1962-03-24 |
| ES267225A1 (es) | 1961-11-01 |
| US3137615A (en) | 1964-06-16 |
| GB944960A (en) | 1963-12-18 |
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