NO118921B - - Google Patents
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- Publication number
- NO118921B NO118921B NO168540A NO16854067A NO118921B NO 118921 B NO118921 B NO 118921B NO 168540 A NO168540 A NO 168540A NO 16854067 A NO16854067 A NO 16854067A NO 118921 B NO118921 B NO 118921B
- Authority
- NO
- Norway
- Prior art keywords
- soil
- nematodes
- organisms
- dioxide
- plants
- Prior art date
Links
- 239000002689 soil Substances 0.000 claims description 29
- 241000244206 Nematoda Species 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000013543 active substance Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000000945 filler Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 15
- 239000007788 liquid Substances 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- MBDNRNMVTZADMQ-UHFFFAOYSA-N sulfolene Chemical compound O=S1(=O)CC=CC1 MBDNRNMVTZADMQ-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 241000227653 Lycopersicon Species 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- LFHISGNCFUNFFM-UHFFFAOYSA-N chloropicrin Chemical compound [O-][N+](=O)C(Cl)(Cl)Cl LFHISGNCFUNFFM-UHFFFAOYSA-N 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000002361 compost Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- -1 fuller's earth Chemical compound 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000005645 nematicide Substances 0.000 description 2
- 244000045947 parasite Species 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 2
- 229920000053 polysorbate 80 Polymers 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- UATYTNIKGIQPOE-UHFFFAOYSA-N 2,2-dichloropropane 1,1-dichloroprop-1-ene Chemical compound ClC(C)(C)Cl.ClC(=CC)Cl UATYTNIKGIQPOE-UHFFFAOYSA-N 0.000 description 1
- BPTGGFRVUKNIBY-UHFFFAOYSA-N 3,4-dibromo-3-chlorothiolane 1,1-dioxide Chemical compound ClC1(Br)CS(=O)(=O)CC1Br BPTGGFRVUKNIBY-UHFFFAOYSA-N 0.000 description 1
- CGWKQCYAMPDEGC-UHFFFAOYSA-N 3,4-dibromothiolane 1,1-dioxide Chemical compound BrC1CS(=O)(=O)CC1Br CGWKQCYAMPDEGC-UHFFFAOYSA-N 0.000 description 1
- JCUQWSIALJCIEE-UHFFFAOYSA-N 3,4-dichlorothiolane 1,1-dioxide Chemical compound ClC1CS(=O)(=O)CC1Cl JCUQWSIALJCIEE-UHFFFAOYSA-N 0.000 description 1
- SEZJAAIKYHZWCH-UHFFFAOYSA-N 3-chlorothiolane 1,1-dioxide Chemical compound ClC1CCS(=O)(=O)C1 SEZJAAIKYHZWCH-UHFFFAOYSA-N 0.000 description 1
- OIPVZGSYIJYEGU-UHFFFAOYSA-N 4-chloro-1,1-dioxothiolan-3-ol Chemical compound OC1CS(=O)(=O)CC1Cl OIPVZGSYIJYEGU-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000258963 Diplopoda Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- HSRJKNPTNIJEKV-UHFFFAOYSA-N Guaifenesin Chemical compound COC1=CC=CC=C1OCC(O)CO HSRJKNPTNIJEKV-UHFFFAOYSA-N 0.000 description 1
- 101000756346 Homo sapiens RE1-silencing transcription factor Proteins 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000243786 Meloidogyne incognita Species 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical compound ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 102100022940 RE1-silencing transcription factor Human genes 0.000 description 1
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 1
- 239000004147 Sorbitan trioleate Substances 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- URXDZIFZXGLYIT-UHFFFAOYSA-N decylbenzene;sodium Chemical compound [Na].CCCCCCCCCCC1=CC=CC=C1 URXDZIFZXGLYIT-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 206010014881 enterobiasis Diseases 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000003864 humus Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 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
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920001993 poloxamer 188 Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000006283 soil fumigant Substances 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/91—Nitro radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO246069A NO120034B (es) | 1966-06-10 | 1969-06-13 | |
| NO246169A NO120035B (es) | 1966-06-10 | 1969-06-13 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55658566A | 1966-06-10 | 1966-06-10 | |
| US84007769A | 1969-04-23 | 1969-04-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO118921B true NO118921B (es) | 1970-03-02 |
Family
ID=27071183
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO168540A NO118921B (es) | 1966-06-10 | 1967-06-09 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US3468902A (es) |
| AT (4) | AT278005B (es) |
| BE (1) | BE699358A (es) |
| CH (2) | CH508632A (es) |
| DE (1) | DE1695189A1 (es) |
| DK (1) | DK130585B (es) |
| ES (1) | ES341604A1 (es) |
| FI (1) | FI48083C (es) |
| FR (1) | FR6691M (es) |
| GB (1) | GB1139455A (es) |
| IL (1) | IL28090A (es) |
| NL (1) | NL6708044A (es) |
| NO (1) | NO118921B (es) |
| SE (1) | SE345454B (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2037610A1 (de) * | 1970-07-29 | 1972-02-03 | Bayer Ag | Neue alpha-substituierte Benzyl-azole, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| US3852301A (en) * | 1973-06-21 | 1974-12-03 | Squibb & Sons Inc | Enol betaines of imidazoles |
| DE2350123C2 (de) * | 1973-10-05 | 1983-04-14 | Bayer Ag, 5090 Leverkusen | 1-Propyl-imidazol-Derivate und deren Salze, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide |
| JPS5692887A (en) * | 1979-12-05 | 1981-07-27 | Sumitomo Chem Co Ltd | N-substituted imidazole derivative |
| US4358571A (en) * | 1981-03-10 | 1982-11-09 | Mobil Oil Corporation | Chemically modified imidazole curing catalysts for epoxy resin and powder coatings containing them |
| DE3216894A1 (de) * | 1982-05-06 | 1983-11-10 | Henkel KGaA, 4000 Düsseldorf | Substituierte 2-(3-iod-2-propinyloxy)ethanole, ihre herstellung und ihre verwendung als antimikrobielle substanzen |
| DE3218130A1 (de) * | 1982-05-14 | 1983-11-17 | Basf Ag, 6700 Ludwigshafen | Azolylmethyloxirane, verfahren zu ihrer herstellung und diese enthaltende fungizide |
| US5532380A (en) * | 1992-12-18 | 1996-07-02 | Pola Chemical Industries, Inc. | R,R,S,S-2-nitroimidazole derivatives |
| US5728843A (en) * | 1993-10-04 | 1998-03-17 | Wallace Technologies | (2'-nitro-1'-imidazolyl)-2,3-isopropylidene-y-tosylbutanol, a precursor to 18 F!fluoroerythronitroimidazole PET imaging agent |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1445963A1 (de) * | 1962-04-06 | 1969-12-04 | Klosa Dipl Chem Dr Josef | Verfahren zur Herstellung eines neuen Imidazolderivates |
-
1966
- 1966-06-10 US US556585A patent/US3468902A/en not_active Expired - Lifetime
-
1967
- 1967-05-25 CH CH84771A patent/CH508632A/de unknown
- 1967-05-25 CH CH748467A patent/CH503741A/de not_active IP Right Cessation
- 1967-05-27 DE DE19671695189 patent/DE1695189A1/de active Pending
- 1967-05-29 AT AT999268A patent/AT278005B/de not_active IP Right Cessation
- 1967-05-29 AT AT09990/68A patent/AT278003B/de not_active IP Right Cessation
- 1967-05-29 AT AT999168A patent/AT278004B/de not_active IP Right Cessation
- 1967-05-29 AT AT999368A patent/AT278777B/de not_active IP Right Cessation
- 1967-05-30 SE SE7578/67A patent/SE345454B/xx unknown
- 1967-05-31 IL IL28090A patent/IL28090A/en unknown
- 1967-06-01 BE BE699358D patent/BE699358A/xx unknown
- 1967-06-07 FR FR109375A patent/FR6691M/fr not_active Expired
- 1967-06-09 ES ES341604A patent/ES341604A1/es not_active Expired
- 1967-06-09 NL NL6708044A patent/NL6708044A/xx unknown
- 1967-06-09 FI FI671632A patent/FI48083C/fi active
- 1967-06-09 DK DK303467AA patent/DK130585B/da unknown
- 1967-06-09 GB GB26766/67A patent/GB1139455A/en not_active Expired
- 1967-06-09 NO NO168540A patent/NO118921B/no unknown
-
1969
- 1969-04-23 US US840077*A patent/US3549653A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AT278004B (de) | 1970-01-26 |
| NL6708044A (es) | 1967-12-11 |
| BE699358A (es) | 1967-12-01 |
| GB1139455A (en) | 1969-01-08 |
| FI48083B (es) | 1974-02-28 |
| AT278777B (de) | 1970-02-10 |
| AT278005B (de) | 1970-01-26 |
| DE1695189A1 (de) | 1971-04-08 |
| AT278003B (de) | 1970-01-26 |
| FI48083C (fi) | 1974-06-10 |
| US3549653A (en) | 1970-12-22 |
| ES341604A1 (es) | 1968-12-01 |
| CH503741A (de) | 1971-02-28 |
| DK130585B (da) | 1975-03-10 |
| SE345454B (es) | 1972-05-29 |
| DK130585C (es) | 1975-08-11 |
| US3468902A (en) | 1969-09-23 |
| CH508632A (de) | 1971-06-15 |
| FR6691M (es) | 1969-02-10 |
| IL28090A (en) | 1971-11-29 |
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