CH645511A5 - Soluzioni e formulazioni di carbammati antiparassitari stabili nel tempo e che resistono a basse ed alte temperature. - Google Patents
Soluzioni e formulazioni di carbammati antiparassitari stabili nel tempo e che resistono a basse ed alte temperature. Download PDFInfo
- Publication number
- CH645511A5 CH645511A5 CH557880A CH557880A CH645511A5 CH 645511 A5 CH645511 A5 CH 645511A5 CH 557880 A CH557880 A CH 557880A CH 557880 A CH557880 A CH 557880A CH 645511 A5 CH645511 A5 CH 645511A5
- Authority
- CH
- Switzerland
- Prior art keywords
- carbamate
- solvent
- solutions
- solutions according
- formulations
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 22
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 title claims description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 26
- 239000002904 solvent Substances 0.000 claims description 21
- UOHMMEJUHBCKEE-UHFFFAOYSA-N prehnitene Chemical compound CC1=CC=C(C)C(C)=C1C UOHMMEJUHBCKEE-UHFFFAOYSA-N 0.000 claims description 12
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 claims description 10
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 6
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 5
- 239000000575 pesticide Substances 0.000 claims description 5
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 4
- -1 aliphatic ketones Chemical class 0.000 claims description 4
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 claims description 4
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 claims description 4
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 claims description 4
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- 229940007550 benzyl acetate Drugs 0.000 claims description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- ODLMAHJVESYWTB-UHFFFAOYSA-N ethylmethylbenzene Natural products CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 claims description 2
- 239000002563 ionic surfactant Substances 0.000 claims description 2
- 229940095102 methyl benzoate Drugs 0.000 claims description 2
- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 235000005985 organic acids Nutrition 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- CFXQEHVMCRXUSD-UHFFFAOYSA-N 1,2,3-Trichloropropane Chemical compound ClCC(Cl)CCl CFXQEHVMCRXUSD-UHFFFAOYSA-N 0.000 claims 2
- 150000004996 alkyl benzenes Chemical class 0.000 claims 1
- 229940113088 dimethylacetamide Drugs 0.000 claims 1
- 238000000034 method Methods 0.000 description 8
- 238000009472 formulation Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000005594 Phenmedipham Substances 0.000 description 4
- 239000013543 active substance Substances 0.000 description 4
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 4
- 229960005286 carbaryl Drugs 0.000 description 4
- 239000002917 insecticide Substances 0.000 description 4
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 description 4
- 238000004809 thin layer chromatography Methods 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000002141 anti-parasite Effects 0.000 description 2
- 239000003096 antiparasitic agent Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- QBSJMKIUCUGGNG-UHFFFAOYSA-N isoprocarb Chemical compound CNC(=O)OC1=CC=CC=C1C(C)C QBSJMKIUCUGGNG-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000013112 stability test Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000005503 Desmedipham Substances 0.000 description 1
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Polymers CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 1
- NWGKJDSIEKMTRX-MDZDMXLPSA-N Sorbitan oleate Polymers CCCCCCCC\C=C\CCCCCCCC(=O)OCC(O)C1OCC(O)C1O NWGKJDSIEKMTRX-MDZDMXLPSA-N 0.000 description 1
- NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Polymers CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 description 1
- AMRQXHFXNZFDCH-UHFFFAOYSA-N [1-(ethylamino)-1-oxopropan-2-yl] n-phenylcarbamate Chemical compound CCNC(=O)C(C)OC(=O)NC1=CC=CC=C1 AMRQXHFXNZFDCH-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- WZJZMXBKUWKXTQ-UHFFFAOYSA-N desmedipham Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=CC=CC=2)=C1 WZJZMXBKUWKXTQ-UHFFFAOYSA-N 0.000 description 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GIOQLVUHIQGITJ-UHFFFAOYSA-N methyl n-carbamoyloxy-n-[3-(3-methylphenyl)phenyl]carbamate Chemical compound COC(=O)N(OC(N)=O)C1=CC=CC(C=2C=C(C)C=CC=2)=C1 GIOQLVUHIQGITJ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT24733/79A IT1163687B (it) | 1979-07-27 | 1979-07-27 | Soluzioni e formulazioni di carbammati antiparassitari stabili nel tempo e che resistono a basse ed alte temperature |
Publications (1)
Publication Number | Publication Date |
---|---|
CH645511A5 true CH645511A5 (it) | 1984-10-15 |
Family
ID=11214561
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH557880A CH645511A5 (it) | 1979-07-27 | 1980-07-22 | Soluzioni e formulazioni di carbammati antiparassitari stabili nel tempo e che resistono a basse ed alte temperature. |
Country Status (19)
Country | Link |
---|---|
US (1) | US4452630A (en:Method) |
JP (1) | JPS5620503A (en:Method) |
BE (1) | BE884482A (en:Method) |
CA (1) | CA1153694A (en:Method) |
CH (1) | CH645511A5 (en:Method) |
CS (1) | CS236769B2 (en:Method) |
DD (1) | DD152271A5 (en:Method) |
DE (1) | DE3027767A1 (en:Method) |
DK (1) | DK313480A (en:Method) |
ES (1) | ES493737A0 (en:Method) |
FI (1) | FI802296A7 (en:Method) |
FR (1) | FR2462101B1 (en:Method) |
GR (1) | GR82410B (en:Method) |
IL (1) | IL60665A0 (en:Method) |
IT (1) | IT1163687B (en:Method) |
NL (1) | NL8004178A (en:Method) |
PL (1) | PL125190B1 (en:Method) |
SE (1) | SE8005272L (en:Method) |
SU (1) | SU1367835A3 (en:Method) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1195941B (it) * | 1982-07-16 | 1988-11-03 | Montedison Spa | Composizioni liquide stabili di meta-bis-carbammati erbicidi |
ES8604495A1 (es) * | 1983-09-20 | 1986-02-01 | Koege Kemisk Vaerk | Un procedimiento para preparar fenil-carbamatos sustituidos |
US5246912A (en) * | 1984-02-29 | 1993-09-21 | Berol Nobel (Suisse) S.A. | Herbicidal compositions of phenmedipham and desmedipham |
SK278523B6 (en) * | 1984-02-29 | 1997-08-06 | Erik Nielsen | A stabilised liquid herbicidal agent and method for killing weed plants |
FR2577387B1 (fr) * | 1985-02-19 | 1987-09-11 | Raffineries Soufre Reunies | Nouvelles compositions herbicides a base de carbamoyloxy-phenyl-carbamates et d'huile minerale de petrole |
FR2590119B1 (fr) * | 1985-03-14 | 1988-07-29 | Rhone Poulenc Agrochimie | Compositions herbicides liquides stabilisees, a base de biscarbamate |
FR2597720A1 (fr) * | 1986-04-29 | 1987-10-30 | Rhone Poulenc Agrochimie | Compositions herbicides liquides stabilisees a base de m-bis-carbamates et leur utilisation. |
FR2599593A1 (fr) * | 1986-06-06 | 1987-12-11 | Rhone Poulenc Agrochimie | Compositions herbicides liquides stabilisees a base de m-bis-carbamates et leur utilisation |
IT1199818B (it) * | 1986-12-19 | 1989-01-05 | Agrimont Spa | Composizioni di metil-3-(3'-metilfenil-carbamoilossi)feniclcarbammato stabili in emulsione acquosa |
HU207197B (en) * | 1987-07-16 | 1993-03-29 | Chinoin Gyogyszer Es Vegyeszet | Plant protecting solution and aquous suspension containing water insoluble active component |
USRE35993E (en) * | 1989-02-27 | 1998-12-15 | Gierveld Beheer B.V. | Frame for a skate, method for the manufacture thereof, skating shoe and skate |
GB8921515D0 (en) * | 1989-09-22 | 1989-11-08 | Wellcome Found | Pesticidal compositions |
GB2243551A (en) * | 1990-05-01 | 1991-11-06 | Kemira Oy | Herbicidal solution |
DE19516522A1 (de) * | 1995-05-05 | 1996-11-07 | Bayer Ag | Neue Flüssigformulierungen |
GB2446644B (en) * | 2007-02-15 | 2009-03-04 | William Anthony Jonfia-Essien | An antifeedant agent with insecticidal effect |
EA022368B1 (ru) * | 2010-05-27 | 2015-12-30 | Акцо Нобель Кемикалз Интернэшнл Б.В. | Сельскохозяйственные препараты с ацилморфолинами и полярными апротонными сорастворителями |
WO2013076200A1 (en) * | 2011-11-24 | 2013-05-30 | Akzo Nobel Chemicals International B.V. | Agricultural formulations with amides and acyl morpholines |
RU2606798C2 (ru) * | 2011-11-24 | 2017-01-10 | Акцо Нобель Кемикалз Интернэшнл Б.В. | Сельскохозяйственные составы с ароматическими растворителями и ацилморфолинами |
CN108552171B (zh) * | 2012-02-27 | 2020-07-17 | 胡茨曼澳大利亚股份有限公司 | 乳油配制剂 |
CN103004756B (zh) * | 2012-12-28 | 2015-04-22 | 深圳诺普信农化股份有限公司 | 农药溶剂及其制备方法和应用 |
RU2709725C2 (ru) * | 2014-12-30 | 2019-12-19 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Фунгицидные соединения |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3068142A (en) * | 1962-12-11 | Solvent system comprising dimethyl | ||
US30578A (en) * | 1860-11-06 | Henry johnson | ||
GB852610A (en) * | 1958-12-19 | 1960-10-26 | Shell Res Ltd | Liquid seed dressing compositions |
US3404975A (en) * | 1964-12-18 | 1968-10-08 | Fmc Corp | m-(carbamoyloxy)-carbanilates as herbicides |
BE683901A (en:Method) * | 1965-07-14 | 1967-01-09 | ||
NL6915231A (en:Method) * | 1968-10-24 | 1970-04-28 | ||
NL6917222A (en:Method) * | 1969-11-14 | 1971-05-18 | ||
IL33580A (en) * | 1968-12-25 | 1973-05-31 | Philips Nv | Single-phase pesticidal u.l.v.preparations |
DE2128225C3 (de) * | 1971-06-07 | 1980-06-12 | C.H. Boehringer Sohn, 6507 Ingelheim | Lösungskonzentrate mit fungizider und akarizider Wirkung |
US4093447A (en) | 1971-06-23 | 1978-06-06 | Bayer Aktiengesellschaft | N-Arylcarbamic acid esters and plant growth regulant compositions and methods |
US4163662A (en) * | 1973-01-02 | 1979-08-07 | E. I. Du Pont De Nemours And Company | Liquid formulations of 1-(3,4-dichlorophenyl)-3-methoxy-3-methylurea and selected chloroacetamides |
LU66864A1 (en:Method) * | 1973-01-19 | 1974-08-19 | ||
NL178647C (nl) * | 1974-03-08 | 1986-05-01 | Duphar Int Res | Werkwijze ter bereiding van een de plantengroei bevorderende vloeibare samenstelling. |
IT1111151B (it) * | 1978-01-10 | 1986-01-13 | Sipcam Spa | Composizione erbicida liquida emulsionabile in acqua |
CA1106202A (en) * | 1978-12-13 | 1981-08-04 | Lawrence J. Giilck | Herbicidal concentrate containing ketone and amide solvent |
-
1979
- 1979-07-27 IT IT24733/79A patent/IT1163687B/it active
-
1980
- 1980-07-21 DK DK313480A patent/DK313480A/da not_active Application Discontinuation
- 1980-07-21 FI FI802296A patent/FI802296A7/fi not_active Application Discontinuation
- 1980-07-21 SE SE8005272A patent/SE8005272L/xx not_active Application Discontinuation
- 1980-07-21 NL NL8004178A patent/NL8004178A/nl not_active Application Discontinuation
- 1980-07-22 JP JP9944280A patent/JPS5620503A/ja active Granted
- 1980-07-22 FR FR8016093A patent/FR2462101B1/fr not_active Expired
- 1980-07-22 CH CH557880A patent/CH645511A5/it not_active IP Right Cessation
- 1980-07-22 DE DE19803027767 patent/DE3027767A1/de not_active Ceased
- 1980-07-23 PL PL1980225836A patent/PL125190B1/pl unknown
- 1980-07-23 IL IL60665A patent/IL60665A0/xx unknown
- 1980-07-23 CA CA000356867A patent/CA1153694A/en not_active Expired
- 1980-07-25 BE BE0/201532A patent/BE884482A/fr not_active IP Right Cessation
- 1980-07-25 CS CS805259A patent/CS236769B2/cs unknown
- 1980-07-25 GR GR62542A patent/GR82410B/el unknown
- 1980-07-25 SU SU802953004A patent/SU1367835A3/ru active
- 1980-07-25 DD DD80222882A patent/DD152271A5/de not_active IP Right Cessation
- 1980-07-26 ES ES493737A patent/ES493737A0/es active Granted
-
1981
- 1981-11-17 US US06/322,202 patent/US4452630A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
IT1163687B (it) | 1987-04-08 |
US4452630A (en) | 1984-06-05 |
BE884482A (fr) | 1981-01-26 |
FR2462101A1 (fr) | 1981-02-13 |
IL60665A0 (en) | 1980-09-16 |
DE3027767A1 (de) | 1981-02-19 |
JPS5620503A (en) | 1981-02-26 |
CS236769B2 (en) | 1985-05-15 |
DD152271A5 (de) | 1981-11-25 |
FR2462101B1 (fr) | 1985-07-12 |
SE8005272L (sv) | 1981-01-28 |
SU1367835A3 (ru) | 1988-01-15 |
ES8104794A1 (es) | 1981-05-16 |
IT7924733A0 (it) | 1979-07-27 |
DK313480A (da) | 1981-01-28 |
PL225836A1 (en:Method) | 1981-05-22 |
ES493737A0 (es) | 1981-05-16 |
GR82410B (en:Method) | 1984-12-13 |
FI802296A7 (fi) | 1981-01-01 |
CA1153694A (en) | 1983-09-13 |
NL8004178A (nl) | 1981-01-29 |
JPH0135801B2 (en:Method) | 1989-07-27 |
PL125190B1 (en) | 1983-04-30 |
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