IL33014A - Fungicidal compositions comprising sucrose and 1-alkylaminocarbonyl-2-alkoxycarbonylaminobenzimidazoles - Google Patents
Fungicidal compositions comprising sucrose and 1-alkylaminocarbonyl-2-alkoxycarbonylaminobenzimidazolesInfo
- Publication number
- IL33014A IL33014A IL33014A IL3301469A IL33014A IL 33014 A IL33014 A IL 33014A IL 33014 A IL33014 A IL 33014A IL 3301469 A IL3301469 A IL 3301469A IL 33014 A IL33014 A IL 33014A
- Authority
- IL
- Israel
- Prior art keywords
- compounds
- sucrose
- plants
- mites
- mite
- Prior art date
Links
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- 241001286670 Ulmus x hollandica Species 0.000 description 1
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- 241000509513 Ustilago hordei Species 0.000 description 1
- JYBGVFYNRAPJRJ-UHFFFAOYSA-N [1-(butylcarbamoyl)benzimidazol-2-yl]carbamic acid Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(O)=O)=NC2=C1 JYBGVFYNRAPJRJ-UHFFFAOYSA-N 0.000 description 1
- DJYWNBIJMHTYFH-UHFFFAOYSA-N [1-(hexylcarbamoyl)benzimidazol-2-yl]carbamic acid Chemical compound C(CCCCC)NC(=O)N1C(=NC2=C1C=CC=C2)NC(=O)O DJYWNBIJMHTYFH-UHFFFAOYSA-N 0.000 description 1
- JQEGDMWMPRDBRR-UHFFFAOYSA-N [1-(methylcarbamoyl)benzimidazol-2-yl]carbamic acid Chemical compound C1=CC=C2N(C(=O)NC)C(NC(O)=O)=NC2=C1 JQEGDMWMPRDBRR-UHFFFAOYSA-N 0.000 description 1
- WEUHFCALMYALAY-UHFFFAOYSA-N [1-(octylcarbamoyl)benzimidazol-2-yl]carbamic acid Chemical compound C(CCCCCCC)NC(=O)N1C(=NC2=C1C=CC=C2)NC(=O)O WEUHFCALMYALAY-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- 235000021028 berry Nutrition 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000001465 calcium Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 208000002925 dental caries Diseases 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000004492 dustable powder Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 244000037666 field crops Species 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 239000004459 forage Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 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 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical class OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000001055 magnesium Nutrition 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 235000021017 pears Nutrition 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 235000021018 plums Nutrition 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Chemical class 0.000 description 1
- 239000001267 polyvinylpyrrolidone Chemical class 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009291 secondary effect Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 description 1
- HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical class [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229960005349 sulfur Drugs 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- ACWBQPMHZXGDFX-QFIPXVFZSA-N valsartan Chemical class C1=CC(CN(C(=O)CCCC)[C@@H](C(C)C)C(O)=O)=CC=C1C1=CC=CC=C1C1=NN=NN1 ACWBQPMHZXGDFX-QFIPXVFZSA-N 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
- C07D235/32—Benzimidazole-2-carbamic acids, unsubstituted or substituted; Esters thereof; Thio-analogues thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US76602868A | 1968-10-02 | 1968-10-02 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL33014A0 IL33014A0 (en) | 1969-11-30 |
| IL33014A true IL33014A (en) | 1972-06-28 |
Family
ID=25075175
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL33014A IL33014A (en) | 1968-10-02 | 1969-09-17 | Fungicidal compositions comprising sucrose and 1-alkylaminocarbonyl-2-alkoxycarbonylaminobenzimidazoles |
Country Status (14)
| Country | Link |
|---|---|
| AT (1) | AT299612B (da) |
| BE (1) | BE739690A (da) |
| BR (1) | BR6912907D0 (da) |
| CH (1) | CH499267A (da) |
| DE (1) | DE1949846A1 (da) |
| DK (1) | DK122923B (da) |
| ES (1) | ES372015A1 (da) |
| FR (1) | FR2019722A1 (da) |
| GB (1) | GB1269970A (da) |
| IE (1) | IE33319B1 (da) |
| IL (1) | IL33014A (da) |
| NL (1) | NL147613B (da) |
| PH (1) | PH9215A (da) |
| SE (1) | SE376535B (da) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6210004A (ja) * | 1985-07-05 | 1987-01-19 | Sumitomo Chem Co Ltd | フザリウム病害防除剤 |
| US4857541A (en) * | 1986-08-07 | 1989-08-15 | Canadian Patents And Development Limited/Societe Canadienne Des Brevets Et D'exploitation Limitee | Substituted benzimidazole fungicide |
-
1969
- 1969-09-16 IE IE1297/69A patent/IE33319B1/xx unknown
- 1969-09-17 PH PH10730*UA patent/PH9215A/en unknown
- 1969-09-17 IL IL33014A patent/IL33014A/en unknown
- 1969-09-23 CH CH1437069A patent/CH499267A/de not_active IP Right Cessation
- 1969-09-26 SE SE6913265A patent/SE376535B/xx unknown
- 1969-09-29 ES ES372015A patent/ES372015A1/es not_active Expired
- 1969-09-30 DK DK520769AA patent/DK122923B/da not_active IP Right Cessation
- 1969-09-30 GB GB48112/69A patent/GB1269970A/en not_active Expired
- 1969-10-01 BR BR212907/69A patent/BR6912907D0/pt unknown
- 1969-10-01 BE BE739690D patent/BE739690A/xx not_active IP Right Cessation
- 1969-10-01 NL NL696914841A patent/NL147613B/xx not_active IP Right Cessation
- 1969-10-02 DE DE19691949846 patent/DE1949846A1/de active Pending
- 1969-10-02 AT AT932169A patent/AT299612B/de not_active IP Right Cessation
- 1969-10-02 FR FR6933703A patent/FR2019722A1/fr active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| FR2019722A1 (da) | 1970-07-03 |
| PH9215A (en) | 1975-07-10 |
| ES372015A1 (es) | 1971-10-16 |
| GB1269970A (en) | 1972-04-12 |
| NL6914841A (da) | 1970-04-06 |
| AT299612B (de) | 1972-06-26 |
| CH499267A (de) | 1970-11-30 |
| BR6912907D0 (pt) | 1973-03-01 |
| DK122923B (da) | 1972-05-01 |
| DE1949846A1 (de) | 1970-04-09 |
| SE376535B (da) | 1975-06-02 |
| BE739690A (da) | 1970-03-16 |
| IE33319B1 (en) | 1974-05-15 |
| IE33319L (en) | 1970-04-02 |
| IL33014A0 (en) | 1969-11-30 |
| NL147613B (nl) | 1975-11-17 |
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