IL28185A - Noble converted trichloroacetaldehyde - Google Patents
Noble converted trichloroacetaldehydeInfo
- Publication number
- IL28185A IL28185A IL28185A IL2818567A IL28185A IL 28185 A IL28185 A IL 28185A IL 28185 A IL28185 A IL 28185A IL 2818567 A IL2818567 A IL 2818567A IL 28185 A IL28185 A IL 28185A
- Authority
- IL
- Israel
- Prior art keywords
- active
- aminal
- fungus
- composition
- admixture
- Prior art date
Links
- -1 Acylated trichloracetaldehyde aminals Chemical class 0.000 title claims description 6
- 150000007854 aminals Chemical class 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 13
- 239000003085 diluting agent Substances 0.000 claims description 12
- 241000233866 Fungi Species 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 5
- 230000000855 fungicidal effect Effects 0.000 claims description 5
- 241000607479 Yersinia pestis Species 0.000 claims description 4
- 239000012442 inert solvent Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 15
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
- 241000196324 Embryophyta Species 0.000 description 9
- 206010061217 Infestation Diseases 0.000 description 8
- 239000000243 solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 240000008067 Cucumis sativus Species 0.000 description 3
- 241000220225 Malus Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000221785 Erysiphales Species 0.000 description 2
- 241000221787 Erysiphe Species 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 241000896238 Oidium Species 0.000 description 2
- 241000896242 Podosphaera Species 0.000 description 2
- 241001337928 Podosphaera leucotricha Species 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 241000579741 Sphaerotheca <fungi> Species 0.000 description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Chemical group 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- ADAKRBAJFHTIEW-UHFFFAOYSA-N 1-chloro-4-isocyanatobenzene Chemical compound ClC1=CC=C(N=C=O)C=C1 ADAKRBAJFHTIEW-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- 241001480059 Erysiphaceae Species 0.000 description 1
- 241000896246 Golovinomyces cichoracearum Species 0.000 description 1
- 241000896218 Golovinomyces orontii Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 235000021016 apples Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229960004424 carbon dioxide Drugs 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229940084434 fungoid Drugs 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- ACZVWYLTJHGUCP-UHFFFAOYSA-N n-(2,2,2-trichloro-1-hydroxyethyl)formamide Chemical compound ClC(Cl)(Cl)C(O)NC=O ACZVWYLTJHGUCP-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- CMXPERZAMAQXSF-UHFFFAOYSA-M sodium;1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate;1,8-dihydroxyanthracene-9,10-dione Chemical compound [Na+].O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=CC=C2O.CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC CMXPERZAMAQXSF-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 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
- 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
- A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (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 |
|---|---|---|---|
| DEF0049691 | 1966-07-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL28185A true IL28185A (en) | 1971-01-28 |
Family
ID=7103207
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL28185A IL28185A (en) | 1966-07-14 | 1967-06-23 | Noble converted trichloroacetaldehyde |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US3520927A (de) |
| AT (1) | AT268776B (de) |
| BE (1) | BE701322A (de) |
| CH (1) | CH488659A (de) |
| DK (1) | DK120757B (de) |
| ES (1) | ES342996A1 (de) |
| GB (1) | GB1123850A (de) |
| IL (1) | IL28185A (de) |
| MY (1) | MY6900193A (de) |
| NL (1) | NL6709836A (de) |
| SE (2) | SE352226B (de) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3960947A (en) * | 1971-01-22 | 1976-06-01 | Ciba-Geigy Corporation | Condensation products |
| US3716587A (en) * | 1971-03-25 | 1973-02-13 | Boehringer Sohn Ingelheim | N-(phenyl or benzyl)-n,n'-bis-(1-amino-2,2,2-trichloro)-ethyl)alkyleniamines |
| US4146646A (en) * | 1976-02-12 | 1979-03-27 | Fisons Limited | Bis-amide fungicidal compounds |
-
1967
- 1967-06-20 CH CH873267A patent/CH488659A/de not_active IP Right Cessation
- 1967-06-23 IL IL28185A patent/IL28185A/en unknown
- 1967-06-27 GB GB29632/67A patent/GB1123850A/en not_active Expired
- 1967-06-30 SE SE15837/69A patent/SE352226B/xx unknown
- 1967-06-30 SE SE10038/67*A patent/SE337211B/xx unknown
- 1967-07-11 US US652410A patent/US3520927A/en not_active Expired - Lifetime
- 1967-07-12 AT AT1119567A patent/AT268776B/de active
- 1967-07-12 DK DK361067AA patent/DK120757B/da unknown
- 1967-07-13 BE BE701322D patent/BE701322A/xx unknown
- 1967-07-13 ES ES342996A patent/ES342996A1/es not_active Expired
- 1967-07-14 NL NL6709836A patent/NL6709836A/xx unknown
-
1969
- 1969-06-24 US US845118A patent/US3629458A/en not_active Expired - Lifetime
- 1969-12-31 MY MY1969193A patent/MY6900193A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SE337211B (de) | 1971-08-02 |
| NL6709836A (de) | 1968-01-15 |
| US3629458A (en) | 1971-12-21 |
| BE701322A (de) | 1968-01-15 |
| CH488659A (de) | 1970-04-15 |
| SE352226B (de) | 1972-12-27 |
| GB1123850A (en) | 1968-08-14 |
| US3520927A (en) | 1970-07-21 |
| AT268776B (de) | 1969-02-25 |
| MY6900193A (en) | 1969-12-31 |
| DK120757B (da) | 1971-07-12 |
| ES342996A1 (es) | 1968-08-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0251082B1 (de) | Substituierte Acrylsäureester und Fungizide, die diese Verbindungen enthalten | |
| CS203928B2 (en) | Fungicide means and method of making the active substance | |
| IL31302A (en) | N-tritylimidazoles,their preparation and use for combatting fungi | |
| EP0130366B1 (de) | Arylalkylimidazolium- und -triazoliumsalze, Verfahren zu ihrer Herstellung und ihre Verwendung als Mikrozide | |
| EP0111234A2 (de) | Fungizide Mittel, deren Herstellung und Verwendung | |
| EP0146064A2 (de) | 1,1-Diphenyl-2-triazolyl-2-alkyl-ethane, ihre Herstellung und ihre Verwendung als Biozide | |
| EP0015502A2 (de) | Azolsubstituierte Atropasäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenschutzmittel | |
| CS249138B2 (en) | Fungicide | |
| IL28185A (en) | Noble converted trichloroacetaldehyde | |
| EP0007010A1 (de) | 1,2,4-Triazolderivate, Verfahren zu deren Herstellung, deren Verwendung als Schädlingsbekämpfungsmittel und Pflanzenwuchsregulatoren und diese Derivate enthaltende Schädlingsbekämpfungsmittel | |
| DE1767924A1 (de) | 1-Phenyl-4,4-dialkyl-thiosemicarbazide | |
| EP0061037A1 (de) | Fungizide Mittel auf Basis von 1,2-Oxazolylalkylphosphaten und die Verwendung dieser Wirkstoffe zur Bekämpfung von Pilzen | |
| US4560694A (en) | Fungicidal alkylene(cycloalkylene)-bis-heterocyclyl-biguanides | |
| US4166854A (en) | Substituted 1-pyridinyloxy-1-(imidazolyl)-2-butanone compounds and their use as fungicides | |
| EP0031962B1 (de) | Fungizide Azolyl-silyl-glykolether, ihre Herstellung, ihre Verwendung zur Bekämpfung von Fungi und Mittel dafür | |
| EP0071095B1 (de) | Phenylketenacetale und diese enthaltende Fungizide | |
| DE2502932C2 (de) | Metallkomplexe von N-Trityl-azolen, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide | |
| DE2025412A1 (de) | Amidophenylisothiohamstoffe, Verfahren zu ihrer Herstellung und ihre fungizide Verwendung | |
| EP0069289B1 (de) | Azolderivate, Verfahren zu ihrer Herstellung und diese enthaltende Fungizide | |
| EP0126380A1 (de) | Substituierte Tetrahydrothiopyran-3,5-dion-4-carboxamide | |
| EP0121183B1 (de) | Azolylierte Halogen-keten-O,N-acetale, Verfahren zu ihrer Herstellung, diese enthaltende Fungizide und Verfahren zur Bekämpfung von Pilzen mit ihnen | |
| US4212869A (en) | Substituted 1-pyridinyloxy-1-(imidazolyl)-2-butanone compounds and their use as fungicides | |
| EP0015498A2 (de) | Triazolsubstituierte Hydratropasäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenschutzmittel | |
| EP0077300B1 (de) | Triorganozinnhydantoin-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung | |
| EP0093274A1 (de) | Organosilyl-Verbindungen und ihre Verwendung als Fungizide |