IL29325A - Alkylsulphuric acid salts of tetradecylguanidine - Google Patents
Alkylsulphuric acid salts of tetradecylguanidineInfo
- Publication number
- IL29325A IL29325A IL2932568A IL2932568A IL29325A IL 29325 A IL29325 A IL 29325A IL 2932568 A IL2932568 A IL 2932568A IL 2932568 A IL2932568 A IL 2932568A IL 29325 A IL29325 A IL 29325A
- Authority
- IL
- Israel
- Prior art keywords
- process according
- compound
- active compound
- reaction
- active
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title claims description 17
- HEPBMDUSWIMDBM-UHFFFAOYSA-N 2-tetradecylguanidine Chemical class CCCCCCCCCCCCCCN=C(N)N HEPBMDUSWIMDBM-UHFFFAOYSA-N 0.000 title claims description 7
- 239000002253 acid Substances 0.000 title description 6
- 150000001875 compounds Chemical class 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 23
- 241000196324 Embryophyta Species 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- 241000233866 Fungi Species 0.000 claims description 9
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 9
- 206010039509 Scab Diseases 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 claims description 6
- 239000003085 diluting agent Substances 0.000 claims description 6
- 230000000855 fungicidal effect Effects 0.000 claims description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- LMEDOLJKVASKTP-UHFFFAOYSA-N dibutyl sulfate Chemical compound CCCCOS(=O)(=O)OCCCC LMEDOLJKVASKTP-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 240000001987 Pyrus communis Species 0.000 claims description 2
- 235000014443 Pyrus communis Nutrition 0.000 claims description 2
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 claims description 2
- 239000012442 inert solvent Substances 0.000 claims description 2
- 230000003071 parasitic effect Effects 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims description 2
- 239000002689 soil Substances 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 244000141359 Malus pumila Species 0.000 claims 2
- 239000004480 active ingredient Substances 0.000 claims 2
- 235000011430 Malus pumila Nutrition 0.000 claims 1
- 235000015103 Malus silvestris Nutrition 0.000 claims 1
- 241000220324 Pyrus Species 0.000 claims 1
- 235000021016 apples Nutrition 0.000 claims 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical group COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims 1
- 238000011065 in-situ storage Methods 0.000 claims 1
- 235000021017 pears Nutrition 0.000 claims 1
- 239000001117 sulphuric acid Substances 0.000 claims 1
- 206010061217 Infestation Diseases 0.000 description 9
- 241000220225 Malus Species 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- -1 that is Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 241000489964 Fusicladium Species 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-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
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000011081 inoculation Methods 0.000 description 3
- 239000006072 paste Substances 0.000 description 3
- HILAYQUKKYWPJW-UHFFFAOYSA-N 1-dodecylguanidine Chemical class CCCCCCCCCCCCN=C(N)N HILAYQUKKYWPJW-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- HWBLTYHIEYOAOL-UHFFFAOYSA-N Diisopropyl sulfate Chemical compound CC(C)OS(=O)(=O)OC(C)C HWBLTYHIEYOAOL-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- BPMPPVUBRPXMNX-UHFFFAOYSA-N butyl carbamimidothioate Chemical compound CCCCSC(N)=N BPMPPVUBRPXMNX-UHFFFAOYSA-N 0.000 description 1
- ZTHQBROSBNNGPU-UHFFFAOYSA-M butyl sulfate(1-) Chemical compound CCCCOS([O-])(=O)=O ZTHQBROSBNNGPU-UHFFFAOYSA-M 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011814 protection agent Substances 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
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Landscapes
- 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 |
|---|---|---|---|
| DEF0051480 | 1967-02-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL29325A true IL29325A (en) | 1971-03-24 |
Family
ID=7104639
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL2932568A IL29325A (en) | 1967-02-10 | 1968-01-17 | Alkylsulphuric acid salts of tetradecylguanidine |
Country Status (7)
| Country | Link |
|---|---|
| AT (1) | AT278033B (en。) |
| BE (1) | BE710579A (en。) |
| ES (1) | ES350292A1 (en。) |
| FR (1) | FR1568888A (en。) |
| GB (1) | GB1169133A (en。) |
| IL (1) | IL29325A (en。) |
| NL (1) | NL6801664A (en。) |
-
1968
- 1968-01-17 IL IL2932568A patent/IL29325A/en unknown
- 1968-01-26 GB GB425168A patent/GB1169133A/en not_active Expired
- 1968-02-06 NL NL6801664A patent/NL6801664A/xx unknown
- 1968-02-08 ES ES350292A patent/ES350292A1/es not_active Expired
- 1968-02-09 FR FR1568888D patent/FR1568888A/fr not_active Expired
- 1968-02-09 AT AT123968A patent/AT278033B/de not_active IP Right Cessation
- 1968-02-09 BE BE710579D patent/BE710579A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR1568888A (en。) | 1969-05-30 |
| NL6801664A (en。) | 1968-08-12 |
| AT278033B (de) | 1970-01-26 |
| ES350292A1 (es) | 1969-04-16 |
| BE710579A (en。) | 1968-08-09 |
| GB1169133A (en) | 1969-10-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3501578A (en) | Fungicidal composition containing phenyl - mercaptomethane-sulfonamide and method of using the same | |
| KR890000368B1 (ko) | (티오-)우레아의 제조방법 | |
| EP0068144B1 (de) | 1,1-Diphenyl-2-triazolyl-ethane, ihre Herstellung und ihre Verwendung als Fungizide | |
| US4521412A (en) | Pesticidal iodopropargylammonium salts | |
| CS227695B2 (en) | Fungicide | |
| US2971884A (en) | Method for the control of fungal organisms | |
| US3421883A (en) | Pesticidal preparation and method of use | |
| EP0032879A1 (de) | Neue Benzthiazolyl-harnstoffderivate, deren Herstellung, sie enthaltende Mittel und deren Verwendung als Herbizide | |
| US3766243A (en) | Ureidophenylisothioureas | |
| EP0001271B1 (de) | Heterocyclische Norbornanderivate, Mittel zur Beeinflussung des Pflanzenwachstums die diese Verbindungen enthalten, und Verfahren zur Herstellung dieser Mittel | |
| IL29325A (en) | Alkylsulphuric acid salts of tetradecylguanidine | |
| US4560694A (en) | Fungicidal alkylene(cycloalkylene)-bis-heterocyclyl-biguanides | |
| NZ204239A (en) | Halogenopropargylformamides and pesticidal compositions | |
| US4496575A (en) | Fungicidal N-sulphenylated hydantoins | |
| DE1518692B2 (de) | N-a-Methyl-4-bromphenyl)-N\ N'dimethylformamidin enthaltende Schädlingsbekämpfungsmittel | |
| US4267186A (en) | Combating fungi with substituted spiro-derivatives of 3-(3,5-dihalogenophenyl)-oxazolidine-2,4-diones (thione-ones) | |
| US4378371A (en) | Combating fungi with N-alkyl-carbamic acid 1,1,2-trimethyl-5-substituted-indan-4-yl esters | |
| PL87004B1 (en。) | ||
| IL31307A (en) | O-halophenylcarbamates,their preparation and use as fungicides | |
| US4291046A (en) | Preparation of novel fungicidally active spiro derivatives of 3-(3,5-dihalogenophenyl)-oxazolidine-2-thion-4-ones | |
| US4255437A (en) | Combating fungi with 2-aryl-5-alkyl-3,4-dioxo-1,2,5-thiazolidine-1-oxides | |
| IL28185A (en) | Noble converted trichloroacetaldehyde | |
| IL28238A (en) | Dodecylguanidine alkylsulphuric acid salts and their preparation | |
| EP0008731B1 (de) | N-sulfenylierte Formanilide, ihre Herstellung und ihre Anwendung als Fungizide | |
| IL30561A (en) | Sulphonic acid salts of substituted guanidines |