IL29204A - Agents for retarding the growth of plants and changing their habit containing quaternary ammonium compounds - Google Patents
Agents for retarding the growth of plants and changing their habit containing quaternary ammonium compoundsInfo
- Publication number
- IL29204A IL29204A IL29204A IL2920467A IL29204A IL 29204 A IL29204 A IL 29204A IL 29204 A IL29204 A IL 29204A IL 2920467 A IL2920467 A IL 2920467A IL 29204 A IL29204 A IL 29204A
- Authority
- IL
- Israel
- Prior art keywords
- radical
- plants
- growth
- agents
- retarding
- Prior art date
Links
- 230000008635 plant growth Effects 0.000 title claims description 5
- 230000000979 retarding effect Effects 0.000 title claims description 4
- 150000003856 quaternary ammonium compounds Chemical class 0.000 title 1
- -1 alkyl radical Chemical class 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Natural products C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- HNVIQLPOGUDBSU-UHFFFAOYSA-N 2,6-dimethylmorpholine Chemical compound CC1CNCC(C)O1 HNVIQLPOGUDBSU-UHFFFAOYSA-N 0.000 claims description 2
- OCBFFGCSTGGPSQ-UHFFFAOYSA-N [CH2]CC Chemical compound [CH2]CC OCBFFGCSTGGPSQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 22
- 239000002689 soil Substances 0.000 description 15
- 241000196324 Embryophyta Species 0.000 description 13
- 238000002474 experimental method Methods 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000012010 growth Effects 0.000 description 6
- 241000209219 Hordeum Species 0.000 description 5
- 241000894007 species Species 0.000 description 5
- 235000007340 Hordeum vulgare Nutrition 0.000 description 4
- 230000000459 effect on growth Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 241000209140 Triticum Species 0.000 description 3
- 235000021307 Triticum Nutrition 0.000 description 3
- 150000001350 alkyl halides Chemical class 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- KJDRSWPQXHESDQ-UHFFFAOYSA-N 1,4-dichlorobutane Chemical compound ClCCCCCl KJDRSWPQXHESDQ-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 241000227653 Lycopersicon Species 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 239000002168 alkylating agent Substances 0.000 description 2
- 229940100198 alkylating agent Drugs 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 2
- 230000031018 biological processes and functions Effects 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 150000004985 diamines Chemical group 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000002780 morpholines Chemical class 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- OPHVSASGPNDWOP-UHFFFAOYSA-N 4-amino-2-(dimethylamino)-4-oxobutanoic acid Chemical compound CN(C)C(C(O)=O)CC(N)=O OPHVSASGPNDWOP-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- NOQGZXFMHARMLW-UHFFFAOYSA-N Daminozide Chemical compound CN(C)NC(=O)CCC(O)=O NOQGZXFMHARMLW-UHFFFAOYSA-N 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 1
- 125000004982 dihaloalkyl group Chemical group 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical group 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/037—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements with quaternary ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cultivation Of Plants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Fertilizers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB0090597 | 1967-01-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL29204A true IL29204A (en) | 1972-02-29 |
Family
ID=6985381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL29204A IL29204A (en) | 1967-01-04 | 1967-12-24 | Agents for retarding the growth of plants and changing their habit containing quaternary ammonium compounds |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US3542538A (is") |
| AT (1) | AT277656B (is") |
| BE (1) | BE708691A (is") |
| CH (1) | CH502760A (is") |
| CS (1) | CS171669B2 (is") |
| DK (1) | DK120978B (is") |
| ES (1) | ES348753A1 (is") |
| FI (1) | FI46016C (is") |
| FR (1) | FR1550622A (is") |
| GB (1) | GB1203171A (is") |
| IL (1) | IL29204A (is") |
| MY (1) | MY7100103A (is") |
| NL (1) | NL6717743A (is") |
| SE (1) | SE337959B (is") |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2842220A1 (de) | 1978-09-28 | 1980-04-17 | Bayer Ag | Mittel zur wuchshemmung bei getreide |
| DE2913523A1 (de) * | 1979-04-04 | 1980-10-23 | Basf Ag | Substituierte alkylammoniumsalze, ihre herstellung und verwendung zur regulierung des pflanzenwachstums |
| US4474965A (en) * | 1980-01-25 | 1984-10-02 | Monsanto Company | 3-Substituted aminoalkyl-2-benzothiazolinones |
| US4371388A (en) * | 1980-01-25 | 1983-02-01 | Monsanto Company | 3-Substituted aminoalkyl-2-benzothiazolinones as plant growth regulants |
| JPH0672081B2 (ja) * | 1985-06-07 | 1994-09-14 | 三菱瓦斯化学株式会社 | 植物生長促進剤 |
| US5461077A (en) * | 1993-10-21 | 1995-10-24 | Great Lakes Chemical Corp. | Use of perbromides to control diseases in plants |
| DE10060383A1 (de) * | 2000-12-05 | 2002-06-13 | Basf Ag | Mittel auf Basis einer homogenen Phase und deren Stabilisierung durch Ammoniumnitrat sowie Verwendung der Mittel als Bioregulatoren |
| EP1423007B1 (de) * | 2001-04-12 | 2007-06-06 | Basf Aktiengesellschaft | Bioregulatorische wirkstoffkombination |
| CA2495567C (en) * | 2002-08-19 | 2011-11-15 | Basf Aktiengesellschaft | Agents containing carboxylic acid and the use of the same in plant cultivation |
| CN105585561B (zh) * | 2014-10-21 | 2018-08-31 | 沈阳中化农药化工研发有限公司 | 一种双季铵盐(碱)类化合物及其用途 |
| RU2633699C2 (ru) * | 2015-10-20 | 2017-10-17 | Общество С Ограниченной Ответственностью "Ниармедик Плюс" | Пиримидил-ди(диазадиспироалкан)ы с противовирусной активностью |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3156554A (en) * | 1959-08-10 | 1964-11-10 | Research Corp | Method of controlling relative stem growth of plants |
| US3156555A (en) * | 1961-07-17 | 1964-11-10 | Research Corp | Method of controlling relative stem growth |
| DE1199048B (de) * | 1964-03-13 | 1965-08-19 | Basf Ag | Mischung zur Beeinflussung des Pflanzenwachstums |
| US3402039A (en) * | 1966-12-05 | 1968-09-17 | Dow Chemical Co | Piperazinium salts as plant stunting agents |
-
1967
- 1967-12-21 CH CH1793867A patent/CH502760A/de not_active IP Right Cessation
- 1967-12-22 US US692675A patent/US3542538A/en not_active Expired - Lifetime
- 1967-12-24 IL IL29204A patent/IL29204A/en unknown
- 1967-12-26 FR FR1550622D patent/FR1550622A/fr not_active Expired
- 1967-12-28 NL NL6717743A patent/NL6717743A/xx unknown
- 1967-12-28 FI FI673473A patent/FI46016C/fi active
- 1967-12-28 BE BE708691D patent/BE708691A/xx unknown
- 1967-12-29 ES ES348753A patent/ES348753A1/es not_active Expired
- 1967-12-29 DK DK661967AA patent/DK120978B/da unknown
-
1968
- 1968-01-03 GB GB418/68A patent/GB1203171A/en not_active Expired
- 1968-01-04 CS CS81*YA patent/CS171669B2/cs unknown
- 1968-01-04 SE SE00111/68A patent/SE337959B/xx unknown
- 1968-01-04 AT AT8568A patent/AT277656B/de not_active IP Right Cessation
-
1971
- 1971-12-30 MY MY103/71A patent/MY7100103A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US3542538A (en) | 1970-11-24 |
| DK120978B (da) | 1971-08-09 |
| DE1642215A1 (de) | 1972-03-09 |
| MY7100103A (en) | 1971-12-31 |
| BE708691A (is") | 1968-06-28 |
| ES348753A1 (es) | 1969-03-16 |
| FI46016C (fi) | 1972-12-11 |
| CH502760A (de) | 1971-02-15 |
| GB1203171A (en) | 1970-08-26 |
| FI46016B (is") | 1972-08-31 |
| FR1550622A (is") | 1968-12-20 |
| NL6717743A (is") | 1968-07-05 |
| AT277656B (de) | 1970-01-12 |
| CS171669B2 (is") | 1976-10-29 |
| SE337959B (is") | 1971-08-23 |
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