ZA200508327B - Use of acylcyclohexanedione derivatives for improving the tolerance of plants to cold and/or frost - Google Patents
Use of acylcyclohexanedione derivatives for improving the tolerance of plants to cold and/or frost Download PDFInfo
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- ZA200508327B ZA200508327B ZA200508327A ZA200508327A ZA200508327B ZA 200508327 B ZA200508327 B ZA 200508327B ZA 200508327 A ZA200508327 A ZA 200508327A ZA 200508327 A ZA200508327 A ZA 200508327A ZA 200508327 B ZA200508327 B ZA 200508327B
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- South Africa
- Prior art keywords
- use according
- compounds
- formula
- frost
- plants
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- 125000002704 decyl 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])* 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 210000002257 embryonic structure Anatomy 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 230000035784 germination Effects 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
- 239000008187 granular material Substances 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 235000021251 pulses Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000037380 skin damage Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 229930003802 tocotrienol Natural products 0.000 description 1
- 239000011731 tocotrienol Substances 0.000 description 1
- 229940068778 tocotrienols Drugs 0.000 description 1
- 235000019148 tocotrienols Nutrition 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 1
- DFFWZNDCNBOKDI-UHFFFAOYSA-N trinexapac Chemical compound O=C1CC(C(=O)O)CC(=O)C1=C(O)C1CC1 DFFWZNDCNBOKDI-UHFFFAOYSA-N 0.000 description 1
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-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
- 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
- A01N37/42—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 within the same carbon skeleton a carboxylic group or a thio analogue, or a derivative thereof, and a carbon atom having only two bonds to hetero atoms with at the most one bond to halogen, e.g. keto-carboxylic acids
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Cultivation Of Plants (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10311689A DE10311689A1 (de) | 2003-03-17 | 2003-03-17 | Verwendung von Acylcyclohexandion-Derivaten zur Verbesserung der Toleranz von Pflanzen gegenüber Kälte und/oder Frost |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200508327B true ZA200508327B (en) | 2007-02-28 |
Family
ID=32920857
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200508327A ZA200508327B (en) | 2003-03-17 | 2005-10-14 | Use of acylcyclohexanedione derivatives for improving the tolerance of plants to cold and/or frost |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7686975B2 (ja) |
| EP (1) | EP1605751B1 (ja) |
| JP (1) | JP4463800B2 (ja) |
| KR (1) | KR20050120650A (ja) |
| AR (1) | AR043626A1 (ja) |
| AT (1) | ATE443446T1 (ja) |
| AU (1) | AU2004222562B2 (ja) |
| BR (1) | BRPI0408305A (ja) |
| CA (1) | CA2518928A1 (ja) |
| CL (1) | CL2004000540A1 (ja) |
| DE (2) | DE10311689A1 (ja) |
| ES (1) | ES2332133T3 (ja) |
| NZ (1) | NZ542350A (ja) |
| PL (1) | PL1605751T3 (ja) |
| PT (1) | PT1605751E (ja) |
| WO (1) | WO2004082379A1 (ja) |
| ZA (1) | ZA200508327B (ja) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2690833A1 (en) * | 2007-06-18 | 2008-12-24 | The University Of Alabama | Plant cryoprotectant compositions and methods of use |
| US8288437B2 (en) * | 2008-07-24 | 2012-10-16 | Valent Biosciences Corporation | Salts, aqueous liquid compositions containing salts of abscisic acid analogs and methods of their preparation |
| JP2014150744A (ja) * | 2013-02-06 | 2014-08-25 | Yamanashi Prefecture | バラ科作物の果実の結実促進方法 |
| CN105272612A (zh) * | 2015-10-27 | 2016-01-27 | 丹阳市香逸林果专业合作社 | 一种紫薇防冻营养液 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2961798A (en) * | 1959-03-09 | 1960-11-29 | Dumas Milner Corp | Protection of plants against frost damage |
| HU176764B (en) * | 1978-05-23 | 1981-05-28 | Chinoin Gyogyszer Es Vegyeszet | Process for influencing the germination of plant seed and the growth of plants evolved therefrom by the application of dextrins |
| US4383845A (en) * | 1982-01-15 | 1983-05-17 | Rutherford Joseph P | Foliar growth promoting mixture |
| JPS59196840A (ja) * | 1983-04-22 | 1984-11-08 | Kumiai Chem Ind Co Ltd | シクロヘキサン誘導体および植物生長調節剤 |
| DE3821520A1 (de) * | 1988-06-25 | 1989-12-28 | Basf Ag | Mittel zur verbesserung des pflanzlichen stressverhaltens |
| JP3266674B2 (ja) * | 1992-11-19 | 2002-03-18 | クミアイ化学工業株式会社 | 植物成長調整剤組成物 |
| DE4437945A1 (de) * | 1993-10-22 | 1995-04-27 | Georg Dr Noga | Vitamin E enthaltendes Pflanzenstärkungsmittel und seine Verwendung |
| US6022831A (en) * | 1997-07-15 | 2000-02-08 | Basf Corporation | Control of Erwinia amylovora in plants |
| DE19904703A1 (de) * | 1999-02-05 | 2000-08-24 | Georg Noga | Tocopherol und/oder Tocopherol-Derivate sowie Methoxyzimtsäure(-Derivate) enthaltendes wäßriges Pflanzenstärkungsmittel |
-
2003
- 2003-03-17 DE DE10311689A patent/DE10311689A1/de not_active Withdrawn
-
2004
- 2004-03-16 KR KR1020057017476A patent/KR20050120650A/ko not_active Application Discontinuation
- 2004-03-16 CL CL200400540A patent/CL2004000540A1/es unknown
- 2004-03-16 DE DE502004010110T patent/DE502004010110D1/de not_active Expired - Lifetime
- 2004-03-16 PL PL04720874T patent/PL1605751T3/pl unknown
- 2004-03-16 AU AU2004222562A patent/AU2004222562B2/en not_active Ceased
- 2004-03-16 ES ES04720874T patent/ES2332133T3/es not_active Expired - Lifetime
- 2004-03-16 WO PCT/EP2004/002713 patent/WO2004082379A1/de active Search and Examination
- 2004-03-16 US US10/549,171 patent/US7686975B2/en not_active Expired - Fee Related
- 2004-03-16 JP JP2006500064A patent/JP4463800B2/ja not_active Expired - Fee Related
- 2004-03-16 PT PT04720874T patent/PT1605751E/pt unknown
- 2004-03-16 CA CA002518928A patent/CA2518928A1/en not_active Abandoned
- 2004-03-16 AT AT04720874T patent/ATE443446T1/de active
- 2004-03-16 NZ NZ542350A patent/NZ542350A/en not_active IP Right Cessation
- 2004-03-16 AR ARP040100872A patent/AR043626A1/es unknown
- 2004-03-16 BR BRPI0408305-9A patent/BRPI0408305A/pt not_active Application Discontinuation
- 2004-03-16 EP EP04720874A patent/EP1605751B1/de not_active Expired - Lifetime
-
2005
- 2005-10-14 ZA ZA200508327A patent/ZA200508327B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US7686975B2 (en) | 2010-03-30 |
| PL1605751T3 (pl) | 2010-03-31 |
| BRPI0408305A (pt) | 2006-03-07 |
| CL2004000540A1 (es) | 2005-05-06 |
| CA2518928A1 (en) | 2004-09-30 |
| NZ542350A (en) | 2009-11-27 |
| KR20050120650A (ko) | 2005-12-22 |
| PT1605751E (pt) | 2009-10-22 |
| AU2004222562B2 (en) | 2010-03-04 |
| JP2006520188A (ja) | 2006-09-07 |
| EP1605751B1 (de) | 2009-09-23 |
| ES2332133T3 (es) | 2010-01-27 |
| AU2004222562A1 (en) | 2004-09-30 |
| US20070066485A1 (en) | 2007-03-22 |
| DE502004010110D1 (de) | 2009-11-05 |
| ATE443446T1 (de) | 2009-10-15 |
| JP4463800B2 (ja) | 2010-05-19 |
| AR043626A1 (es) | 2005-08-03 |
| WO2004082379A1 (de) | 2004-09-30 |
| EP1605751A1 (de) | 2005-12-21 |
| DE10311689A1 (de) | 2004-09-30 |
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