DD218542A5 - Zusammensetzung zur sterilisierung der staubbeutel einer pflanze - Google Patents
Zusammensetzung zur sterilisierung der staubbeutel einer pflanze Download PDFInfo
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- DD218542A5 DD218542A5 DD84259474A DD25947484A DD218542A5 DD 218542 A5 DD218542 A5 DD 218542A5 DD 84259474 A DD84259474 A DD 84259474A DD 25947484 A DD25947484 A DD 25947484A DD 218542 A5 DD218542 A5 DD 218542A5
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- DD
- German Democratic Republic
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- compound
- hydrogen atom
- formula
- optionally substituted
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- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 150000001539 azetidines Chemical class 0.000 description 1
- 125000002393 azetidinyl group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical class [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000009838 combustion analysis Methods 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000003113 dilution method Methods 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- MYBGIDBPYOOYGS-UHFFFAOYSA-N ethyl 2-(azetidin-1-yl)acetate Chemical compound CCOC(=O)CN1CCC1 MYBGIDBPYOOYGS-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000035558 fertility Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000005094 fruit set 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
- 150000002334 glycols Chemical class 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000010196 hermaphroditism Effects 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000007163 homologation reaction Methods 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 235000012243 magnesium silicates Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum 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
- 125000006368 phosphonoyl group Chemical group [*:1]P([*:2])=O 0.000 description 1
- 230000008119 pollen development Effects 0.000 description 1
- 230000007198 pollen germination Effects 0.000 description 1
- 230000010152 pollination Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 230000010153 self-pollination Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- MNWBNISUBARLIT-UHFFFAOYSA-N sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- KLILRMJUKZYUBK-UHFFFAOYSA-M sodium;2-(azetidin-1-yl)acetate Chemical compound [Na+].[O-]C(=O)CN1CCC1 KLILRMJUKZYUBK-UHFFFAOYSA-M 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000002426 superphosphate Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 150000007970 thio esters Chemical class 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
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/44—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom three- or four-membered rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Health & Medical Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Saccharide Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Cleaning Implements For Floors, Carpets, Furniture, Walls, And The Like (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB838301702A GB8301702D0 (en) | 1983-01-21 | 1983-01-21 | Azetidine compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
DD218542A5 true DD218542A5 (de) | 1985-02-13 |
Family
ID=10536724
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DD84259474A DD218542A5 (de) | 1983-01-21 | 1984-01-18 | Zusammensetzung zur sterilisierung der staubbeutel einer pflanze |
Country Status (26)
Country | Link |
---|---|
US (1) | US4620866A (en, 2012) |
EP (1) | EP0114706B1 (en, 2012) |
JP (1) | JPS59137458A (en, 2012) |
AR (1) | AR240312A1 (en, 2012) |
AT (1) | ATE29489T1 (en, 2012) |
AU (1) | AU563161B2 (en, 2012) |
BR (1) | BR8400238A (en, 2012) |
CA (1) | CA1270491A (en, 2012) |
CS (1) | CS253587B2 (en, 2012) |
DD (1) | DD218542A5 (en, 2012) |
DE (1) | DE3465986D1 (en, 2012) |
DK (1) | DK23884A (en, 2012) |
ES (1) | ES8504698A1 (en, 2012) |
GB (1) | GB8301702D0 (en, 2012) |
GR (1) | GR79786B (en, 2012) |
HU (1) | HU191583B (en, 2012) |
IE (1) | IE56549B1 (en, 2012) |
IL (1) | IL70722A (en, 2012) |
MA (1) | MA20014A1 (en, 2012) |
NO (1) | NO164023C (en, 2012) |
NZ (1) | NZ206889A (en, 2012) |
PH (1) | PH20411A (en, 2012) |
PL (1) | PL141848B1 (en, 2012) |
PT (1) | PT77974B (en, 2012) |
TR (1) | TR21934A (en, 2012) |
ZA (1) | ZA84401B (en, 2012) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8419084D0 (en) * | 1984-07-26 | 1984-08-30 | Shell Int Research | Azetidine derivatives |
WO1998025920A1 (en) * | 1996-12-10 | 1998-06-18 | Abbott Laboratories | 3-pyridyl enantiomers and their use as analgesics |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1567153A (en) * | 1975-09-16 | 1980-05-14 | Shell Int Research | Method of sterilizing male anthers of angiosperms |
JPS5461151A (en) * | 1977-10-25 | 1979-05-17 | Shionogi & Co Ltd | Novel aminoglycoside derivative |
CA1261858A (en) * | 1979-11-16 | 1989-09-26 | Barry R.J. Devlin | Method of producing male sterility in plants |
-
1983
- 1983-01-21 GB GB838301702A patent/GB8301702D0/en active Pending
-
1984
- 1984-01-04 CA CA000444671A patent/CA1270491A/en not_active Expired - Fee Related
- 1984-01-11 AT AT84200038T patent/ATE29489T1/de active
- 1984-01-11 DE DE8484200038T patent/DE3465986D1/de not_active Expired
- 1984-01-11 EP EP84200038A patent/EP0114706B1/en not_active Expired
- 1984-01-12 PH PH30099A patent/PH20411A/en unknown
- 1984-01-18 PT PT77974A patent/PT77974B/pt not_active IP Right Cessation
- 1984-01-18 DD DD84259474A patent/DD218542A5/de not_active IP Right Cessation
- 1984-01-19 AR AR295481A patent/AR240312A1/es active
- 1984-01-19 DK DK23884A patent/DK23884A/da not_active Application Discontinuation
- 1984-01-19 ZA ZA84401A patent/ZA84401B/xx unknown
- 1984-01-19 ES ES528988A patent/ES8504698A1/es not_active Expired
- 1984-01-19 GR GR73560A patent/GR79786B/el unknown
- 1984-01-19 TR TR21934A patent/TR21934A/xx unknown
- 1984-01-19 BR BR8400238A patent/BR8400238A/pt unknown
- 1984-01-19 CS CS84425A patent/CS253587B2/cs unknown
- 1984-01-19 NO NO840195A patent/NO164023C/no unknown
- 1984-01-19 AU AU23594/84A patent/AU563161B2/en not_active Ceased
- 1984-01-19 IL IL70722A patent/IL70722A/xx not_active IP Right Cessation
- 1984-01-19 NZ NZ206889A patent/NZ206889A/en unknown
- 1984-01-19 JP JP59006412A patent/JPS59137458A/ja active Pending
- 1984-01-19 HU HU84203A patent/HU191583B/hu not_active IP Right Cessation
- 1984-01-19 PL PL1984245816A patent/PL141848B1/pl unknown
- 1984-01-19 IE IE120/84A patent/IE56549B1/xx unknown
- 1984-01-20 MA MA20235A patent/MA20014A1/fr unknown
- 1984-08-13 US US06/639,986 patent/US4620866A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
NO164023B (no) | 1990-05-14 |
GR79786B (en, 2012) | 1984-10-31 |
DE3465986D1 (en) | 1987-10-15 |
IL70722A (en) | 1987-07-31 |
AR240312A1 (es) | 1990-03-30 |
JPS59137458A (ja) | 1984-08-07 |
PH20411A (en) | 1987-01-11 |
ZA84401B (en) | 1984-08-29 |
AU563161B2 (en) | 1987-07-02 |
MA20014A1 (fr) | 1984-10-01 |
CS253587B2 (en) | 1987-11-12 |
AU2359484A (en) | 1984-07-26 |
NO164023C (no) | 1990-08-22 |
ES528988A0 (es) | 1985-05-01 |
EP0114706B1 (en) | 1987-09-09 |
NO840195L (no) | 1984-07-23 |
EP0114706A1 (en) | 1984-08-01 |
DK23884D0 (da) | 1984-01-19 |
IL70722A0 (en) | 1984-04-30 |
DK23884A (da) | 1984-07-22 |
GB8301702D0 (en) | 1983-02-23 |
ATE29489T1 (de) | 1987-09-15 |
HU191583B (en) | 1987-03-30 |
BR8400238A (pt) | 1984-08-28 |
CA1270491A (en) | 1990-06-19 |
ES8504698A1 (es) | 1985-05-01 |
US4620866A (en) | 1986-11-04 |
IE840120L (en) | 1984-07-21 |
PT77974A (en) | 1984-02-01 |
TR21934A (tr) | 1985-11-22 |
PL245816A1 (en) | 1985-05-21 |
PT77974B (en) | 1986-03-25 |
IE56549B1 (en) | 1991-08-28 |
NZ206889A (en) | 1986-10-08 |
PL141848B1 (en) | 1987-08-31 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
ENJ | Ceased due to non-payment of renewal fee |