SK287567B6 - Kompozície na báze homogénnej fázy a ich stabilizácia dusičnanom amónnym, spôsob ich prípravy a použitie týchto kompozícií ako bioregulátorov - Google Patents

Kompozície na báze homogénnej fázy a ich stabilizácia dusičnanom amónnym, spôsob ich prípravy a použitie týchto kompozícií ako bioregulátorov Download PDF

Info

Publication number: SK287567B6
Authority: SK; Slovakia
Prior art keywords: formula; alkyl; weight; composition according; active ingredient
Prior art date: 2000-12-05

Application number

SK849-2003A

Other languages

English (en)

Slovak (sk)

Other versions

SK8492003A3 (en

Inventor

Reiner Kober

Wilhelm Rademacher

Hans-Michael Fricke

Original Assignee

Basf Aktiengesellschaft

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2000-12-05

Filing date

2001-12-05

Publication date

2011-02-04

2001-12-05 Application filed by Basf Aktiengesellschaft filed Critical Basf Aktiengesellschaft

2003-12-02 Publication of SK8492003A3 publication Critical patent/SK8492003A3/sk

2011-02-04 Publication of SK287567B6 publication Critical patent/SK287567B6/sk

Links

PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 title claims abstract description 26
230000006641 stabilisation Effects 0.000 title description 6
229920001400 block copolymer Polymers 0.000 claims abstract description 25
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 12
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 12
239000000203 mixture Substances 0.000 claims description 129
239000004480 active ingredient Substances 0.000 claims description 70
-1 2-thienylmethyl Chemical group 0.000 claims description 52
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
239000004094 surface-active agent Substances 0.000 claims description 21
150000003254 radicals Chemical class 0.000 claims description 20
125000004432 carbon atom Chemical group C* 0.000 claims description 16
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 14
239000000546 pharmaceutical excipient Substances 0.000 claims description 12
229910052739 hydrogen Inorganic materials 0.000 claims description 11
238000000034 method Methods 0.000 claims description 11
229920000642 polymer Polymers 0.000 claims description 11
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 10
229910052801 chlorine Inorganic materials 0.000 claims description 10
229910052731 fluorine Inorganic materials 0.000 claims description 10
239000002736 nonionic surfactant Substances 0.000 claims description 10
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 9
239000000600 sorbitol Substances 0.000 claims description 9
239000002253 acid Substances 0.000 claims description 8
229910052794 bromium Inorganic materials 0.000 claims description 8
239000003085 diluting agent Substances 0.000 claims description 8
239000001257 hydrogen Substances 0.000 claims description 8
239000002904 solvent Substances 0.000 claims description 8
125000000129 anionic group Chemical group 0.000 claims description 7
229910000019 calcium carbonate Inorganic materials 0.000 claims description 7
159000000007 calcium salts Chemical class 0.000 claims description 7
239000004359 castor oil Substances 0.000 claims description 7
235000019438 castor oil Nutrition 0.000 claims description 7
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 claims description 7
NLKUPINTOLSSLD-UHFFFAOYSA-L calcium;4-(1-oxidopropylidene)-3,5-dioxocyclohexane-1-carboxylate Chemical compound [Ca+2].CCC([O-])=C1C(=O)CC(C([O-])=O)CC1=O NLKUPINTOLSSLD-UHFFFAOYSA-L 0.000 claims description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 6
150000003839 salts Chemical class 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
239000003337 fertilizer Substances 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
229920005862 polyol Polymers 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 4
239000004202 carbamide Substances 0.000 claims description 3
229910052799 carbon Inorganic materials 0.000 claims description 3
150000001768 cations Chemical class 0.000 claims description 3
239000002738 chelating agent Substances 0.000 claims description 3
UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 claims description 3
239000008187 granular material Substances 0.000 claims description 3
239000004615 ingredient Substances 0.000 claims description 3
KWIBFFTYDWCTFM-UHFFFAOYSA-M 1-chloroethyl(trimethyl)azanium;chloride Chemical compound [Cl-].CC(Cl)[N+](C)(C)C KWIBFFTYDWCTFM-UHFFFAOYSA-M 0.000 claims description 2
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 2
238000012272 crop production Methods 0.000 claims description 2
125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 claims description 2
238000003898 horticulture Methods 0.000 claims description 2
HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 claims description 2
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 2
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
150000002431 hydrogen Chemical class 0.000 claims 2
XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical class CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 claims 1
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
239000012071 phase Substances 0.000 abstract description 50
239000003795 chemical substances by application Substances 0.000 abstract description 15
150000001875 compounds Chemical class 0.000 abstract description 11
239000008346 aqueous phase Substances 0.000 abstract description 2
239000013543 active substance Substances 0.000 abstract 2
239000004698 Polyethylene Substances 0.000 description 60
239000004546 suspension concentrate Substances 0.000 description 24
125000000217 alkyl group Chemical group 0.000 description 18
238000009472 formulation Methods 0.000 description 18
241000196324 Embryophyta Species 0.000 description 15
238000002360 preparation method Methods 0.000 description 15
229920005682 EO-PO block copolymer Polymers 0.000 description 14
239000000047 product Substances 0.000 description 14
150000002148 esters Chemical class 0.000 description 11
239000003630 growth substance Substances 0.000 description 11
239000007788 liquid Substances 0.000 description 10
239000002245 particle Substances 0.000 description 10
229920001983 poloxamer Polymers 0.000 description 10
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 9
235000014113 dietary fatty acids Nutrition 0.000 description 9
239000000194 fatty acid Substances 0.000 description 9
229930195729 fatty acid Natural products 0.000 description 9
230000012010 growth Effects 0.000 description 9
239000003921 oil Substances 0.000 description 9
235000019198 oils Nutrition 0.000 description 9
230000002829 reductive effect Effects 0.000 description 9
239000000460 chlorine Substances 0.000 description 8
150000002430 hydrocarbons Chemical class 0.000 description 8
239000007787 solid Substances 0.000 description 8
230000000694 effects Effects 0.000 description 7
238000003860 storage Methods 0.000 description 7
239000000126 substance Substances 0.000 description 7
DARPYRSDRJYGIF-PTNGSMBKSA-N (Z)-3-ethoxy-2-naphthalen-2-ylsulfonylprop-2-enenitrile Chemical compound C1=CC=CC2=CC(S(=O)(=O)C(\C#N)=C/OCC)=CC=C21 DARPYRSDRJYGIF-PTNGSMBKSA-N 0.000 description 6
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
229920003171 Poly (ethylene oxide) Polymers 0.000 description 6
239000012141 concentrate Substances 0.000 description 6
235000013399 edible fruits Nutrition 0.000 description 6
238000000227 grinding Methods 0.000 description 6
230000001965 increasing effect Effects 0.000 description 6
229920000056 polyoxyethylene ether Polymers 0.000 description 6
PWVXXGRKLHYWKM-UHFFFAOYSA-N 5-[2-(benzenesulfonyl)ethyl]-3-[(1-methylpyrrolidin-2-yl)methyl]-1h-indole Chemical compound CN1CCCC1CC(C1=C2)=CNC1=CC=C2CCS(=O)(=O)C1=CC=CC=C1 PWVXXGRKLHYWKM-UHFFFAOYSA-N 0.000 description 5
125000003545 alkoxy group Chemical group 0.000 description 5
150000003868 ammonium compounds Chemical class 0.000 description 5
239000000010 aprotic solvent Substances 0.000 description 5
239000003093 cationic surfactant Substances 0.000 description 5
229920001577 copolymer Polymers 0.000 description 5
238000009826 distribution Methods 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
238000011105 stabilization Methods 0.000 description 5
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
239000000654 additive Substances 0.000 description 4
150000003863 ammonium salts Chemical class 0.000 description 4
230000001164 bioregulatory effect Effects 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
235000013339 cereals Nutrition 0.000 description 4
230000002708 enhancing effect Effects 0.000 description 4
238000007046 ethoxylation reaction Methods 0.000 description 4
150000004820 halides Chemical class 0.000 description 4
238000003306 harvesting Methods 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
229910052500 inorganic mineral Inorganic materials 0.000 description 4
239000011707 mineral Substances 0.000 description 4
235000010755 mineral Nutrition 0.000 description 4
238000002156 mixing Methods 0.000 description 4
229910052760 oxygen Inorganic materials 0.000 description 4
238000005191 phase separation Methods 0.000 description 4
229920001296 polysiloxane Polymers 0.000 description 4
230000008569 process Effects 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
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 3
229930191978 Gibberellin Natural products 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
125000003342 alkenyl group Chemical group 0.000 description 3
150000008051 alkyl sulfates Chemical class 0.000 description 3
239000003945 anionic surfactant Substances 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
125000002091 cationic group Chemical group 0.000 description 3
244000038559 crop plants Species 0.000 description 3
125000000753 cycloalkyl group Chemical group 0.000 description 3
239000003448 gibberellin Substances 0.000 description 3
IXORZMNAPKEEDV-OBDJNFEBSA-N gibberellin A3 Chemical class C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@]2(C=C[C@@H]3O)[C@H]1[C@]3(C)C(=O)O2 IXORZMNAPKEEDV-OBDJNFEBSA-N 0.000 description 3
239000011521 glass Substances 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
150000002790 naphthalenes Chemical class 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
125000001117 oleyl 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])=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 3
150000003077 polyols Chemical class 0.000 description 3
229940051841 polyoxyethylene ether Drugs 0.000 description 3
238000004062 sedimentation Methods 0.000 description 3
239000007790 solid phase Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
230000007704 transition Effects 0.000 description 3
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 2
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
239000002028 Biomass Substances 0.000 description 2
240000002791 Brassica napus Species 0.000 description 2
244000025254 Cannabis sativa Species 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
229920002472 Starch Polymers 0.000 description 2
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
238000007259 addition reaction Methods 0.000 description 2
230000002411 adverse Effects 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
150000008052 alkyl sulfonates Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
235000019270 ammonium chloride Nutrition 0.000 description 2
239000002280 amphoteric surfactant Substances 0.000 description 2
125000001204 arachidyl 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])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])C([H])([H])[H] 0.000 description 2
239000011324 bead Substances 0.000 description 2
230000008901 benefit Effects 0.000 description 2
230000004071 biological effect Effects 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
235000020971 citrus fruits Nutrition 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000002285 corn oil Substances 0.000 description 2
235000005687 corn oil Nutrition 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
230000001186 cumulative effect Effects 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
238000011161 development Methods 0.000 description 2
230000018109 developmental process Effects 0.000 description 2
150000001991 dicarboxylic acids Chemical class 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
239000003792 electrolyte Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
239000003925 fat Substances 0.000 description 2
235000019197 fats Nutrition 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
229930182478 glucoside Natural products 0.000 description 2
125000001188 haloalkyl group Chemical group 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
239000008240 homogeneous mixture Substances 0.000 description 2
125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
239000000787 lecithin Substances 0.000 description 2
235000010445 lecithin Nutrition 0.000 description 2
239000012669 liquid formulation Substances 0.000 description 2
239000007791 liquid phase Substances 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
239000002798 polar solvent Substances 0.000 description 2
229960000502 poloxamer Drugs 0.000 description 2
229920001451 polypropylene glycol Polymers 0.000 description 2
BUCOQPHDYUOJSI-UHFFFAOYSA-N prohexadione Chemical class CCC(=O)C1C(=O)CC(C(O)=O)CC1=O BUCOQPHDYUOJSI-UHFFFAOYSA-N 0.000 description 2
230000002035 prolonged effect Effects 0.000 description 2
230000001737 promoting effect Effects 0.000 description 2
239000003586 protic polar solvent Substances 0.000 description 2
238000005086 pumping Methods 0.000 description 2
VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000004550 soluble concentrate Substances 0.000 description 2
239000008107 starch Substances 0.000 description 2
125000004079 stearyl 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])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])[H] 0.000 description 2
150000003871 sulfonates Chemical class 0.000 description 2
150000003460 sulfonic acids Chemical class 0.000 description 2
YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
230000009105 vegetative growth Effects 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 1
AVBJHQDHVYGQLS-AWEZNQCLSA-N (2s)-2-(dodecanoylamino)pentanedioic acid Chemical compound CCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O AVBJHQDHVYGQLS-AWEZNQCLSA-N 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
PUNFIBHMZSHFKF-KTKRTIGZSA-N (z)-henicos-12-ene-1,2,3-triol Chemical compound CCCCCCCC\C=C/CCCCCCCCC(O)C(O)CO PUNFIBHMZSHFKF-KTKRTIGZSA-N 0.000 description 1
ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
ZSGCBBCGHYYEGU-UHFFFAOYSA-N 1-dimethylphosphoryltetradecane Chemical compound CCCCCCCCCCCCCCP(C)(C)=O ZSGCBBCGHYYEGU-UHFFFAOYSA-N 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
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229940114930 potassium stearate Drugs 0.000 description 1
ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
235000013772 propylene glycol Nutrition 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
238000013138 pruning Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
230000005070 ripening Effects 0.000 description 1
235000005713 safflower oil Nutrition 0.000 description 1
239000003813 safflower oil Substances 0.000 description 1
239000012266 salt solution Substances 0.000 description 1
108700004121 sarkosyl Proteins 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
238000004904 shortening Methods 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000010802 sludge Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000000344 soap Substances 0.000 description 1
KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
229940045885 sodium lauroyl sarcosinate Drugs 0.000 description 1
239000004317 sodium nitrate Substances 0.000 description 1
235000010344 sodium nitrate Nutrition 0.000 description 1
SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 description 1
239000001593 sorbitan monooleate Substances 0.000 description 1
235000011069 sorbitan monooleate Nutrition 0.000 description 1
229940035049 sorbitan monooleate Drugs 0.000 description 1
239000001589 sorbitan tristearate Substances 0.000 description 1
235000011078 sorbitan tristearate Nutrition 0.000 description 1
229960004129 sorbitan tristearate Drugs 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
229940114926 stearate Drugs 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
230000036435 stunted growth Effects 0.000 description 1
150000003900 succinic acid esters Chemical class 0.000 description 1
150000005846 sugar alcohols Chemical class 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000011885 synergistic combination Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
125000005329 tetralinyl group Chemical class C1(CCCC2=CC=CC=C12)* 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
210000001519 tissue Anatomy 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
229910052723 transition metal Inorganic materials 0.000 description 1
150000003624 transition metals Chemical class 0.000 description 1
238000002054 transplantation Methods 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
125000005208 trialkylammonium group Chemical group 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
230000008511 vegetative development Effects 0.000 description 1
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229940082509 xanthan gum Drugs 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
- 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
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

Landscapes

Life Sciences & Earth Sciences (AREA)
Environmental Sciences (AREA)
Health & Medical Sciences (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Zoology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Cultivation Of Plants (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Saccharide Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Compositions Of Macromolecular Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Medicinal Preparation (AREA)

SK849-2003A 2000-12-05 2001-12-05 Kompozície na báze homogénnej fázy a ich stabilizácia dusičnanom amónnym, spôsob ich prípravy a použitie týchto kompozícií ako bioregulátorov SK287567B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE10060383A DE10060383A1 (de)	2000-12-05	2000-12-05	Mittel auf Basis einer homogenen Phase und deren Stabilisierung durch Ammoniumnitrat sowie Verwendung der Mittel als Bioregulatoren
PCT/EP2001/014289 WO2002045504A2 (de)	2000-12-05	2001-12-05	Mittel auf basis einer homogenen phase und deren stabilisierung durch ammoniumnitrat sowie verwendung der mittel als bioregulatoren

Publications (2)

Publication Number	Publication Date
SK8492003A3 SK8492003A3 (en)	2003-12-02
SK287567B6 true SK287567B6 (sk)	2011-02-04

Family

ID=7665841

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK849-2003A SK287567B6 (sk)	2000-12-05	2001-12-05	Kompozície na báze homogénnej fázy a ich stabilizácia dusičnanom amónnym, spôsob ich prípravy a použitie týchto kompozícií ako bioregulátorov

Country Status (13)

Country	Link
US (1)	US6878673B2 (cs)
EP (1)	EP1339284B1 (cs)
JP (1)	JP4256161B2 (cs)
AT (1)	ATE275339T1 (cs)
AU (1)	AU2002227991A1 (cs)
CA (1)	CA2437001C (cs)
CZ (1)	CZ305201B6 (cs)
DE (2)	DE10060383A1 (cs)
DK (1)	DK1339284T3 (cs)
HU (1)	HU225809B1 (cs)
PL (1)	PL204146B1 (cs)
SK (1)	SK287567B6 (cs)
WO (1)	WO2002045504A2 (cs)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20080026944A1 (en) *	2003-06-05	2008-01-31	Biomagic, Inc.	Compositions and Methods For Enhancing Plant Growth by Chemical Oxygenation of Soils
US7637054B2 (en) *	2003-06-05	2009-12-29	Bio Magic, Inc.	Compositions and methods for enhancing plant growth by chemical oxygenation of soils
NZ570645A (en) *	2006-01-27	2011-07-29	Nat Univ Corp Tottori Univ	Method of promoting thickening growth of agricultural or horticultural crop
BR112013008445A2 (pt)	2010-10-11	2016-06-28	Basf Se	''composição,processo para a produção de composição,uso do éter de policarboxilato,semente,métodos de controle de fungos fitopatogênicos,de revestimento de semente e de controle de infestação de ácaro''
TWI634840B (zh) *	2011-03-31	2018-09-11	先正達合夥公司	植物生長調節組成物及使用其之方法
GB201902551D0 (en) *	2019-02-26	2019-04-10	Syngenta Crop Protection Ag	Formulation
AU2019101065B4 (en) *	2019-09-16	2023-08-24	Adama Australia Pty Limited	Mepiquat Formulations
GB201918088D0 (en) *	2019-12-10	2020-01-22	Gama Healthcare Ltd	Universal formulation
WO2024019955A1 (en) *	2022-07-22	2024-01-25	Basf Se	Compatibilizers for agrochemical compositions including fertilizers and active ingredients

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL254741A (cs)	1959-08-10
CH502760A (de) *	1967-01-04	1971-02-15	Basf Ag	Mittel zur Hemmung des Pflanzenwachstums und zur Änderung des Pflanzenhabitus
BE795534A (fr) *	1972-02-18	1973-08-16	Basf Ag	Agents pour la regulation de la croissance des plantes, contenant comme principe actif un sel azote
JP2673211B2 (ja)	1988-05-19	1997-11-05	クミアイ化学工業株式会社	植物生長調節組成物
ATE253822T1 (de) *	1998-07-31	2003-11-15	Basf Ag	Wachstumsregulierende wässrige zusammensetzungen

2000
- 2000-12-05 DE DE10060383A patent/DE10060383A1/de not_active Withdrawn
2001
- 2001-12-05 US US10/433,427 patent/US6878673B2/en not_active Expired - Lifetime
- 2001-12-05 WO PCT/EP2001/014289 patent/WO2002045504A2/de not_active Ceased
- 2001-12-05 EP EP01989578A patent/EP1339284B1/de not_active Expired - Lifetime
- 2001-12-05 PL PL365325A patent/PL204146B1/pl unknown
- 2001-12-05 AU AU2002227991A patent/AU2002227991A1/en not_active Abandoned
- 2001-12-05 SK SK849-2003A patent/SK287567B6/sk not_active IP Right Cessation
- 2001-12-05 CA CA2437001A patent/CA2437001C/en not_active Expired - Lifetime
- 2001-12-05 CZ CZ2003-1574A patent/CZ305201B6/cs not_active IP Right Cessation
- 2001-12-05 DK DK01989578T patent/DK1339284T3/da active
- 2001-12-05 HU HU0302551A patent/HU225809B1/hu not_active IP Right Cessation
- 2001-12-05 JP JP2002547304A patent/JP4256161B2/ja not_active Expired - Fee Related
- 2001-12-05 AT AT01989578T patent/ATE275339T1/de active
- 2001-12-05 DE DE50103566T patent/DE50103566D1/de not_active Expired - Lifetime

Also Published As

Publication number	Publication date
CA2437001A1 (en)	2002-06-13
DE10060383A1 (de)	2002-06-13
PL365325A1 (en)	2004-12-27
EP1339284A2 (de)	2003-09-03
WO2002045504A3 (de)	2002-08-22
JP2004522719A (ja)	2004-07-29
US6878673B2 (en)	2005-04-12
CZ20031574A3 (cs)	2004-01-14
ATE275339T1 (de)	2004-09-15
PL204146B1 (pl)	2009-12-31
SK8492003A3 (en)	2003-12-02
EP1339284B1 (de)	2004-09-08
HUP0302551A2 (hu)	2003-11-28
JP4256161B2 (ja)	2009-04-22
CZ305201B6 (cs)	2015-06-10
WO2002045504A2 (de)	2002-06-13
DK1339284T3 (da)	2005-01-17
CA2437001C (en)	2010-09-14
HU225809B1 (hu)	2007-10-29
US20040031305A1 (en)	2004-02-19
AU2002227991A1 (en)	2002-06-18
DE50103566D1 (de)	2004-10-14

Legal Events

Date	Code	Title	Description
2016-09-05	MM4A	Patent lapsed due to non-payment of maintenance fees	Effective date: 20151205

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SK287567B6 (sk)	2011-02-04	Kompozície na báze homogénnej fázy a ich stabilizácia dusičnanom amónnym, spôsob ich prípravy a použitie týchto kompozícií ako bioregulátorov
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