CS261895B2 - Agent for plants growth regulation and method of efficient substance production - Google Patents

Agent for plants growth regulation and method of efficient substance production Download PDF

Info

Publication number: CS261895B2
Authority: CS; Czechoslovakia
Prior art keywords: formula; hydrogen; succinate; growth; phenoxyethyl
Prior art date: 1985-06-03

Application number

CS864323A

Other languages

Czech (cs)

English (en)

Other versions

CS432386A2 (en

Inventor

Gyorgy Dr Matolcsy

Gyula Dr Kerekes

Tamas Dr Buban

Endre Dr Vasarhelyi

Janos Ing Kovacs

Ivan Dr Belai

Original Assignee

Reanal Finomvegyszergyar

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.)

1985-06-03

Filing date

1986-06-11

Publication date

1989-02-10

1985-06-03 Priority claimed from HU214285A external-priority patent/HU193768B/hu

1986-06-11 Application filed by Reanal Finomvegyszergyar filed Critical Reanal Finomvegyszergyar

1988-06-15 Publication of CS432386A2 publication Critical patent/CS432386A2/cs

1989-02-10 Publication of CS261895B2 publication Critical patent/CS261895B2/cs

Links

238000000034 method Methods 0.000 title claims description 13
239000000126 substance Substances 0.000 title description 3
230000026267 regulation of growth Effects 0.000 title 1
-1 naphthoxyethyl group Chemical group 0.000 claims abstract description 19
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 14
239000001257 hydrogen Substances 0.000 claims abstract description 14
230000008635 plant growth Effects 0.000 claims abstract description 11
150000003839 salts Chemical class 0.000 claims abstract description 11
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims abstract description 9
229940014800 succinic anhydride Drugs 0.000 claims abstract description 9
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 6
150000002431 hydrogen Chemical group 0.000 claims abstract description 6
239000000203 mixture Substances 0.000 claims description 40
239000004480 active ingredient Substances 0.000 claims description 20
238000002360 preparation method Methods 0.000 claims description 9
QZFAJHYRQCRHGT-UHFFFAOYSA-N 4-oxo-4-(2-phenoxyethoxy)butanoic acid Chemical compound OC(=O)CCC(=O)OCCOC1=CC=CC=C1 QZFAJHYRQCRHGT-UHFFFAOYSA-N 0.000 claims description 8
230000008569 process Effects 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 6
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
150000003900 succinic acid esters Chemical class 0.000 claims description 5
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
230000001105 regulatory effect Effects 0.000 abstract description 4
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
125000001475 halogen functional group Chemical group 0.000 abstract 2
150000003443 succinic acid derivatives Chemical class 0.000 abstract 2
150000001875 compounds Chemical class 0.000 description 20
239000013543 active substance Substances 0.000 description 19
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
230000012010 growth Effects 0.000 description 15
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
235000011430 Malus pumila Nutrition 0.000 description 11
235000015103 Malus silvestris Nutrition 0.000 description 11
244000141359 Malus pumila Species 0.000 description 10
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 10
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
239000000843 powder Substances 0.000 description 9
239000004094 surface-active agent Substances 0.000 description 9
239000007787 solid Substances 0.000 description 8
239000000243 solution Substances 0.000 description 8
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
241000196324 Embryophyta Species 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
238000003306 harvesting Methods 0.000 description 6
239000000047 product Substances 0.000 description 6
238000010992 reflux Methods 0.000 description 6
229910052708 sodium Inorganic materials 0.000 description 6
239000011734 sodium Substances 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
239000003085 diluting agent Substances 0.000 description 5
238000009472 formulation Methods 0.000 description 5
239000007788 liquid Substances 0.000 description 5
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 5
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 5
239000005995 Aluminium silicate Substances 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
244000046052 Phaseolus vulgaris Species 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
239000000654 additive Substances 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
150000005690 diesters Chemical class 0.000 description 4
235000013399 edible fruits Nutrition 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000007689 inspection Methods 0.000 description 4
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
239000000725 suspension Substances 0.000 description 4
240000008067 Cucumis sativus Species 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
240000008415 Lactuca sativa Species 0.000 description 3
229920001732 Lignosulfonate Polymers 0.000 description 3
235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
239000008187 granular material Substances 0.000 description 3
239000005648 plant growth regulator Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
230000000638 stimulation Effects 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000004563 wettable powder Substances 0.000 description 3
UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 2
TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical compound C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 description 2
UTRWHMSWIKTXQT-UHFFFAOYSA-N 2-(2-phenoxyethyl)butanedioic acid Chemical compound O(C1=CC=CC=C1)CCC(CC(=O)O)C(=O)O UTRWHMSWIKTXQT-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
241000167854 Bourreria succulenta Species 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
235000009849 Cucumis sativus Nutrition 0.000 description 2
NOQGZXFMHARMLW-UHFFFAOYSA-N Daminozide Chemical compound CN(C)NC(=O)CCC(O)=O NOQGZXFMHARMLW-UHFFFAOYSA-N 0.000 description 2
DKMROQRQHGEIOW-UHFFFAOYSA-N Diethyl succinate Chemical compound CCOC(=O)CCC(=O)OCC DKMROQRQHGEIOW-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
239000005909 Kieselgur Substances 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
231100000674 Phytotoxicity Toxicity 0.000 description 2
150000007513 acids 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
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
239000011575 calcium Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
235000019693 cherries Nutrition 0.000 description 2
239000004927 clay Substances 0.000 description 2
229910052570 clay Inorganic materials 0.000 description 2
230000001276 controlling effect Effects 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000004495 emulsifiable concentrate Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
210000003754 fetus Anatomy 0.000 description 2
238000000227 grinding Methods 0.000 description 2
239000003630 growth substance Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
235000010446 mineral oil Nutrition 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000002420 orchard Substances 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
239000010452 phosphate Substances 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
230000000885 phytotoxic effect Effects 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
230000009467 reduction Effects 0.000 description 2
235000012045 salad Nutrition 0.000 description 2
229910000029 sodium carbonate Inorganic materials 0.000 description 2
239000012265 solid product Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
239000001384 succinic acid Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
238000009736 wetting Methods 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
RAKDYZRIBBIDEK-UHFFFAOYSA-N 1-(4-bromophenoxy)ethanol Chemical compound CC(O)OC1=CC=C(Br)C=C1 RAKDYZRIBBIDEK-UHFFFAOYSA-N 0.000 description 1
GOHPTLYPQCTZSE-UHFFFAOYSA-N 2,2-dimethylsuccinic acid Chemical compound OC(=O)C(C)(C)CC(O)=O GOHPTLYPQCTZSE-UHFFFAOYSA-N 0.000 description 1
DSUPUOGOCIFZBG-UHFFFAOYSA-N 2-(phenylcarbamoyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)NC1=CC=CC=C1 DSUPUOGOCIFZBG-UHFFFAOYSA-N 0.000 description 1
BQPBZDSDFCDSAO-UHFFFAOYSA-N 2-naphthalen-2-yloxyethanol Chemical compound C1=CC=CC2=CC(OCCO)=CC=C21 BQPBZDSDFCDSAO-UHFFFAOYSA-N 0.000 description 1
QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
IGPROYLOGZTOAM-UHFFFAOYSA-N 3-phenylsulfanylpropanoic acid Chemical class OC(=O)CCSC1=CC=CC=C1 IGPROYLOGZTOAM-UHFFFAOYSA-N 0.000 description 1
ZFNYBQWNSDAQCG-UHFFFAOYSA-N CCC(C(C(=O)O)OC1=CC=CC=C1)C(=O)O Chemical compound CCC(C(C(=O)O)OC1=CC=CC=C1)C(=O)O ZFNYBQWNSDAQCG-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 1
235000003228 Lactuca sativa Nutrition 0.000 description 1
244000070406 Malus silvestris Species 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
208000025174 PANDAS Diseases 0.000 description 1
208000021155 Paediatric autoimmune neuropsychiatric disorders associated with streptococcal infection Diseases 0.000 description 1
240000004718 Panda Species 0.000 description 1
235000016496 Panda oleosa Nutrition 0.000 description 1
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
RNCAJLLRSYSZAM-UHFFFAOYSA-N diazinane-3,6-dione Chemical compound O=C1CCC(=O)NN1 RNCAJLLRSYSZAM-UHFFFAOYSA-N 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
230000001605 fetal effect Effects 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000007710 freezing Methods 0.000 description 1
230000008014 freezing Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
230000006872 improvement Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000002245 particle Substances 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
229960005323 phenoxyethanol Drugs 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000008654 plant damage Effects 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
ARENMZZMCSLORU-UHFFFAOYSA-N propan-2-yl naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)OC(C)C)=CC=CC2=C1 ARENMZZMCSLORU-UHFFFAOYSA-N 0.000 description 1
230000001603 reducing effect Effects 0.000 description 1
230000000979 retarding effect Effects 0.000 description 1
230000002786 root growth Effects 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000011343 solid material Substances 0.000 description 1
230000005082 stem growth Effects 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
150000003445 sucroses Chemical class 0.000 description 1
230000001629 suppression Effects 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone

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)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS864323A 1985-06-03 1986-06-11 Agent for plants growth regulation and method of efficient substance production CS261895B2 (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
HU214285A HU193768B (en)	1985-06-03	1985-06-03	Compositions for controlling growth of plants containing derivatives of succinic acid and process for producing succinic acid derivatives
DD86291160A DD254877A5 (de)	1985-06-03	1986-06-10	Zusammensetzung und verfahren zur regulierung des pflanzenwachstums
DD86304091A DD257255A5 (de)	1985-06-03	1986-06-10	Verfahren zur herstellung von neuen mono- oder di-(aryloxyethyl)succinaten

Publications (2)

Publication Number	Publication Date
CS432386A2 CS432386A2 (en)	1988-06-15
CS261895B2 true CS261895B2 (en)	1989-02-10

Family

ID=27179886

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS864323A CS261895B2 (en)	1985-06-03	1986-06-11	Agent for plants growth regulation and method of efficient substance production

Country Status (5)

Country	Link
US (1)	US4846883A (de)
EP (1)	EP0224551A1 (de)
CS (1)	CS261895B2 (de)
DD (2)	DD254877A5 (de)
WO (1)	WO1986007354A1 (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2290809C2 (ru) *	2005-03-25	2007-01-10	Иван Семёнович Новиков	Стимулятор плодообразования "томатон"
US20070130991A1 (en) *	2005-12-14	2007-06-14	Chevron U.S.A. Inc.	Liquefaction of associated gas at moderate conditions
US7786057B2 (en)	2007-02-08	2010-08-31	Infineum International Limited	Soot dispersants and lubricating oil compositions containing same
RU2013133873A (ru)	2010-12-21	2015-01-27	БАЙЕР КРОПСАЙЕНС ЭлПи	ШЕРОХОВАТЫЕ МУТАНТЫ Bacillus И СПОСОБЫ ИХ ПРИМЕНЕНИЯ ДЛЯ УСКОРЕНИЯ РОСТА РАСТЕНИЙ, УЛУЧШЕНИЯ ЗДОРОВЬЯ РАСТЕНИЙ И БОРЬБЫ С БОЛЕЗНЯМИ И ВРЕДИТЕЛЯМИ
BR112014005654A2 (pt)	2011-09-12	2017-03-28	Bayer Cropscience Lp	métodos para melhorar a saúde e promover o crescimento de uma planta e/ou de melhorar o amadurecimento da fruta
AU2019337472A1 (en) *	2018-09-11	2021-03-04	Shrikant Kumar Burje	Alternative oxidase activity stimulating chemical composition and a method for reducing hypoxia in plants

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE708768C (de) *	1939-11-01	1941-07-29	Hoffmann La Roche & Co Akt Ges	Verfahren zur Darstellung von sauren Estern der alkylierten 1, 4-Naphthohydrochinone
NL173233B (nl) *	1951-11-03		Lely Nv C Van Der	Verrijdbare inrichting voor het verspreiden van vloeistoffen, in het bijzonder mengmest.
US3085078A (en) *	1958-10-22	1963-04-09	Thompson Chemical Company	Ester of a dicarboxylic acid and vinyl chloride resin plasticized therewith
US4036984A (en) *	1974-04-30	1977-07-19	Nissan Chemical Industries, Ltd.	Soil fungi inhibiting agent
US4456721A (en) *	1982-12-02	1984-06-26	Borg-Warner Chemicals, Inc.	Flame-retarded acrylonitrile-butadiene-styrene copolymer compositions comprising bis(beta-pentabromophenoxyethyl) succinate
DE3321529A1 (de) *	1983-06-15	1984-12-20	Bayer Ag, 5090 Leverkusen	Mittel zur regulierung des pflanzenwachstums

1986
- 1986-06-03 EP EP86903535A patent/EP0224551A1/de not_active Withdrawn
- 1986-06-03 WO PCT/HU1986/000036 patent/WO1986007354A1/en not_active Ceased
- 1986-06-03 US US07/018,903 patent/US4846883A/en not_active Expired - Fee Related
- 1986-06-10 DD DD86291160A patent/DD254877A5/de not_active IP Right Cessation
- 1986-06-10 DD DD86304091A patent/DD257255A5/de not_active IP Right Cessation
- 1986-06-11 CS CS864323A patent/CS261895B2/cs unknown

Also Published As

Publication number	Publication date
WO1986007354A1 (en)	1986-12-18
EP0224551A1 (de)	1987-06-10
US4846883A (en)	1989-07-11
DD257255A5 (de)	1988-06-08
DD254877A5 (de)	1988-03-16
CS432386A2 (en)	1988-06-15

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DE2546251C3 (de)	1980-10-02
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