CS201519B2 - Means for regulation of the growth of plants and method of making the active component - Google Patents

Means for regulation of the growth of plants and method of making the active component Download PDF

Info

Publication number: CS201519B2
Authority: CS; Czechoslovakia
Prior art keywords: growth; plants; acid; active; active ingredient
Prior art date: 1977-11-19

Application number

CS787496A

Other languages

Czech (cs)

English (en)

Inventor

Rolf Schroeder

Klaus Luerssen

Original Assignee

Bayer Ag

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.)

1977-11-19

Filing date

1978-11-16

Publication date

1980-11-28

1978-11-16 Application filed by Bayer Ag filed Critical Bayer Ag

1980-11-28 Publication of CS201519B2 publication Critical patent/CS201519B2/cs

Links

230000008635 plant growth Effects 0.000 title claims description 10
238000004519 manufacturing process Methods 0.000 title description 2
239000004480 active ingredient Substances 0.000 claims description 30
239000002904 solvent Substances 0.000 claims description 27
239000000203 mixture Substances 0.000 claims description 19
125000004432 carbon atom Chemical group C* 0.000 claims description 12
238000000034 method Methods 0.000 claims description 11
239000002253 acid Substances 0.000 claims description 10
238000002360 preparation method Methods 0.000 claims description 7
150000003839 salts Chemical class 0.000 claims description 6
150000008044 alkali metal hydroxides Chemical class 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
239000011734 sodium Substances 0.000 claims description 4
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 claims description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
125000005907 alkyl ester group Chemical group 0.000 claims description 2
125000002947 alkylene group Chemical group 0.000 claims description 2
125000000286 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
229910052700 potassium Inorganic materials 0.000 claims description 2
239000011591 potassium Substances 0.000 claims description 2
229910052708 sodium Inorganic materials 0.000 claims description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
241000196324 Embryophyta Species 0.000 description 54
239000013543 active substance Substances 0.000 description 45
230000012010 growth Effects 0.000 description 26
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 24
150000001875 compounds Chemical class 0.000 description 22
-1 α-isocyan-β-methylcaproic acid Chemical compound 0.000 description 21
230000000694 effects Effects 0.000 description 20
239000003995 emulsifying agent Substances 0.000 description 20
239000003630 growth substance Substances 0.000 description 18
239000000126 substance Substances 0.000 description 15
235000013399 edible fruits Nutrition 0.000 description 12
230000009036 growth inhibition Effects 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
229920000742 Cotton Polymers 0.000 description 9
241000219146 Gossypium Species 0.000 description 9
244000061176 Nicotiana tabacum Species 0.000 description 9
235000002637 Nicotiana tabacum Nutrition 0.000 description 9
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
239000005648 plant growth regulator Substances 0.000 description 8
238000003306 harvesting Methods 0.000 description 7
239000000843 powder Substances 0.000 description 7
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
230000000052 comparative effect Effects 0.000 description 6
239000008187 granular material Substances 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
230000000638 stimulation Effects 0.000 description 5
230000009105 vegetative growth Effects 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
235000007688 Lycopersicon esculentum Nutrition 0.000 description 4
229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
240000003768 Solanum lycopersicum Species 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 4
230000001105 regulatory effect Effects 0.000 description 4
239000007858 starting material Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
RRSCOUPNURHZBJ-UHFFFAOYSA-N 2-chloroethanesulfinic acid Chemical compound OS(=O)CCCl RRSCOUPNURHZBJ-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
LLVUVAFIZLGBRB-UHFFFAOYSA-N C(CCCCCCCCCCC)O.C(CCCCCCCCC)O.C(CCCCCCC)O.C(CCCCC)O Chemical compound C(CCCCCCCCCCC)O.C(CCCCCCCCC)O.C(CCCCCCC)O.C(CCCCC)O LLVUVAFIZLGBRB-UHFFFAOYSA-N 0.000 description 3
235000010469 Glycine max Nutrition 0.000 description 3
240000005979 Hordeum vulgare Species 0.000 description 3
235000007340 Hordeum vulgare Nutrition 0.000 description 3
229920001213 Polysorbate 20 Polymers 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
241000209140 Triticum Species 0.000 description 3
230000001133 acceleration Effects 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000000354 decomposition reaction Methods 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
239000000945 filler Substances 0.000 description 3
239000006260 foam Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 3
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 3
230000005070 ripening Effects 0.000 description 3
239000000779 smoke Substances 0.000 description 3
239000002689 soil Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
230000001629 suppression Effects 0.000 description 3
239000000725 suspension Substances 0.000 description 3
RMHLITODGAKLHU-UHFFFAOYSA-N 2-isocyanopropanoic acid Chemical compound [C-]#[N+]C(C)C(O)=O RMHLITODGAKLHU-UHFFFAOYSA-N 0.000 description 2
244000099147 Ananas comosus Species 0.000 description 2
235000007119 Ananas comosus Nutrition 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
244000068988 Glycine max Species 0.000 description 2
240000002024 Gossypium herbaceum Species 0.000 description 2
235000004341 Gossypium herbaceum Nutrition 0.000 description 2
206010053759 Growth retardation Diseases 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical group [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
235000013339 cereals Nutrition 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
238000004040 coloring Methods 0.000 description 2
244000038559 crop plants Species 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
230000006378 damage Effects 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 2
239000000975 dye Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
125000004494 ethyl ester group Chemical group 0.000 description 2
239000007954 growth retardant Substances 0.000 description 2
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
239000004816 latex Substances 0.000 description 2
229920000126 latex Polymers 0.000 description 2
229940070765 laurate Drugs 0.000 description 2
235000012054 meals Nutrition 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
230000004060 metabolic process Effects 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
230000017066 negative regulation of growth Effects 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
230000017363 positive regulation of growth Effects 0.000 description 2
229910001414 potassium ion Chemical group 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
229910001415 sodium ion Inorganic materials 0.000 description 2
239000004575 stone Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
YXBFCLYILRJMIR-UHFFFAOYSA-N 1-isocyanocyclopropane-1-carboxylic acid Chemical compound OC(=O)C1([N+]#[C-])CC1 YXBFCLYILRJMIR-UHFFFAOYSA-N 0.000 description 1
GHERKZSZPVSWBQ-UHFFFAOYSA-N 2-ethyl-2-isocyanobutanoic acid Chemical compound CCC(CC)([N+]#[C-])C(O)=O GHERKZSZPVSWBQ-UHFFFAOYSA-N 0.000 description 1
YTJURFIZKYIJJB-UHFFFAOYSA-N 2-isocyano-2-methylbutanoic acid Chemical compound CCC(C)([N+]#[C-])C(O)=O YTJURFIZKYIJJB-UHFFFAOYSA-N 0.000 description 1
GNHRTWYZEIYCRW-UHFFFAOYSA-N 2-isocyano-2-methylpropanoic acid Chemical compound [C-]#[N+]C(C)(C)C(O)=O GNHRTWYZEIYCRW-UHFFFAOYSA-N 0.000 description 1
OYCJHELUKJMXIN-UHFFFAOYSA-N 2-isocyano-3-methylbutanoic acid Chemical compound CC(C)C([N+]#[C-])C(O)=O OYCJHELUKJMXIN-UHFFFAOYSA-N 0.000 description 1
CFCNTIFLYGKEIO-UHFFFAOYSA-N 2-isocyanoacetic acid Chemical compound OC(=O)C[N+]#[C-] CFCNTIFLYGKEIO-UHFFFAOYSA-N 0.000 description 1
HBLAXMITNSURQX-UHFFFAOYSA-N 2-isocyanobutanoic acid Chemical compound CCC([N+]#[C-])C(O)=O HBLAXMITNSURQX-UHFFFAOYSA-N 0.000 description 1
XRNVIFDBCJXAPN-UHFFFAOYSA-N 2-isocyanopentanoic acid Chemical compound CCCC([N+]#[C-])C(O)=O XRNVIFDBCJXAPN-UHFFFAOYSA-N 0.000 description 1
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 description 1
244000215068 Acacia senegal Species 0.000 description 1
RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
241000209134 Arundinaria Species 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
235000016068 Berberis vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
239000004604 Blowing Agent Substances 0.000 description 1
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
240000007154 Coffea arabica Species 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
244000043261 Hevea brasiliensis Species 0.000 description 1
101000652359 Homo sapiens Spermatogenesis-associated protein 2 Proteins 0.000 description 1
101000642464 Homo sapiens Spermatogenesis-associated protein 2-like protein Proteins 0.000 description 1
OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical compound N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 description 1
235000019738 Limestone Nutrition 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
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
108010009736 Protein Hydrolysates Proteins 0.000 description 1
102100030254 Spermatogenesis-associated protein 2 Human genes 0.000 description 1
LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
208000027418 Wounds and injury Diseases 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000006978 adaptation Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000002969 artificial stone Substances 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
239000001273 butane Substances 0.000 description 1
DJIBHHGQPSAZCY-UHFFFAOYSA-N butoxy-bis(butylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCOP(=S)(SCCCC)SCCCC DJIBHHGQPSAZCY-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
230000035613 defoliation Effects 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000010410 dusting Methods 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
230000004345 fruit ripening Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003966 growth inhibitor Substances 0.000 description 1
231100000001 growth retardation Toxicity 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
208000014674 injury Diseases 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
230000011890 leaf development Effects 0.000 description 1
230000002015 leaf growth Effects 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000006028 limestone Substances 0.000 description 1
150000002696 manganese Chemical class 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
230000035800 maturation Effects 0.000 description 1
UFGJMIRODOAASM-UHFFFAOYSA-N methyl 2-isocyanopropanoate Chemical compound COC(=O)C(C)[N+]#[C-] UFGJMIRODOAASM-UHFFFAOYSA-N 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
239000005445 natural material Substances 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000011368 organic material Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000002245 particle Substances 0.000 description 1
238000003359 percent control normalization Methods 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
QMYAUOGCTFKFIV-UHFFFAOYSA-M potassium;1-isocyanocyclopropane-1-carboxylate Chemical compound [K+].[O-]C(=O)C1([N+]#[C-])CC1 QMYAUOGCTFKFIV-UHFFFAOYSA-M 0.000 description 1
CQKHUQUTXVGQGJ-UHFFFAOYSA-M potassium;2-isocyano-2-methylpropanoate Chemical compound [K+].[C-]#[N+]C(C)(C)C([O-])=O CQKHUQUTXVGQGJ-UHFFFAOYSA-M 0.000 description 1
230000002028 premature Effects 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000013558 reference substance Substances 0.000 description 1
230000033764 rhythmic process Effects 0.000 description 1
230000007226 seed germination Effects 0.000 description 1
238000004904 shortening Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
HLMMCKMTLSIMBC-UHFFFAOYSA-M sodium;1-isocyanocyclopropane-1-carboxylate Chemical compound [Na+].[O-]C(=O)C1([N+]#[C-])CC1 HLMMCKMTLSIMBC-UHFFFAOYSA-M 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000010186 staining Methods 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
230000005068 transpiration Effects 0.000 description 1
229940005605 valeric acid Drugs 0.000 description 1
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS787496A 1977-11-19 1978-11-16 Means for regulation of the growth of plants and method of making the active component CS201519B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19772751783 DE2751783A1 (de)	1977-11-19	1977-11-19	Alpha-isocyanocarbonsaeure-salze, verfahren zu ihrer herstellung und ihre verwendung als pflanzenwachstumsregulatoren

Publications (1)

Publication Number	Publication Date
CS201519B2 true CS201519B2 (en)	1980-11-28

Family

ID=6024140

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS787496A CS201519B2 (en)	1977-11-19	1978-11-16	Means for regulation of the growth of plants and method of making the active component

Country Status (22)

Country	Link
US (1)	US4292072A (fr)
EP (1)	EP0002014B1 (fr)
JP (1)	JPS5479230A (fr)
AT (1)	AT361017B (fr)
AU (1)	AU4168978A (fr)
BR (1)	BR7807547A (fr)
CA (1)	CA1114836A (fr)
CS (1)	CS201519B2 (fr)
DD (1)	DD141254A5 (fr)
DE (2)	DE2751783A1 (fr)
DK (1)	DK513178A (fr)
ES (1)	ES475189A1 (fr)
GR (1)	GR72770B (fr)
IL (1)	IL55962A (fr)
IT (1)	IT1101706B (fr)
NZ (1)	NZ188929A (fr)
OA (1)	OA06103A (fr)
PL (1)	PL110796B1 (fr)
PT (1)	PT68799A (fr)
RO (1)	RO79084A (fr)
TR (1)	TR20095A (fr)
ZA (1)	ZA786469B (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2842639A1 (de) *	1978-09-29	1980-04-10	Bayer Ag	Alpha -isocyano-carbonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als pflanzenwachstumsregulatoren
EP2654433B1 (fr)	2010-12-21	2017-08-30	Bayer Cropscience LP	Les mutants "papier émeri" de bacillus et des méthodes d'application pour la promotion de la croissance des plantes, de la santé des plants et pour le contrôl des maladies et des parasites
MX2014002890A (es)	2011-09-12	2015-01-19	Bayer Cropscience Lp	Metodo para mejorar la salud y/o promover el crecimiento de una planta y/o mejorar la maduracion de frutos.
JP6164610B2 (ja) *	2013-08-26	2017-07-19	国立大学法人東京農工大学	アミノ酸イソニトリル骨格を有する水中付着生物の防汚剤
KR101886053B1 (ko) *	2016-08-22	2018-08-07	서울과학기술대학교 산학협력단	벅 부스트 컨버터
CN116924943B (zh) *	2022-03-31	2026-04-10	中国科学院理化技术研究所	氨基酸类异氰酸盐衍生物的制备及应用

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2749231A (en) *	1952-05-06	1956-06-05	Ethyl Corp	Bromophenyl cyanoacrylic acids and derivatives
US3201466A (en) *	1963-03-08	1965-08-17	Gulf Oil Corp	Substituted cyclopropanecarboxanilide herbicides
CH495111A (de) *	1968-03-14	1970-08-31	Ciba Geigy	Schädlingsbekämpfungsmittel
US3597469A (en) *	1968-07-29	1971-08-03	Gaf Corp	Cycloalkyl unsaturated esters
US3584037A (en) *	1969-05-21	1971-06-08	Velsicol Chemical Corp	1-carboxy-3-methylene-1,2,2,4,5-pentachloropent-4-ene
JPS5220473B1 (fr) *	1970-06-29	1977-06-03
DE2043666A1 (en) *	1970-09-03	1972-03-09		Cyano-amino-polycarboxylic acids and their esters - prepn from isocyanoalkane esters and unsatd esters
US3773824A (en) *	1971-06-14	1973-11-20	Mobil Oil Corp	3-(4-methyl-3-cyclohexenyl)butyl esters of organic acids
DE2147707A1 (de) *	1971-09-24	1973-03-29	Basf Ag	Verfahren zur herstellung von carbonsaeuren
DE2218009A1 (de) *	1972-04-14	1973-11-08	Agfa Gevaert Ag	Verfahren zur haertung gelatinehaltiger schichten
DE2349108A1 (de) *	1973-09-29	1975-04-03	Hoechst Ag	2,2-difluorcyclopropancarbonitrile und verfahren zu deren herstellung
DE2405819A1 (de) *	1974-02-07	1975-08-21	Agfa Gevaert Ag	Verfahren zum fixieren von photographischen materialien
US4098600A (en) *	1976-05-24	1978-07-04	Monsanto Company	Isocyanoacylamides
US4083863A (en) *	1976-06-01	1978-04-11	American Cyanamid Corporation	Process for the preparation of cyclopropane carboxylic acids and esters
GB1578139A (en) *	1976-07-07	1980-11-05	Ici Ltd	Preparation of alicyclic compounds

1977
- 1977-11-19 DE DE19772751783 patent/DE2751783A1/de not_active Withdrawn
1978
- 1978-10-27 US US05/955,435 patent/US4292072A/en not_active Expired - Lifetime
- 1978-10-30 CA CA314,682A patent/CA1114836A/fr not_active Expired
- 1978-11-04 EP EP78101306A patent/EP0002014B1/fr not_active Expired
- 1978-11-04 DE DE7878101306T patent/DE2860381D1/de not_active Expired
- 1978-11-10 DD DD78209019A patent/DD141254A5/de unknown
- 1978-11-15 RO RO7895687A patent/RO79084A/fr unknown
- 1978-11-16 OA OA56660A patent/OA06103A/fr unknown
- 1978-11-16 NZ NZ188929A patent/NZ188929A/xx unknown
- 1978-11-16 IL IL55962A patent/IL55962A/xx unknown
- 1978-11-16 CS CS787496A patent/CS201519B2/cs unknown
- 1978-11-17 ES ES475189A patent/ES475189A1/es not_active Expired
- 1978-11-17 ZA ZA00786469A patent/ZA786469B/xx unknown
- 1978-11-17 GR GR57670A patent/GR72770B/el unknown
- 1978-11-17 PT PT68799A patent/PT68799A/pt unknown
- 1978-11-17 DK DK513178A patent/DK513178A/da not_active Application Discontinuation
- 1978-11-17 TR TR20095A patent/TR20095A/xx unknown
- 1978-11-17 AU AU41689/78A patent/AU4168978A/en active Pending
- 1978-11-17 BR BR7807547A patent/BR7807547A/pt unknown
- 1978-11-17 AT AT822778A patent/AT361017B/de not_active IP Right Cessation
- 1978-11-17 JP JP14123678A patent/JPS5479230A/ja active Pending
- 1978-11-17 IT IT29894/78A patent/IT1101706B/it active
- 1978-11-18 PL PL1978211045A patent/PL110796B1/pl unknown

Also Published As

Publication number	Publication date
ZA786469B (en)	1979-10-31
IL55962A0 (en)	1979-01-31
PL110796B1 (en)	1980-07-31
PL211045A1 (pl)	1979-06-18
DK513178A (da)	1979-05-20
OA06103A (fr)	1981-06-30
NZ188929A (en)	1980-05-08
BR7807547A (pt)	1979-07-24
ES475189A1 (es)	1979-04-16
TR20095A (tr)	1980-07-08
IT7829894A0 (it)	1978-11-17
US4292072A (en)	1981-09-29
PT68799A (pt)	1978-12-01
EP0002014B1 (fr)	1981-01-28
DD141254A5 (de)	1980-04-23
CA1114836A (fr)	1981-12-22
DE2751783A1 (de)	1979-05-23
IT1101706B (it)	1985-10-07
RO79084A (fr)	1982-06-25
AU4168978A (en)	1979-05-24
ATA822778A (de)	1980-07-15
AT361017B (de)	1981-02-10
IL55962A (en)	1982-09-30
EP0002014A1 (fr)	1979-05-30
DE2860381D1 (en)	1981-03-19
GR72770B (fr)	1983-12-05
JPS5479230A (en)	1979-06-25

Publication	Publication Date	Title
JPH0413349B2 (fr)	1992-03-09
KR840001772B1 (ko)	1984-10-19	1-하이드록시에틸-아졸 유도체의 제조방법
US4554017A (en)	1985-11-19	Method and compositions for regulating plant growth using cycloalkane-carboxylic acid compounds
US4367344A (en)	1983-01-04	Process for the preparation of 1-amino-cyclopropane-carboxylic acid compounds
US4525204A (en)	1985-06-25	Method and compositions for regulating plant growth using pyrimidine-butanol compounds
CS236691B2 (en)	1985-05-15	Agent for regulation of plant growth and fungicide agent and production method of its efficient components
US4457870A (en)	1984-07-03	Regulating plant growth with novel 1-amino-cyclopropanecarboxylic acid metal complexes
US4227918A (en)	1980-10-14	Novel halogenoethyl sulphones and their use as plant growth regulators
US4292072A (en)	1981-09-29	Novel α-isocyanocarboxylic acid compounds and plant growth regulant compositions
CS230598B2 (en)	1984-08-13	Fungicid agent and for regulation of growing of plants and method manufacture of efficient compound
CS201518B2 (en)	1980-11-28	Means for regulation of the plants growth
CS236695B2 (en)	1985-05-15	Fungicide agent and for regulation of plant growth and production method of its efficient components
CS214799B2 (cs)	1982-05-28	Prostředek k regulaci růstu rostlin a způsob výroby účinných látek
US4261731A (en)	1981-04-14	Alpha-isocyano-carboxylic acid amide compounds and plant growth regulant compositions
US3979204A (en)	1976-09-07	Plant growth regulant compositions comprising 2-cyano-bicyclo[2,2,1]heptane
US4293331A (en)	1981-10-06	Novel acyloxamides and plant growth regulant compositions
JPS5946248A (ja)	1984-03-15	４−トリフルオロメチルベンジルアンモニウム塩
JPH0881310A (ja)	1996-03-26	植物生長調節剤
JPS61145185A (ja)	1986-07-02	新規複素環化合物、その製法並びに農園芸用殺菌剤及び植物生長調整剤
CS208499B2 (en)	1981-09-15	Means for regulation of the plants growth,particularly the vegetables
PL100337B1 (pl)	1978-09-30	Srodek do regulowania wzrostu roslin
GB1574430A (en)	1980-09-10	Plant growth regulating 3-phenyl-1,2,4-thiadiazol derivate
PL94237B1 (fr)	1977-07-30
JPH01151582A (ja)	1989-06-14	アゾリルスピロ化合物
CS241499B2 (cs)	1986-03-13	Prostředek k regulaci růstu rostlin a fungicidní prostředek a způsob výroby účinné složky