IL38891A - A method for the regulation of plant growth with 2-haloethanesulfinic acid and some derivatives thereof - Google Patents
A method for the regulation of plant growth with 2-haloethanesulfinic acid and some derivatives thereofInfo
- Publication number
- IL38891A IL38891A IL38891A IL3889172A IL38891A IL 38891 A IL38891 A IL 38891A IL 38891 A IL38891 A IL 38891A IL 3889172 A IL3889172 A IL 3889172A IL 38891 A IL38891 A IL 38891A
- Authority
- IL
- Israel
- Prior art keywords
- admixture
- carrier
- compound
- growth
- formula
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims description 10
- 238000000034 method Methods 0.000 title claims description 10
- 230000008635 plant growth Effects 0.000 title claims description 6
- 230000033228 biological regulation Effects 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 85
- 239000003085 diluting agent Substances 0.000 claims description 42
- 239000000203 mixture Substances 0.000 claims description 26
- 239000007788 liquid Substances 0.000 claims description 22
- 239000007787 solid Substances 0.000 claims description 20
- 239000004094 surface-active agent Substances 0.000 claims description 19
- 239000004480 active ingredient Substances 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 230000012010 growth Effects 0.000 claims description 11
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 6
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- 230000001105 regulatory effect Effects 0.000 claims description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 2
- 125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 claims description 2
- 239000002689 soil Substances 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims 1
- RRSCOUPNURHZBJ-UHFFFAOYSA-N 2-chloroethanesulfinic acid Chemical compound OS(=O)CCCl RRSCOUPNURHZBJ-UHFFFAOYSA-N 0.000 description 25
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 239000002904 solvent Substances 0.000 description 19
- -1 2-chloroethanesulphinic acid isooctyl ester Chemical class 0.000 description 16
- 241000196324 Embryophyta Species 0.000 description 16
- 239000003995 emulsifying agent Substances 0.000 description 16
- 150000002148 esters Chemical class 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 235000013399 edible fruits Nutrition 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- 230000009758 senescence Effects 0.000 description 10
- 230000009036 growth inhibition Effects 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
- 230000001133 acceleration Effects 0.000 description 7
- 230000017066 negative regulation of growth Effects 0.000 description 7
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- 230000005070 ripening Effects 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 229940035044 sorbitan monolaurate Drugs 0.000 description 6
- FKUBZQOURSEZDB-UHFFFAOYSA-N 2-chloroethanesulfinyl chloride Chemical compound ClCCS(Cl)=O FKUBZQOURSEZDB-UHFFFAOYSA-N 0.000 description 5
- 235000003276 Apios tuberosa Nutrition 0.000 description 5
- 244000105624 Arachis hypogaea Species 0.000 description 5
- 235000010777 Arachis hypogaea Nutrition 0.000 description 5
- 235000010744 Arachis villosulicarpa Nutrition 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 241000234295 Musa Species 0.000 description 4
- 235000021015 bananas Nutrition 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 230000035784 germination Effects 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 240000005979 Hordeum vulgare Species 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
- 244000211187 Lepidium sativum Species 0.000 description 3
- 235000007849 Lepidium sativum Nutrition 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 240000003768 Solanum lycopersicum Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000003630 growth substance Substances 0.000 description 3
- 238000003306 harvesting Methods 0.000 description 3
- 230000000977 initiatory effect Effects 0.000 description 3
- 239000005648 plant growth regulator Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- AAFAGAHZFPLKOI-UHFFFAOYSA-N ethyl 2-chloroethanesulfinate Chemical compound CCOS(=O)CCCl AAFAGAHZFPLKOI-UHFFFAOYSA-N 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- OVTJMPMILNESKM-UHFFFAOYSA-N methyl 2-bromoethanesulfinate Chemical compound COS(=O)CCBr OVTJMPMILNESKM-UHFFFAOYSA-N 0.000 description 2
- DXVLGOVMHHQZFV-UHFFFAOYSA-N methyl 2-chloroethanesulfinate Chemical compound COS(=O)CCCl DXVLGOVMHHQZFV-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- KBRIJYGGGXRJDH-UHFFFAOYSA-N propan-2-yl 2-chloroethanesulfinate Chemical compound CC(C)OS(=O)CCCl KBRIJYGGGXRJDH-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 230000005068 transpiration Effects 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- JXJMYPUDIPBWSB-UHFFFAOYSA-N 2-bromoethanesulfinic acid Chemical class OS(=O)CCBr JXJMYPUDIPBWSB-UHFFFAOYSA-N 0.000 description 1
- BFLHFAIQYRSXFX-UHFFFAOYSA-N 2-bromoethanesulfinyl chloride Chemical compound BrCCS(=O)Cl BFLHFAIQYRSXFX-UHFFFAOYSA-N 0.000 description 1
- HZVAMSNIACUQNK-UHFFFAOYSA-N 2-chloroethanesulfinyl bromide Chemical compound ClCCS(Br)=O HZVAMSNIACUQNK-UHFFFAOYSA-N 0.000 description 1
- MBSNTMGVGKCVOD-UHFFFAOYSA-N 2-chloroethyl 2-chloroethanesulfinate Chemical compound ClCCOS(=O)CCCl MBSNTMGVGKCVOD-UHFFFAOYSA-N 0.000 description 1
- YAUXBKSFOXSMFY-UHFFFAOYSA-N 2-methylpropyl 2-chloroethanesulfinate Chemical compound CC(C)COS(=O)CCCl YAUXBKSFOXSMFY-UHFFFAOYSA-N 0.000 description 1
- XRPNCCZDBMFDJC-UHFFFAOYSA-N 3-chloropropyl 2-chloroethanesulfinate Chemical compound ClCCCOS(=O)CCCl XRPNCCZDBMFDJC-UHFFFAOYSA-N 0.000 description 1
- KXSQKSVIFDJCLV-UHFFFAOYSA-N 3-methylbutyl 2-chloroethanesulfinate Chemical compound CC(C)CCOS(=O)CCCl KXSQKSVIFDJCLV-UHFFFAOYSA-N 0.000 description 1
- PWNPBNQPDGZNST-UHFFFAOYSA-N C(CCCCCCCC)OS(=O)CCCl Chemical compound C(CCCCCCCC)OS(=O)CCCl PWNPBNQPDGZNST-UHFFFAOYSA-N 0.000 description 1
- JZXDOJGVQFMZRS-UHFFFAOYSA-N CC(C)(C)COS(CCCl)=O Chemical compound CC(C)(C)COS(CCCl)=O JZXDOJGVQFMZRS-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 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
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 230000015709 bud dormancy process Effects 0.000 description 1
- YYHLBTHZFWSZLD-UHFFFAOYSA-N butyl 2-chloroethanesulfinate Chemical compound CCCCOS(=O)CCCl YYHLBTHZFWSZLD-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- WBLIXGSTEMXDSM-UHFFFAOYSA-N chloromethane Chemical compound Cl[CH2] WBLIXGSTEMXDSM-UHFFFAOYSA-N 0.000 description 1
- NKRJYXRBFNKHHT-UHFFFAOYSA-N chloromethyl 2-chloroethanesulfinate Chemical compound ClCOS(=O)CCCl NKRJYXRBFNKHHT-UHFFFAOYSA-N 0.000 description 1
- 238000012505 colouration Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- IADJAZLSGXNUKK-UHFFFAOYSA-N cyclohexyl 2-chloroethanesulfinate Chemical compound ClCCS(=O)OC1CCCCC1 IADJAZLSGXNUKK-UHFFFAOYSA-N 0.000 description 1
- NJEFCKWCNIQKRP-UHFFFAOYSA-N decyl 2-chloroethanesulfinate Chemical compound CCCCCCCCCCOS(=O)CCCl NJEFCKWCNIQKRP-UHFFFAOYSA-N 0.000 description 1
- 230000035613 defoliation Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- QNGCMDVCEXVOMM-UHFFFAOYSA-N dodecyl 2-chloroethanesulfinate Chemical compound CCCCCCCCCCCCOS(=O)CCCl QNGCMDVCEXVOMM-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- RQIFXTOWUNAUJC-UHFFFAOYSA-N ethanesulfinic acid Chemical compound CCS(O)=O RQIFXTOWUNAUJC-UHFFFAOYSA-N 0.000 description 1
- WWXAPKPPJWNEJJ-UHFFFAOYSA-N ethenyl 2-chloroethanesulfinate Chemical compound ClCCS(=O)OC=C WWXAPKPPJWNEJJ-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 230000004345 fruit ripening Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- KJBLMTNFRDSZOY-UHFFFAOYSA-N heptyl 2-chloroethanesulfinate Chemical compound CCCCCCCOS(=O)CCCl KJBLMTNFRDSZOY-UHFFFAOYSA-N 0.000 description 1
- HZINEDNLYLGGLR-UHFFFAOYSA-N hexadecyl 2-chloroethanesulfinate Chemical compound CCCCCCCCCCCCCCCCOS(=O)CCCl HZINEDNLYLGGLR-UHFFFAOYSA-N 0.000 description 1
- VTGAFTYVPGUPPM-UHFFFAOYSA-N hexyl 2-chloroethanesulfinate Chemical compound CCCCCCOS(=O)CCCl VTGAFTYVPGUPPM-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- VFLYOLOQOBMHLI-UHFFFAOYSA-N octyl 2-chloroethanesulfinate Chemical compound CCCCCCCCOS(=O)CCCl VFLYOLOQOBMHLI-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- QONFYQVYLWBOGF-UHFFFAOYSA-N pentyl 2-chloroethanesulfinate Chemical compound CCCCCOS(=O)CCCl QONFYQVYLWBOGF-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BXASJHHFQZPVQH-UHFFFAOYSA-N prop-1-enyl 2-chloroethanesulfinate Chemical compound C(=CC)OS(=O)CCCl BXASJHHFQZPVQH-UHFFFAOYSA-N 0.000 description 1
- SQPYNGUNZZYGKA-UHFFFAOYSA-N prop-2-ynyl 2-chloroethanesulfinate Chemical compound ClCCS(=O)OCC#C SQPYNGUNZZYGKA-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- SDOPFTQRUFYRPP-UHFFFAOYSA-N propyl 2-chloroethanesulfinate Chemical compound CCCOS(=O)CCCl SDOPFTQRUFYRPP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 230000002786 root growth Effects 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 230000014284 seed dormancy process Effects 0.000 description 1
- 230000007226 seed germination Effects 0.000 description 1
- 230000021217 seedling development Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CTNLUPWKAFSZPW-UHFFFAOYSA-N tetradecyl 2-chloroethanesulfinate Chemical compound CCCCCCCCCCCCCCOS(=O)CCCl CTNLUPWKAFSZPW-UHFFFAOYSA-N 0.000 description 1
- LSNIQTHIIZWHJE-UHFFFAOYSA-N undecyl 2-chloroethanesulfinate Chemical compound C(CCCCCCCCCC)OS(=O)CCCl LSNIQTHIIZWHJE-UHFFFAOYSA-N 0.000 description 1
- 230000009105 vegetative growth Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C313/00—Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C313/02—Sulfinic acids; Derivatives thereof
- C07C313/04—Sulfinic acids; Esters thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712110773 DE2110773C3 (de) | 1971-03-06 | Verwendung von 2-Halogenäthansulfinsäuren und deren Derivaten zur Regulierung des Pflanzenwachstums |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL38891A0 IL38891A0 (en) | 1972-05-30 |
| IL38891A true IL38891A (en) | 1974-12-31 |
Family
ID=5800736
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL38891A IL38891A (en) | 1971-03-06 | 1972-03-03 | A method for the regulation of plant growth with 2-haloethanesulfinic acid and some derivatives thereof |
Country Status (24)
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3927062A (en) * | 1972-05-15 | 1975-12-16 | Shell Oil Co | Plant growth regulators |
| DE2657380C3 (de) * | 1976-12-17 | 1981-02-05 | Bayer Ag, 5090 Leverkusen | Halogenäthyl-sulfone, Verfahren zu ihrer Herstellung sowie ihre Verwendung zur Regulierung des Pflanzenwachstums |
| US4357159A (en) * | 1977-01-12 | 1982-11-02 | Ciba-Geigy Corporation | Haloethylthienylsulphonates for the regulation of plant metabolism |
| CH622404A5 (enrdf_load_stackoverflow) * | 1977-01-12 | 1981-04-15 | Ciba Geigy Ag | |
| FR2442833A1 (fr) * | 1978-11-29 | 1980-06-27 | Conservatoire Nal Arts Metiers | Procede de preparation de sels d'acides sulfiniques organiques |
| US4359334A (en) * | 1980-04-28 | 1982-11-16 | Gaf Corporation | Composition for plant growth regulation |
| US4427439A (en) | 1980-04-28 | 1984-01-24 | Gaf Corporation | Composition for plant growth regulation |
| WO1987005781A2 (en) | 1986-03-31 | 1987-10-08 | Rhone-Poulenc Nederlands B.V. | Synergistic plant growth regulator compositions |
| US5123951A (en) * | 1986-03-31 | 1992-06-23 | Rhone-Poulenc Nederland B.V. | Synergistic plant growth regulator compositions |
| GB9705120D0 (en) * | 1997-03-12 | 1997-04-30 | Zeneca Ltd | Sulfur-containing acids and derivatives |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2654667A (en) * | 1950-11-29 | 1953-10-06 | Phillips Petroleum Co | Sulfoxides as plant defoliants |
| US2999105A (en) * | 1957-05-20 | 1961-09-05 | Phillips Petroleum Co | Process for preparation of esters of thiosulfinic acids |
| US3463803A (en) * | 1966-10-28 | 1969-08-26 | Chemagro Corp | Polyhaloethyl and polyhalovinyl sulfinate and thiosulfinate esters |
-
1972
- 1972-02-25 SU SU1752211A patent/SU512691A3/ru active
- 1972-02-26 EG EG70/72A patent/EG10407A/xx active
- 1972-02-29 US US230505A patent/US3885951A/en not_active Expired - Lifetime
- 1972-03-01 TR TR16683A patent/TR16683A/xx unknown
- 1972-03-01 RO RO7269945A patent/RO70848A/ro unknown
- 1972-03-03 ZA ZA721461A patent/ZA721461B/xx unknown
- 1972-03-03 AT AT178972A patent/AT314271B/de not_active IP Right Cessation
- 1972-03-03 CA CA136,160A patent/CA987127A/en not_active Expired
- 1972-03-03 CH CH317172A patent/CH568003A5/xx not_active IP Right Cessation
- 1972-03-03 BR BR1239/72*[A patent/BR7201239D0/pt unknown
- 1972-03-03 DD DD161302A patent/DD96626A5/xx unknown
- 1972-03-03 IL IL38891A patent/IL38891A/en unknown
- 1972-03-03 NL NLAANVRAGE7202864,A patent/NL169401C/xx not_active IP Right Cessation
- 1972-03-04 HU HUBA2709A patent/HU164190B/hu unknown
- 1972-03-04 ES ES400452A patent/ES400452A1/es not_active Expired
- 1972-03-04 PL PL1972153870A patent/PL83269B1/pl unknown
- 1972-03-04 IT IT21449/72A patent/IT953442B/it active
- 1972-03-06 GB GB1030772A patent/GB1320667A/en not_active Expired
- 1972-03-06 JP JP2239872A patent/JPS5618562B1/ja active Pending
- 1972-03-06 FR FR7207690A patent/FR2128660B1/fr not_active Expired
- 1972-03-06 CS CS1485A patent/CS176188B2/cs unknown
- 1972-03-06 BE BE780256A patent/BE780256A/xx unknown
-
1975
- 1975-12-30 MY MY57/75A patent/MY7500057A/xx unknown
-
1976
- 1976-04-13 KE KE2617*UA patent/KE2617A/xx unknown
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