IL35249A - The use of 2-chloroethane-phosphonic and thiono-phosphonic acid amido compounds as agents for the regulation of plant growth - Google Patents
The use of 2-chloroethane-phosphonic and thiono-phosphonic acid amido compounds as agents for the regulation of plant growthInfo
- Publication number
- IL35249A IL35249A IL7035249A IL3524970A IL35249A IL 35249 A IL35249 A IL 35249A IL 7035249 A IL7035249 A IL 7035249A IL 3524970 A IL3524970 A IL 3524970A IL 35249 A IL35249 A IL 35249A
- Authority
- IL
- Israel
- Prior art keywords
- chloroethane
- phosphonic acid
- thiono
- phosphonic
- agents
- Prior art date
Links
- 239000003795 chemical substances by application Substances 0.000 title description 3
- 230000008635 plant growth Effects 0.000 title description 3
- 230000033228 biological regulation Effects 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 19
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000002904 solvent Substances 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 9
- 241000196324 Embryophyta Species 0.000 description 8
- -1 nitro, methyl Chemical group 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 235000013399 edible fruits Nutrition 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
- 230000012010 growth Effects 0.000 description 6
- 244000046052 Phaseolus vulgaris Species 0.000 description 5
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 230000035613 defoliation Effects 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 239000005648 plant growth regulator Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IRCBUFATUTYVLO-UHFFFAOYSA-N CCCl.OP(N=S)=O.Cl Chemical class CCCl.OP(N=S)=O.Cl IRCBUFATUTYVLO-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 230000009036 growth inhibition Effects 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- JQVRXKKZYHDRFT-UHFFFAOYSA-N n-butyl-(2-chloroethyl)phosphonamidic acid Chemical compound CCCCNP(O)(=O)CCCl JQVRXKKZYHDRFT-UHFFFAOYSA-N 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000008055 phosphate buffer solution Substances 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- BUCIWTBCUUHRHZ-UHFFFAOYSA-K potassium;disodium;dihydrogen phosphate;hydrogen phosphate Chemical compound [Na+].[Na+].[K+].OP(O)([O-])=O.OP([O-])([O-])=O BUCIWTBCUUHRHZ-UHFFFAOYSA-K 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- LOUZURPQCYZSJH-UHFFFAOYSA-N 1-chloro-2-dichlorophosphorylethane Chemical compound ClCCP(Cl)(Cl)=O LOUZURPQCYZSJH-UHFFFAOYSA-N 0.000 description 1
- MEGNXINOZSBVFU-UHFFFAOYSA-N 2-chloroethyl-N-phenylphosphonamidic acid Chemical compound C1(=CC=CC=C1)NP(O)(=O)CCCl MEGNXINOZSBVFU-UHFFFAOYSA-N 0.000 description 1
- AHEJETSIRUFWPC-UHFFFAOYSA-N 2-chloroethyl-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound OP(O)(=S)CCCl AHEJETSIRUFWPC-UHFFFAOYSA-N 0.000 description 1
- OGOPMOUFAUXUHE-UHFFFAOYSA-N 2-chloroethyl-n-ethylphosphonamidic acid Chemical compound CCNP(O)(=O)CCCl OGOPMOUFAUXUHE-UHFFFAOYSA-N 0.000 description 1
- PLXRCLLRGBJTMY-UHFFFAOYSA-N 2-chloroethyl-n-methylphosphonamidic acid Chemical compound CNP(O)(=O)CCCl PLXRCLLRGBJTMY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- RGUUYBLWZURQQG-UHFFFAOYSA-N C(C(C)C)NP(O)(=O)CCCl Chemical compound C(C(C)C)NP(O)(=O)CCCl RGUUYBLWZURQQG-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- YMDQMMGRBWZOET-UHFFFAOYSA-N Cl.CC(C)NP(O)(=O)CCCl Chemical compound Cl.CC(C)NP(O)(=O)CCCl YMDQMMGRBWZOET-UHFFFAOYSA-N 0.000 description 1
- ZSQRKBJNPOZLLB-UHFFFAOYSA-N Cl.CCCCNP(O)(=O)CCCl Chemical compound Cl.CCCCNP(O)(=O)CCCl ZSQRKBJNPOZLLB-UHFFFAOYSA-N 0.000 description 1
- PIJXPOIMVYIAAL-UHFFFAOYSA-N Cl.CNP(O)(=O)CCCl Chemical compound Cl.CNP(O)(=O)CCCl PIJXPOIMVYIAAL-UHFFFAOYSA-N 0.000 description 1
- NJLHHACGWKAWKL-UHFFFAOYSA-N ClP(Cl)=O Chemical compound ClP(Cl)=O NJLHHACGWKAWKL-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- MMCPOSDMTGQNKG-UHFFFAOYSA-N anilinium chloride Chemical compound Cl.NC1=CC=CC=C1 MMCPOSDMTGQNKG-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015709 bud dormancy process Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000460 chlorine Chemical group 0.000 description 1
- 229910052801 chlorine Chemical group 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000004426 flaxseed Nutrition 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 230000002015 leaf growth Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 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
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- FUWGSUOSJRCEIV-UHFFFAOYSA-N phosphonothioic O,O-acid Chemical compound OP(O)=S FUWGSUOSJRCEIV-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- ISYORFGKSZLPNW-UHFFFAOYSA-N propan-2-ylazanium;chloride Chemical compound [Cl-].CC(C)[NH3+] ISYORFGKSZLPNW-UHFFFAOYSA-N 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 230000002786 root growth Effects 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
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000000967 suction filtration 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
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000005068 transpiration Effects 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/44—Amides thereof
- C07F9/4403—Amides thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4407—Amides of acyclic saturated acids which can have further substituents on alkyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19691950100 DE1950100B2 (de) | 1969-10-04 | 1969-10-04 | Verwendung von 2-chloraethan-(thiono)- phosphonsaeureamido-verbindungen zur beeinflussung des pflanzenwachstums |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL35249A0 IL35249A0 (en) | 1970-11-30 |
| IL35249A true IL35249A (en) | 1973-01-30 |
Family
ID=5747300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL7035249A IL35249A (en) | 1969-10-04 | 1970-09-07 | The use of 2-chloroethane-phosphonic and thiono-phosphonic acid amido compounds as agents for the regulation of plant growth |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US3901679A (cs) |
| AT (1) | AT296683B (cs) |
| BE (1) | BE756981A (cs) |
| CA (1) | CA977176A (cs) |
| CH (1) | CH528208A (cs) |
| CS (1) | CS161992B2 (cs) |
| DE (1) | DE1950100B2 (cs) |
| DK (1) | DK129754B (cs) |
| ES (1) | ES384232A1 (cs) |
| FR (1) | FR2064143B1 (cs) |
| GB (1) | GB1275496A (cs) |
| HU (1) | HU175568B (cs) |
| IL (1) | IL35249A (cs) |
| MY (1) | MY7500053A (cs) |
| NL (1) | NL7014255A (cs) |
| PL (1) | PL81094B1 (cs) |
| RO (1) | RO60623A (cs) |
| SE (1) | SE393736B (cs) |
| ZA (1) | ZA706226B (cs) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4065288A (en) * | 1970-03-04 | 1977-12-27 | Bayer Aktiengesellschaft | Novel 2-chloroethane-(thiono)-phosphonic acid amido compounds and plant growth inhibiting compositions |
| NL152266B (nl) * | 1971-12-23 | 1977-02-15 | Vnii Chim Sredstv Zaschity | Werkwijze ter bereiding van herbicide werkzame amido-esters van thiofosfonzuur en werkwijze ter bereiding van herbicide werkzame preparaten. |
| JPS5516124B2 (cs) * | 1972-02-19 | 1980-04-30 | ||
| JPS5312980B2 (cs) * | 1973-10-27 | 1978-05-06 | ||
| DE2408863A1 (de) * | 1974-02-23 | 1975-09-11 | Basf Ag | 2-chloraethanphosphonsaeurederivate |
| US3972915A (en) * | 1974-08-14 | 1976-08-03 | Monsanto Company | N-phosphonomethylglycine phenyl hydrazides |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3531549A (en) * | 1967-02-23 | 1970-09-29 | Gaf Corp | Catechol half esters of beta-haloethylphosphonic acid |
| US3551528A (en) * | 1967-02-23 | 1970-12-29 | Gaf Corp | Phosphonic acid esters and the methol for their preparation |
| US3600435A (en) * | 1968-01-26 | 1971-08-17 | Gaf Corp | Bis aliphatic phosphonic acid anhydrides |
| US3733192A (en) * | 1968-03-28 | 1973-05-15 | Scottish Agricultural Ind Ltd | Plant foods |
| US3679780A (en) * | 1969-12-02 | 1972-07-25 | Gaf Corp | N-substituted-p-(2-chloroethyl)-phosphonamidates |
-
1969
- 1969-10-04 DE DE19691950100 patent/DE1950100B2/de active Granted
-
1970
- 1970-09-07 IL IL7035249A patent/IL35249A/en unknown
- 1970-09-11 ZA ZA706226A patent/ZA706226B/xx unknown
- 1970-09-11 CH CH1357370A patent/CH528208A/de not_active IP Right Cessation
- 1970-09-18 CA CA093,471A patent/CA977176A/en not_active Expired
- 1970-09-22 CS CS6436A patent/CS161992B2/cs unknown
- 1970-09-25 DK DK491570AA patent/DK129754B/da unknown
- 1970-09-28 NL NL7014255A patent/NL7014255A/xx not_active Application Discontinuation
- 1970-09-29 US US076595A patent/US3901679A/en not_active Expired - Lifetime
- 1970-10-02 GB GB47010/70A patent/GB1275496A/en not_active Expired
- 1970-10-02 FR FR7035722A patent/FR2064143B1/fr not_active Expired
- 1970-10-02 AT AT892270A patent/AT296683B/de not_active IP Right Cessation
- 1970-10-02 SE SE7013409A patent/SE393736B/xx unknown
- 1970-10-02 BE BE756981D patent/BE756981A/xx unknown
- 1970-10-03 HU HU70BA2476A patent/HU175568B/hu unknown
- 1970-10-03 ES ES384232A patent/ES384232A1/es not_active Expired
- 1970-10-03 PL PL1970143787A patent/PL81094B1/pl unknown
- 1970-10-05 RO RO64599A patent/RO60623A/ro unknown
-
1975
- 1975-12-30 MY MY53/75A patent/MY7500053A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES384232A1 (es) | 1973-01-01 |
| IL35249A0 (en) | 1970-11-30 |
| CA977176A (en) | 1975-11-04 |
| RO60623A (cs) | 1976-10-15 |
| GB1275496A (en) | 1972-05-24 |
| US3901679A (en) | 1975-08-26 |
| BE756981A (cs) | 1971-04-02 |
| DK129754B (da) | 1974-11-18 |
| DE1950100A1 (de) | 1971-04-15 |
| PL81094B1 (cs) | 1975-08-30 |
| MY7500053A (en) | 1975-12-31 |
| ZA706226B (en) | 1971-04-28 |
| CH528208A (de) | 1972-09-30 |
| NL7014255A (cs) | 1971-04-06 |
| DK129754C (cs) | 1975-04-28 |
| AT296683B (de) | 1972-02-25 |
| FR2064143A1 (cs) | 1971-07-16 |
| SE393736B (sv) | 1977-05-23 |
| HU175568B (hu) | 1980-09-28 |
| DE1950100B2 (de) | 1976-12-02 |
| FR2064143B1 (cs) | 1974-10-11 |
| CS161992B2 (cs) | 1975-06-10 |
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