IL48598A - Method for increasing the sucrose content of growing plants by applying an aminomethylene phosphonic acid derivativ - Google Patents
Method for increasing the sucrose content of growing plants by applying an aminomethylene phosphonic acid derivativInfo
- Publication number
- IL48598A IL48598A IL48598A IL4859875A IL48598A IL 48598 A IL48598 A IL 48598A IL 48598 A IL48598 A IL 48598A IL 4859875 A IL4859875 A IL 4859875A IL 48598 A IL48598 A IL 48598A
- Authority
- IL
- Israel
- Prior art keywords
- trichloroacetyl
- acid
- salt
- plants
- aminomethylenephosphonic acid
- Prior art date
Links
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 title claims abstract description 13
- 229930006000 Sucrose Natural products 0.000 title claims abstract description 13
- 239000005720 sucrose Substances 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title claims description 20
- -1 aminomethylene phosphonic acid Chemical compound 0.000 title claims description 8
- 239000002253 acid Substances 0.000 claims abstract description 32
- 150000003839 salts Chemical class 0.000 claims abstract description 16
- 241000196324 Embryophyta Species 0.000 claims abstract description 14
- 238000003306 harvesting Methods 0.000 claims abstract description 11
- 240000000111 Saccharum officinarum Species 0.000 claims abstract description 10
- 125000003047 N-acetyl group Chemical group 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 16
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 3
- VIUDTWATMPPKEL-UHFFFAOYSA-N 3-(trifluoromethyl)aniline Chemical class NC1=CC=CC(C(F)(F)F)=C1 VIUDTWATMPPKEL-UHFFFAOYSA-N 0.000 claims description 2
- XFDUHJPVQKIXHO-UHFFFAOYSA-N 3-aminobenzoic acid Chemical class NC1=CC=CC(C(O)=O)=C1 XFDUHJPVQKIXHO-UHFFFAOYSA-N 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 150000001448 anilines Chemical class 0.000 claims description 2
- 150000002169 ethanolamines Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 abstract description 7
- 125000002668 chloroacetyl group Chemical group ClCC(=O)* 0.000 abstract description 4
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 12
- 150000007513 acids Chemical class 0.000 description 7
- 239000007788 liquid Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 235000007201 Saccharum officinarum Nutrition 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000003862 amino acid derivatives Chemical class 0.000 description 1
- 239000008365 aqueous carrier Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 229940042400 direct acting antivirals phosphonic acid derivative Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- HWJHZLJIIWOTGZ-UHFFFAOYSA-N n-(hydroxymethyl)acetamide Chemical class CC(=O)NCO HWJHZLJIIWOTGZ-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 150000003007 phosphonic acid derivatives Chemical class 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009105 vegetative growth Effects 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)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—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)
- Saccharide Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/534,268 US3961934A (en) | 1974-12-19 | 1974-12-19 | Method for increasing the sucrose content of growing plants |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL48598A0 IL48598A0 (en) | 1976-02-29 |
| IL48598A true IL48598A (en) | 1977-11-30 |
Family
ID=24129367
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL48598A IL48598A (en) | 1974-12-19 | 1975-12-03 | Method for increasing the sucrose content of growing plants by applying an aminomethylene phosphonic acid derivativ |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3961934A (enExample) |
| JP (1) | JPS51118640A (enExample) |
| BE (1) | BE836804A (enExample) |
| BR (1) | BR7508428A (enExample) |
| CA (1) | CA1044913A (enExample) |
| DE (1) | DE2557139A1 (enExample) |
| FR (1) | FR2294640A1 (enExample) |
| GB (1) | GB1486156A (enExample) |
| IL (1) | IL48598A (enExample) |
| IT (1) | IT1051191B (enExample) |
| NL (1) | NL160473C (enExample) |
| PH (1) | PH12454A (enExample) |
| ZA (1) | ZA757898B (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4120688A (en) * | 1976-04-05 | 1978-10-17 | The Proctor & Gamble Company | Method of increasing sucrose yield of sugarcane |
| GB2097001A (en) * | 1981-04-16 | 1982-10-27 | Ici Plc | Herbicidal compounds |
| US4579691A (en) * | 1983-04-21 | 1986-04-01 | Ciba-Geigy Corporation | Haloacylaminoalkylphosphonates |
| US4569802A (en) * | 1983-06-27 | 1986-02-11 | Stauffer Chemical Company | Method for preparation of N-phosphonomethylglycine |
| JPS6174015A (ja) * | 1984-09-19 | 1986-04-16 | Saginomiya Johnson Control Kk | 自動圧力制御方式 |
| US5041627A (en) * | 1988-11-25 | 1991-08-20 | Monsanto Company | Preparation of N-acyl-aminomethylphosphonates |
| US8883865B2 (en) * | 2006-09-05 | 2014-11-11 | Cerion Technology, Inc. | Cerium-containing nanoparticles |
| US9169279B2 (en) | 2009-07-31 | 2015-10-27 | Thar Pharmaceuticals, Inc. | Crystallization method and bioavailability |
| WO2011014781A1 (en) | 2009-07-31 | 2011-02-03 | Thar Pharmaceuticals, Inc. | Novel oral forms of a phosphonic acid derivative |
| US20160016982A1 (en) | 2009-07-31 | 2016-01-21 | Thar Pharmaceuticals, Inc. | Crystallization method and bioavailability |
| EP3295935B1 (en) | 2009-07-31 | 2020-07-22 | Grünenthal GmbH | Crystallization method and bioavailability |
| WO2012071517A2 (en) | 2010-11-24 | 2012-05-31 | Thar Pharmaceuticals, Inc. | Novel crystalline forms |
| US10195218B2 (en) | 2016-05-31 | 2019-02-05 | Grunenthal Gmbh | Crystallization method and bioavailability |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2304156A (en) * | 1940-03-07 | 1942-12-08 | Du Pont | Organic compound and process of preparing the same |
| US2328358A (en) * | 1941-01-23 | 1943-08-31 | Du Pont | Organic compound and process for preparing the same |
| US3556762A (en) * | 1968-10-21 | 1971-01-19 | Monsanto Co | Increasing carbohydrate deposition in plants with aminophosphonates |
| US3619166A (en) * | 1969-04-01 | 1971-11-09 | Du Pont | Method of increasing sugar content of crops |
| US3853530A (en) * | 1971-03-10 | 1974-12-10 | Monsanto Co | Regulating plants with n-phosphonomethylglycine and derivatives thereof |
| US3826641A (en) * | 1973-02-12 | 1974-07-30 | Monsanto Co | Method for increasing the sucrose content of growing plants |
| DE2315886C3 (de) * | 1973-03-30 | 1980-07-31 | Bayer Ag, 5090 Leverkusen | Verwendung von Aminomethanphosphonsaure zur Hemmung des vegetativen Pflanzenwachstums |
| US3894861A (en) * | 1973-05-21 | 1975-07-15 | Procter & Gamble | Grass growth control compositions |
-
1974
- 1974-12-19 US US05/534,268 patent/US3961934A/en not_active Expired - Lifetime
-
1975
- 1975-12-03 IL IL48598A patent/IL48598A/en unknown
- 1975-12-17 NL NL7514702.A patent/NL160473C/xx not_active IP Right Cessation
- 1975-12-18 FR FR7538884A patent/FR2294640A1/fr active Granted
- 1975-12-18 JP JP50151190A patent/JPS51118640A/ja active Granted
- 1975-12-18 BR BR7508428*A patent/BR7508428A/pt unknown
- 1975-12-18 DE DE19752557139 patent/DE2557139A1/de not_active Withdrawn
- 1975-12-18 CA CA242,237A patent/CA1044913A/en not_active Expired
- 1975-12-18 PH PH17885A patent/PH12454A/en unknown
- 1975-12-18 GB GB51796/75A patent/GB1486156A/en not_active Expired
- 1975-12-18 IT IT30455/75A patent/IT1051191B/it active
- 1975-12-18 ZA ZA757898A patent/ZA757898B/xx unknown
- 1975-12-18 BE BE162878A patent/BE836804A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BE836804A (fr) | 1976-06-18 |
| BR7508428A (pt) | 1976-08-24 |
| GB1486156A (en) | 1977-09-21 |
| IT1051191B (it) | 1981-04-21 |
| JPS51118640A (en) | 1976-10-18 |
| CA1044913A (en) | 1978-12-26 |
| FR2294640A1 (fr) | 1976-07-16 |
| DE2557139A1 (de) | 1976-07-01 |
| US3961934A (en) | 1976-06-08 |
| IL48598A0 (en) | 1976-02-29 |
| FR2294640B1 (enExample) | 1978-10-06 |
| NL160473C (nl) | 1979-11-15 |
| NL160473B (nl) | 1979-06-15 |
| JPS5654287B2 (enExample) | 1981-12-24 |
| AU8766275A (en) | 1976-11-25 |
| PH12454A (en) | 1979-03-08 |
| NL7514702A (nl) | 1976-06-22 |
| ZA757898B (en) | 1976-11-24 |
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