SU308602A1 - Herbicide - Google Patents
Herbicide Download PDFInfo
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- SU308602A1 SU308602A1 SU701416162A SU1416162A SU308602A1 SU 308602 A1 SU308602 A1 SU 308602A1 SU 701416162 A SU701416162 A SU 701416162A SU 1416162 A SU1416162 A SU 1416162A SU 308602 A1 SU308602 A1 SU 308602A1
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Abstract
Применение замещенньтх амиаоэфировгиофосфоновой кислоты общей формупыII-P-0К'Ж11\ где R - апкип с чиспом атомов угперодаот 1 до 4 ипи гапоидапкип;R -апкип нормального ипи изострое-ни с чиспом атомов угперодаот 1 до 4;водород, алкип ипи гапоид;гапоид нпи нитрогруппа, При этом У и R " одновременно не могут быть гапоидом, в качестве гербицидов.R V!3(Лс:The use of substituted amide esters of phosphoric acid of the general formupi II-P-0K'Zh11 \ where R is an upkip with a number of atoms of 1 to 4 atoms, or a normal or an isostroy with a number of atoms from 1 to 4, hydrogen, an acid, and an isothermal with a number of atoms from 1 to 4; NPI nitro group, At the same time Y and R "cannot simultaneously be a hapoid, as herbicides. RV! 3 (Ls:
Description
со оwith about
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о Изобретение относитс к области при менени в качестве i-юрбици ов фосфорорганических соединений, в частности эфироамидов апкип (гапоидапкип) тиофос фоновых кис по т, Известно испопьзование дп этой цепи эфироамида алкип (гапоидапкип) тиофосфоновой киспоты,. содержащего моноипи попигапоидфенипьный радикал, напри мер изофоса (0-2,4 - дихпорфенил - N изопропипами охлорметипгиофосфоната), С целью изыскани бопее активных препаратов предлагаетс испопьзбвагь в качестве гербицида эфироамидов алкил (галоидапкил) тиофосфоновой кислоты, содержащих в арильном радикале нитрогруппу или два заместител алкил и галоид, алкил и нитрогруппу, галоид и нитрогруппу, общей формулы КтР-0 где R - алкил с числом атомов углерода от 1 до 4 или гапоидапкил; алкил нормального или изостроени с числом атомов углерода от 1 до 4; водород, алкип или галоид; Y - галоид или нитрогруппа. При этом У и R одновременно не могут быть галоидом. Исгхытани гербидидной активности соединений проводились в лабораторных услови х. В качестве тест-объектов использовали пшеницу, овес, просо, редис, которые выращивали в чашках . Препараты вносили в агар-агар в виде эмульсии. Контролем служили растени , выращенные на чистой агаровой среде, Результаты опытов приведены в та5п пице, Наиболее сильными гербицидными свойствами обладают О -.2 - хлор - 4 метилфенил - N -втор,бутиламидохлорм©тил-тиофосфонат , О - 2 - нитро - 4 хлорфешт . - N.- втор.бутиламидохлорме-. тилтиофосфонат, 0-2 - нитрофенип - N изопропиламидохпорметиптиофосфонат , которые в дозе 0,ООЗ-О,ОО8 кг/га подавл ют рост корней однодольных расте Соединени , могут быть использованы, в виде различных препаративных форм.o The invention relates to the use of organophosphorus compounds, i.e., i-jerbits, in particular the ester amides of the acid booth (hapoidapic) of the thiophosphate backdrops, the use of this chain of the ether of amide alkypus (hapoidapkip) of the thiophosphonic acid, known containing mono-type popigaphopenphenic radical, for example isophos (0-2.4 - dihporpenyl - N with isopropyls of chloromethyphosphonate), in order to find breeders, bakers are offered as an herbicide of ester amide alkyl (halogidopkyl) asp, and as a baker has breeders, asparagus, as the herbicide of alkyl amide (halogidopkyl) tetra bladders, is offered by drawing breeders, as well as drawing bladders, asparagens, as is the herbicide of alkyl ether and halo, alkyl and nitro, halo and nitro, of the general formula KtP-0 where R is alkyl with 1 to 4 carbon atoms or hapoidapkyl; normal or iso-alkyl with 1 to 4 carbon atoms; hydrogen, alkyp or halo; Y is a halogen or nitro group. In this case, Y and R at the same time can not be halogen. The gerbid activity of the compounds was carried out under laboratory conditions. Wheat, oats, millet, and radish, which were grown in cups, were used as test objects. The preparations were applied to the agar-agar in the form of an emulsion. The plants grown on a pure agar medium served as controls. The results of the experiments are given in step 5, O-2 - chlorine - 4 methylphenyl - N - second, butylamidochlorine tyl tiophosphonate, O - 2 - nitro - 4 chlorofest have the strongest herbicidal properties. . - N.- sec. Butylamidochlorme-. tylthiophosphonate, 0-2-nitrophenip-N isopropylamido-hydroxyphosphate, which, at a dose of 0, OOZ-O, OO8 kg / ha, suppresses root growth of monocotyledonous plants of the Compound, can be used in the form of various preparative forms.
1one
1one
1one
1one
1one
1one
0,30.3
10ten
10ten
1one
8,58.5
11eleven
10ten
ОД О,005 О.ООЗOD O, 005 O.OOZ
О,007 0,8 Oh, 007 0.8
1 О,ОО8 11 Oh, OO8 1
О-2 нитрофенип-N-изопропипамидохлорметилтиофосфонат0 ,8 О,007 0,25 О,005O-2 nitrophenip-N-isopropipamidochloromethylthiophosphonate, 0, 007 0.25, 005
О,007 1 Примечание: доза препаратов - кг/га, роста растений. O, 007 1 Note: dose of drugs - kg / ha, plant growth.
Проаолжение габпипыGabpips continuation
0,ОО5 О,35 0,ОО8 10, OO5 O, 35 0, OO8 1
1one
0,005 10,005 1
0,30.3
1one
1one
0,3 О,0.3 Oh,
0,50.5
0,005 10,005 1
0,40.4
1one
1 что вызывает 50%-ное угнетение1 that causes 50% depression
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU701416162A SU308602A1 (en) | 1970-03-18 | 1970-03-18 | Herbicide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU701416162A SU308602A1 (en) | 1970-03-18 | 1970-03-18 | Herbicide |
Publications (1)
Publication Number | Publication Date |
---|---|
SU308602A1 true SU308602A1 (en) | 1983-08-23 |
Family
ID=20450954
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU701416162A SU308602A1 (en) | 1970-03-18 | 1970-03-18 | Herbicide |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU308602A1 (en) |
-
1970
- 1970-03-18 SU SU701416162A patent/SU308602A1/en active
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