SU308602A1 - Herbicide - Google Patents

Herbicide Download PDF

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Publication number
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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SU
USSR - Soviet Union
Prior art keywords
colspan
sprouts
roots
atoms
text
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Application number
SU701416162A
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Russian (ru)
Inventor
Л.А. Бакуменко
А.Ф. Грапов
Т.Ф. Козлов
Н.Н. Мельников
В.П. Покатун
Л.Д. Стонов
Т.А. Сергеева
Л.М. Титова
Original Assignee
Bakumenko L A
Grapov A F
Kozlov T F
Melnikov N N
Pokatun V P
Stonov L D
Sergeeva T A
Titova L M
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Application filed by Bakumenko L A, Grapov A F, Kozlov T F, Melnikov N N, Pokatun V P, Stonov L D, Sergeeva T A, Titova L M filed Critical Bakumenko L A
Priority to SU701416162A priority Critical patent/SU308602A1/en
Application granted granted Critical
Publication of SU308602A1 publication Critical patent/SU308602A1/en

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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

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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

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1one

1one

0,30.3

10ten

10ten

1one

8,58.5

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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)

<claim-text><table border="1"> <tbody><tr><td rowspan="2"> </td><td colspan="3"> Пшеница</td><td colspan="2"> Овес</td><td colspan="2"> Просо</td><td colspan="2"> Редис</td></tr> <tr><td colspan="2"> проростки</td><td> корни</td><td> проростки</td><td> корни</td><td> проростки</td><td> корни</td><td> проростки</td><td> корни</td></tr> <tr><td> 0-2-нитро-4хпорфенип-Νвтор.бутиламидохлорметиптиофосфонат</td><td> &gt;1</td><td colspan="2"> 0,007</td><td> 0,8</td><td> 0,005</td><td> 0,35</td><td> 0,008</td><td> &gt;1</td><td> &gt;1</td></tr> <tr><td> О-2-хпор-4нитрофенил-N втор.бутйл амидохлорметилтиофосфонат</td><td> &gt;1</td><td colspan="2"> 0,008</td><td> &gt;1</td><td> 0,005</td><td> &gt;1</td><td> 0,3</td><td> &gt;1</td><td> &gt;1</td></tr> <tr><td> 0-2-нигрофенил—N -изопропилам идохлорметилтиофосфонат</td><td> 0,8</td><td> </td><td> 0,007</td><td> 0,25</td><td> 0,005</td><td> 0,3</td><td colspan="2"> 0,005 &gt;1</td><td> 0,5</td></tr> <tr><td> О-2-хлор-4нитрофенип- Νизопропипамидохпорметилтиофосфонат</td><td> М</td><td> </td><td> 0,007</td><td> &gt;1</td><td> 0,005</td><td> &gt;1</td><td> 0,4</td><td> &gt;1</td><td> ?1</td></tr> </tbody></table> <claim-text>Примечание; доза препаратов - кг/га, что вызывает 50%-ное угнетение роста растений.</claim-text><claim-text> <table border = "1"> <tbody> <tr> <td rowspan = "2"> </ td> <td colspan = "3"> Wheat </ td> <td colspan = "2"> Oats </ td> <td colspan = "2"> Millet </ td> <td colspan = "2"> Radish </ td> </ tr> <tr> <td colspan = "2"> sprouts </ td> <td> roots </ td> <td> sprouts </ td> <td> roots </ td> <td> sprouts </ td> <td> roots </ td> <td> sprouts </ td> <td> roots </ td> </ tr> <tr> <td> 0-2-nitro-4xporpenip-Νvth.butylamidochlormetyptiofosfonat </ td> <td> &gt; 1 </ td> <td colspan = "2"> 0.007 </ td> <td> 0.8 </ td> <td> 0.005 </ td> <td> 0.35 </ td> <td> 0.008 </ td> <td> &gt; 1 </ td> <td> &gt; 1 </ td> </ tr> <tr> <td> O-2-hpor-4nitrophenyl-N sec.butyl amidochloromethylthiophosphonate </ td> <td> &gt; 1 </ td> <td colspan = "2"> 0.008 </ td> <td> &gt; 1 </ td> <td> 0.005 </ td> <td> &gt; 1 </ td> <td> 0.3 </ td> <td> &gt; 1 </ td> <td> &gt; 1 </ td> </ tr> <tr> <td> 0-2-nigrophenyl — N-isopropyl idochlormethylthiophosphonate </ td> <td> 0.8 </ td> <td> </ td> <td> 0.007 </ td> <td> 0.25 </ td> <td> 0.005 </ td> <td> 0.3 </ td> <td colspan = "2"> 0.005 &gt; 1 </ td> <td> 0.5 </ td> </ tr> <tr> <td> O-2-chloro-4 nitrofenip-Ν isopropipamide-hydroxy-thiophosphate </ td> M </ td> <td> </ td> <td> 0.007 </ td> <td> &gt; 1 </ td> <td> 0.005 </ td> <td> &gt; 1 </ td> <td> 0.4 </ td> <td> &gt; 1 </ td> <td> ? 1 </ td> </ tr> </ tbody> </ table> <claim-text> Note; dose of drugs - kg / ha, which causes 50% inhibition of plant growth. </ claim-text>
SU701416162A 1970-03-18 1970-03-18 Herbicide SU308602A1 (en)

Priority Applications (1)

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Application Number Priority Date Filing Date Title
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