SU461485A3 - Herbicidal composition - Google Patents
Herbicidal compositionInfo
- Publication number
- SU461485A3 SU461485A3 SU1967069A SU1967069A SU461485A3 SU 461485 A3 SU461485 A3 SU 461485A3 SU 1967069 A SU1967069 A SU 1967069A SU 1967069 A SU1967069 A SU 1967069A SU 461485 A3 SU461485 A3 SU 461485A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- herbicidal composition
- weeks
- derivatives
- herbicide
- rice
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title description 12
- 239000000203 mixture Substances 0.000 title description 8
- 241000209094 Oryza Species 0.000 description 5
- 239000004009 herbicide Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- -1 2-methylpiperidyl Chemical group 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical class OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-N 0.000 description 1
- NNWUEBIEOFQMSS-UHFFFAOYSA-N 2-Methylpiperidine Chemical compound CC1CCCCN1 NNWUEBIEOFQMSS-UHFFFAOYSA-N 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 241000131095 Oniscidea Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 230000005080 plant death Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A63—SPORTS; GAMES; AMUSEMENTS
- A63B—APPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
- A63B67/00—Sporting games or accessories therefor, not provided for in groups A63B1/00 - A63B65/00
- A63B67/10—Games with thread-suspended or swingably-mounted bodies, e.g. balls, pointed bodies shaped as birds, animals, or the like, for aiming at and hitting targets ; Games using tethered bodies, e.g. balls, not otherwise provided for
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Physical Education & Sports Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
(54) ГЕРБИЦИДНЫЙ СОСТАВ(54) HERBICIDE STRUCTURE
Изобретение относитс к химическим средствам борьбы с нежелательной растительностью в посевах возделываемых культур.This invention relates to chemical means of controlling undesirable vegetation in crops of cultivated crops.
Известен гербицид, представл ющий собой производные дитиофосфата формулыKnown herbicide, which is a derivative of dithiophosphate of the formula
цидный состав на основе производных феноксиуксусной кислоты общей формулы:cide composition based on phenoxyacetic acid derivatives of the general formula:
О-Ш,-СО-OR2 ,OW, -CO-OR2,
(N-CO-CH -S-PlO-H-C.(N-CO-CH -S-PlO-H-C.
где цикл с (N - остаток циклогексаметиленимина или 2-метилпиперидина.where a cycle with (N is a residue of cyclohexamethyleneimine or 2-methylpiperidine.
Также известен гербицидный состав на основе производных феноксиуксусной кислоты общей формулыAlso known herbicide composition based on derivatives of phenoxyacetic acid of General formula
С1 О -СНг-СО - OR ,C1 O-SNG-CO - OR,
где К - водород или фенил, алкил, алкенил ,алкинил.where K is hydrogen or phenyl, alkyl, alkenyl, alkynyl.
Однако известный гербицидный состав не обладает достаточно высокой гербицидной активностью .However, the known herbicidal composition does not have a sufficiently high herbicidal activity.
Дл усилени гербицидной активности и избирательности действи предлагаетс гербигде RI - атом хлора или метил и R2 - водород , атом щелочного металла или алкил с 1 - 8 атомами углерода,To enhance the herbicidal activity and selectivity of action, a herbicide is offered: RI is a chlorine atom or methyl and R2 is hydrogen, an alkali metal atom or alkyl with 1-8 carbon atoms,
и производных дитиофосфата общей формулы:and dithiophosphate derivatives of the general formula:
1515
SS
ф-СО-СН г8-Р(о-Н-СзНт)5, ,f-CO-CH g8-P (o-H-CzNt) 5,
2020
где цикл с (N - остаток циклогексаметиленамина или 2-метилпиперидил, причем весовые соотношени компонентов составл ют от 1 : 10 до 3: 1 соответственно.where the cycle is with (N is the residue of cyclohexamethylene amine or 2-methylpiperidyl, and the weight ratios of the components are from 1: 10 to 3: 1, respectively.
Форма приготовлени гербицидного препарата обычна в виде раствора, дуста или концентрата эмульсий.The form of preparation of a herbicidal preparation is usually in the form of a solution, dust, or emulsion concentrate.
Пример 1. Рисовые растени 3-4 недели высотой 12-15 см, выращенные в рисовомExample 1. Rice plants 3-4 weeks tall 12-15 cm grown in rice
поле, пересаживают на опытный участок, который покрыт слоем воды в 3-5 см.field, transplanted to the experimental area, which is covered with a layer of water in 3-5 cm.
Послевсходова обработка - через 8-12 суток участок с по вившимис за это врем всходами куриного проса и мокрицы обрабатывают один раз испытуемым действующим началом и смесью действующих начал соответственно .Post-harvest treatment — after 8–12 days, the area with seedlings of chicken millet and woodlice that occurred during this time is treated once with the test active ingredient and a mixture of active principles, respectively.
Довсходова обработка - через 4 суток во Примечание. Pre-emergence treatment - after 4 days in Note.
аблица 2 10table 2 10
) Нет повреждени риса.No rice damage.
врем по влени сорных растений участок обрабатывают один раз испытуемым действующим началом и смесью действующих начал.The time of occurrence of weed plants is treated area once with the test active principle and a mixture of active principles.
Результаты опыта обрабатывают в каждом случае через 7-8 недель после обработки гербицидом .The results of the experiment are treated in each case 7-8 weeks after the treatment with the herbicide.
Показатели довсходовой обработки приведены в табл. 1, послевсходовой обработки - в табл. 2.Indicators pre-emergence treatment are given in table. 1, post-harvest processing - in table. 2
Таблица 1Table 1
Пример 2. Рисовые растени 3-4 недели высотой 12-15 см, выращенные в рисовом поле, пересаживают на опытный участок, который покрыт слоем воды в 3-5 см.Example 2. Rice plants 3–4 weeks in height 12–15 cm grown in a paddy field are transplanted to an experimental plot which is covered with a layer of water of 3–5 cm.
Через 4 суток до по влени всходов участок обрабатывают действующим началом и смесью действующих начал.After 4 days before the emergence of shoots, the area is treated with the active principle and a mixture of active principles.
Результаты опыта (обрабатывают через б недель) и показатели урожайности (определ ют через 17 недель) приведены в табл. 3.The results of the experiment (processed after b weeks) and the yield indicators (determined after 17 weeks) are given in Table. 3
Таблица 3Table 3
В табл. I, 2 и 3 прин ты следующие условные обозначени : 1А - 0,0-ди-н-пропил-дитиоПоказатель фитотоксичности оцениваетс по 5-балльной шкале: О-нет повреждени риса; 1,5-заметные повреждени (отдельные п тна); 3-сильные повреждени (растени ув дают); 5-полна гибель растени .In tab. I, 2, and 3, the following conventions are adopted: 1A - 0.0-di-n-propyl-dithio. The phytotoxicity index is estimated on a 5-point scale: O-no damage to rice; 1,5-noticeable damage (single spots); 3-strong damage (plants give uv); 5 is full of plant death.
фосфорил-ацетоциклогексаметиленимид; IB - 0,0-ди-н-пропил - дитиофосфорил - ацето-2-метилпиперидид; ПА - изопропиловый эфир 2,4-дихлорфеноксиуксусной кислоты.phosphoryl acetocyclohexamethyleneimide; IB - 0,0-di-n-propyl - dithiophosphoryl - aceto-2-methylpiperidide; PA - isopropyl ester of 2,4-dichlorophenoxyacetic acid.
Предмет изобретени Subject invention
Гербицидный состав на основе производных феноксиуксусной кислоты формулыHerbicidal composition based on derivatives of phenoxyacetic acid of the formula
RIRI
С.1- Vo-€H,-CO-OR,C.1- Vo- € H, -CO-OR,
где RI - атом хлора или метил;where RI is a chlorine atom or methyl;
R2 - водород, атом щелочного металла, или алкил с циклом атом углерода от 1 до 8,R2 is hydrogen, an alkali metal atom, or an alkyl with a carbon atom cycle of from 1 to 8,
отличающийс тем, что, с целью цовышени гербицидной активности, в него введены производные дитиофосфата общей формулыcharacterized in that, in order to increase herbicidal activity, dithiophosphate derivatives of the general formula are introduced into it
SS
II (N - СО - СНг - S -Р(0 - Н - С,Н,),II (N - CO - SNg - S - P (0 - H - C, H,),
где цикл с (N - остаток циклогексаметиленимина или 2-метилпиперидила,where cycle c (N is a residue of cyclohexamethyleneimine or 2-methylpiperidyl,
причем весовые соотношени компонентовmoreover, the weight ratio of the components
составл ют от 1 : 10 до 3: 1 соответственно.range from 1: 10 to 3: 1, respectively.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1533871A CH559506A5 (en) | 1971-10-21 | 1971-10-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU461485A3 true SU461485A3 (en) | 1975-02-25 |
Family
ID=4408284
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1838978A SU495802A3 (en) | 1971-10-21 | 1972-10-19 | Herbicidal composition |
SU1967069A SU461485A3 (en) | 1971-10-21 | 1972-10-19 | Herbicidal composition |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1838978A SU495802A3 (en) | 1971-10-21 | 1972-10-19 | Herbicidal composition |
Country Status (13)
Country | Link |
---|---|
US (1) | US3873298A (en) |
JP (1) | JPS568009B2 (en) |
CH (1) | CH559506A5 (en) |
EG (1) | EG10638A (en) |
ES (1) | ES407797A1 (en) |
FR (1) | FR2156837B1 (en) |
GB (1) | GB1353878A (en) |
HK (1) | HK15877A (en) |
IT (1) | IT969767B (en) |
MY (1) | MY7700199A (en) |
OA (1) | OA04204A (en) |
PH (2) | PH10083A (en) |
SU (2) | SU495802A3 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4137065A (en) * | 1972-11-30 | 1979-01-30 | Sumitomo Chemical Company, Ltd. | Amido phosphorothiolate pesticide |
JPS52118429A (en) * | 1976-03-31 | 1977-10-04 | Sumitomo Chem Co Ltd | (di)thiophosphates, their preparation and herbicidal composition containing the same |
JPS5251028A (en) * | 1975-10-22 | 1977-04-23 | Nippon Tokushu Noyaku Seizo Kk | Herbicide |
DE2963654D1 (en) * | 1978-02-03 | 1982-11-04 | Ciba Geigy Ag | 2-methylthio-4-cyclopropylamino-6-(alpha,beta-dimethylpropylamino)-s-triazine and the use of triazine derivatives as seewater algicides |
JPS56128704A (en) * | 1980-03-14 | 1981-10-08 | Takeda Chem Ind Ltd | Herbicidal composition for rice paddy |
IL74654A (en) * | 1985-03-20 | 1989-03-31 | Agan Chemical Manufacturers | Herbicides comprising a mixture of 1,3,5-triazine derivatives |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3295947A (en) * | 1963-11-26 | 1967-01-03 | Stauffer Chemical Co | Herbicidal mixture comprising an s-triazine derivative and nu-(b-omicron, omicron-di-isopropylidithiophosphorylethyl) benzenesulfonamide |
US3393991A (en) * | 1967-11-07 | 1968-07-23 | Monsanto Co | Herbicidal composition and method |
-
1971
- 1971-10-21 CH CH1533871A patent/CH559506A5/xx not_active IP Right Cessation
-
1972
- 1972-10-05 US US295408A patent/US3873298A/en not_active Expired - Lifetime
- 1972-10-19 FR FR7237093A patent/FR2156837B1/fr not_active Expired
- 1972-10-19 SU SU1838978A patent/SU495802A3/en active
- 1972-10-19 EG EG435/72A patent/EG10638A/en active
- 1972-10-19 PH PH14027A patent/PH10083A/en unknown
- 1972-10-19 SU SU1967069A patent/SU461485A3/en active
- 1972-10-20 OA OA54727A patent/OA04204A/en unknown
- 1972-10-20 IT IT30759/72A patent/IT969767B/en active
- 1972-10-20 GB GB4851372A patent/GB1353878A/en not_active Expired
- 1972-10-20 ES ES407797A patent/ES407797A1/en not_active Expired
- 1972-10-21 JP JP10576872A patent/JPS568009B2/ja not_active Expired
-
1976
- 1976-02-25 PH PH18142A patent/PH11465A/en unknown
-
1977
- 1977-04-07 HK HK158/77A patent/HK15877A/en unknown
- 1977-12-30 MY MY199/77A patent/MY7700199A/en unknown
Also Published As
Publication number | Publication date |
---|---|
JPS4849929A (en) | 1973-07-14 |
JPS568009B2 (en) | 1981-02-20 |
IT969767B (en) | 1974-04-10 |
SU495802A3 (en) | 1975-12-15 |
OA04204A (en) | 1979-12-31 |
ES407797A1 (en) | 1975-10-01 |
EG10638A (en) | 1976-09-30 |
MY7700199A (en) | 1977-12-31 |
US3873298A (en) | 1975-03-25 |
PH10083A (en) | 1976-08-12 |
FR2156837A1 (en) | 1973-06-01 |
CH559506A5 (en) | 1975-03-14 |
FR2156837B1 (en) | 1977-01-14 |
PH11465A (en) | 1978-02-01 |
HK15877A (en) | 1977-04-15 |
GB1353878A (en) | 1974-05-22 |
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