SU736855A3 - Herbicidic composition - Google Patents
Herbicidic composition Download PDFInfo
- Publication number
- SU736855A3 SU736855A3 SU752171863A SU2171863A SU736855A3 SU 736855 A3 SU736855 A3 SU 736855A3 SU 752171863 A SU752171863 A SU 752171863A SU 2171863 A SU2171863 A SU 2171863A SU 736855 A3 SU736855 A3 SU 736855A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acid
- chloro
- salt
- ester
- dichloro
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 19
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 17
- 150000003839 salts Chemical class 0.000 claims abstract description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000002148 esters Chemical class 0.000 claims abstract description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 abstract description 9
- 241000196324 Embryophyta Species 0.000 abstract description 5
- 244000042664 Matricaria chamomilla Species 0.000 abstract description 3
- 239000004480 active ingredient Substances 0.000 abstract description 3
- 150000007513 acids Chemical class 0.000 abstract description 2
- 125000004494 ethyl ester group Chemical group 0.000 abstract description 2
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 abstract 2
- OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-N 0.000 abstract 1
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 abstract 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 abstract 1
- 235000007639 Anthemis cotula Nutrition 0.000 abstract 1
- 240000002791 Brassica napus Species 0.000 abstract 1
- 235000006008 Brassica napus var napus Nutrition 0.000 abstract 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 description 7
- HYJSGOXICXYZGS-UHFFFAOYSA-N benazolin Chemical compound C1=CC=C2SC(=O)N(CC(=O)O)C2=C1Cl HYJSGOXICXYZGS-UHFFFAOYSA-N 0.000 description 4
- 239000004009 herbicide Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- AFZMKBLOQNTBOT-UHFFFAOYSA-N 3,4-dichloropyridine-2-carboxylic acid Chemical compound OC(=O)C1=NC=CC(Cl)=C1Cl AFZMKBLOQNTBOT-UHFFFAOYSA-N 0.000 description 2
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 2
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 208000037909 invasive meningococcal disease Diseases 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000005080 plant death Effects 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
(54) ГЕРБИЦИДНАЯ КОМПОЗИЦИЯ(54) HERBICIDE COMPOSITION
tt
Изобретение относитс к химичес КИМ средствам ДТ1Я борьбы с нежелательной растительностью в, посевах возделываемых культур, в частности к составам на основе 3 6-дихлор-пи капиновой-2 кислоты в смеси с производными феноксиалкановых .кислсэт.This invention relates to chemical IMDs of DTLI for controlling undesirable vegetation in crops of cultivated crops, in particular, compositions based on 3 6-dichloro-capanoic-2 acid in a mixture with phenoxyalkanoic acid derivatives.
Известна гербидидна композици на основе 3,6-дихлорпиколиновой-2 кислоты и ее соли или метилового эфира 1.The herbicidal composition based on 3,6-dichloropicolinic-2 acid and its salt or methyl ester 1 is known.
Известна также гербицйдна композици , содержаща в качестве действующего вещества 4-хлороксО бензтиазолинон-2-ил-3-уксусной кислоты 2 . Also known is the herbicide composition containing benzthiazolinone-2-yl-3-acetic acid 2 as the active ingredient 4-chlorooxO.
Изаестна гербицйдна композици включающа смесь трихлоруксусной и арилоксиалкановой кислоты (3 . .Однако известные гербицидные комn-rmiuHH недостаточно активны в отнои .знии двудольных сорных растений в посеэах злаковых культур,The foreign gerbit composition includes a mixture of trichloroacetic and aryloxyalkanoic acid (3. However, the well-known herbicidal com-rmiuHH are not sufficiently active in relation to the dicotyledonous weed plants in the cereal crops,
С целью усилени гербицидной актив -:ости и избирательности действи предлагаетс гербицйдна композици на основе 3,6 дихлор -2-пиколиновой кислоты или ее соли,вклю .чающа 4-хлор-2-оксобензотиазолин-3-йл-уксусную кислоту или ее соль или сложный эфир, причем весовые соотношени компонентов равны 1:25 до 1:1.-In order to enhance the herbicidal asset -: spine and selectivity of action, a herbicide composition based on 3.6 dichloro-2-picolinic acid or its salt, including the preferred 4-chloro-2-oxobenzothiazoline-3-yl-acetic acid or its salt or an ester, and the weight ratios of the components are 1:25 to 1: 1.-
Пример 1. Растени ровой пшеницы Б стадии выхода в трубку и горца обрабатывают в дозе 140, 210, 420 г/га вз тыми каждый в отдельпос;ти ИЛИ В. смеси в дозе 140 + 1DO., Example 1. Plants of wheat wheat B at the tube exit stage and mountaineer are treated at a dose of 140, 210, 420 g / ha each taken separately; or OR B. the mixture at a dose of 140 + 1DO.,
0 210 + 25, 210 + 100, 420 + 12,5, 420 + 25. г/га соединени ми - 1: 4-хлор-2-оксобензотиазолин-З-ил-уксусной кислоты и № 2: 3,6 диХлор-2-пиколиновой кислоты.0 210 + 25, 210 + 100, 420 + 12.5, 420 + 25. g / ha with compounds: 1: 4-chloro-2-oxobenzothiazolin-3-yl-acetic acid and no. 2: 3.6 dichloro 2-picolinic acid.
tsts
Спуст две недели провод т учет гербицидной активности в баллах по дес тибальной шкале: О-нет поражени , 10-полна гибель растений.After two weeks, the herbicidal activity was scored in points according to the decimal scale: O-no lesion, 10 is full of plant death.
Результаты испытаний представлены Test results are presented
20 в табл. 1..20 in the table. one..
Пример 2.-Растени ржи в фазе 4-7 листьев и ромашки о рабатывают сложным этиловым эфиром 4-хлор-2-оксо-бензоти аз олин-3-ил-у Ксусной Example 2.-Rye plants in the phase of 4-7 leaves and chamomile are diluted with 4-chloro-2-oxo-benzothiaz olin-3-yl-y Xusna ethyl ester
кислоты .(соединени 3) и с|эбдинением № 2, указанным выше в дозе 650 г/га или их сглесью в дозе 560 + 25, 560 + 86, 560 + 50 г/га.acids. (Compounds 3) and with | Ebdinenie number 2, indicated above at a dose of 650 g / ha or their mixture in a dose of 560 + 25, 560 + 86, 560 + 50 g / ha.
Спуст 2 недели провод т учет After 2 weeks, an account is taken.
3D гербицидной активности в баллах по3D herbicide activity in points
двс тибальиой шкале. РезультатыICE scale tibalyi. results
представлены а табл. 2,presented a table. 2,
При мер J. Растени озимой пшеницы в фазе всходов, а также ромашки обрабатывают калиевой солью 4-хлор-2-оксо-бензотиазолин-3-ил-уксусной кислоты (соединением 4) и моноэтаноламиновой солью 3,6-дихлор-2-пик6линовой кислоты (соединение 5) в дозе 70 и 100 г/га, а таже их смесью в дозе 70 + 30 и 100 + 30 Г/ГЙ1. Спуст две недели . лровод т учет гербицидной актибнрсги по дес тибал ьной шкале.Example J. Winter wheat plants in the seedling as well as chamomile phase are treated with the potassium salt of 4-chloro-2-oxo-benzothiazolin-3-yl-acetic acid (compound 4) and the monoethanolamine salt of 3,6-dichloro-2-peak 6-linear acid (compound 5) at a dose of 70 and 100 g / ha, as well as their mixture at a dose of 70 + 30 and 100 + 30 G / GY1. After two weeks. A record of the herbicidal aktibnrsgi on a ten-year scale is carried out.
Результата испытаний указаны в табл. 3, The results of the tests are shown in Table. 3,
Гербицидна активность, балЛHerbicidal activity, ball
доза, г/гаdose, g / ha
Соединение 1 .Compound 1.
Т7ГT7G
100100
Z10Z10
3,23.2
2525
210 + 25210 + 25
210210
3/23/2
100100
210 + 100210 + 100
420420
6,26.2
12,5 . 420 + 12,512.5. 420 + 12.5
420 25420 25
6,26.2
420 + 25420 + 25
560 + 25 560560 + 25 560
3636
Пример 4. Растени репса в фазе прорастани обрабатывают соединением № 3 и соединением № 5,указанным выше в дозе 300, 400, 500, 600 и 700 r/rS а также их смесью в дозе 30 + 25, 30D + 50, 400 + 25, + 25, 500 + 50, Example 4. Repro plants in the germination phase are treated with Compound No. 3 and Compound No. 5, indicated above at a dose of 300, 400, 500, 600 and 700 r / rS, as well as their mixture at a dose of 30 + 25, 30D + 50, 400 + 25 , + 25, 500 + 50,
400 -f- 50, 500 + 50, 700 + 25, 600 + 25, 600 700 + 50 г/га.400 -f- 50, 500 + 50, 700 + 25, 600 + 25, 600 700 + 50 g / ha.
Спуст две недели провод т учет гербицидной активности по дес тибальной шкале. Результаты испытаний представлены в табл. 4.After two weeks, the herbicidal activity was recorded on a ten-point scale. The test results are presented in Table. four.
т а.блица 1Table 1
бмесь соединенийbatch of compounds
Соединение 2Connection 2
..2..2
9,59.5
8,58.5
Т а б Л и ц а 2Table 2
8,258.25
2,52.5
2/32/3
4.34.3
Доза, г/гаDose, g / ha
Соединение 3+ 25 Compound 3+ 25
+ 50 + 50
+ 25 + 25
+ 50 + 50
25 25
f 50 25f 50 25
Таблица 3Table 3
2,72.7
8,08.0
2,72.7
8,88,8
Таблица 4Table 4
Гербицидна активность, баллHerbicidal activity, score
Смесь соединеСоединение 5 ний 4 и 5Mixture of compounds 5 connections 4 and 5
1,31,3
7,77.7
5,25.2
9/09/0
1,31,3
8,88,8
5,25.2
9,39.3
1,31,3
9,09.0
5,25.2
9,89.8
1,31,3
9,69.6
73685587368558
Гербицидна композици на основе 3,б-дцхлор-2-пуколиновой Кислоты или ее соли; о т л и ч а ю щ: а с тем, что, с целью усилени гёр15йцидной активности и избирательйостн действи , она дополнительно содержит 4-хлор-2оксобензотиазоЛ|1 н-3 ил-уксусную кислоту или ее соль или сложный эфир при следующих A herbicidal composition based on 3, b-dchlor-2-pucolic acid or its salt; About tl and h and y: with the fact that, in order to enhance the gericidal activity and electoral effect, it additionally contains 4-chloro-2-oxobenzothiazo | 1 n-3 or acetic acid or its salt or ester with
Продолжение табл. 4Continued table. four
1:25 до,1;1.1:25 to, 1; 1.
Источники информации, прин тые во внимание при экспертизеSources of information taken into account in the examination
1.Патент ФРГ 1228848, кл. 452 19/02, 07.11,66.1. The patent of the Federal Republic of Germany 1228848, cl. 452 19/02, 07.11,66.
2.Мельников Н.Н. „Хими и технологи -пестицидов , М., Хими , 1974, с, 629. :2. Melnikov N.N. “Chemistry and pesticide technology, M., Himi, 1974, p. 629.:
3.Патент Японии, кл, 30-F-932, 10.07.70. , .3. The patent of Japan, class, 30-F-932, 07/10/70. ,
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB40337/74A GB1518672A (en) | 1974-09-17 | 1974-09-17 | Herbicidal composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU736855A3 true SU736855A3 (en) | 1980-05-25 |
Family
ID=10414396
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU752171863A SU736855A3 (en) | 1974-09-17 | 1975-09-16 | Herbicidic composition |
Country Status (17)
| Country | Link |
|---|---|
| JP (1) | JPS5157825A (en) |
| AT (1) | AT343403B (en) |
| BE (1) | BE833218A (en) |
| BR (1) | BR7505905A (en) |
| CA (1) | CA1104843A (en) |
| CS (1) | CS191279B2 (en) |
| DD (1) | DD120346A5 (en) |
| DE (1) | DE2540364A1 (en) |
| DK (1) | DK139801B (en) |
| ES (1) | ES440973A1 (en) |
| FR (1) | FR2285071A1 (en) |
| GB (1) | GB1518672A (en) |
| HU (1) | HU177800B (en) |
| IT (1) | IT1047110B (en) |
| NL (1) | NL7510866A (en) |
| SE (1) | SE7510351L (en) |
| SU (1) | SU736855A3 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3242487A1 (en) * | 1982-11-18 | 1984-05-24 | Hoechst Ag, 6230 Frankfurt | HERBICIDAL AGENTS |
| EA021029B1 (en) | 2009-11-23 | 2015-03-31 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Improved process for preparing soluble granules of salts of pyridine containing carboxylic acids |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL244642A (en) * | 1958-10-29 | |||
| DE1228848B (en) * | 1963-03-25 | 1966-11-17 | Dow Chemical Co | Use of 3, 6-dichloro-2-picolinic acid compounds as a total herbicide |
| FR1426923A (en) * | 1964-07-20 | 1966-02-04 | Prod Chim Ind Et Agricoles Pro | New herbicide mixtures |
| US3544302A (en) * | 1967-09-15 | 1970-12-01 | Monsanto Co | Phytotoxic compositions and methods |
| GB1494205A (en) * | 1974-06-05 | 1977-12-07 | Dow Chemical Co | Herbicidal compositions |
-
1974
- 1974-09-17 GB GB40337/74A patent/GB1518672A/en not_active Expired
-
1975
- 1975-09-09 BE BE159865A patent/BE833218A/en not_active IP Right Cessation
- 1975-09-10 DE DE19752540364 patent/DE2540364A1/en active Granted
- 1975-09-12 FR FR7528056A patent/FR2285071A1/en active Granted
- 1975-09-15 IT IT51339/75A patent/IT1047110B/en active
- 1975-09-15 AT AT707775A patent/AT343403B/en not_active IP Right Cessation
- 1975-09-15 CA CA235,478A patent/CA1104843A/en not_active Expired
- 1975-09-15 DD DD188342A patent/DD120346A5/xx unknown
- 1975-09-15 HU HU75BO1571A patent/HU177800B/en not_active IP Right Cessation
- 1975-09-15 BR BR7505905*A patent/BR7505905A/en unknown
- 1975-09-16 JP JP50112015A patent/JPS5157825A/ja active Pending
- 1975-09-16 SU SU752171863A patent/SU736855A3/en active
- 1975-09-16 SE SE7510351A patent/SE7510351L/en not_active Application Discontinuation
- 1975-09-16 NL NL7510866A patent/NL7510866A/en not_active Application Discontinuation
- 1975-09-16 ES ES440973A patent/ES440973A1/en not_active Expired
- 1975-09-16 DK DK412675AA patent/DK139801B/en not_active IP Right Cessation
- 1975-09-17 CS CS756300A patent/CS191279B2/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DK139801C (en) | 1979-10-01 |
| DK412675A (en) | 1976-03-18 |
| CA1104843A (en) | 1981-07-14 |
| BR7505905A (en) | 1976-08-03 |
| DK139801B (en) | 1979-04-23 |
| CS191279B2 (en) | 1979-06-29 |
| ES440973A1 (en) | 1977-07-01 |
| JPS5157825A (en) | 1976-05-20 |
| ATA707775A (en) | 1977-09-15 |
| HU177800B (en) | 1981-12-28 |
| BE833218A (en) | 1976-03-09 |
| FR2285071B1 (en) | 1980-04-18 |
| NL7510866A (en) | 1976-03-19 |
| AT343403B (en) | 1978-05-26 |
| DD120346A5 (en) | 1976-06-12 |
| GB1518672A (en) | 1978-07-19 |
| FR2285071A1 (en) | 1976-04-16 |
| IT1047110B (en) | 1980-09-10 |
| SE7510351L (en) | 1976-03-18 |
| DE2540364C2 (en) | 1988-03-24 |
| DE2540364A1 (en) | 1976-03-25 |
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