WO2001003506A1 - Herbicide - Google Patents
Herbicide Download PDFInfo
- Publication number
- WO2001003506A1 WO2001003506A1 PCT/CN2000/000192 CN0000192W WO0103506A1 WO 2001003506 A1 WO2001003506 A1 WO 2001003506A1 CN 0000192 W CN0000192 W CN 0000192W WO 0103506 A1 WO0103506 A1 WO 0103506A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- herbicide
- isoprolong
- benzsulfuron
- weight
- detergent
- Prior art date
Links
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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
Definitions
- the invention belongs to the technical field of pesticides, and relates to a herbicide, in particular to a multi-purpose herbicide product with broad-spectrum efficacy, which can be used in paddy fields and dry fields.
- the herbicides currently in use mainly include acetochlor, ketofuran, glyphosate, propachlor, butachlor and their combinations.
- the use of these herbicides is mostly limited. For example, some can only be used in seedlings. Used before, after the seedlings will kill the crops; some can only be used in dry fields, and have no effect on weeds in paddy fields; some are effective on monocotyledon weeds, but not effective on dicotyledonous weeds; otherwise, some It is effective against dicotyledonous weeds.
- no multipurpose herbicide Prior to the present invention, no multipurpose herbicide has been used or reported.
- the object of the present invention is to provide a herbicide with a broad-spectrum herbicidal effect, good safety, strong adaptability, and can be used in paddy fields and dry fields.
- isoprolong As the main agent, and repeatedly added components that may have new effects to isoprolong herbicides. After observing and comparing, they finally proposed to use isoprolong
- the invention is a main agent, which is compounded with benzsulfuron-methyl as an active ingredient in an appropriate ratio. Herbicide formulation.
- the herbicide provided by the present invention includes isoprolong and benzsulfuron in a proper ratio, and conventional auxiliaries, that is, the active ingredients in its composition include isoprolong and benzsulfuron.
- the herbicide composition of the present invention may include isoprolong 95% by weight and benzsulfuron 0.1 to 20% by weight, and the remaining minor components include auxiliary agents and fillers.
- the formula includes 20-80% by weight of isoprolong, 0.2 ⁇ : bensulfuron-methyl by 10% by weight.
- Isoprolong itself is a dryland herbicide. Its chemical name is 3- (4-isopropylphenyl) -1,1-difluorenyl urea. Its chemical structural formula is
- Bemsulfuron itself is a more commonly used herbicide that is safe for rice and broad-spectrum and effective for controlling broad-leaved weeds.
- Isoprone has the effect of inhibiting photosynthesis. It is used for weeding in paddy fields, and its weed killing activity has doubled. When the weed killing effect is basically the same, its usage is only less than 32% in dry land, so it is safe to use. It is significantly improved, but isoprolong is less effective in controlling broad-leaved weeds, and bensulfuron-methyl's mechanism of action is to inhibit plant cell division. Therefore, the present invention uses isoprolong as the main agent and benzsulfuron-methyl as a compatibilizer.
- test results found that the two compounds were used in weeding, and each of them did not interfere with each other's efficacy, but also had a synergistic effect of inhibiting photosynthesis and inhibiting plant cell division, which greatly improved their respective pharmacological activities.
- the broad-spectrum effect has increased significantly, and the range of herbicidal effects has also expanded, especially in direct seeding fields and small seedling fields.
- the actual application effect has proved that after applying the herbicide of the present invention, the more harmful herbicides such as acetochlor, prachlor, butachlor can be eliminated, and its herbicidal effect is significantly better than that of Surachlor, Prochlora, Butachlor, and their compounding agents, thus realizing safe weeding.
- the scope of application of the herbicide of the present invention can be used in rice fields (including direct seedling fields, seedling throwing fields, small seedling fields, etc.), and also in crop fields such as wheat fields. Whether in the south or the north, regardless of the use of poisonous soil and fertilizer, or spray use, it can reach The ideal effect, its adaptability is rare in herbicides. Best Mode for Carrying Out the Invention
- the herbicide provided by the present invention achieves broad-spectrum and high-efficiency herbicide control through the compounding of isoprolong and benzsulfuron-methyl.
- the compounding ratio of isoprolong and benzylsulfone is 50 ⁇ 70: 1 ⁇ 5 ( Weight ratio), and its more preferred compounding ratio is 55 ⁇ 60: 3 ⁇ 5.
- the conventional auxiliaries include lubricants, dispersants, detergents and fillers.
- a formula composition of the herbicide includes:
- Dispersant 1 ⁇ 10%
- the rest are conventional fillers.
- BBU is a lubricant used to increase the lubricating effect. Its chemical structure is: C 9 H 19 — ⁇ 2 ⁇ 0— (CH 2 CH 2 0) 3 H
- the role of the detergent is to improve the wetting and suspension rate of the herbicide, and the dispersant can make the various components fully mixed.
- the choice of detergent and dispersant in the present invention is not particularly limited. The technicians can determine through experiments and comparisons. Through screening of comparative tests, the present invention preferably uses detergent LS and dispersant NNO.
- the chemical structure of detergent LS is:
- the component of the dispersant NNO is sodium methylene perylene naphthalenesulfonate.
- the preferred herbicide formulation of the present invention may be:
- the rest is filler.
- a more preferred herbicide formulation of the present invention includes:
- the rest are conventional fillers.
- the invention provides a broad-spectrum safe new herbicide product.
- a wettable powder containing 50-75% by weight of active ingredients is used.
- the amount of application needs to be adjusted.
- the amount of the herbicide is determined based on the content of the active ingredients (that is, the sum of isoprolong and benzsulfuron content).
- the content of the active ingredients that is, the sum of isoprolong and benzsulfuron content.
- the herbicide product used per acre is converted to the active ingredient.
- the content should be 30 to 80 grams, which can achieve the desired herbicidal effect. This dosage range is obtained after comprehensive consideration by the inventor after a large number of effect tests and safety tests.
- Determination of the amount of active ingredients Use herbicides with an active ingredient content of 60%, and use benzulsulfuron 0.3, 0.6, 0.9, 1.2, 1.5 grams per acre, and isoprene 11, 17, 23, 29, 35 grams per acre after conversion. Each dose is combined with each other, with the drug-free area as a control.
- Test method In the pot method, grass weeds are labeled with thousands of gold, and each pot is planted with 0.05 g (about 340 grains), and the medicine is used the day after sowing. Broad-leaf weeds use water peanuts as a bar label. Cut the water peanuts into sections and insert them in plastic pots. Each plant contains 4 plants. Repeat three times. When 4 new leaves grow and the height reaches 5-6 cm, use it. The soil surface is moist, without water accumulation, and the water consumption is 50kg / mu.
- Table 1 shows the control effect on Bachelor's weed under various dosages.
- the control effect on water peanut is basically consistent with the above results.
- Table 2 is based on the determination that isoprolong is effective for Thousand Gold.
- the effective amount of isoprolong is fixed at 15 g / mu, and then different amounts of benzsulfuron are added.
- the effective amount of benzsulfuron is set at 0.5, 0.75, 1.0, 1.25, 1.5, 2.0 grams. Effects of the Proportion of Isoprone and Bensulfuron-methyl on the Control Effect of Water Peanuts
- the herbicide of the present invention with isoprolong and benzsulfuron with different ratios was used.
- the content of the active ingredient was 60% (weight ), 60% wettable powder made by adding auxiliaries, converted into effective dosages of 31.5 g / mu, 36.5 g / mu, 41.5 g / mu, 37 g / mu and 32.5 g / mu for application at 120 g / mu 10% Dingnong was used as the control drug, with no drug treatment as the control, and applied with the poisonous soil method.
- the seedlings were planted with one heart, the water was kept in the basin for 1-2 cm, and the water was kept for 6-7 days.
- the safety of the herbicides at all levels of the present invention is generally higher than that of young grasshoppers, but the number of seedlings and plant height of 50 grams per mu is lower than other treatments. Therefore, the herbicide The dosage of the agent in the seedling stage should be less than 50 g / mu, and it is safe between 20 and 50 grams (that is, the amount of active ingredients is 12 to 30 grams).
- This herbicide is made by mixing isoprolong with benzsulfuron and adding an auxiliary agent. Taking into account the composition ratio (active ingredient) of prolong and benzsulfuron is 50 ⁇ 70: 1-5, preferably at 55 ⁇ 60: 3 ⁇ 5.
- Paddy field weeding uses the herbicide product with an effective ingredient amount of 10-30 grams per acre to achieve the desired herbicidal effect. Preferably, the effective ingredient amount used for weeding per acre is 12-24 grams. Additives are usually used as wettable powders as needed. Examples 1 to 3
- Example 2 and Example 1 used the herbicides of Example 2 and Example 1 (referred to as 60% Caoshuai and 70% Caoshuai), respectively, with the representative propachlor herbicides vermicillin and upland herbicide Long single agent is used as a control group, and the case without medicine is used as a reference.
- the herbicide (grass master) of the present invention has a control effect of more than 90% on various weeds in the paddy field, especially the control effect on grasses and broadleaf grasses is significantly better than that of herbicides.
- its dosage is only 60% of carbamazepam, so it is basically harmless to the seedlings, and the cost is only about 50% of carbamazeb, which is indeed a good medicine, safe to use, original and suitable for modernization.
- the ideal herbicide for farming has good promotion and application value.
- the application was performed about 7 to 5 days after sowing in the wheat field, and 2 months after the application, the herbicidal efficacy test was performed. The results are shown in Table 6.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (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)
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU56706/00A AU5670600A (en) | 1999-07-12 | 2000-07-07 | Herbicide |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN99114323.X | 1999-07-12 | ||
CN99114323A CN1078443C (zh) | 1999-07-12 | 1999-07-12 | 除草剂 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2001003506A1 true WO2001003506A1 (fr) | 2001-01-18 |
Family
ID=5277423
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2000/000192 WO2001003506A1 (fr) | 1999-07-12 | 2000-07-07 | Herbicide |
Country Status (3)
Country | Link |
---|---|
CN (1) | CN1078443C (zh) |
AU (1) | AU5670600A (zh) |
WO (1) | WO2001003506A1 (zh) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101884335A (zh) * | 2010-07-17 | 2010-11-17 | 陕西合和种业科技有限公司 | 一种十字花科作物化学杀雄剂组合物及其应用方法 |
CN105580824A (zh) * | 2016-03-08 | 2016-05-18 | 钱永康 | 苄嘧·异丙隆除草剂及其生产方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0449751A1 (fr) * | 1990-03-20 | 1991-10-02 | Rhone-Poulenc Agrochimie | Association herbicide comprenant l'aclonifen et au moins une urée substituée |
DD297762A5 (de) * | 1988-12-08 | 1992-01-23 | Biologische Zentralanstalt Berlin,De | Herbizides mittel |
CN1203740A (zh) * | 1998-06-05 | 1999-01-06 | 钱永康 | 异缘隆除草剂 |
CN1204455A (zh) * | 1998-06-05 | 1999-01-13 | 钱永康 | 异甲隆除草剂及其制作工艺 |
CN1209272A (zh) * | 1997-08-22 | 1999-03-03 | 浙江乐吉化工厂 | 一次性水稻育秧及直播田复配除草剂 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1189294A (zh) * | 1998-01-23 | 1998-08-05 | 姚东瑞 | 苄嘧黄隆复配除草剂 |
-
1999
- 1999-07-12 CN CN99114323A patent/CN1078443C/zh not_active Expired - Lifetime
-
2000
- 2000-07-07 AU AU56706/00A patent/AU5670600A/en not_active Abandoned
- 2000-07-07 WO PCT/CN2000/000192 patent/WO2001003506A1/zh active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DD297762A5 (de) * | 1988-12-08 | 1992-01-23 | Biologische Zentralanstalt Berlin,De | Herbizides mittel |
EP0449751A1 (fr) * | 1990-03-20 | 1991-10-02 | Rhone-Poulenc Agrochimie | Association herbicide comprenant l'aclonifen et au moins une urée substituée |
CN1209272A (zh) * | 1997-08-22 | 1999-03-03 | 浙江乐吉化工厂 | 一次性水稻育秧及直播田复配除草剂 |
CN1203740A (zh) * | 1998-06-05 | 1999-01-06 | 钱永康 | 异缘隆除草剂 |
CN1204455A (zh) * | 1998-06-05 | 1999-01-13 | 钱永康 | 异甲隆除草剂及其制作工艺 |
Also Published As
Publication number | Publication date |
---|---|
CN1078443C (zh) | 2002-01-30 |
CN1242938A (zh) | 2000-02-02 |
AU5670600A (en) | 2001-01-30 |
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