CN1977604A - Imidacloprid preparation and Nonyl pheno Ethoxylate use in said preparation - Google Patents
Imidacloprid preparation and Nonyl pheno Ethoxylate use in said preparation Download PDFInfo
- Publication number
- CN1977604A CN1977604A CN 200610156925 CN200610156925A CN1977604A CN 1977604 A CN1977604 A CN 1977604A CN 200610156925 CN200610156925 CN 200610156925 CN 200610156925 A CN200610156925 A CN 200610156925A CN 1977604 A CN1977604 A CN 1977604A
- Authority
- CN
- China
- Prior art keywords
- imidacloprid
- ether
- preparation
- polyoxyethylene
- surfactant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000005906 Imidacloprid Substances 0.000 title claims abstract description 74
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 title claims abstract description 74
- 229940056881 imidacloprid Drugs 0.000 title claims abstract description 74
- 238000002360 preparation method Methods 0.000 title claims abstract description 29
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 title description 10
- 239000004094 surface-active agent Substances 0.000 claims abstract description 29
- -1 polyoxyethylene nonylphenol Polymers 0.000 claims description 19
- RNMDNPCBIKJCQP-UHFFFAOYSA-N 5-nonyl-7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-ol Chemical compound C(CCCCCCCC)C1=C2C(=C(C=C1)O)O2 RNMDNPCBIKJCQP-UHFFFAOYSA-N 0.000 claims description 15
- 239000007788 liquid Substances 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000002917 insecticide Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 4
- 239000000375 suspending agent Substances 0.000 claims description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
- 239000004530 micro-emulsion Substances 0.000 claims description 3
- 238000009736 wetting Methods 0.000 claims description 3
- 239000008267 milk Substances 0.000 claims description 2
- 210000004080 milk Anatomy 0.000 claims description 2
- 235000013336 milk Nutrition 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 230000002195 synergetic effect Effects 0.000 abstract description 15
- 239000000575 pesticide Substances 0.000 abstract description 4
- 229940051841 polyoxyethylene ether Drugs 0.000 abstract description 4
- 229920000056 polyoxyethylene ether Polymers 0.000 abstract description 4
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 abstract 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 104
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 26
- 239000003814 drug Substances 0.000 description 18
- DTPCFIHYWYONMD-UHFFFAOYSA-N decaethylene glycol Polymers OCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO DTPCFIHYWYONMD-UHFFFAOYSA-N 0.000 description 15
- 239000007921 spray Substances 0.000 description 13
- 239000003905 agrochemical Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 241001600408 Aphis gossypii Species 0.000 description 7
- 241000018137 Trialeurodes vaporariorum Species 0.000 description 7
- 238000012545 processing Methods 0.000 description 7
- 238000005507 spraying Methods 0.000 description 7
- 241001414989 Thysanoptera Species 0.000 description 5
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 241000238631 Hexapoda Species 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 230000003449 preventive effect Effects 0.000 description 4
- 238000011160 research Methods 0.000 description 4
- 241000819999 Nymphes Species 0.000 description 3
- 230000003213 activating effect Effects 0.000 description 3
- 230000008485 antagonism Effects 0.000 description 3
- 239000002199 base oil Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000005286 illumination Methods 0.000 description 3
- 231100000636 lethal dose Toxicity 0.000 description 3
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 3
- 229920000053 polysorbate 80 Polymers 0.000 description 3
- 230000004083 survival effect Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 231100000419 toxicity Toxicity 0.000 description 3
- 230000001988 toxicity Effects 0.000 description 3
- 231100000820 toxicity test Toxicity 0.000 description 3
- 230000001018 virulence Effects 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- 241001674048 Phthiraptera Species 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 230000000857 drug effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- MUHFRORXWCGZGE-KTKRTIGZSA-N 2-hydroxyethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCO MUHFRORXWCGZGE-KTKRTIGZSA-N 0.000 description 1
- 102000012440 Acetylcholinesterase Human genes 0.000 description 1
- 108010022752 Acetylcholinesterase Proteins 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- 206010034133 Pathogen resistance Diseases 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 229940022698 acetylcholinesterase Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- UXGNZZKBCMGWAZ-UHFFFAOYSA-N dimethylformamide dmf Chemical compound CN(C)C=O.CN(C)C=O UXGNZZKBCMGWAZ-UHFFFAOYSA-N 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 235000021332 kidney beans Nutrition 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000010148 water-pollination Effects 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Form and proportioning | LC 50(PPM) | Co-toxicity coefficient | Remarks |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (4) ether 1 | 0.181 | 286.8 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (4) ether 2 | 0.179 | 289.4 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (4) ether 4 | 0.016 | 320.5 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (4) ether 6 | 0.156 | 331.1 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (4) ether 8 | 0.142 | 365.6 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (4) ether 10 | 0.089 | 580.2 | |
Imidacloprid 10+ is right-n-nonyl phenol-polyoxyethylene (4) ether 1 | 0.162 | 321.7 | |
Imidacloprid 8+ is right-n-nonyl phenol-polyoxyethylene (4) ether 1 | 0.254 | 204.6 | |
Imidacloprid 6+ is right-n-nonyl phenol-polyoxyethylene (4) ether 1 | 0.274 | 189.7 | |
Imidacloprid 4+ is right-n-nonyl phenol-polyoxyethylene (4) ether 1 | 0.301 | 172.5 | |
Imidacloprid 2+ is right-n-nonyl phenol-polyoxyethylene (4) ether 1 | |||
Right-n-nonyl phenol-polyoxyethylene (4) ether | Actual invalid | ||
Imidacloprid | 0.52 | ||
1 Imidacloprid+2 Tween 80s | 0.51 |
Form and proportioning | LC 50(PPM) | Co-toxicity coefficient | Remarks |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (10) ether 1 | 0.965 | 242.4 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (10) ether 2 | 0.874 | 267.8 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (10) ether 4 | 0.749 | 312.3 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (10) ether 6 | 0.557 | 420.3 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (10) ether 8 | 0.433 | 540.1 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (10) ether 10 | 0.403 | 580.9 | |
Imidacloprid 10+ is right-n-nonyl phenol-polyoxyethylene (10) ether 1 | 1.648 | 142.0 | |
Imidacloprid 8+ is right-n-nonyl phenol-polyoxyethylene (10) ether 1 | 1.449 | 161.5 | |
Imidacloprid 6+ is right-n-nonyl phenol-polyoxyethylene (10) ether 1 | 1.300 | 180.0 | |
Imidacloprid 4+ is right-n-nonyl phenol-polyoxyethylene (10) ether 1 | 1.162 | 201.4 | |
Imidacloprid 2+ is right-n-nonyl phenol-polyoxyethylene (10) ether 1 | 1.124 | 208.2 | |
Right-n-nonyl phenol-polyoxyethylene (10) ether | Actual invalid | ||
Imidacloprid | 2.34 | ||
1 Imidacloprid+2 surfactant JFC | 2.32 |
Form and proportioning | LC 50(PPM) | Co-toxicity coefficient | Remarks |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (15) ether 1 | 0.675 | 203.0 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (15) ether 2 | 0.563 | 243.3 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (15) ether 4 | 0.441 | 310.7 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (15) ether 6 | 0.323 | 452.6 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (15) ether 8 | 0.268 | 510.5 | |
Imidacloprid 1+ is right-n-nonyl phenol-polyoxyethylene (15) ether 10 | 0.199 | 686.6 | |
Imidacloprid 10+ is right-n-nonyl phenol-polyoxyethylene (15) ether 1 | 0.962 | 142.4 | |
Imidacloprid 8+ is right-n-nonyl phenol-polyoxyethylene (15) ether 1 | 0.845 | 162.1 | |
Imidacloprid 6+ is right-n-nonyl phenol-polyoxyethylene (15) ether 1 | 0.755 | 181.5 | |
Imidacloprid 4+ is right-n-nonyl phenol-polyoxyethylene (15) ether 1 | 0.712 | 192.3 | |
Imidacloprid 2+ is right-n-nonyl phenol-polyoxyethylene (15) ether 1 | 0.657 | 208.5 | |
Right-n-nonyl phenol-polyoxyethylene (15) ether | Actual invalid | ||
Imidacloprid | 1.37 | ||
1 Imidacloprid+2 fast penetrant Ts | 1.35 |
Claims (7)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2006101569250A CN100571516C (en) | 2006-11-17 | 2006-11-17 | A kind of Imidacloprid preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2006101569250A CN100571516C (en) | 2006-11-17 | 2006-11-17 | A kind of Imidacloprid preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1977604A true CN1977604A (en) | 2007-06-13 |
CN100571516C CN100571516C (en) | 2009-12-23 |
Family
ID=38129041
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2006101569250A Active CN100571516C (en) | 2006-11-17 | 2006-11-17 | A kind of Imidacloprid preparation |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100571516C (en) |
-
2006
- 2006-11-17 CN CNB2006101569250A patent/CN100571516C/en active Active
Also Published As
Publication number | Publication date |
---|---|
CN100571516C (en) | 2009-12-23 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
EE01 | Entry into force of recordation of patent licensing contract |
Assignee: CHENGDU HUANGPAI CROP SCIENCE Co.,Ltd. Assignor: SHENZHEN NOPOSION AGROCHEMICALS Co.,Ltd. Contract record no.: 2010510000060 Denomination of invention: Imidacloprid preparation and Nonyl pheno Ethoxylate use in said preparation Granted publication date: 20091223 License type: Exclusive License Open date: 20070613 Record date: 20100816 |
|
CP03 | Change of name, title or address | ||
CP03 | Change of name, title or address |
Address after: 518102 No. 113 Reservoir Road, Baoan District, Guangdong, Shenzhen, Xixiang Patentee after: Shenzhen Novozon Crop Science Co.,Ltd. Country or region after: China Address before: 518102 No. 113 Reservoir Road, Baoan District, Guangdong, Shenzhen, Xixiang Patentee before: SHENZHEN NOPOSION AGROCHEMICALS Co.,Ltd. Country or region before: China |