CA1131129A - Pesticide et methode de lutte contre les parasites - Google Patents

Pesticide et methode de lutte contre les parasites

Info

Publication number: CA1131129A
Authority: CA; Canada
Prior art keywords: group; carbon atoms; alkyl; composition; general formula
Prior art date: 1979-01-15
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.): Expired

Application number

CA319,656A

Other languages

English (en)

Inventor

John S. Badmin

Robert J. Knight

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Shell Canada Ltd

Original Assignee

Shell Canada Ltd

Priority date (The priority date 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 date listed.)

1979-01-15

Filing date

1979-01-15

Publication date

1982-09-07

1979-01-15 Application filed by Shell Canada Ltd filed Critical Shell Canada Ltd

1979-01-15 Priority to CA319,656A priority Critical patent/CA1131129A/fr

1982-09-07 Application granted granted Critical

1982-09-07 Publication of CA1131129A publication Critical patent/CA1131129A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 45
230000000361 pesticidal effect Effects 0.000 title claims abstract description 9
238000000034 method Methods 0.000 title claims description 8
241000607479 Yersinia pestis Species 0.000 title claims description 6
125000000217 alkyl group Chemical class 0.000 claims abstract description 14
239000002728 pyrethroid Substances 0.000 claims abstract description 11
125000003710 aryl alkyl group Chemical class 0.000 claims abstract description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 8
239000002917 insecticide Substances 0.000 claims abstract description 8
125000003342 alkenyl group Chemical group 0.000 claims abstract description 7
125000004104 aryloxy group Chemical group 0.000 claims abstract description 5
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 5
125000000753 cycloalkyl group Chemical class 0.000 claims abstract description 4
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Chemical group C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims abstract description 3
125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims abstract description 3
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
239000001257 hydrogen Substances 0.000 claims abstract description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 19
150000001875 compounds Chemical class 0.000 claims description 18
-1 alpha-isopropyl-4-chlorobenzyl group Chemical group 0.000 claims description 10
239000000460 chlorine Substances 0.000 claims description 5
125000002947 alkylene group Chemical group 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
229910052705 radium Inorganic materials 0.000 claims description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
125000001246 bromo group Chemical group Br* 0.000 claims description 2
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims 2
DZROWLGJQLYJMN-UHFFFAOYSA-N n'-[(2,4-dimethylanilino)methyl]-n-(2,4-dimethylphenyl)-n'-methylmethanediamine Chemical compound C=1C=C(C)C=C(C)C=1NCN(C)CNC1=CC=C(C)C=C1C DZROWLGJQLYJMN-UHFFFAOYSA-N 0.000 claims 1
230000002195 synergetic effect Effects 0.000 abstract description 4
QXAITBQSYVNQDR-UHFFFAOYSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1N=CN(C)C=NC1=CC=C(C)C=C1C QXAITBQSYVNQDR-UHFFFAOYSA-N 0.000 abstract description 3
241000238876 Acari Species 0.000 abstract 1
QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 description 10
229960002587 amitraz Drugs 0.000 description 10
230000001988 toxicity Effects 0.000 description 8
231100000419 toxicity Toxicity 0.000 description 8
241001454293 Tetranychus urticae Species 0.000 description 7
239000004480 active ingredient Substances 0.000 description 6
239000002270 dispersing agent Substances 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
239000000654 additive Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000009472 formulation Methods 0.000 description 4
239000000575 pesticide Substances 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
125000004429 atom Chemical group 0.000 description 3
239000000969 carrier Substances 0.000 description 3
239000000428 dust Substances 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
239000008187 granular material Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000004563 wettable powder Substances 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
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 2
230000000895 acaricidal effect Effects 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
230000009916 joint effect Effects 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000011343 solid material Substances 0.000 description 2
239000004546 suspension concentrate Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical class C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 1
DGXRGGUNBXNJRI-UHFFFAOYSA-N 2-methyl-4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C(C)=C1 DGXRGGUNBXNJRI-UHFFFAOYSA-N 0.000 description 1
VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 1
NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
108010053481 Antifreeze Proteins Proteins 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
239000004141 Sodium laurylsulphate Substances 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
239000013504 Triton X-100 Substances 0.000 description 1
229920004890 Triton X-100 Polymers 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000011149 active material Substances 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000005667 attractant Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
238000011278 co-treatment Methods 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000013270 controlled release Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
239000006184 cosolvent Substances 0.000 description 1
239000013530 defoamer Substances 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
235000013601 eggs Nutrition 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
235000012041 food component Nutrition 0.000 description 1
239000005417 food ingredient Substances 0.000 description 1
239000000727 fraction Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
125000000262 haloalkenyl group Chemical group 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000011344 liquid material Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
239000003607 modifier Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000006259 organic additive Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000003016 pheromone Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical class OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)

CA319,656A 1979-01-15 1979-01-15 Pesticide et methode de lutte contre les parasites Expired CA1131129A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA319,656A CA1131129A (fr)	1979-01-15	1979-01-15	Pesticide et methode de lutte contre les parasites

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA319,656A CA1131129A (fr)	1979-01-15	1979-01-15	Pesticide et methode de lutte contre les parasites

Publications (1)

Publication Number	Publication Date
CA1131129A true CA1131129A (fr)	1982-09-07

Family

ID=4113332

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA319,656A Expired CA1131129A (fr)	1979-01-15	1979-01-15	Pesticide et methode de lutte contre les parasites

Country Status (1)

Country	Link
CA (1)	CA1131129A (fr)

1979
- 1979-01-15 CA CA319,656A patent/CA1131129A/fr not_active Expired

Legal Events

Date	Code	Title	Description
1999-09-07	MKEX	Expiry

Publication	Publication Date	Title
GB2058569A (en)	1981-04-15	Liquid insecticide compositions containing synthetic pyrethroids
US4179518A (en)	1979-12-18	Synergistic pesticidal composition
CA1111760A (fr)	1981-11-03	Pesticides
US4305934A (en)	1981-12-15	Pyrethroid pesticidal compositions
EP0000962B1 (fr)	1981-11-18	Composition pesticide et procédé pour détruire les organismes nuisibles
EP0008474B1 (fr)	1985-10-02	Compositions pesticides contenant un sulfure d'acide carbamique et un insecticide pyréthroide synthétique et leur utilisation
US4311838A (en)	1982-01-19	Tetrahydro-2-nitrimino-2H-1,3-thiazine
AU600847B2 (en)	1990-08-23	Stabilised pesticidal composition
US4308262A (en)	1981-12-29	Pyrethroid pesticidal compositions
US4424233A (en)	1984-01-03	Pyrethroid pesticidal composition
US4374833A (en)	1983-02-22	Pyrethroid pesticidal composition
US4346091A (en)	1982-08-24	Insecticidal combinations
US4346092A (en)	1982-08-24	Insecticidal combinations
US4188400A (en)	1980-02-12	Furylmethyloxime ethers
EP0013582A1 (fr)	1980-07-23	Compositions pesticides et leur utilisation
EP0002091B1 (fr)	1981-06-10	Méthode de lutte contre les organismes nuisibles de l'ordre des acariens au moyen d'esters d'acides cyclopropanecarboxyliques, l'utilisation de tels esters comme acaricides, et un de ces esters comme nouveau composé
EP0011893B1 (fr)	1982-06-09	Composition pesticide et procédé de lutte contre des parasites
US4175134A (en)	1979-11-20	Phenoxybenzyl ester pesticides
KR840000533B1 (ko)	1984-04-20	살충제 조성물
USRE31623E (en)	1984-07-03	Pesticidal cinnolines
KR840000837B1 (ko)	1984-06-19	살충성 조성물
GB2187385A (en)	1987-09-09	Method of combatting colorado beetles using chemical compounds and compositions containing the chemical compounds
GB2059771A (en)	1981-04-29	Pesticidal compositions
GB2059772A (en)	1981-04-29	Pesticidal compositions
DK159802B (da)	1990-12-10	Acaricidt praeparat