CH619350A5 - Insecticidal preparation - Google Patents
Insecticidal preparation Download PDFInfo
- Publication number
- CH619350A5 CH619350A5 CH1098676A CH1098676A CH619350A5 CH 619350 A5 CH619350 A5 CH 619350A5 CH 1098676 A CH1098676 A CH 1098676A CH 1098676 A CH1098676 A CH 1098676A CH 619350 A5 CH619350 A5 CH 619350A5
- Authority
- CH
- Switzerland
- Prior art keywords
- connection
- insecticide
- activation factor
- activator
- insecticidal
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title description 19
- 230000000749 insecticidal effect Effects 0.000 title description 13
- 239000002917 insecticide Substances 0.000 description 50
- 230000004913 activation Effects 0.000 description 48
- 239000012190 activator Substances 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 14
- 239000004480 active ingredient Substances 0.000 description 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000013543 active substance Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 230000000361 pesticidal effect Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 241000567412 Estigmene acrea Species 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 4
- -1 mercaptomethyl Chemical group 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 241000255925 Diptera Species 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- 241000238631 Hexapoda Species 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 240000008415 Lactuca sativa Species 0.000 description 2
- 235000003228 Lactuca sativa Nutrition 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 2
- 241000255993 Trichoplusia ni Species 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 241001425390 Aphis fabae Species 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 241000219198 Brassica Species 0.000 description 1
- 235000011331 Brassica Nutrition 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- 241000256244 Heliothis virescens Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- STECJAGHUSJQJN-USLFZFAMSA-N LSM-4015 Chemical compound C1([C@@H](CO)C(=O)OC2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-USLFZFAMSA-N 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- 241000257159 Musca domestica Species 0.000 description 1
- 240000005407 Nasturtium officinale Species 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 240000007113 Rumex obtusifolius Species 0.000 description 1
- 235000009422 Rumex obtusifolius Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241000256248 Spodoptera Species 0.000 description 1
- 241000256247 Spodoptera exigua Species 0.000 description 1
- 241000985245 Spodoptera litura Species 0.000 description 1
- 241000208241 Tropaeolum Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- UJTMLNARSPORHR-UHFFFAOYSA-N oc2h5 Chemical compound C=C=[O+] UJTMLNARSPORHR-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 125000003884 phenylalkyl group Chemical group 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- NESLWCLHZZISNB-UHFFFAOYSA-M sodium phenolate Chemical compound [Na+].[O-]C1=CC=CC=C1 NESLWCLHZZISNB-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/18—Esters of thiophosphoric acids with hydroxyaryl compounds
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/14—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Biochemistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US05/609,865 US4004001A (en) | 1974-01-14 | 1975-09-02 | Phosphorus containing insecticide activators |
Publications (1)
Publication Number | Publication Date |
---|---|
CH619350A5 true CH619350A5 (en) | 1980-09-30 |
Family
ID=24442667
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH1098676A CH619350A5 (en) | 1975-09-02 | 1976-08-30 | Insecticidal preparation |
Country Status (21)
Country | Link |
---|---|
JP (1) | JPS5239628A (nl) |
AR (1) | AR216447A1 (nl) |
BE (1) | BE845794A (nl) |
BR (1) | BR7605696A (nl) |
CA (1) | CA1081615A (nl) |
CH (1) | CH619350A5 (nl) |
CS (1) | CS189029B2 (nl) |
DD (1) | DD126876A5 (nl) |
DE (1) | DE2639408A1 (nl) |
DK (1) | DK379176A (nl) |
ES (1) | ES451163A1 (nl) |
FR (1) | FR2322869A1 (nl) |
GR (1) | GR63183B (nl) |
HU (1) | HU178722B (nl) |
IN (1) | IN142443B (nl) |
NL (1) | NL7609670A (nl) |
PH (1) | PH11361A (nl) |
PL (1) | PL100062B1 (nl) |
PT (1) | PT65540B (nl) |
RO (1) | RO70090A (nl) |
SU (1) | SU803846A3 (nl) |
-
1976
- 1976-08-23 IN IN1539/CAL/76A patent/IN142443B/en unknown
- 1976-08-23 DK DK379176A patent/DK379176A/da not_active Application Discontinuation
- 1976-08-24 JP JP51101029A patent/JPS5239628A/ja active Pending
- 1976-08-26 CA CA259,917A patent/CA1081615A/en not_active Expired
- 1976-08-26 CS CS765547A patent/CS189029B2/cs unknown
- 1976-08-27 RO RO7687383A patent/RO70090A/ro unknown
- 1976-08-27 AR AR264494A patent/AR216447A1/es active
- 1976-08-27 HU HU76SA2967A patent/HU178722B/hu unknown
- 1976-08-30 CH CH1098676A patent/CH619350A5/de not_active IP Right Cessation
- 1976-08-30 BR BR7605696A patent/BR7605696A/pt unknown
- 1976-08-31 NL NL7609670A patent/NL7609670A/nl not_active Application Discontinuation
- 1976-08-31 PH PH18851A patent/PH11361A/en unknown
- 1976-08-31 PT PT65540A patent/PT65540B/pt unknown
- 1976-08-31 DD DD194539A patent/DD126876A5/xx unknown
- 1976-09-01 DE DE19762639408 patent/DE2639408A1/de not_active Withdrawn
- 1976-09-01 FR FR7626354A patent/FR2322869A1/fr active Granted
- 1976-09-01 GR GR51595A patent/GR63183B/el unknown
- 1976-09-02 ES ES451163A patent/ES451163A1/es not_active Expired
- 1976-09-02 BE BE7000877A patent/BE845794A/nl unknown
- 1976-09-02 PL PL1976192162A patent/PL100062B1/pl unknown
- 1976-09-02 SU SU762393508A patent/SU803846A3/ru active
Also Published As
Publication number | Publication date |
---|---|
DD126876A5 (nl) | 1977-08-17 |
PH11361A (en) | 1977-11-02 |
CS189029B2 (en) | 1979-03-30 |
FR2322869B1 (nl) | 1980-11-07 |
CA1081615A (en) | 1980-07-15 |
BR7605696A (pt) | 1977-08-23 |
NL7609670A (nl) | 1977-03-04 |
IN142443B (nl) | 1977-07-09 |
JPS5239628A (en) | 1977-03-28 |
DE2639408A1 (de) | 1977-03-10 |
DK379176A (da) | 1977-03-03 |
PT65540B (en) | 1978-02-22 |
GR63183B (en) | 1979-10-03 |
RO70090A (ro) | 1982-09-09 |
BE845794A (nl) | 1977-03-02 |
AR216447A1 (es) | 1979-12-28 |
HU178722B (en) | 1982-06-28 |
PL100062B1 (pl) | 1978-08-31 |
PT65540A (en) | 1976-09-01 |
ES451163A1 (es) | 1977-09-01 |
FR2322869A1 (fr) | 1977-04-01 |
SU803846A3 (ru) | 1981-02-07 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PL | Patent ceased |