DE1695128A1 - Schaedlingsbekaempfungsmittel - Google Patents

Schaedlingsbekaempfungsmittel

Info

Publication number: DE1695128A1
Authority: DE; Germany
Prior art keywords: active ingredient; pesticides; dispersant; dimethyl; concentrate
Prior art date: 1965-01-11
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.): Pending

Application number

DE19661695128

Other languages

German (de)

English (en)

Inventor

Haubein Albert Howard

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.)

Hercules LLC

Original Assignee

Hercules LLC

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.)

1965-01-11

Filing date

1966-01-11

Publication date

1970-12-10

1966-01-11 Application filed by Hercules LLC filed Critical Hercules LLC

1970-12-10 Publication of DE1695128A1 publication Critical patent/DE1695128A1/de

Status Pending legal-status Critical Current

Links

241000607479 Yersinia pestis Species 0.000 title claims description 3
239000004480 active ingredient Substances 0.000 claims description 20
239000000839 emulsion Substances 0.000 claims description 17
239000012141 concentrate Substances 0.000 claims description 15
239000000575 pesticide Substances 0.000 claims description 15
239000004094 surface-active agent Substances 0.000 claims description 15
239000000654 additive Substances 0.000 claims description 9
230000000996 additive effect Effects 0.000 claims description 9
241000238631 Hexapoda Species 0.000 claims description 7
239000002270 dispersing agent Substances 0.000 claims description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
-1 1-succinimidoethyl Chemical group 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
238000000034 method Methods 0.000 claims description 5
239000003960 organic solvent Substances 0.000 claims description 5
239000002253 acid Substances 0.000 claims description 4
230000000749 insecticidal effect Effects 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
150000003863 ammonium salts Chemical class 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims description 2
238000002360 preparation method Methods 0.000 claims description 2
239000006185 dispersion Substances 0.000 claims 1
150000003839 salts Chemical class 0.000 claims 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
235000008504 concentrate Nutrition 0.000 description 14
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
230000000694 effects Effects 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000000428 dust Substances 0.000 description 6
235000014666 liquid concentrate Nutrition 0.000 description 6
239000003921 oil Substances 0.000 description 6
241000255925 Diptera Species 0.000 description 5
239000007788 liquid Substances 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
NAGJZTKCGNOGPW-UHFFFAOYSA-K dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [O-]P([O-])([S-])=S NAGJZTKCGNOGPW-UHFFFAOYSA-K 0.000 description 4
239000003208 petroleum Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
239000002917 insecticide Substances 0.000 description 3
230000005923 long-lasting effect Effects 0.000 description 3
239000000203 mixture Substances 0.000 description 3
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
229910001220 stainless steel Inorganic materials 0.000 description 2
239000010935 stainless steel Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
231100000331 toxic Toxicity 0.000 description 2
230000002588 toxic effect Effects 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
VOCDJQSAMZARGX-UHFFFAOYSA-N 1-ethenylpyrrolidine-2,5-dione Chemical compound C=CN1C(=O)CCC1=O VOCDJQSAMZARGX-UHFFFAOYSA-N 0.000 description 1
241000238876 Acari Species 0.000 description 1
244000045232 Canavalia ensiformis Species 0.000 description 1
229940126062 Compound A Drugs 0.000 description 1
241000532642 Conotrachelus nenuphar Species 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
101100117236 Drosophila melanogaster speck gene Proteins 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
241000462639 Epilachna varivestis Species 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
244000141359 Malus pumila Species 0.000 description 1
241000257226 Muscidae Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
235000010617 Phaseolus lunatus Nutrition 0.000 description 1
235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
235000011613 Pinus brutia Nutrition 0.000 description 1
241000018646 Pinus brutia Species 0.000 description 1
229920001213 Polysorbate 20 Polymers 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
241001454293 Tetranychus urticae Species 0.000 description 1
239000011149 active material Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
235000021016 apples Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 1
230000035622 drinking Effects 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000010687 lubricating oil Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000005416 organic matter Substances 0.000 description 1
150000002903 organophosphorus compounds Chemical class 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000002688 persistence Effects 0.000 description 1
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/5537—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom the heteroring containing the structure -C(=O)-N-C(=O)- (both carbon atoms belong to the heteroring)
- 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
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic 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)

DE19661695128 1965-01-11 1966-01-11 Schaedlingsbekaempfungsmittel Pending DE1695128A1 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US424843A US3316145A (en)	1965-01-11	1965-01-11	O, o-dimethyl s-(1-succinimidoethyl) phos-phorodithioate and insecticidal compositions containing the same

Publications (1)

Publication Number	Publication Date
DE1695128A1 true DE1695128A1 (de)	1970-12-10

Family

ID=23684094

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19661695128 Pending DE1695128A1 (de)	1965-01-11	1966-01-11	Schaedlingsbekaempfungsmittel

Country Status (10)

Country	Link
US (1)	US3316145A (pl)
BE (1)	BE674914A (pl)
CH (1)	CH453790A (pl)
DE (1)	DE1695128A1 (pl)
DK (1)	DK124411B (pl)
ES (1)	ES321588A1 (pl)
FR (1)	FR1469250A (pl)
GB (1)	GB1098548A (pl)
IL (1)	IL24877A (pl)
NL (1)	NL6600295A (pl)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE930446C (de) *	1953-02-09	1955-07-18	Bayer Ag	Verfahren zur Herstellung von Thiophosphorsaeureestern
BE547771A (pl) *	1955-05-13
CH388319A (de) *	1958-07-15	1965-02-28	Basf Ag	Verfahren zur Herstellung von O,O-Dialkyl-thiol- und O,O-Dialkyl-dithiophosphorsäureestern von N-alkylsubstituierten Laktamen und Thiolaktamen

1965
- 1965-01-11 US US424843A patent/US3316145A/en not_active Expired - Lifetime
- 1965-12-27 IL IL24877A patent/IL24877A/en unknown
1966
- 1966-01-05 GB GB556/66A patent/GB1098548A/en not_active Expired
- 1966-01-07 FR FR46803A patent/FR1469250A/fr not_active Expired
- 1966-01-10 NL NL6600295A patent/NL6600295A/xx unknown
- 1966-01-10 ES ES0321588A patent/ES321588A1/es not_active Expired
- 1966-01-10 BE BE674914D patent/BE674914A/xx unknown
- 1966-01-11 DK DK13966AA patent/DK124411B/da unknown
- 1966-01-11 DE DE19661695128 patent/DE1695128A1/de active Pending
- 1966-01-11 CH CH31166A patent/CH453790A/fr unknown

Also Published As

Publication number	Publication date
FR1469250A (fr)	1967-02-10
ES321588A1 (es)	1967-01-01
NL6600295A (pl)	1966-07-12
US3316145A (en)	1967-04-25
DK124411B (da)	1972-10-16
IL24877A (en)	1969-11-12
GB1098548A (en)	1968-01-10
BE674914A (pl)	1966-07-11
CH453790A (fr)	1968-03-31

Publication	Publication Date	Title
DE2603877C2 (de)	1985-03-07	Oxadiazolinonverbindungen, ihre Herstellung und sie enthaltendes Mittel
EP0446464A1 (de)	1991-09-18	Köder für Stubenfliegen
DE1208115B (de)	1965-12-30	Insektizide Mittel
DE3717467A1 (de)	1988-12-01	Biologisches insektizidspray
DE1089209B (de)	1960-09-15	Schaedlingsbekaempfungsmittel
DE1252962B (de)	1967-10-26	Insektizide Zubereitung
DE1493646A1 (de)	1969-11-06	Verfahren zur Herstellung von Cumarany-N-methylcarbaminsaeureestern
DE2730340A1 (de)	1978-02-02	Pestizide
DE1695128A1 (de)	1970-12-10	Schaedlingsbekaempfungsmittel
DE3513180A1 (de)	1985-10-24	Abwehrmittel gegen insekten, zecken und milben
DE1017848B (de)	1957-10-17	Insektizide Mittel
DE1147439B (de)	1963-04-18	Phosphorsaeureester als insektizide Mittel
DE1812762C3 (pl)	1978-05-03
DE2609704A1 (de)	1976-09-23	Thioamidverbindungen, verfahren zu ihrer herstellung und ihre verwendung zur schaedlingsbekaempfung
EP0005227B1 (de)	1981-04-29	Akarizide und insektizide Mittel sowie deren Verwendung zur Schädlingsbekämpfung
DE1277624B (de)	1968-09-12	Insenkticides und acaricides Mittel
DE1226363B (de)	1966-10-06	Alkylthiophosphonsaeurearylester enthaltende Insektizide
DE1200060B (de)	1965-09-02	Insektizides und acarizides Mittel
DE1642339C (de)	1972-08-24	Insektizide Mittel
DE1643996A1 (de)	1971-04-15	Verfahren zur Herstellung eines 3-Isopropyl-4-methylphenyl-N-methylcarbamats
AT253861B (de)	1967-04-25	Insektizide Mischung
DE2712333A1 (de)	1977-09-29	Dispirocyclopropancarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung zur schaedlingsbekaempfung
DE1668194A1 (de)	1971-07-22	Phenylcarbamate,insbesondere deren Verwendung als Schaedlingsbekaempfungsmittel
DE1910588A1 (de)	1970-09-17	N-Methyl-O-(2-aethylmercapto-methyl)-phenylcarbaminsaeureester,Verfahren zu seiner Herstellung sowie seine Verwendung als Insektizid
DE1493276C3 (de)	1974-01-17	Sulfitdiester, Verfahren zu deren Herstellung und ihrer Verwendung