GB979888A - Improvements in or relating to insecticidal compositions - Google Patents
Improvements in or relating to insecticidal compositionsInfo
- Publication number
- GB979888A GB979888A GB22895/62A GB2289562A GB979888A GB 979888 A GB979888 A GB 979888A GB 22895/62 A GB22895/62 A GB 22895/62A GB 2289562 A GB2289562 A GB 2289562A GB 979888 A GB979888 A GB 979888A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- alkyl group
- aryl
- aralkyl
- phosphate
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title abstract 4
- 230000000749 insecticidal effect Effects 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 5
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 abstract 4
- 229910019142 PO4 Inorganic materials 0.000 abstract 3
- 229960003742 phenol Drugs 0.000 abstract 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 3
- 239000010452 phosphate Substances 0.000 abstract 3
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 abstract 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 abstract 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 abstract 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 abstract 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 2
- BEWYHVAWEKZDPP-UHFFFAOYSA-N bornane Chemical compound C1CC2(C)CCC1C2(C)C BEWYHVAWEKZDPP-UHFFFAOYSA-N 0.000 abstract 2
- CRPUJAZIXJMDBK-UHFFFAOYSA-N camphene Chemical compound C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 abstract 2
- -1 carbocyclic organic compound Chemical class 0.000 abstract 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 239000002917 insecticide Substances 0.000 abstract 2
- LPNBBFKOUUSUDB-UHFFFAOYSA-N p-toluic acid Chemical compound CC1=CC=C(C(O)=O)C=C1 LPNBBFKOUUSUDB-UHFFFAOYSA-N 0.000 abstract 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 abstract 2
- 229940079877 pyrogallol Drugs 0.000 abstract 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- DWCLZPVTOUGAER-UHFFFAOYSA-N (1,2-dibromo-2,2-dichloroethyl) dihydrogen phosphate Chemical compound OP(O)(=O)OC(Br)C(Cl)(Cl)Br DWCLZPVTOUGAER-UHFFFAOYSA-N 0.000 abstract 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 abstract 1
- GBDZXPJXOMHESU-UHFFFAOYSA-N 1,2,3,4-tetrachlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1Cl GBDZXPJXOMHESU-UHFFFAOYSA-N 0.000 abstract 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 abstract 1
- ZBQZXTBAGBTUAD-UHFFFAOYSA-N 1,5-dichloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1Cl ZBQZXTBAGBTUAD-UHFFFAOYSA-N 0.000 abstract 1
- CEDZMDSZTVUPSP-UHFFFAOYSA-N 1,6-dichloronaphthalene Chemical compound ClC1=CC=CC2=CC(Cl)=CC=C21 CEDZMDSZTVUPSP-UHFFFAOYSA-N 0.000 abstract 1
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 abstract 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 abstract 1
- NJQADTYRAYFBJN-UHFFFAOYSA-N 2-bromo-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical compound C1CC2(C)C(=O)C(Br)C1C2(C)C NJQADTYRAYFBJN-UHFFFAOYSA-N 0.000 abstract 1
- APSMUYYLXZULMS-UHFFFAOYSA-N 2-bromonaphthalene Chemical compound C1=CC=CC2=CC(Br)=CC=C21 APSMUYYLXZULMS-UHFFFAOYSA-N 0.000 abstract 1
- CGYGETOMCSJHJU-UHFFFAOYSA-N 2-chloronaphthalene Chemical compound C1=CC=CC2=CC(Cl)=CC=C21 CGYGETOMCSJHJU-UHFFFAOYSA-N 0.000 abstract 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 abstract 1
- 239000005711 Benzoic acid Substances 0.000 abstract 1
- 229930185605 Bisphenol Natural products 0.000 abstract 1
- 241000723346 Cinnamomum camphora Species 0.000 abstract 1
- UIOFUWFRIANQPC-JKIFEVAISA-N Floxacillin Chemical compound N([C@@H]1C(N2[C@H](C(C)(C)S[C@@H]21)C(O)=O)=O)C(=O)C1=C(C)ON=C1C1=C(F)C=CC=C1Cl UIOFUWFRIANQPC-JKIFEVAISA-N 0.000 abstract 1
- XETQTCAMTVHYPO-UHFFFAOYSA-N Isocamphan von ungewisser Konfiguration Natural products C1CC2C(C)(C)C(C)C1C2 XETQTCAMTVHYPO-UHFFFAOYSA-N 0.000 abstract 1
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 abstract 1
- PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 abstract 1
- LUSZGTFNYDARNI-UHFFFAOYSA-N Sesamol Natural products OC1=CC=C2OCOC2=C1 LUSZGTFNYDARNI-UHFFFAOYSA-N 0.000 abstract 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003368 amide group Chemical group 0.000 abstract 1
- 235000010233 benzoic acid Nutrition 0.000 abstract 1
- 229950011260 betanaphthol Drugs 0.000 abstract 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract 1
- 229930006742 bornane Natural products 0.000 abstract 1
- 229930006739 camphene Natural products 0.000 abstract 1
- ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 abstract 1
- 229930008380 camphor Natural products 0.000 abstract 1
- 229960000846 camphor Drugs 0.000 abstract 1
- 125000005111 carboxyalkoxy group Chemical group 0.000 abstract 1
- 239000002781 deodorant agent Substances 0.000 abstract 1
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical class COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 abstract 1
- 150000005171 halobenzenes Chemical class 0.000 abstract 1
- 230000026030 halogenation Effects 0.000 abstract 1
- 238000005658 halogenation reaction Methods 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052753 mercury Inorganic materials 0.000 abstract 1
- AFZFXRLFDQLEAL-UHFFFAOYSA-N methyl 3-phosphonooxybut-2-enoate Chemical compound COC(=O)C=C(C)OP(O)(O)=O AFZFXRLFDQLEAL-UHFFFAOYSA-N 0.000 abstract 1
- CEOCDNVZRAIOQZ-UHFFFAOYSA-N pentachlorobenzene Chemical compound ClC1=CC(Cl)=C(Cl)C(Cl)=C1Cl CEOCDNVZRAIOQZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000008379 phenol ethers Chemical class 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 abstract 1
- 229960001553 phloroglucinol Drugs 0.000 abstract 1
- 239000004014 plasticizer Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 229940075579 propyl gallate Drugs 0.000 abstract 1
- 235000010388 propyl gallate Nutrition 0.000 abstract 1
- 239000000473 propyl gallate Substances 0.000 abstract 1
- 229960001755 resorcinol Drugs 0.000 abstract 1
- 229930003799 tocopherol Natural products 0.000 abstract 1
- 239000011732 tocopherol Substances 0.000 abstract 1
- 235000019149 tocopherols Nutrition 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 abstract 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
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/113—Esters of phosphoric acids with unsaturated acyclic alcohols
-
- 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
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 |
|---|---|---|---|
| US11766661A | 1961-06-16 | 1961-06-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB979888A true GB979888A (en) | 1965-01-06 |
Family
ID=22374155
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB22895/62A Expired GB979888A (en) | 1961-06-16 | 1962-06-14 | Improvements in or relating to insecticidal compositions |
Country Status (8)
| Country | Link |
|---|---|
| BE (1) | BE618972A (ja) |
| CH (1) | CH442860A (ja) |
| DE (1) | DE1567076A1 (ja) |
| ES (1) | ES278297A1 (ja) |
| FR (1) | FR1332161A (ja) |
| GB (1) | GB979888A (ja) |
| NL (1) | NL279704A (ja) |
| OA (1) | OA00415A (ja) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1258155A (ja) * | 1969-05-28 | 1971-12-22 | ||
| FR2092898A1 (en) * | 1970-06-29 | 1972-01-28 | Aries Robert | Sustained release pesticides - esp volatile phosphorus pesticide absorbed in a carrier block together with release rate controlling ag |
| JPS50126838A (ja) * | 1974-01-17 | 1975-10-06 | ||
| US4233161A (en) * | 1976-12-25 | 1980-11-11 | Idemitsu Kosan Company Limited | Sublimable composition |
-
0
- FR FR1332161D patent/FR1332161A/fr not_active Expired
- BE BE618972D patent/BE618972A/xx unknown
- NL NL279704D patent/NL279704A/xx unknown
-
1962
- 1962-06-14 CH CH713562A patent/CH442860A/de unknown
- 1962-06-14 DE DE19621567076 patent/DE1567076A1/de not_active Withdrawn
- 1962-06-14 ES ES278297A patent/ES278297A1/es not_active Expired
- 1962-06-14 GB GB22895/62A patent/GB979888A/en not_active Expired
-
1964
- 1964-10-28 OA OA50492A patent/OA00415A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH442860A (de) | 1967-08-31 |
| BE618972A (ja) | |
| DE1567076A1 (de) | 1970-07-30 |
| ES278297A1 (es) | 1962-12-01 |
| NL279704A (ja) | |
| OA00415A (fr) | 1966-05-15 |
| FR1332161A (ja) | 1963-12-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4015017A (en) | Certain biphenyl derivatives used to treat disorders caused by increased capillary permeability | |
| CA1051459A (en) | Halogenated 4-trifluoromethyl-4'-nitro-diphenyl-ethers, process for their preparation, and their use as herbicides | |
| GB979888A (en) | Improvements in or relating to insecticidal compositions | |
| GB1058309A (en) | Improvements in or relating to cyclopropane carboxylic acid esters | |
| SE8303013L (sv) | B-gamma-dihydropolyprenylalkoholderivat och farmaceutisk komposition innehallande en polyprenylforening | |
| Bordwell et al. | Enhancement of the equilibrium acidities of carbon acids by polyfluoroaryl substituents | |
| US3364105A (en) | Vapour emissive compositions containing dimethyl dichlorovinyl phosphate | |
| CA1055041A (en) | Ketone derivatives | |
| US3683005A (en) | Cyclopropanecarboxylic acid esters | |
| CA1201127A (en) | Biphenylylpropionic acid derivative, process for preparing the same and pharmaceutical composition containing the same | |
| Sundstrom | Metabolic hydroxylation of the aromatic rings of 1, 1-dichloro-2, 2-bis (4-chlorophenyl) ethylene (p, p'-DDE) by the rat | |
| ES2091957T3 (es) | Compuestos de fenona, procedimiento para su preparacion y preparaciones farmaceuticas que los contienen. | |
| Meltzer et al. | 3-(Alkoxyphenoxy)-1, 2-propanediols | |
| GB2161163A (en) | Insecticidally active phenylacetic acid ester derivatives | |
| Stephenson et al. | 67. Chemical investigations of the insecticide “DDT” and its analogues. Part II. Symmetrical analogues | |
| US3806602A (en) | Inhalant analgesic and anesthetic method and composition | |
| Gilman et al. | Use of the Halogen—Metal Interconversion Reaction for the Preparation of an Aromatic Iodo Compound | |
| Hatch et al. | Allylic Chlorides. XI. Cuprous Chloride Catalyzed Hydrolysis of Several Allylic Chlorides1 | |
| US3213127A (en) | Cyclooctyl trichloroacetate | |
| Cristol et al. | Isolation of the o, o'-DDT Isomer from Technical DDT1, 2 | |
| GB938815A (en) | Iodine-containing benzoic acid derivatives | |
| BR112018015378B1 (pt) | Líquido aquoso para controle de pragas compreendendo compostos piretróides e método para controle de pragas compreendendo a vaporização do mesmo | |
| US3257471A (en) | Ddt derivatives | |
| US3723467A (en) | Sesamolyl ethers and thioethers | |
| US4118424A (en) | Biodegradable insecticides |