GB799905A - Improvements in or relating to insecticidal composition - Google Patents
Improvements in or relating to insecticidal compositionInfo
- Publication number
- GB799905A GB799905A GB4555/56A GB455556A GB799905A GB 799905 A GB799905 A GB 799905A GB 4555/56 A GB4555/56 A GB 4555/56A GB 455556 A GB455556 A GB 455556A GB 799905 A GB799905 A GB 799905A
- Authority
- GB
- United Kingdom
- Prior art keywords
- weight
- per cent
- pyrethrins
- mixture
- petroleum ether
- 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 8
- 230000000749 insecticidal effect Effects 0.000 title abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 4
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 abstract 4
- 239000003208 petroleum Substances 0.000 abstract 4
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 abstract 4
- 229940070846 pyrethrins Drugs 0.000 abstract 4
- 239000002728 pyrethroid Substances 0.000 abstract 4
- 231100000167 toxic agent Toxicity 0.000 abstract 3
- 239000003440 toxic substance Substances 0.000 abstract 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 229940080817 rotenone Drugs 0.000 abstract 2
- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 abstract 2
- HBQPGVWPSQGTJK-TWELXNIESA-N (1s,4r)-1,2,2,3,3,4,7-heptachloro-5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptane Chemical compound ClC1[C@]2(Cl)C(C)(C)C(=C)[C@@]1(Cl)C(Cl)(Cl)C2(Cl)Cl HBQPGVWPSQGTJK-TWELXNIESA-N 0.000 abstract 1
- WRQROVPSTYSDFL-UHFFFAOYSA-N 1-methoxy-4-[2,2,2-tris(chloranyl)-1-(4-methoxyphenyl)ethyl]benzene Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1.C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 WRQROVPSTYSDFL-UHFFFAOYSA-N 0.000 abstract 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 abstract 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 abstract 1
- 241000238631 Hexapoda Species 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 abstract 1
- -1 aliphatic alcohols Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 abstract 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229960005235 piperonyl butoxide Drugs 0.000 abstract 1
- 239000003380 propellant Substances 0.000 abstract 1
- 150000003505 terpenes Chemical class 0.000 abstract 1
- 235000007586 terpenes Nutrition 0.000 abstract 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
An insecticidal composition adapted for use against house and garden insects by dispersing from a low-pressure system comprises at least about 5 per cent by weight of a toxicant, from 0.5 to 5 per cent by weight of pyrethrins, a synergist for the pyrethrins in the ratio of about 5 parts for each part of pyrethrins and the major proportion by weight of a volatile carrier consisting of a liquid boiling between 85 DEG and 200 DEG F., e.g. substituted or unsubstituted aliphatic hydrocarbons of less than 8 carbon atoms, aliphatic alcohols, ketones, ethers or simple aliphatic esters. An alternative composition comprises about 5 per cent by weight of a toxicant, from 0.25-1.75 per cent by weight of rotenone, from 0.5-5 per cent by weight of pyrethrins, together with a synergist and volatile carrier as in the composition above. Specified toxicants are methoxychlor (1,1,1-trichloro-2,2 bis [paramethoxyphenyl] ethane); "strobane," which is a mixture of chlorinated terpenes containing about 66 per cent chlorine; chlordane (octachlorodihydrocyclopentadiene), rotenone, DDT. Specified synergists are piperonyl butoxide [butyl carbitol] [6-propylpiperonly] ether. Specified carriers are petroleum ether, isopropanol, a mixture of petroleum ether and methylene chloride, or a mixture of petroleum ether, methylene chloride and isopropanol, methyl acetate, chloroform, a mixture of ethanol and petroleum ether. A propellant such as fluorotrichloromethane and dichlorodifluoromethane may also be incorporated.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US799905XA | 1955-02-18 | 1955-02-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB799905A true GB799905A (en) | 1958-08-13 |
Family
ID=22154090
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4555/56A Expired GB799905A (en) | 1955-02-18 | 1956-02-14 | Improvements in or relating to insecticidal composition |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB799905A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1285093B (en) * | 1966-07-01 | 1968-12-12 | Roehner Gottfried | Means for killing coccidial oocysts and worm eggs |
-
1956
- 1956-02-14 GB GB4555/56A patent/GB799905A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1285093B (en) * | 1966-07-01 | 1968-12-12 | Roehner Gottfried | Means for killing coccidial oocysts and worm eggs |
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