HU182802B - Fotostabil delousing (insecticide) composition containing synthetic piretroides - Google Patents
Fotostabil delousing (insecticide) composition containing synthetic piretroides Download PDFInfo
- Publication number
- HU182802B HU182802B HU80430A HU43080A HU182802B HU 182802 B HU182802 B HU 182802B HU 80430 A HU80430 A HU 80430A HU 43080 A HU43080 A HU 43080A HU 182802 B HU182802 B HU 182802B
- Authority
- HU
- Hungary
- Prior art keywords
- weight
- composition
- permethrin
- active ingredient
- castor oil
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 31
- 239000002917 insecticide Substances 0.000 title description 2
- 229960000490 permethrin Drugs 0.000 claims abstract description 26
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 claims abstract description 26
- QAQSNXHKHKONNS-UHFFFAOYSA-N 1-ethyl-2-hydroxy-4-methyl-6-oxopyridine-3-carboxamide Chemical compound CCN1C(O)=C(C(N)=O)C(C)=CC1=O QAQSNXHKHKONNS-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000004359 castor oil Substances 0.000 claims abstract description 14
- 235000019438 castor oil Nutrition 0.000 claims abstract description 14
- 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 abstract description 14
- 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 claims abstract description 14
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229960002483 decamethrin Drugs 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims abstract description 7
- 239000012153 distilled water Substances 0.000 claims abstract description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 23
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 17
- 235000019441 ethanol Nutrition 0.000 claims description 15
- 239000004480 active ingredient Substances 0.000 claims description 11
- 241001674048 Phthiraptera Species 0.000 claims description 6
- 239000002728 pyrethroid Substances 0.000 claims description 6
- -1 alcohol ester Chemical class 0.000 claims description 5
- VTJMSIIXXKNIDJ-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-methylbutyric acid Chemical compound CC(C)C(C(O)=O)C1=CC=C(Cl)C=C1 VTJMSIIXXKNIDJ-UHFFFAOYSA-N 0.000 claims description 2
- LLMLSUSAKZVFOA-UHFFFAOYSA-N 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(O)=O LLMLSUSAKZVFOA-UHFFFAOYSA-N 0.000 claims description 2
- MDIQXIJPQWLFSD-UHFFFAOYSA-N 3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Br)Br)C1C(O)=O MDIQXIJPQWLFSD-UHFFFAOYSA-N 0.000 claims 1
- 125000005909 ethyl alcohol group Chemical group 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000002304 perfume Substances 0.000 claims 1
- 210000004209 hair Anatomy 0.000 abstract description 17
- 230000000694 effects Effects 0.000 abstract description 16
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 abstract description 9
- 239000003205 fragrance Substances 0.000 abstract description 7
- DVBJBNKEBPCGSY-UHFFFAOYSA-M cetylpyridinium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 DVBJBNKEBPCGSY-UHFFFAOYSA-M 0.000 abstract description 6
- 230000002195 synergetic effect Effects 0.000 abstract description 3
- 239000000126 substance Substances 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract 3
- 239000003599 detergent Substances 0.000 abstract 2
- 235000015112 vegetable and seed oil Nutrition 0.000 abstract 2
- 239000008158 vegetable oil Substances 0.000 abstract 2
- 125000002091 cationic group Chemical group 0.000 abstract 1
- 230000001256 tonic effect Effects 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 6
- 239000006210 lotion Substances 0.000 description 5
- 241000255925 Diptera Species 0.000 description 4
- 206010040880 Skin irritation Diseases 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 230000036556 skin irritation Effects 0.000 description 4
- 231100000475 skin irritation Toxicity 0.000 description 4
- 230000004071 biological effect Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 238000003197 gene knockdown Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- ABFDKXBSQCTIKH-UHFFFAOYSA-M 1-ethylpyridin-1-ium;bromide Chemical compound [Br-].CC[N+]1=CC=CC=C1 ABFDKXBSQCTIKH-UHFFFAOYSA-M 0.000 description 2
- 206010015946 Eye irritation Diseases 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 231100000013 eye irritation Toxicity 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 230000002147 killing effect Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound 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 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 2
- 125000003003 spiro group Chemical group 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- ZEMPKEQAKRGZGQ-AAKVHIHISA-N 2,3-bis[[(z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (z)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCC(O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 241000238366 Cephalopoda Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 231100000111 LD50 Toxicity 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241000257159 Musca domestica Species 0.000 description 1
- 241000282339 Mustela Species 0.000 description 1
- 206010033799 Paralysis Diseases 0.000 description 1
- 241000517325 Pediculus Species 0.000 description 1
- 241000269978 Pleuronectiformes Species 0.000 description 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
- 208000035415 Reinfection Diseases 0.000 description 1
- 240000004460 Tanacetum coccineum Species 0.000 description 1
- 206010052428 Wound Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- ROVGZAWFACYCSP-MQBLHHJJSA-N [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 Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 description 1
- 230000037374 absorbed through the skin Effects 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000002009 allergenic effect Effects 0.000 description 1
- 230000000172 allergic effect Effects 0.000 description 1
- 239000012871 anti-fungal composition Substances 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Substances OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- NEUSVAOJNUQRTM-UHFFFAOYSA-N cetylpyridinium Chemical compound CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 NEUSVAOJNUQRTM-UHFFFAOYSA-N 0.000 description 1
- 229960004830 cetylpyridinium Drugs 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000008029 eradication Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 231100000640 hair analysis Toxicity 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 239000000321 herbal drug Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 210000003800 pharynx Anatomy 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- 229940048383 pyrethrum extract Drugs 0.000 description 1
- BBFCIBZLAVOLCF-UHFFFAOYSA-N pyridin-1-ium;bromide Chemical compound Br.C1=CC=NC=C1 BBFCIBZLAVOLCF-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/23—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
-
- 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)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Epidemiology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Emergency Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cosmetics (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU80430A HU182802B (en) | 1980-02-26 | 1980-02-26 | Fotostabil delousing (insecticide) composition containing synthetic piretroides |
| AT0073481A AT372244B (de) | 1980-02-26 | 1981-02-18 | Laeuse-vertilgungsmittel mit synergetischer wirkung und dessen verwendung |
| BE1/10146A BE887600A (fr) | 1980-02-26 | 1981-02-20 | Produit de destruction des poux |
| GB8105466A GB2072013B (en) | 1980-02-26 | 1981-02-20 | Louse-killing composition containing a pyrethroid |
| FR8103379A FR2476486A1 (fr) | 1980-02-26 | 1981-02-20 | Produit de destruction des poux |
| NL8100876A NL8100876A (nl) | 1980-02-26 | 1981-02-23 | Bestrijdingsmiddel tegen luizen. |
| DD81227835A DD156511A5 (de) | 1980-02-26 | 1981-02-24 | Laeusevernichtungsmittel |
| PL1981229837A PL125709B1 (en) | 1980-02-26 | 1981-02-24 | Agent fighting against louses |
| RO103518A RO81516B (ro) | 1980-02-26 | 1981-02-25 | Compozitie sinergetica pentru distrugerea paduchilor |
| CH1259/81A CH647650A5 (de) | 1980-02-26 | 1981-02-25 | Laeusevernichtungsmittel. |
| CS811351A CS226422B2 (en) | 1980-02-26 | 1981-02-25 | De-lousing composition |
| DE19813107129 DE3107129A1 (de) | 1980-02-26 | 1981-02-26 | Insektizide, insbesondere laeusevernichtungsmittel, und deren verwendung |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU80430A HU182802B (en) | 1980-02-26 | 1980-02-26 | Fotostabil delousing (insecticide) composition containing synthetic piretroides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU182802B true HU182802B (en) | 1984-03-28 |
Family
ID=10949564
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU80430A HU182802B (en) | 1980-02-26 | 1980-02-26 | Fotostabil delousing (insecticide) composition containing synthetic piretroides |
Country Status (12)
| Country | Link |
|---|---|
| AT (1) | AT372244B (cs) |
| BE (1) | BE887600A (cs) |
| CH (1) | CH647650A5 (cs) |
| CS (1) | CS226422B2 (cs) |
| DD (1) | DD156511A5 (cs) |
| DE (1) | DE3107129A1 (cs) |
| FR (1) | FR2476486A1 (cs) |
| GB (1) | GB2072013B (cs) |
| HU (1) | HU182802B (cs) |
| NL (1) | NL8100876A (cs) |
| PL (1) | PL125709B1 (cs) |
| RO (1) | RO81516B (cs) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3208334A1 (de) * | 1982-03-09 | 1983-09-15 | Bayer Ag, 5090 Leverkusen | Pestizide pour-on-formulierungen |
| DE3208333A1 (de) * | 1982-03-09 | 1983-09-15 | Bayer Ag, 5090 Leverkusen | Pestizide formulierungen |
| DE3478397D1 (en) * | 1983-03-31 | 1989-07-06 | T & R Chemicals Inc | Pyrethroid-containing pharmaceutical compositions |
| AU596867B2 (en) * | 1986-09-29 | 1990-05-17 | Del Laboratories, Inc. | Pediculicidal/ovicidal shampoo composition |
| DE19528529A1 (de) * | 1995-08-03 | 1997-02-06 | Bayer Ag | Schädlingsbekämpfungsmittel |
| CN115968876B (zh) * | 2023-01-12 | 2024-11-22 | 中山榄菊日化实业有限公司 | 一种长效杀虫的超低容量液剂及其制备方法 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB660131A (en) * | 1947-09-18 | 1951-10-31 | Mckesson & Robbins Inc | Parasiticidal lotions |
| US3492402A (en) * | 1967-02-01 | 1970-01-27 | Mclaughlin Gormley King Co | Pyrethroid insecticidal compositions containing an emulsifier and a bacterio-fungistat |
| US3864388A (en) * | 1970-12-29 | 1975-02-04 | Sumitomo Chemical Co | Alkynyl esters of {60 -alkoxy-{60 -phenyl alkenoic acid |
| GB1511646A (en) * | 1974-05-08 | 1978-05-24 | Wellcome Found | Method for insecticide use |
| US3966959A (en) * | 1975-02-13 | 1976-06-29 | American Cyanamid Company | Insecticidal and acaricidal, pyrethroid compounds |
| FR2341307A1 (fr) * | 1976-02-19 | 1977-09-16 | Roussel Uclaf | Pyrethrinoides a titre de medicaments et compositions pharmaceutiques les renfermant |
| GB1574609A (en) * | 1976-07-06 | 1980-09-10 | Inchcape Chemco Ltd | Pesticidal compositions |
| SE441179B (sv) * | 1976-09-21 | 1985-09-16 | Roussel Uclaf | Nya cyklopropankarboxylsyror med polyhalogenerad substituent, sett for framstellning derav samt anvendning derav i pesticidkompositioner |
| GB1591105A (en) * | 1976-12-24 | 1981-06-17 | Wellcome Found | Pest control |
| GB1591106A (en) * | 1976-12-24 | 1981-06-17 | Wellcome Found | Pest control |
| FR2377198A2 (fr) * | 1977-01-13 | 1978-08-11 | Roussel Uclaf | Pyrethrinoides a titre de medicaments et compositions pharmaceutiques les renfermant |
| DE2704066A1 (de) * | 1977-02-01 | 1978-08-03 | Neudorff & Co Chem Fab W | Insektizidgemisch |
| GB1602971A (en) * | 1977-03-11 | 1981-11-18 | Wellcome Found | Synergistic pesticidal compositions |
| GB2012585B (en) * | 1977-12-20 | 1982-04-15 | Ici Ltd | Insecticidal formulations |
| GB2021416A (en) * | 1978-05-16 | 1979-12-05 | Wellcome Found | Pest control |
| EP0006630A1 (de) * | 1978-07-03 | 1980-01-09 | Ciba-Geigy Ag | Alpha-phenyl-alpha-cyclopropylacetate, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung |
| DE2844271A1 (de) * | 1978-10-11 | 1980-04-24 | Bayer Ag | 3-chlorostyryl-2,2-dimethyl-cyclopropancarbonsaeure-(4-fluoro-3-phenoxy- alpha -cyano-benzyl)-ester, verfahren zu ihrer herstellung und ihre verwendung als ektoparasitizide |
| FR2484256B1 (fr) * | 1979-06-29 | 1986-10-24 | Roussel Uclaf | Procede de lutte contre les parasites des animaux a sang chaud |
| IT1123122B (it) * | 1979-09-12 | 1986-04-30 | Montedison Spa | Composizioni liquide insetticide contenenti piretroidi sintetici |
-
1980
- 1980-02-26 HU HU80430A patent/HU182802B/hu unknown
-
1981
- 1981-02-18 AT AT0073481A patent/AT372244B/de not_active IP Right Cessation
- 1981-02-20 GB GB8105466A patent/GB2072013B/en not_active Expired
- 1981-02-20 BE BE1/10146A patent/BE887600A/fr not_active IP Right Cessation
- 1981-02-20 FR FR8103379A patent/FR2476486A1/fr active Granted
- 1981-02-23 NL NL8100876A patent/NL8100876A/nl not_active Application Discontinuation
- 1981-02-24 DD DD81227835A patent/DD156511A5/de not_active IP Right Cessation
- 1981-02-24 PL PL1981229837A patent/PL125709B1/pl unknown
- 1981-02-25 RO RO103518A patent/RO81516B/ro unknown
- 1981-02-25 CH CH1259/81A patent/CH647650A5/de not_active IP Right Cessation
- 1981-02-25 CS CS811351A patent/CS226422B2/cs unknown
- 1981-02-26 DE DE19813107129 patent/DE3107129A1/de not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| GB2072013B (en) | 1984-11-07 |
| DD156511A5 (de) | 1982-09-01 |
| CS226422B2 (en) | 1984-03-19 |
| DE3107129A1 (de) | 1981-12-24 |
| NL8100876A (nl) | 1981-09-16 |
| PL229837A1 (cs) | 1981-11-13 |
| ATA73481A (de) | 1983-02-15 |
| BE887600A (fr) | 1981-08-20 |
| FR2476486A1 (fr) | 1981-08-28 |
| GB2072013A (en) | 1981-09-30 |
| AT372244B (de) | 1983-09-12 |
| PL125709B1 (en) | 1983-06-30 |
| FR2476486B1 (cs) | 1984-11-23 |
| RO81516B (ro) | 1983-04-30 |
| CH647650A5 (de) | 1985-02-15 |
| RO81516A (ro) | 1983-04-29 |
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| HU90 | Patent valid on 900628 |