GB638662A - Combating acarida, and more especially compositions for use therein - Google Patents
Combating acarida, and more especially compositions for use thereinInfo
- Publication number
- GB638662A GB638662A GB2241546A GB2241546A GB638662A GB 638662 A GB638662 A GB 638662A GB 2241546 A GB2241546 A GB 2241546A GB 2241546 A GB2241546 A GB 2241546A GB 638662 A GB638662 A GB 638662A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethyl
- acid
- methyl
- active
- carrier
- 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 3
- 241000238876 Acari Species 0.000 title 1
- -1 bole Chemical compound 0.000 abstract 9
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 4
- 239000003925 fat Substances 0.000 abstract 4
- 239000000194 fatty acid Substances 0.000 abstract 4
- 229930195729 fatty acid Natural products 0.000 abstract 4
- 239000007787 solid Substances 0.000 abstract 4
- 239000013543 active substance Substances 0.000 abstract 3
- 239000000969 carrier Substances 0.000 abstract 3
- 239000003995 emulsifying agent Substances 0.000 abstract 3
- 238000002360 preparation method Methods 0.000 abstract 3
- 239000000344 soap Substances 0.000 abstract 3
- 239000002904 solvent Substances 0.000 abstract 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- 235000004443 Ricinus communis Nutrition 0.000 abstract 2
- 230000000895 acaricidal effect Effects 0.000 abstract 2
- 239000004480 active ingredient Substances 0.000 abstract 2
- 239000011149 active material Substances 0.000 abstract 2
- 230000000844 anti-bacterial effect Effects 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 abstract 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 abstract 2
- 239000002270 dispersing agent Substances 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 150000004665 fatty acids Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- 150000002790 naphthalenes Chemical class 0.000 abstract 2
- 239000003921 oil Substances 0.000 abstract 2
- 235000019198 oils Nutrition 0.000 abstract 2
- 239000002674 ointment Substances 0.000 abstract 2
- 235000019271 petrolatum Nutrition 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- 239000000454 talc Substances 0.000 abstract 2
- 235000012222 talc Nutrition 0.000 abstract 2
- 229910052623 talc Inorganic materials 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 abstract 2
- 235000013311 vegetables Nutrition 0.000 abstract 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 abstract 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 abstract 1
- XWTUFPFWNHRJNF-UHFFFAOYSA-N 1,2-dimethylthianthrene Chemical compound C1=CC=C2SC3=C(C)C(C)=CC=C3SC2=C1 XWTUFPFWNHRJNF-UHFFFAOYSA-N 0.000 abstract 1
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 abstract 1
- NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 abstract 1
- COSYXLHTXXMVGM-UHFFFAOYSA-N 2-butyl-4-chlorophenol Chemical compound CCCCC1=CC(Cl)=CC=C1O COSYXLHTXXMVGM-UHFFFAOYSA-N 0.000 abstract 1
- MVRPPTGLVPEMPI-UHFFFAOYSA-N 2-cyclohexylphenol Chemical compound OC1=CC=CC=C1C1CCCCC1 MVRPPTGLVPEMPI-UHFFFAOYSA-N 0.000 abstract 1
- YYPNJNDODFVZLE-UHFFFAOYSA-N 3-methylbut-2-enoic acid Chemical compound CC(C)=CC(O)=O YYPNJNDODFVZLE-UHFFFAOYSA-N 0.000 abstract 1
- CFKMVGJGLGKFKI-UHFFFAOYSA-N 4-chloro-m-cresol Chemical compound CC1=CC(O)=CC=C1Cl CFKMVGJGLGKFKI-UHFFFAOYSA-N 0.000 abstract 1
- 239000005995 Aluminium silicate Substances 0.000 abstract 1
- VVZBFOKBSDGVGZ-UHFFFAOYSA-N BENZALKONIUM Chemical compound CCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 VVZBFOKBSDGVGZ-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 239000005749 Copper compound Substances 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 241000282414 Homo sapiens Species 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 abstract 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 240000007817 Olea europaea Species 0.000 abstract 1
- 239000005662 Paraffin oil Substances 0.000 abstract 1
- 244000000231 Sesamum indicum Species 0.000 abstract 1
- 235000003434 Sesamum indicum Nutrition 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract 1
- 229920002472 Starch Polymers 0.000 abstract 1
- 235000021355 Stearic acid Nutrition 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 239000000642 acaricide Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 239000000443 aerosol Substances 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
- 235000012211 aluminium silicate Nutrition 0.000 abstract 1
- SMYKVLBUSSNXMV-UHFFFAOYSA-K aluminum;trihydroxide;hydrate Chemical compound O.[OH-].[OH-].[OH-].[Al+3] SMYKVLBUSSNXMV-UHFFFAOYSA-K 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 150000003931 anilides Chemical class 0.000 abstract 1
- 239000000440 bentonite Substances 0.000 abstract 1
- 229910000278 bentonite Inorganic materials 0.000 abstract 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 abstract 1
- 229960002903 benzyl benzoate Drugs 0.000 abstract 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 abstract 1
- 239000004327 boric acid Substances 0.000 abstract 1
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract 1
- 235000010216 calcium carbonate Nutrition 0.000 abstract 1
- 239000001506 calcium phosphate Substances 0.000 abstract 1
- 239000010624 camphor oil Substances 0.000 abstract 1
- 239000005018 casein Substances 0.000 abstract 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 1
- 235000021240 caseins Nutrition 0.000 abstract 1
- 239000004359 castor oil Substances 0.000 abstract 1
- 229920003086 cellulose ether Polymers 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000007859 condensation product Substances 0.000 abstract 1
- 150000001880 copper compounds Chemical class 0.000 abstract 1
- 239000007799 cork Substances 0.000 abstract 1
- 239000006071 cream Substances 0.000 abstract 1
- 239000007857 degradation product Substances 0.000 abstract 1
- 239000000645 desinfectant Substances 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 230000001804 emulsifying effect Effects 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 235000013861 fat-free Nutrition 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 239000003292 glue Chemical class 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000008101 lactose Substances 0.000 abstract 1
- 229940100892 mercury compound Drugs 0.000 abstract 1
- 150000002731 mercury compounds Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 150000005002 naphthylamines Chemical class 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 1
- 239000004006 olive oil Substances 0.000 abstract 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 239000006072 paste Substances 0.000 abstract 1
- 239000002304 perfume Substances 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical compound N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 abstract 1
- 229920006391 phthalonitrile polymer Polymers 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 abstract 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical class C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 abstract 1
- 239000011347 resin Chemical class 0.000 abstract 1
- 229920005989 resin Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000008159 sesame oil Substances 0.000 abstract 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 abstract 1
- 239000008107 starch Substances 0.000 abstract 1
- 235000019698 starch Nutrition 0.000 abstract 1
- 239000008117 stearic acid Substances 0.000 abstract 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 abstract 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 abstract 1
- 229940078499 tricalcium phosphate Drugs 0.000 abstract 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 abstract 1
- 235000019731 tricalcium phosphate Nutrition 0.000 abstract 1
- UAXOELSVPTZZQG-UHFFFAOYSA-N trimethyl acrylic acid Chemical class CC(C)=C(C)C(O)=O UAXOELSVPTZZQG-UHFFFAOYSA-N 0.000 abstract 1
- 235000015112 vegetable and seed oil Nutrition 0.000 abstract 1
- 239000008158 vegetable oil Substances 0.000 abstract 1
- 239000001993 wax Substances 0.000 abstract 1
- 238000009736 wetting Methods 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Acaricidal and disinfectant compositions for treating pests on plants, animals and human beings comprise an active ingredient of general formula <FORM:0638662/VI/1> where R1 and R2 represent hydrogen or a methyl group; R3 represents hydrogen or an alkyl group, R4 represents a phenyl radical, substituted if desired, with non-salt-forming groups, alone or with other effective substances, in admixture with at least one inert solid, or semi-solid, or not easily inflammable liquid, diluent or carrier, characterized in that the said active ingredient is finely divided, the particle size being below 300 microns. Such amides are prepared by the methods disclosed in Specification 615,137, [Group IV (b)]. For the preparation of dusts the active agent and the carrier, either separately or in admixture, may be milled to the required degree or the finely ground carrier may be impregnated with a solution of the active material in a volatile solvent which is subsequently removed. Fine dispersions are also obtained by emulsifying the active agent or a solution thereof. Aerosols are produced by dissolving in an inert carrier such as difluodichloro-methane which boils below room temperature at atmospheric pressures. The inert solid carriers comprise materials of inorganic or vegetable nature, e.g., tricalcium phosphate, calcium carbonate, kaolin, bole, bentonite, talcum, calcined magnesia, kieselguhr, boric acid, powdered cork and powdered wood, which may be employed in admixture with wetting or dispersing agents. Inert liquids comprise oils of vegetable origin, e.g., castor and solvents such as carbon tetrachloride, ethylene dichloride, tetrachlorethane, hydrogenated naphthalenes, alkylated naphthalenes, solvent naphtha and the like. Dispersing or emulsifying agents comprise natural or synthetic soaps, turkey red oil, fatty alcohol sulphonates, sulphated fats, esters of fatty acids, high molecular quaternary ammonium compounds and condensation products of aliphatic or araliphatic compounds and ethylene anide. The products may include additives such as casein, salts of fatty acids, glue, resins, fats, albumen degradation products, solubility promotors, dyestuffs and perfumes. Other organic synthetic acaricides, insecticides, oricides, fungicides or bactericidal substances may be added, e.g., benzyl benzoate, dimethyl thianthrene, phthalonitrile, a a -bis (p-chlorophenyl) b b b trichlorethane, b b -dichlorethane, 4:6-dinitro-o-cresol, mixtures of nitrated naphthylamines, mercury compound, copper compounds and sulphur. For special purposes semi-solid carriers of the nature of a cream, ointment, paste or wax may be employed into which the active substance can be worked with or without the aid of solubility promotors and/or of emulsifying agents. Such carriers are typified by soft soap and petroleum jelly. Materials suitable for incorporating in veterinary preparations comprise paraffin oil, vegetable oils, e.g., olive, castor, sesame and camphor oils, glycerine, petroleum jelly, wool fat and emulsifying agents such as soaps, sulphonated fats, fatty acid esters, fatty alcohol sulphonates, alkylated aromatic and halogenated aromatic sulphonic acids, higher molecular alkoxy carboxylic acids and esters of phosphoric acid. Emulsions of ointment-like consistency may be produced by employing stearic acid and fatty acid salts, e.g., sodium stearate. For fat-free ointments, cellulose ethers, aluminium hydroxide gel and the like may be used. Talcum, starch, lactose and the like may be added. The bactericidal action may be increased by the addition of phenols, e.g., p-chlor-m-cresol, o-butyl p-chlor phenol, o-benzyl p-chlorphenol, cyclohexylphenol, dodecyl-benzyl-trimethyl-ammonium metho sulphate, oxyquinoline derivatives, colloidal silver preparations and thiocyanic acid. Specified active materials of the invention are the anilide, -N-methyl and ethyl o- and ptoluidides, N-ethyl M-toluidide, -N- methyl and ethyl anilide, -N- methyl and ethyl o-chloranilide, -N-ethyl p-bromanilide, -N- ethyl 3,4 dichloranilide, -N- ethyl 2 chlor 6 methyl anilide, o-anisidide, -N-methyl p-anisidide, -N-ethyl o-anisidide, -N- isoamyl o-toluidide -N-ethyl p-phenetidide of crotonic acid; and b ,b -dimethylacrylic acid and trimethyl acrylic acid derivatives similar to the crotonic acid derivatives above.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE474164D BE474164A (en) | 1946-07-27 | ||
GB2241546A GB638662A (en) | 1946-07-27 | 1946-07-27 | Combating acarida, and more especially compositions for use therein |
FR948614D FR948614A (en) | 1946-07-27 | 1947-06-27 | Products for combating mites and having a disinfectant power and process for preparing these products |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2241546A GB638662A (en) | 1946-07-27 | 1946-07-27 | Combating acarida, and more especially compositions for use therein |
Publications (1)
Publication Number | Publication Date |
---|---|
GB638662A true GB638662A (en) | 1950-06-14 |
Family
ID=10178994
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2241546A Expired GB638662A (en) | 1946-07-27 | 1946-07-27 | Combating acarida, and more especially compositions for use therein |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE474164A (en) |
FR (1) | FR948614A (en) |
GB (1) | GB638662A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4217363A (en) * | 1978-08-17 | 1980-08-12 | Givaudan Corporation | Preservation of aqueous systems with α-chloro-β-aminocrotonamide |
EP0566495A1 (en) * | 1992-04-16 | 1993-10-20 | Pierre Fabre Sante | Potentiation of pyrethrinoid by crotamiton, useful for the treatment of pediculosis |
FR2723291A1 (en) * | 1994-08-03 | 1996-02-09 | Fabre Pierre Sante | SYNERGISTIC ACARICIDE COMPOSITION |
-
0
- BE BE474164D patent/BE474164A/xx unknown
-
1946
- 1946-07-27 GB GB2241546A patent/GB638662A/en not_active Expired
-
1947
- 1947-06-27 FR FR948614D patent/FR948614A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4217363A (en) * | 1978-08-17 | 1980-08-12 | Givaudan Corporation | Preservation of aqueous systems with α-chloro-β-aminocrotonamide |
EP0566495A1 (en) * | 1992-04-16 | 1993-10-20 | Pierre Fabre Sante | Potentiation of pyrethrinoid by crotamiton, useful for the treatment of pediculosis |
FR2690048A1 (en) * | 1992-04-16 | 1993-10-22 | Fabre Sante Pierre | Potentiation of pyrethroid by the crotamiton useful in the treatment of pediculosis. |
US5441980A (en) * | 1992-04-16 | 1995-08-15 | Pierre Fabre Sante | Potentialization of pyrethroid by crotamiton which is useful in the treatment of pediculosis |
FR2723291A1 (en) * | 1994-08-03 | 1996-02-09 | Fabre Pierre Sante | SYNERGISTIC ACARICIDE COMPOSITION |
WO1996003874A1 (en) * | 1994-08-03 | 1996-02-15 | Pierre Fabre Sante | Acaricidal composition |
Also Published As
Publication number | Publication date |
---|---|
BE474164A (en) | |
FR948614A (en) | 1949-08-05 |
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