GB638662A - Combating acarida, and more especially compositions for use therein - Google Patents

Combating acarida, and more especially compositions for use therein

Info

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
Application number
GB2241546A
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.)
Novartis AG
Original Assignee
JR Geigy AG
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.)
Filing date
Publication date
Priority to BE474164D priority Critical patent/BE474164A/xx
Application filed by JR Geigy AG filed Critical JR Geigy AG
Priority to GB2241546A priority patent/GB638662A/en
Priority to FR948614D priority patent/FR948614A/en
Publication of GB638662A publication Critical patent/GB638662A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic 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.
GB2241546A 1946-07-27 1946-07-27 Combating acarida, and more especially compositions for use therein Expired GB638662A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (6)

* Cited by examiner, † Cited by third party
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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