GB503507A - Manufacture of improved insecticidal compositions - Google Patents

Manufacture of improved insecticidal compositions

Info

Publication number
GB503507A
GB503507A GB34656/38A GB3465638A GB503507A GB 503507 A GB503507 A GB 503507A GB 34656/38 A GB34656/38 A GB 34656/38A GB 3465638 A GB3465638 A GB 3465638A GB 503507 A GB503507 A GB 503507A
Authority
GB
United Kingdom
Prior art keywords
acid
morpholine
kerosene
acids
dodecylamide
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
GB34656/38A
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of GB503507A publication Critical patent/GB503507A/en
Expired legal-status Critical Current

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

503,507. Insecticidal compositions; acid amides. IMPERIAL 'CHEMICAL INDUSTRIES, Ltd. Oct. 4-, 1937, No. 84656/38. Convention date, Oct. 3, 1936. Divided out of 503,490. [Class 81 (i)] [Also in Group IV] Insecticidal compositions comprise an amide of the formula R.CO.N<<R1>R11, wherein at least one of the groups R, R<1> and R<11> contains a heterocyclic residue or R<1> and R<11> are linked by a closed carbon chain which may be interrupted by oxygen or sulphur atoms so as to form with the nitrogen atom a heterocyclic ring and wherein at least one R is an aliphatic or cycloaliphatic hydrocarbon radicle having at least six carbon atoms, R, R<1> and R<11> being otherwise hydrogen or aliphatic or cycloaliphatic. hydrocarbon radicles, together with a known solid insecticidal substance and together, if desired, with a solvent or carrier. The amides are prepared by reacting acids, acid chlorides or esters with . ammonia or amines. Thus, alpha-picolinic acid n-dodecylamide is obtained by. heating ethyl alpha-picolinate with n-dodecylamine, 4.(10: : 11-undecylenoy 1),-morpholine by reacting 10: 11-undecylenic acid chloride with morpholine in the presence of benzene and sodium hydroxide solution, 1- laurylpiperidine by heating lauric acid with piperidine in the presence of m-cresol, and 4-laurylmorpholine by reacting lauric acid chloride with morpholine in the presence of benzene and aqueous sodium hydroxide. Further amides mentioned are furoic acid dodecylamide, octanoic acid tetrahydrofurfurylamide,-lauric acid thiodiphenylamide, 4- oleylmorpholine, 1-heptanoylpiperidine, 1-lauryldecahydroquinoline, the pipendides of linseed oil acids, the morpholidee of china wood oil acids and soya bean oil acids, nicotinic acid hexylamide, tetrahydrofuroic acid dodecylamide, the 5-ethoxybenzthiazyl-1-amide of octanoic, acid, 1-octanoyl-2-(3<1>-pyridyl)-piperidine and the reaction products of lauric acid with hydrogenated nicotines and hydrogenated nitrogen bases from shale oil distillation. The following further components of the compositions are specified: as insecticidal sub-. stances, pyrethrum, derris, thiocyanates and phthalates; as solvents, kerosene, gasoline and pine - oil ; as a carrier, talc. Thus, fly . sprays are prepared by dissolving the ingredients in kerosene or other petroleum product with an amide concentration of 0'01. to 5'0 per cent, e.g. a solution of 25 parts by weight of pyrethrins and .500, parts of 1-laurylpiperidine in 100,000 parts of kerosene. Specification 364,046 is referred to. The Specification as open to inspection under Sect. 91 also describes insecticidal compositions containing the amides in admixture with a solvent or carrier, and refers in this connection to kerosene solutions of 1-laurylpiperidine, a mixture of the n-dodecylamine of alpha-picolinic acid or furoic acid with casein, glue and straw oil containing sodium n-dodecyl sulphate as emulsifying agent, and a mixture of alpha-picolinic acid dodecylamide and talc. Mention is .made of hexahydrophthalic acid morpholide, the dimorpholides of sebacic, suberic and azolaic acids, 4-ricinoleylmorpholine and 4-(12-hydroxystearyl)-morpholine. This subject-matter does not appear in the Specification as accepted.
GB34656/38A 1936-10-03 1937-10-04 Manufacture of improved insecticidal compositions Expired GB503507A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US503507XA 1936-10-03 1936-10-03

Publications (1)

Publication Number Publication Date
GB503507A true GB503507A (en) 1939-04-04

Family

ID=21964754

Family Applications (1)

Application Number Title Priority Date Filing Date
GB34656/38A Expired GB503507A (en) 1936-10-03 1937-10-04 Manufacture of improved insecticidal compositions

Country Status (1)

Country Link
GB (1) GB503507A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2605208A (en) * 1949-01-07 1952-07-29 Paul D Bartlett Insect repellents
US3222203A (en) * 1963-11-08 1965-12-07 Evald L Skau N-acyl derivatives of cyclic imines
US3248396A (en) * 1963-02-25 1966-04-26 Evald L Skau Nu-acyl derivatives of cyclic imines

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2605208A (en) * 1949-01-07 1952-07-29 Paul D Bartlett Insect repellents
US3248396A (en) * 1963-02-25 1966-04-26 Evald L Skau Nu-acyl derivatives of cyclic imines
US3222203A (en) * 1963-11-08 1965-12-07 Evald L Skau N-acyl derivatives of cyclic imines

Similar Documents

Publication Publication Date Title
US2166120A (en) Insecticidal composition
CH365079A (en) Process for the production of new guanidines
AT394192B (en) METHOD FOR PRODUCING NEW SUBSTITUTED AMINOGUANIDINE DERIVATIVES
GB503507A (en) Manufacture of improved insecticidal compositions
GB781702A (en) Herbicides and herbicidal compositions
GB224376A (en) Improvements in the manufacture of triarylguanidines
GB819742A (en) Derivatives of dialkyldithiophosphoric acids with a double amide function in the molecule and disinfesting compositions prepared from said compounds
CH449632A (en) Process for the preparation of cyclic diazacycloalkane compounds
CH485680A (en) Process for the production of sulfur-containing amines
CN108640871A (en) A kind of fluorine-containing pyridine piperazine carbamide compounds and its application
US2882197A (en) Sulfurized alkyl thioformal fungicidal compositions
US3067090A (en) Fungicidal preparations and process for preparing the same
DE1543035A1 (en) Process for the preparation of dibenzocycloheptene compounds
US2864682A (en) Selective method of inhibiting preemergent growth of grasses
US3135793A (en) Hydroxyalkylenediminotetracetamides
DE1620325C3 (en) Disubstituted isoxazole compounds
DE3019758A1 (en) TETRAHYDROPHTHALAMIDE DERIVATIVES., PRODUCTION METHOD AND HERBICIDE
US4148901A (en) N-phenyl or n-pyridyl sulfamides and methanesulfonamides
US2948727A (en) Thiobispiperazines
US3576803A (en) 3-amino-2-(aminomethyl)-ar-nitropropiophenones
GB503490A (en) Manufacture of improved insecticidal compositions
CH451952A (en) Process for the preparation of basic alkylated naphthalene- (1,4,5,8) -tetracarboxylic acid diimides
AT336587B (en) METHOD FOR PRODUCING NEW BASIC ESTERS
DE953125C (en) Agent for combating microorganisms such as fungi, bacteria and protozoa
DE99004C (en)