GB503507A - Manufacture of improved insecticidal compositions - Google Patents
Manufacture of improved insecticidal compositionsInfo
- 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
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.
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)
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 |
-
1937
- 1937-10-04 GB GB34656/38A patent/GB503507A/en not_active Expired
Cited By (3)
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 | |
US2545283A (en) | Tertiary diacyl amine insecticides | |
GB503507A (en) | Manufacture of improved insecticidal compositions | |
GB781702A (en) | Herbicides and herbicidal compositions | |
CH449632A (en) | Process for the preparation of cyclic diazacycloalkane compounds | |
CH485680A (en) | Process for the production of sulfur-containing amines | |
US2882197A (en) | Sulfurized alkyl thioformal fungicidal compositions | |
US3067090A (en) | Fungicidal preparations and process for preparing the same | |
US2864682A (en) | Selective method of inhibiting preemergent growth of grasses | |
US3135793A (en) | Hydroxyalkylenediminotetracetamides | |
DE1620325C3 (en) | Disubstituted isoxazole compounds | |
Brookes et al. | The toxicity of organic sulphides to the eggs and larvae of the glasshouse red spider mite. V.—Benzyl phenyl sulphides (non‐halogen substituents) | |
CN114230481B (en) | A low-toxicity bactericidal glycosyl amide ionic liquid and its preparation method and application | |
CH356121A (en) | Process for the preparation of N-monosubstituted amides of α-aminoalkyl-α-phenylacetic acids | |
DE3019758A1 (en) | TETRAHYDROPHTHALAMIDE DERIVATIVES., PRODUCTION METHOD AND HERBICIDE | |
US4148901A (en) | N-phenyl or n-pyridyl sulfamides and methanesulfonamides | |
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 | |
DE953125C (en) | Agent for combating microorganisms such as fungi, bacteria and protozoa | |
AT226691B (en) | Process for the preparation of new 2,5-disubstituted pyrrolidines | |
DE1445409A1 (en) | Process for the preparation of 3-phenyl-5-imino-1,2,4-oxadiazoles | |
DE99004C (en) |