DD267901A5 - Insekten- und milbenabwehrende mittel - Google Patents

Insekten- und milbenabwehrende mittel Download PDF

Info

Publication number: DD267901A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; alkyl; compounds; repellents; insect
Prior art date: 1987-03-12

Application number

DD88313565A

Other languages

German (de)

English (en)

Inventor

Bernd-Wieland Krueger

Klaus Sasse

Franz-Peter Hoever

Guenther Nentwig

Wolfgang Behrenz

Original Assignee

��@��k��

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.)

1987-03-12

Filing date

1988-03-10

Publication date

1989-05-17

1988-03-10 Application filed by ��@��k�� filed Critical ��@��k��

1989-05-17 Publication of DD267901A5 publication Critical patent/DD267901A5/de

Links

241000238631 Hexapoda Species 0.000 title claims abstract description 19
239000005871 repellent Substances 0.000 claims abstract description 31
230000002940 repellent Effects 0.000 claims abstract description 31
238000000034 method Methods 0.000 claims abstract description 5
239000004094 surface-active agent Substances 0.000 claims abstract 3
239000004606 Fillers/Extenders Substances 0.000 claims abstract 2
239000001257 hydrogen Substances 0.000 claims description 20
229910052739 hydrogen Inorganic materials 0.000 claims description 20
238000002360 preparation method Methods 0.000 claims description 19
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
241000238876 Acari Species 0.000 claims description 8
125000000547 substituted alkyl group Chemical group 0.000 claims description 8
125000004429 atom Chemical group 0.000 claims description 7
150000002431 hydrogen Chemical group 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 5
125000002950 monocyclic group Chemical group 0.000 claims description 5
150000001414 amino alcohols Chemical class 0.000 claims description 3
150000001875 compounds Chemical class 0.000 abstract description 37
230000000694 effects Effects 0.000 abstract description 11
239000004480 active ingredient Substances 0.000 abstract description 8
239000003795 chemical substances by application Substances 0.000 abstract description 7
230000002045 lasting effect Effects 0.000 abstract description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 18
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 16
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
241000700199 Cavia porcellus Species 0.000 description 11
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 10
MMOXZBCLCQITDF-UHFFFAOYSA-N N,N-diethyl-m-toluamide Chemical compound CCN(CC)C(=O)C1=CC=CC(C)=C1 MMOXZBCLCQITDF-UHFFFAOYSA-N 0.000 description 10
239000000203 mixture Substances 0.000 description 10
239000002904 solvent Substances 0.000 description 10
-1 carboxylic acid chlorides Chemical class 0.000 description 9
229960001673 diethyltoluamide Drugs 0.000 description 9
241001465754 Metazoa Species 0.000 description 8
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
241000255925 Diptera Species 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000012074 organic phase Substances 0.000 description 6
125000003342 alkenyl group Chemical group 0.000 description 5
239000000460 chlorine Substances 0.000 description 5
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
239000002253 acid Substances 0.000 description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
229910052794 bromium Inorganic materials 0.000 description 4
239000003085 diluting agent Substances 0.000 description 4
238000009472 formulation Methods 0.000 description 4
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
229910000027 potassium carbonate Inorganic materials 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
239000013543 active substance Substances 0.000 description 3
125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000002304 perfume Substances 0.000 description 3
239000000741 silica gel Substances 0.000 description 3
229910002027 silica gel Inorganic materials 0.000 description 3
239000012312 sodium hydride Substances 0.000 description 3
229910000104 sodium hydride Inorganic materials 0.000 description 3
239000000126 substance Substances 0.000 description 3
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
241000257324 Glossina <genus> Species 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
230000010933 acylation Effects 0.000 description 2
238000005917 acylation reaction Methods 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
239000000443 aerosol Substances 0.000 description 2
150000001350 alkyl halides Chemical class 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 2
238000004140 cleaning Methods 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
229910052943 magnesium sulfate Inorganic materials 0.000 description 2
235000019341 magnesium sulphate Nutrition 0.000 description 2
238000002156 mixing Methods 0.000 description 2
125000004368 propenyl group Chemical group C(=CC)* 0.000 description 2
238000000746 purification Methods 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000002390 rotary evaporation Methods 0.000 description 2
239000007921 spray Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
238000010626 work up procedure Methods 0.000 description 2
PBWHJRFXUPLZDS-UHFFFAOYSA-N (1-Ethylpropyl)benzene Chemical compound CCC(CC)C1=CC=CC=C1 PBWHJRFXUPLZDS-UHFFFAOYSA-N 0.000 description 1
YTFGFSUAXNOMKL-UHFFFAOYSA-N 1-[2-(2-hydroxyethyl)piperidin-1-yl]pentan-1-one Chemical compound CCCCC(=O)N1CCCCC1CCO YTFGFSUAXNOMKL-UHFFFAOYSA-N 0.000 description 1
RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 description 1
IUGOPULVANEDRX-UHFFFAOYSA-N 2-ethylhexane-1,1-diol Chemical compound CCCCC(CC)C(O)O IUGOPULVANEDRX-UHFFFAOYSA-N 0.000 description 1
PTHDBHDZSMGHKF-UHFFFAOYSA-N 2-piperidin-2-ylethanol Chemical compound OCCC1CCCCN1 PTHDBHDZSMGHKF-UHFFFAOYSA-N 0.000 description 1
241000256111 Aedes <genus> Species 0.000 description 1
241000256118 Aedes aegypti Species 0.000 description 1
241000238679 Amblyomma Species 0.000 description 1
241000411431 Anobium Species 0.000 description 1
241000256186 Anopheles <genus> Species 0.000 description 1
241000238421 Arthropoda Species 0.000 description 1
241001674044 Blattodea Species 0.000 description 1
241000238678 Boophilus Species 0.000 description 1
125000006414 CCl Chemical group ClC* 0.000 description 1
241000700198 Cavia Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241001124179 Chrysops Species 0.000 description 1
241001327638 Cimex lectularius Species 0.000 description 1
241000933851 Cochliomyia Species 0.000 description 1
241000254173 Coleoptera Species 0.000 description 1
241000256054 Culex <genus> Species 0.000 description 1
241000256057 Culex quinquefasciatus Species 0.000 description 1
241000134316 Culicoides <genus> Species 0.000 description 1
241000202828 Dermatobia hominis Species 0.000 description 1
241001641896 Dermestes lardarius Species 0.000 description 1
241000953886 Fannia canicularis Species 0.000 description 1
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
241000670091 Haematopinus suis Species 0.000 description 1
241000562576 Haematopota Species 0.000 description 1
241000258937 Hemiptera Species 0.000 description 1
241001608644 Hippoboscidae Species 0.000 description 1
241000832178 Hylotrupes Species 0.000 description 1
241000257303 Hymenoptera Species 0.000 description 1
241000543830 Hypoderma bovis Species 0.000 description 1
241000257174 Hypoderma lineatum Species 0.000 description 1
241000256602 Isoptera Species 0.000 description 1
241000238681 Ixodes Species 0.000 description 1
241000948337 Lasius niger Species 0.000 description 1
241000257166 Lucilia cuprina Species 0.000 description 1
240000005265 Lupinus mutabilis Species 0.000 description 1
235000008755 Lupinus mutabilis Nutrition 0.000 description 1
241000257229 Musca <genus> Species 0.000 description 1
241000257226 Muscidae Species 0.000 description 1
208000006123 Myiasis Diseases 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000543819 Oestrus ovis Species 0.000 description 1
241001563696 Orinus Species 0.000 description 1
241000238887 Ornithodoros Species 0.000 description 1
208000002193 Pain Diseases 0.000 description 1
241000517307 Pediculus humanus Species 0.000 description 1
241000238675 Periplaneta americana Species 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical class ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
241000718000 Pulex irritans Species 0.000 description 1
241001509970 Reticulitermes <genus> Species 0.000 description 1
241000304160 Sarcophaga carnaria Species 0.000 description 1
235000019095 Sechium edule Nutrition 0.000 description 1
241000256108 Simulium <genus> Species 0.000 description 1
241000258242 Siphonaptera Species 0.000 description 1
241000254181 Sitophilus Species 0.000 description 1
241001177161 Stegobium paniceum Species 0.000 description 1
241001494115 Stomoxys calcitrans Species 0.000 description 1
241001649251 Supella Species 0.000 description 1
241000255626 Tabanus <genus> Species 0.000 description 1
241000254109 Tenebrio molitor Species 0.000 description 1
244000269722 Thea sinensis Species 0.000 description 1
241001414831 Triatoma infestans Species 0.000 description 1
241001584775 Tunga penetrans Species 0.000 description 1
241000353223 Xenopsylla cheopis Species 0.000 description 1
WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
239000012346 acetyl chloride Substances 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000001273 butane Substances 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000012459 cleaning agent Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000006071 cream Substances 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
230000007123 defense Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000007865 diluting Methods 0.000 description 1
FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
229960001826 dimethylphthalate Drugs 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
239000003480 eluent Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
229960004279 formaldehyde Drugs 0.000 description 1
235000019256 formaldehyde Nutrition 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000000077 insect repellent Substances 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
238000002955 isolation Methods 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000006210 lotion Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000002674 ointment Substances 0.000 description 1
229940037201 oris Drugs 0.000 description 1
239000005022 packaging material Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
150000003053 piperidines Chemical class 0.000 description 1
238000005498 polishing Methods 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
230000001846 repelling effect Effects 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
125000005017 substituted alkenyl group Chemical group 0.000 description 1
239000000516 sunscreening agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000004753 textile Substances 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
239000003039 volatile agent Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring 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
- A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/20—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/44—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom three- or four-membered rings
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/46—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom rings with more than six members
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
- C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/30—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
- C07D211/32—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom by oxygen atoms

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Hydrogenated Pyridines (AREA)
Pyrrole Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

DD88313565A 1987-03-12 1988-03-10 Insekten- und milbenabwehrende mittel DD267901A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19873708033 DE3708033A1 (de)	1987-03-12	1987-03-12	Mittel zur insekten- und milbenabwehr

Publications (1)

Publication Number	Publication Date
DD267901A5 true DD267901A5 (de)	1989-05-17

Family

ID=6322914

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD88313565A DD267901A5 (de)	1987-03-12	1988-03-10	Insekten- und milbenabwehrende mittel

Country Status (25)

Country	Link
US (2)	US4873252A (fr)
EP (1)	EP0281908B1 (fr)
JP (1)	JP2637758B2 (fr)
KR (1)	KR950012166B1 (fr)
AR (1)	AR248067A1 (fr)
AT (1)	ATE62788T1 (fr)
AU (1)	AU608578B2 (fr)
BR (1)	BR8801110A (fr)
CA (1)	CA1327041C (fr)
DD (1)	DD267901A5 (fr)
DE (2)	DE3708033A1 (fr)
DK (1)	DK134888A (fr)
EG (1)	EG18840A (fr)
ES (1)	ES2021772B3 (fr)
FI (1)	FI89323C (fr)
GR (1)	GR3001856T3 (fr)
HU (2)	HU203965B (fr)
IL (1)	IL85686A (fr)
MX (1)	MX168469B (fr)
NO (1)	NO172093C (fr)
NZ (1)	NZ223804A (fr)
PH (1)	PH26328A (fr)
PT (1)	PT86877B (fr)
TR (1)	TR25479A (fr)
ZA (1)	ZA881747B (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3801082A1 (de) *	1987-04-28	1988-11-17	Bayer Ag	Mittel zur insekten- und milbenabwehr
IL90007A0 (en) *	1988-04-22	1989-12-15	Revlon	N-alkoxy-alkylamido derivatives,methods for the preparation thereof and cosmetic preparations containing the same
DE3913939A1 (de) *	1989-04-27	1991-01-17	Bayer Ag	Neue carbonamidgruppen enthaltende (meth)acrylsaeureester, adhaesivkomponenten zur behandlung kollagenhaltiger materialien, enthaltend diese verbindungen, sowie herstellung und anwendung dieser adhaesivkomponenten
CA2047389C (fr) *	1990-07-24	2002-04-23	James R. Mccarthy	Piperidines substituees et leur utilisation comme inhibitrices de la synthese du cholesterol
MX9303636A (es) *	1992-08-07	1994-07-29	Us Agriculture	Composicion y metodo para repeler a las hormigas.
DE19618089A1 (de) *	1996-05-06	1997-11-13	Bayer Ag	Arthropodenrepellents
ATE221726T1 (de) *	1998-06-18	2002-08-15	Novartis Erfind Verwalt Gmbh	Zusammemsetzung zum fernhalten von ungeziefer
KR100594551B1 (ko)	1998-06-18	2006-07-03	노파르티스 아게	해충 방제용 조성물
GB9814827D0 (en)	1998-07-08	1998-09-09	Rolic Ag	Chiral Materials
DE10032879A1 (de) *	2000-07-06	2002-01-17	Bayer Ag	Anthelmintika zur Verhinderung von parasitären Infektionen bei Mensch und Tier II
DE20115729U1 (de)	2001-09-25	2001-12-20	Stubna, Eduard, 80634 München	Detergentmittel mit repelent wirkenden chemischen Substanzen
EP2094079B1 (fr)	2006-11-24	2012-11-14	Novartis AG	Composition servant a repousser et a eloigner des animaux nuisibles
BRPI0809416A2 (pt) *	2007-03-28	2014-09-16	Contech Entpr Inc	Composto com atividade detentoea e repelente de artrópode estoparasita que se alimenta de sangue, composição, e, método para sintetizar um composto
DE102010023586A1 (de) *	2010-06-12	2011-12-15	Saltigo Gmbh	Synergistisch wirkende Mischungen aus α-,ω-Aminalkohol-Enantiomeren, deren Herstellung und ihre Verwendung in insekten- und milbenabwehrenden Zubereitungen

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3178439A (en) *	1963-05-06	1965-04-13	Reilly Tar & Chem Corp	N-alkanoyl and alkenoyl hydroxy alkyl piperidides
US4263321A (en) *	1977-05-31	1981-04-21	Block Drug Company Inc.	Alkanol amide toxicants
US4298612A (en) *	1979-02-02	1981-11-03	The United States Of America As Represented By The Secretary Of Agriculture	Insect repellents
PH18347A (en) *	1979-02-15	1985-06-05	Block Drug Co	Amidoamine toxicants
US4407670A (en) *	1980-02-28	1983-10-04	National Research Development Corporation	Biocidal compounds and compositions

1987
- 1987-03-12 DE DE19873708033 patent/DE3708033A1/de not_active Withdrawn
1988
- 1988-03-02 DE DE8888103119T patent/DE3862490D1/de not_active Expired - Lifetime
- 1988-03-02 PT PT86877A patent/PT86877B/pt not_active IP Right Cessation
- 1988-03-02 EP EP88103119A patent/EP0281908B1/fr not_active Expired - Lifetime
- 1988-03-02 ES ES88103119T patent/ES2021772B3/es not_active Expired - Lifetime
- 1988-03-02 AT AT88103119T patent/ATE62788T1/de active
- 1988-03-03 MX MX010627A patent/MX168469B/es unknown
- 1988-03-07 JP JP63051802A patent/JP2637758B2/ja not_active Expired - Fee Related
- 1988-03-08 EG EG12888A patent/EG18840A/xx active
- 1988-03-09 US US07/165,684 patent/US4873252A/en not_active Expired - Lifetime
- 1988-03-09 TR TR88/0177A patent/TR25479A/xx unknown
- 1988-03-09 NZ NZ223804A patent/NZ223804A/xx unknown
- 1988-03-10 CA CA000561038A patent/CA1327041C/fr not_active Expired - Fee Related
- 1988-03-10 DD DD88313565A patent/DD267901A5/de not_active IP Right Cessation
- 1988-03-10 FI FI881126A patent/FI89323C/fi not_active IP Right Cessation
- 1988-03-10 IL IL85686A patent/IL85686A/xx not_active IP Right Cessation
- 1988-03-11 NO NO881109A patent/NO172093C/no unknown
- 1988-03-11 AU AU13054/88A patent/AU608578B2/en not_active Ceased
- 1988-03-11 KR KR1019880002513A patent/KR950012166B1/ko not_active Expired - Fee Related
- 1988-03-11 PH PH36624A patent/PH26328A/en unknown
- 1988-03-11 BR BR8801110A patent/BR8801110A/pt not_active IP Right Cessation
- 1988-03-11 DK DK134888A patent/DK134888A/da not_active Application Discontinuation
- 1988-03-11 HU HU881186A patent/HU203965B/hu unknown
- 1988-03-11 ZA ZA881747A patent/ZA881747B/xx unknown
- 1988-03-11 HU HU911811A patent/HU206036B/hu not_active IP Right Cessation
- 1988-03-11 AR AR88310289A patent/AR248067A1/es active
1989
- 1989-06-28 US US07/372,801 patent/US4946850A/en not_active Expired - Lifetime
1991
- 1991-04-25 GR GR91400459T patent/GR3001856T3/el unknown

Also Published As

Publication number	Publication date
FI89323C (fi)	1993-09-27
ES2021772B3 (es)	1991-11-16
DK134888A (da)	1988-09-13
HU206036B (en)	1992-08-28
US4946850A (en)	1990-08-07
AR248067A1 (es)	1995-06-30
PT86877A (pt)	1988-04-01
ZA881747B (en)	1988-08-31
BR8801110A (pt)	1988-10-18
DK134888D0 (da)	1988-03-11
TR25479A (tr)	1993-02-17
NO172093B (no)	1993-03-01
MX168469B (es)	1993-05-26
IL85686A (en)	1992-06-21
DE3862490D1 (de)	1991-05-29
PT86877B (pt)	1992-05-29
EP0281908A1 (fr)	1988-09-14
GR3001856T3 (en)	1992-11-23
PH26328A (en)	1992-04-29
NZ223804A (en)	1990-02-26
FI881126A0 (fi)	1988-03-10
EP0281908B1 (fr)	1991-04-24
HU203965B (en)	1991-11-28
CA1327041C (fr)	1994-02-15
KR950012166B1 (ko)	1995-10-14
NO881109D0 (no)	1988-03-11
NO881109L (no)	1988-09-13
NO172093C (no)	1993-06-09
KR880011076A (ko)	1988-10-26
AU1305488A (en)	1988-09-15
FI881126A7 (fi)	1988-09-13
HUT46837A (en)	1988-12-28
EG18840A (en)	1994-06-30
FI89323B (fi)	1993-06-15
ATE62788T1 (de)	1991-05-15
HU911811D0 (en)	1991-12-30
US4873252A (en)	1989-10-10
DE3708033A1 (de)	1988-09-22
AU608578B2 (en)	1991-04-11
JPS63230669A (ja)	1988-09-27
JP2637758B2 (ja)	1997-08-06

Legal Events

Date	Code	Title	Description
1995-07-20	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
EP0289842B1 (fr)	1991-11-27	Remède contre les insectes et les mites
EP0467045B1 (fr)	1998-03-04	Dérivés de morpholino-urées
DD267901A5 (de)	1989-05-17	Insekten- und milbenabwehrende mittel
EP0346709B1 (fr)	1992-11-19	Utilisation de dérivés d'esters -Aminoacides acylés comme agent répulsif contre les insectes et les acariens
DE19618089A1 (de)	1997-11-13	Arthropodenrepellents
DE69902472T2 (de)	2003-05-08	Zusammemsetzung zum fernhalten von ungeziefer
DE1542785A1 (de)	1970-05-06	Insekten- und milbenabweisende Mittel
EP2086327A1 (fr)	2009-08-12	Derives d'alpha-, oméga- aminoalcools enrichis en enantiomeres, leur production et leur utilisation comme agents repulsifs des insectes et des mites
DD281340A5 (de)	1990-08-08	Mittel zur insekten- und milbenabwehr
EP2394511B1 (fr)	2013-08-21	Mélanges à effet synergétique constitués d'énantiomères d'alcool aminé alpha-oméga, leur fabrication et leur utilisation dans des préparations pour la lutte contre les insectes et les acariens
DE1518805A1 (de)	1969-08-21	Insekten- und milbenabweisende Mittel
DE19917948A1 (de)	2000-10-26	Mittel zur Bekämpfung von Arthropoden
FI90765B (fi)	1993-12-15	Asyloidut , -aminoalkoholijohdannaiset ja menetelmä niiden valmistamiseksi
DE19840321A1 (de)	2000-03-09	Mittel zur Bekämpfung von Arthropoden
DE1542784A1 (de)	1970-06-04	Insekten- und milbenabweisende Mittel
DE1795249B2 (de)	1975-11-06	1 -Trityl-1,2,4-triazole