DE1277624B - Insenkticides und acaricides Mittel - Google Patents
Insenkticides und acaricides MittelInfo
- Publication number
- DE1277624B DE1277624B DES85552A DES0085552A DE1277624B DE 1277624 B DE1277624 B DE 1277624B DE S85552 A DES85552 A DE S85552A DE S0085552 A DES0085552 A DE S0085552A DE 1277624 B DE1277624 B DE 1277624B
- Authority
- DE
- Germany
- Prior art keywords
- methylcarbamate
- compound
- tested
- days
- weight
- 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.)
- Pending
Links
- 239000002917 insecticide Substances 0.000 title claims description 13
- 230000000895 acaricidal effect Effects 0.000 title claims description 5
- 239000000642 acaricide Substances 0.000 title claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 28
- 241000238631 Hexapoda Species 0.000 claims description 12
- 239000002689 soil Substances 0.000 claims description 11
- YFZJZJIUKMANKN-UHFFFAOYSA-N methyl n-methyl-n-phenylcarbamate Chemical compound COC(=O)N(C)C1=CC=CC=C1 YFZJZJIUKMANKN-UHFFFAOYSA-N 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 21
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
- AUQAUAIUNJIIEP-UHFFFAOYSA-N 3,4,5-trimethylphenyl methylcarbamate Chemical compound CNC(=O)OC1=CC(C)=C(C)C(C)=C1 AUQAUAIUNJIIEP-UHFFFAOYSA-N 0.000 description 10
- 241000255925 Diptera Species 0.000 description 7
- 241000255967 Helicoverpa zea Species 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- 239000004927 clay Substances 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 241000256187 Anopheles albimanus Species 0.000 description 5
- UFEJKYYYVXYMMS-UHFFFAOYSA-N methylcarbamic acid Chemical compound CNC(O)=O UFEJKYYYVXYMMS-UHFFFAOYSA-N 0.000 description 5
- 231100000419 toxicity Toxicity 0.000 description 5
- 230000001988 toxicity Effects 0.000 description 5
- -1 3,4,5-trimethylphenyl Chemical group 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 241000257226 Muscidae Species 0.000 description 3
- 244000299461 Theobroma cacao Species 0.000 description 3
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000000749 insecticidal effect Effects 0.000 description 3
- GYKXQTKSWLAUIT-UHFFFAOYSA-N m-cumenyl methylcarbamate Chemical compound CNC(=O)OC1=CC=CC(C(C)C)=C1 GYKXQTKSWLAUIT-UHFFFAOYSA-N 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- FDQQNNZKEJIHMS-UHFFFAOYSA-N 3,4,5-trimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1C FDQQNNZKEJIHMS-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 241000258937 Hemiptera Species 0.000 description 2
- 241000257229 Musca <genus> Species 0.000 description 2
- 241000257159 Musca domestica Species 0.000 description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 241000254181 Sitophilus Species 0.000 description 2
- 241000254152 Sitophilus oryzae Species 0.000 description 2
- 235000009470 Theobroma cacao Nutrition 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000002500 effect on skin Effects 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- RVNHHUYYEKSQNX-UHFFFAOYSA-N (3,4,5-trimethylphenyl) carbamate Chemical compound CC1=CC(OC(N)=O)=CC(C)=C1C RVNHHUYYEKSQNX-UHFFFAOYSA-N 0.000 description 1
- NYOKZHDTNBDPOB-UHFFFAOYSA-N 2,3,5-trimethylphenyl methylcarbamate Chemical compound CNC(=O)OC1=CC(C)=CC(C)=C1C NYOKZHDTNBDPOB-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 241000256186 Anopheles <genus> Species 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000256113 Culicidae Species 0.000 description 1
- 241000489973 Diabrotica undecimpunctata Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 241000678550 Helopeltis Species 0.000 description 1
- 240000003293 Magnolia grandiflora Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 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 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910001710 laterite Inorganic materials 0.000 description 1
- 239000011504 laterite Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 231100000636 lethal dose Toxicity 0.000 description 1
- 229940059904 light mineral oil Drugs 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 201000004792 malaria Diseases 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 235000017709 saponins Nutrition 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- 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
- A01N47/08—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 one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US200643A US3130122A (en) | 1962-06-07 | 1962-06-07 | 3, 4, 5-trimethylphenyl methylcarbamate and its use as an insecticide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1277624B true DE1277624B (de) | 1968-09-12 |
Family
ID=22742571
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DES85552A Pending DE1277624B (de) | 1962-06-07 | 1963-06-05 | Insenkticides und acaricides Mittel |
Country Status (7)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3250673A (en) * | 1963-12-10 | 1966-05-10 | Union Carbide Corp | Methods of combating insects of the genus diabrotica |
| GB1046209A (en) * | 1964-07-24 | 1966-10-19 | Shell Int Research | Insecticidal compositions |
| US4511579A (en) * | 1981-03-27 | 1985-04-16 | Union Carbide Corporation | Pest repellant |
| JP2007063182A (ja) * | 2005-08-31 | 2007-03-15 | Nichiha Corp | 防虫性板材 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1097750B (de) * | 1957-08-05 | 1961-01-19 | Union Carbide Corp | Insektenbekaempfungsmittel |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA555686A (en) * | 1958-04-08 | E. Merck | Methyl substituted phenyl carbamates | |
| US2933383A (en) * | 1956-11-23 | 1960-04-19 | Union Carbide Corp | Method of combating weeds using nu-substituted carbamates of 2, 4, 5-trichloro, 6-nitro phenol |
-
0
- NL NL293750D patent/NL293750A/xx unknown
- BE BE633282D patent/BE633282A/xx unknown
-
1962
- 1962-06-07 US US200643A patent/US3130122A/en not_active Expired - Lifetime
-
1963
- 1963-06-05 DE DES85552A patent/DE1277624B/de active Pending
- 1963-06-05 BR BR149674/63A patent/BR6349674D0/pt unknown
- 1963-06-05 CH CH701363A patent/CH445192A/de unknown
- 1963-06-05 GB GB22396/63A patent/GB967620A/en not_active Expired
- 1963-06-07 NL NL63293750A patent/NL139870B/xx not_active IP Right Cessation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1097750B (de) * | 1957-08-05 | 1961-01-19 | Union Carbide Corp | Insektenbekaempfungsmittel |
Also Published As
| Publication number | Publication date |
|---|---|
| GB967620A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1964-08-26 |
| BR6349674D0 (pt) | 1973-06-26 |
| NL293750A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| CH445192A (de) | 1967-10-15 |
| NL139870B (nl) | 1973-10-15 |
| US3130122A (en) | 1964-04-21 |
| BE633282A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69530913T2 (de) | Mikroverkapselte zusammensetzung von chlorpyrifos und endosulfan | |
| DE1097750B (de) | Insektenbekaempfungsmittel | |
| DE2250085A1 (de) | Pesticides gemisch und verwendung von aktiven mischungen dafuer | |
| DE1252962B (de) | Insektizide Zubereitung | |
| DE1277624B (de) | Insenkticides und acaricides Mittel | |
| DE2625808A1 (de) | Schaedlingsbekaempfungsmittel | |
| DE69009862T2 (de) | Köderzusammensetzung für die Schädlingsbekämpfung. | |
| DE1171200B (de) | Insektizide synergistische Gemische | |
| DE1181200B (de) | Verfahren zur Herstellung des N-Mono-methylamids der O, O-Di-(ª-fluoraethyl)-dithiophosphorylessigsaeure | |
| DE834152C (de) | Insekticide und Fungicide | |
| DE2141227A1 (de) | Carbamoyloximverbindungen sowie deren Verwendung | |
| DE2425237A1 (de) | Organophosphorverbindungen | |
| DE1493276C3 (de) | Sulfitdiester, Verfahren zu deren Herstellung und ihrer Verwendung | |
| DE1181978B (de) | Mittel zur Bekaempfung von Arthropoden, Mollusken und Fischen | |
| DE591107C (de) | Bekaempfung von Ruebenaaskaefern und ihren Larven | |
| DE2951037A1 (de) | Verbesserungen im zusammenhang mit insektiziden | |
| DE1200060B (de) | Insektizides und acarizides Mittel | |
| EP0005227B1 (de) | Akarizide und insektizide Mittel sowie deren Verwendung zur Schädlingsbekämpfung | |
| AT253861B (de) | Insektizide Mischung | |
| DE977554C (de) | Schaedlingsbekaempfungsmittel mit insektizider und akarizider Wirkung | |
| DE868375C (de) | Insekticide | |
| DE2426609A1 (de) | Pyrimidinderivate | |
| AT267965B (de) | Akarizides und insektizides Mittel | |
| DE1210240B (de) | Mittel zur Bekaempfung von Insekten | |
| DE2851025A1 (de) | Insektizides mittel |