IL29305A - Pesticidal preparations containing diaralkyl amines - Google Patents

Pesticidal preparations containing diaralkyl amines

Info

Publication number: IL29305A
Authority: IL; Israel
Prior art keywords: formula; compound; parts; active component; pesticidal preparations
Prior art date: 1967-01-17

Application number

IL29305A

Other languages

English (en)

Original Assignee

Ciba 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.)

1967-01-17

Filing date

1968-01-12

Publication date

1971-07-28

1968-01-12 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1971-07-28 Publication of IL29305A publication Critical patent/IL29305A/en

Links

238000002360 preparation method Methods 0.000 title claims description 10
230000000361 pesticidal effect Effects 0.000 title claims 3
150000001412 amines Chemical class 0.000 title description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
241000244206 Nematoda Species 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 7
239000002904 solvent Substances 0.000 claims description 6
239000003995 emulsifying agent Substances 0.000 claims description 5
150000003839 salts Chemical class 0.000 claims description 4
241000238876 Acari Species 0.000 claims description 2
241000534456 Arenaria <Aves> Species 0.000 claims description 2
241000894006 Bacteria Species 0.000 claims description 2
241000195493 Cryptophyta Species 0.000 claims description 2
241000238631 Hexapoda Species 0.000 claims description 2
241000244199 Panagrellus redivivus Species 0.000 claims description 2
241000193943 Pratylenchus Species 0.000 claims description 2
241000607479 Yersinia pestis Species 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
239000000853 adhesive Substances 0.000 claims description 2
230000001070 adhesive effect Effects 0.000 claims description 2
239000011230 binding agent Substances 0.000 claims description 2
239000002270 dispersing agent Substances 0.000 claims description 2
244000079386 endoparasite Species 0.000 claims description 2
244000000008 fungal human pathogen Species 0.000 claims description 2
244000000004 fungal plant pathogen Species 0.000 claims description 2
239000000575 pesticide Substances 0.000 claims description 2
239000002562 thickening agent Substances 0.000 claims description 2
241000399949 Ditylenchus dipsaci Species 0.000 claims 1
125000003545 alkoxy group Chemical group 0.000 claims 1
125000000217 alkyl group Chemical group 0.000 claims 1
125000004414 alkyl thio group Chemical group 0.000 claims 1
125000002947 alkylene group Chemical group 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 claims 1
125000004093 cyano group Chemical group *C#N 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
239000013543 active substance Substances 0.000 description 35
239000000203 mixture Substances 0.000 description 10
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 9
230000001069 nematicidal effect Effects 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 7
239000000839 emulsion Substances 0.000 description 6
239000007787 solid Substances 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
239000000969 carrier Substances 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
239000000126 substance Substances 0.000 description 5
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
229910000019 calcium carbonate Inorganic materials 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 4
238000000034 method Methods 0.000 description 4
239000000243 solution Substances 0.000 description 4
239000008096 xylene Substances 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000010410 dusting Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000000725 suspension Substances 0.000 description 3
KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
239000001506 calcium phosphate Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
239000012895 dilution Substances 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000008187 granular material Substances 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
235000005985 organic acids Nutrition 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
239000000047 product Substances 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
239000004576 sand Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 2
UAZUEJTXWAXSMA-UHFFFAOYSA-N 1,1-dichlorobut-1-ene Chemical compound CCC=C(Cl)Cl UAZUEJTXWAXSMA-UHFFFAOYSA-N 0.000 description 1
ZSNZRVDOTVGDIX-UHFFFAOYSA-N 1,2-dibromo-3-chloroprop-1-ene Chemical compound ClCC(Br)=CBr ZSNZRVDOTVGDIX-UHFFFAOYSA-N 0.000 description 1
QTDIEDOANJISNP-UHFFFAOYSA-N 2-dodecoxyethyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOCCOS(O)(=O)=O QTDIEDOANJISNP-UHFFFAOYSA-N 0.000 description 1
ABMULKFGWTYIIK-UHFFFAOYSA-N 2-hexylphenol Chemical class CCCCCCC1=CC=CC=C1O ABMULKFGWTYIIK-UHFFFAOYSA-N 0.000 description 1
KHEVPDFAQFJIGK-UHFFFAOYSA-N 2-sulfooxyethanesulfonic acid Chemical compound OS(=O)(=O)CCOS(O)(=O)=O KHEVPDFAQFJIGK-UHFFFAOYSA-N 0.000 description 1
IJJWOSAXNHWBPR-HUBLWGQQSA-N 5-[(3as,4s,6ar)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-n-(6-hydrazinyl-6-oxohexyl)pentanamide Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)NCCCCCC(=O)NN)SC[C@@H]21 IJJWOSAXNHWBPR-HUBLWGQQSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241000233866 Fungi Species 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000237852 Mollusca Species 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
239000006004 Quartz sand Substances 0.000 description 1
241001533598 Septoria Species 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical class 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
239000001166 ammonium sulphate Substances 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 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
235000010233 benzoic acid Nutrition 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
239000004327 boric acid Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002170 ethers Chemical class 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
230000000855 fungicidal effect Effects 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
230000005484 gravity Effects 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
238000000338 in vitro Methods 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
-1 loess Chemical class 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
FISRGBICZQXBOD-UHFFFAOYSA-N methane phosphoric acid Chemical compound C.C.OP(O)(O)=O FISRGBICZQXBOD-UHFFFAOYSA-N 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000000843 powder Substances 0.000 description 1
CQBPOPVKDNHISM-UHFFFAOYSA-N propane-1,2,3-triol;propan-2-one Chemical compound CC(C)=O.OCC(O)CO CQBPOPVKDNHISM-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000002689 soil Substances 0.000 description 1
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
238000010998 test method Methods 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
235000019731 tricalcium phosphate Nutrition 0.000 description 1
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/38—Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

IL29305A 1967-01-17 1968-01-12 Pesticidal preparations containing diaralkyl amines IL29305A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH66667A CH480791A (de)	1967-01-17	1967-01-17	Schädlingsbekämpfungsmittel

Publications (1)

Publication Number	Publication Date
IL29305A true IL29305A (en)	1971-07-28

Family

ID=4192298

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL29305A IL29305A (en)	1967-01-17	1968-01-12	Pesticidal preparations containing diaralkyl amines

Country Status (6)

Country	Link
US (1)	US3493662A (fr)
CH (1)	CH480791A (fr)
DE (1)	DE1717104A1 (fr)
FR (1)	FR1551465A (fr)
GB (1)	GB1209961A (fr)
IL (1)	IL29305A (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1430046A (en) *	1974-03-07	1976-03-31	Ici Ltd	Nitrobenzene derivatives
GB1455207A (en) *	1974-11-06	1976-11-10	Ici Ltd	Substituted dinitro-diphenylamines and their pesticidal compositions
US4011344A (en) *	1975-03-14	1977-03-08	Sandoz, Inc.	Iminodimethylene di-tert-alkylophenones and phenols
DE2825961A1 (de) *	1978-06-14	1980-01-03	Basf Ag	Fungizide amine
JP2818958B2 (ja) *	1990-02-23	1998-10-30	塩野義製薬株式会社	４―（４―アルコキシフェニル）―２―ブチルアミン誘導体およびその製造法
US6001884A (en) *	1991-08-23	1999-12-14	Nps Pharmaceuticals, Inc.	Calcium receptor-active molecules
US6313146B1 (en)	1991-08-23	2001-11-06	Nps Pharmaceuticals, Inc.	Calcium receptor-active molecules
US6011068A (en) *	1991-08-23	2000-01-04	Nps Pharmaceuticals, Inc.	Calcium receptor-active molecules
DE122005000033I1 (de)	1994-10-21	2005-09-29	Nps Pharma Inc	Kalzium-Rezeptor aktive Verbindungen.
ES2280460T3 (es) *	1996-05-01	2007-09-16	Nps Pharmaceuticals, Inc.	Compuestos activos frente a receptores de iones inorganicos.

1967
- 1967-01-17 CH CH66667A patent/CH480791A/de not_active IP Right Cessation
1968
- 1968-01-09 DE DE19681717104 patent/DE1717104A1/de active Pending
- 1968-01-12 FR FR1551465D patent/FR1551465A/fr not_active Expired
- 1968-01-12 IL IL29305A patent/IL29305A/en unknown
- 1968-01-15 GB GB2057/68A patent/GB1209961A/en not_active Expired
- 1968-01-15 US US697608A patent/US3493662A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
DE1717104A1 (de)	1971-08-05
FR1551465A (fr)	1968-12-27
US3493662A (en)	1970-02-03
GB1209961A (en)	1970-10-28
CH480791A (de)	1969-11-15

Publication	Publication Date	Title
IL29305A (en)	1971-07-28	Pesticidal preparations containing diaralkyl amines
GB862863A (en)	1961-03-15	Improvements in or relating to preparations for influencing the growth of plants
US3766238A (en)	1973-10-16	3-nitro-4-phenoxy benzonitriles
US3642989A (en)	1972-02-15	Nematocidal preparations containing phosphonium compounds as the ingredient
US3046189A (en)	1962-07-24	Nematocidal agents
US3777024A (en)	1973-12-04	Synergistically activated biocidal compositions
EP0213328A1 (fr)	1987-03-11	Compositions pesticides sèches
DE1147796B (de)	1963-04-25	Mittel zur Bekaempfung von pflanzenparasitaeren Nematoden
US3210423A (en)	1965-10-05	N, n'-di(tetra-substituted-phenyl)-diaminomethanes
US3008869A (en)	1961-11-14	Nematocide compositions
US3421883A (en)	1969-01-14	Pesticidal preparation and method of use
US2923727A (en)	1960-02-02	O-alkyl-s-pentachlorophenyl thiolcarbonate
US3287463A (en)	1966-11-22	Certain 3-chloromethyl-and 3-phenyl-1, 3, 4-thiadiazoles
NO145437B (no)	1981-12-14	Analogifremgangsmaate for fremstilling av en fysiologisk aktiv p-bifenylester av en prostaglandinanalog av e- eller f-serien.
NO122598B (fr)	1971-07-19
US2991221A (en)	1961-07-04	Urea-ethylene dibromide adducts
US3700778A (en)	1972-10-24	Insecticidal composition containing trifluoromethyl substituted benzanilides and method of using the same
GB1247272A (en)	1971-09-22	Novel phosphoroamidothioates and their use as herbicides
JPS6333305A (ja)	1988-02-13	殺虫、殺ダニ組成物
JP4603663B2 (ja)	2010-12-22	高濃度希釈用種子消毒製剤
JP2970666B2 (ja)	1999-11-02	農薬固型製剤
US3642856A (en)	1972-02-15	Dithiocarbamylacetoneoxime carbamates
US3271442A (en)	1966-09-06	5-acenaphthenyl esters of carbamic acid and nu-substituted alkyl carbamic acids
GB2129412A (en)	1984-05-16	Plant growth regulating composition
JPH09309805A (ja)	1997-12-02	除草剤