CA1116076A - Raticides - Google Patents

Raticides

Info

Publication number: CA1116076A
Authority: CA; Canada
Prior art keywords: glycol; solvent; compound; concentrate; bromadiolone
Prior art date: 1976-07-13
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

CA258,561A

Other languages

English (en)

Inventor

Eugene Boschetti

Jean-Claude Lechevin

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.)

Merck Sante SAS

Original Assignee

LIPHA Liyonnaise Industrielle Pharmaceutique

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.)

1976-07-13

Filing date

1976-08-06

Publication date

1982-01-12

1976-08-06 Application filed by LIPHA Liyonnaise Industrielle Pharmaceutique filed Critical LIPHA Liyonnaise Industrielle Pharmaceutique

1982-01-12 Application granted granted Critical

1982-01-12 Publication of CA1116076A publication Critical patent/CA1116076A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 15
230000001119 rodenticidal effect Effects 0.000 title claims abstract description 8
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 81
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 28
150000001875 compounds Chemical class 0.000 claims abstract description 14
239000006184 cosolvent Substances 0.000 claims abstract description 8
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 21
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 11
239000005966 Bromadiolone Substances 0.000 claims description 11
OWNRRUFOJXFKCU-UHFFFAOYSA-N Bromadiolone Chemical compound C=1C=C(C=2C=CC(Br)=CC=2)C=CC=1C(O)CC(C=1C(OC2=CC=CC=C2C=1O)=O)C1=CC=CC=C1 OWNRRUFOJXFKCU-UHFFFAOYSA-N 0.000 claims description 11
-1 polyoxy-ethylene Polymers 0.000 claims description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 9
UDHXJZHVNHGCEC-UHFFFAOYSA-N Chlorophacinone Chemical compound C1=CC(Cl)=CC=C1C(C=1C=CC=CC=1)C(=O)C1C(=O)C2=CC=CC=C2C1=O UDHXJZHVNHGCEC-UHFFFAOYSA-N 0.000 claims description 7
JYGLAHSAISAEAL-UHFFFAOYSA-N Diphenadione Chemical compound O=C1C2=CC=CC=C2C(=O)C1C(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 JYGLAHSAISAEAL-UHFFFAOYSA-N 0.000 claims description 6
229960000267 diphenadione Drugs 0.000 claims description 6
HENZOLWOIZODCT-UHFFFAOYSA-N coumachlor Chemical compound OC=1OC2=CC=CC=C2C(=O)C=1C(CC(=O)C)C1=CC=C(Cl)C=C1 HENZOLWOIZODCT-UHFFFAOYSA-N 0.000 claims 1
VXIXUWQIVKSKSA-UHFFFAOYSA-N 4-hydroxycoumarin Chemical compound C1=CC=CC2=C1OC(=O)C=C2O VXIXUWQIVKSKSA-UHFFFAOYSA-N 0.000 abstract description 8
239000002574 poison Substances 0.000 abstract description 5
231100000614 poison Toxicity 0.000 abstract description 5
WFFZGYRTVIPBFN-UHFFFAOYSA-N 3h-indene-1,2-dione Chemical compound C1=CC=C2C(=O)C(=O)CC2=C1 WFFZGYRTVIPBFN-UHFFFAOYSA-N 0.000 abstract description 4
239000002904 solvent Substances 0.000 abstract description 4
230000000694 effects Effects 0.000 abstract description 3
239000003146 anticoagulant agent Substances 0.000 abstract 1
229940127219 anticoagulant drug Drugs 0.000 abstract 1
239000007788 liquid Substances 0.000 abstract 1
230000014508 negative regulation of coagulation Effects 0.000 abstract 1
239000007787 solid Substances 0.000 abstract 1
239000012141 concentrate Substances 0.000 description 15
235000008504 concentrate Nutrition 0.000 description 15
239000000243 solution Substances 0.000 description 15
241000283984 Rodentia Species 0.000 description 13
229920003171 Poly (ethylene oxide) Polymers 0.000 description 8
238000001816 cooling Methods 0.000 description 6
235000007319 Avena orientalis Nutrition 0.000 description 5
244000075850 Avena orientalis Species 0.000 description 5
DEKWZWCFHUABHE-UHFFFAOYSA-N Coumachlor Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=C(Cl)C=C1 DEKWZWCFHUABHE-UHFFFAOYSA-N 0.000 description 5
238000002156 mixing Methods 0.000 description 5
239000006010 Difenacoum Substances 0.000 description 4
FVQITOLOYMWVFU-UHFFFAOYSA-N Difenacoum Chemical compound O=C1OC=2C=CC=CC=2C(O)=C1C(C1=CC=CC=C1C1)CC1C(C=C1)=CC=C1C1=CC=CC=C1 FVQITOLOYMWVFU-UHFFFAOYSA-N 0.000 description 4
241000209140 Triticum Species 0.000 description 4
235000021307 Triticum Nutrition 0.000 description 4
150000002334 glycols Chemical class 0.000 description 4
231100000331 toxic Toxicity 0.000 description 4
230000002588 toxic effect Effects 0.000 description 4
PJVWKTKQMONHTI-UHFFFAOYSA-N warfarin Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 PJVWKTKQMONHTI-UHFFFAOYSA-N 0.000 description 4
229960005080 warfarin Drugs 0.000 description 4
QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
238000000034 method Methods 0.000 description 3
241000700159 Rattus Species 0.000 description 2
230000006378 damage Effects 0.000 description 2
238000004090 dissolution Methods 0.000 description 2
PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 2
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
239000003128 rodenticide Substances 0.000 description 2
239000008399 tap water Substances 0.000 description 2
235000020679 tap water Nutrition 0.000 description 2
ULSLJYXHZDTLQK-UHFFFAOYSA-N Coumatetralyl Chemical group C1=CC=CC2=C1OC(=O)C(C1C3=CC=CC=C3CCC1)=C2O ULSLJYXHZDTLQK-UHFFFAOYSA-N 0.000 description 1
244000000626 Daucus carota Species 0.000 description 1
235000002767 Daucus carota Nutrition 0.000 description 1
241000551547 Dione <red algae> Species 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
235000007340 Hordeum vulgare Nutrition 0.000 description 1
HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 description 1
244000141359 Malus pumila Species 0.000 description 1
241000699670 Mus sp. Species 0.000 description 1
102100027378 Prothrombin Human genes 0.000 description 1
108010094028 Prothrombin Proteins 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002429 anti-coagulating effect Effects 0.000 description 1
235000021016 apples Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
229940039716 prothrombin Drugs 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
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom

Landscapes

Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

CA258,561A 1976-07-13 1976-08-06 Raticides Expired CA1116076A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR7621377A FR2304290A2 (fr)	1976-07-13	1976-07-13	Nouvelles compositions rodenticides
FR7621.377		1976-07-13

Publications (1)

Publication Number	Publication Date
CA1116076A true CA1116076A (fr)	1982-01-12

Family

ID=9175647

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA258,561A Expired CA1116076A (fr)	1976-07-13	1976-08-06	Raticides

Country Status (4)

Country	Link
CA (1)	CA1116076A (fr)
CS (1)	CS210660B2 (fr)
FR (1)	FR2304290A2 (fr)
IL (1)	IL50226A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN111685110A (zh) *	2020-06-29	2020-09-22	广东省农业科学院植物保护研究所	N,n-二甲基甲酰胺在抗凝血杀鼠剂渗透剂中的应用

1976
- 1976-07-13 FR FR7621377A patent/FR2304290A2/fr active Granted
- 1976-08-06 CA CA258,561A patent/CA1116076A/fr not_active Expired
- 1976-08-09 IL IL5022676A patent/IL50226A/xx unknown
- 1976-08-11 CS CS523776A patent/CS210660B2/cs unknown

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN111685110A (zh) *	2020-06-29	2020-09-22	广东省农业科学院植物保护研究所	N,n-二甲基甲酰胺在抗凝血杀鼠剂渗透剂中的应用

Also Published As

Publication number	Publication date
CS210660B2 (en)	1982-01-29
FR2304290B2 (fr)	1980-03-14
FR2304290A2 (fr)	1976-10-15
IL50226A (en)	1979-10-31

Legal Events

Date	Code	Title	Description
1999-01-12	MKEX	Expiry

Publication	Publication Date	Title
US4985251A (en)	1991-01-15	Flowable insecticidal delivery compositions and methods for controlling insect populations in an aquatic environment
KR20000022165A (ko)	2000-04-25	살충 조성물
JP6193852B2 (ja)	2017-09-06	害虫防除剤
US8440213B2 (en)	2013-05-14	Pesticides formulations
JP2861076B2 (ja)	1999-02-24	殺虫性水性液剤
US4310536A (en)	1982-01-12	Rodenticidal compositions
CA1079630A (fr)	1980-06-17	Rodenticide
CA1116076A (fr)	1982-01-12	Raticides
US3867546A (en)	1975-02-18	Novel rodenticides compositions
JP2636880B2 (ja)	1997-07-30	効力の増強された農業用殺虫殺ダニ剤
JPH0647537B2 (ja)	1994-06-22	アゾ−ル含有乳化性濃厚液
RU2077200C1 (ru)	1997-04-20	Способ приготовления биоцидного гелеобразного препарата, биоцидный гелеобразный препарат, родентицидный гелеобразный препарат "гельцин", родентицидный гелеобразный препарат "гельдан", инсектицидный гелеобразный препарат "инсектогель-а"
US6103793A (en)	2000-08-15	Composition and process for retarding drift and promoting deposition in a spraying operation
JPH0826907A (ja)	1996-01-30	低環境有害性・乳化性濃厚農薬製剤
JP4124993B2 (ja)	2008-07-23	殺虫剤組成物及びエアゾール剤
JPS60104004A (ja)	1985-06-08	低薬害性エアゾ−ル農薬組成物
RU2015671C1 (ru)	1994-07-15	Средство для уничтожения грызунов
WO2025078275A1 (fr)	2025-04-17	Composition agrochimique
KR20090100347A (ko)	2009-09-23	살충제용 침투 증진제
JPS5817721B2 (ja)	1983-04-09	可溶化型木材用防虫防蟻剤
CN108308187A (zh)	2018-07-24	一种农药组合物及其应用
JPH0699249B2 (ja)	1994-12-07	害虫防除剤
CA1307201C (fr)	1992-09-08	Compositions fluidifiables liberant de l'insecticide et methodes pour combattre des populations d'insectes dans un environnement aquatique
JPH07330513A (ja)	1995-12-19	殺虫剤の効力増強剤
CN107821428A (zh)	2018-03-23	一种复合增效农药

CA1116076A - Raticides - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (2)

Publications (1)

Family

ID=9175647

Family Applications (1)

Country Status (4)

Cited By (1)

Cited By (1)

Also Published As

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Legal Events