KR950000003A - Seed treatment using phosphorous acid or one of its inflammations, and the seed so treated - Google Patents

Seed treatment using phosphorous acid or one of its inflammations, and the seed so treated Download PDF

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KR950000003A
KR950000003A KR1019940014506A KR19940014506A KR950000003A KR 950000003 A KR950000003 A KR 950000003A KR 1019940014506 A KR1019940014506 A KR 1019940014506A KR 19940014506 A KR19940014506 A KR 19940014506A KR 950000003 A KR950000003 A KR 950000003A
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seed
group
salts
active substance
pythium
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KR1019940014506A
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KR100353181B1 (en
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샤잘레 모리스
뮈니에 쟈끄
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빠뜨릭 제냉
롱-쁠랑 아그로쉬미
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    • 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
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/26—Phosphorus; Compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/38—Polysiloxanes modified by chemical after-treatment
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
    • C08G77/50—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Inorganic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Plant Pathology (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)
  • Pretreatment Of Seeds And Plants (AREA)

Abstract

트리아졸 2-(4-클로로벤질리덴)-5,5-디메틸-1-(1H-1,2,4-트리아졸-1-일메틸)-1-시클로펜탄올의 부재하에, 아인산 또는 그의 염으로 이루어진 군으로부터 선택된 활성물질의 유효량을 살 진균성 관점으로 곡물의 내부 또는 그 위에 함유하는 것을 특징으로 하는 종자.Phosphoric acid or its in the absence of triazole 2- (4-chlorobenzylidene) -5,5-dimethyl-1- (1H-1,2,4-triazol-1-ylmethyl) -1-cyclopentanol A seed comprising an effective amount of an active substance selected from the group consisting of salts in or on the grains in terms of fungicide.

트리아졸 2-(4-클로로벤질리덴)-5,5-디메틸-1-(1H-1,2,4-트리아졸-1-일메틸)-1-시클로펜탄올의 부재하에, 아인산 또는 그의 염으로 이루어진 군으로부터 선택된 활성물질의 유효량을 살 진균성 관점으로 곡물의 내부 또는 그 위에 함유하는 것을 특징으로 하는 외떡잎 식물 종자.Phosphoric acid or its in the absence of triazole 2- (4-chlorobenzylidene) -5,5-dimethyl-1- (1H-1,2,4-triazol-1-ylmethyl) -1-cyclopentanol A monocotyledonous plant seed characterized by containing an effective amount of an active substance selected from the group consisting of salts in or on the grains in terms of fungicide.

Description

아인산 또는 그의 염중에 하나를 사용한 종자 처리, 및 이와같이 처리된 종자Seed treatment with phosphorous acid or one of its salts, and the seed so treated

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (14)

트리아졸 2-(4-클로로벤질리덴)-5,5-디메틸-1-(1H-1,2,4-트리아졸-1-일메틸)-1-시클로펜탄올의 부재하에, 아인산 또는 그의 염으로 이루어진 군으로부터 선택된 활성물질의 유효량을 살 진균성의 관점으로 곡물의 내부 또는 그위에 함유하는 것을 특징으로 하는 식물 종자.Phosphoric acid or its in the absence of triazole 2- (4-chlorobenzylidene) -5,5-dimethyl-1- (1H-1,2,4-triazol-1-ylmethyl) -1-cyclopentanol A plant seed characterized by containing an effective amount of an active substance selected from the group consisting of salts in or on the grains in terms of fungicide. 트리아졸 2-(4-클로로벤질리덴)-5,5-디메틸-1-(1H-1,2,4-트리아졸-1-일메틸)-1-시클로펜탄올의 부재하에, 아인산 또는 그의 염으로 이루어진 군으로부터 선택된 활성물질의 유효량을 살 진균성 관점으로 곡물의 내부 또는 그위에 함유하는 것을 특징으로 하는 외떡잎 식물 종자.Phosphoric acid or its in the absence of triazole 2- (4-chlorobenzylidene) -5,5-dimethyl-1- (1H-1,2,4-triazol-1-ylmethyl) -1-cyclopentanol A monocotyledonous plant seed characterized by containing an effective amount of an active substance selected from the group consisting of salts in or on the grains in terms of fungicide. 제1 또는 2항에 있어서, 인 활성물질이 아인산 또는 그의 알칼리 금속 또는 암모늄 염중의 하나를 함유하는 것을 특징으로 하는 종자.The seed according to claim 1 or 2, wherein the phosphorus active material contains phosphorous acid or one of its alkali metal or ammonium salts. 제1 또는 2항에 있어서, 인 활성물질이 20℃에서 물에 대한 그의 용해도가 0.1g/1 이상, 바람직하게는 0.5g/1 이상의 양이 되도록 선택되는 것을 특징으로 하는 종자.The seed according to claim 1 or 2, characterized in that the phosphorus active material is selected such that its solubility in water is at least 0.1 g / 1, preferably at least 0.5 g / 1 at 20 ° C. 제1 또는 2항에 있어서, 인 활성물질이 1g/q 내지 1kg/q, 바람직하게는 5 내지 500g/q의 양인 것을 특징으로 하는 종자.Seed according to claim 1 or 2, characterized in that the phosphorus active material is in an amount of 1 g / q to 1 kg / q, preferably 5 to 500 g / q. 제2항에 있어서, 외떡잎 식물이 곡물, 특히 밀, 보리, 호밀, 가을 보리, 귀리, 트리티케일(triticale), 옥수수 또는 벼로 이루어진 군으로 부터 선택되는 것을 특징으로 하는 종자.3. The seed of claim 2, wherein the monocotyledonous plant is selected from the group consisting of cereals, in particular wheat, barley, rye, autumn barley, oats, triticale, corn or rice. 제1 또는 2항에 있어서, *피티움 아르헤노마네스(Pythium arrhenomanes), 피티움 그라미니콜라(Pythium graminicola), 피티움 토룰로숨(Pythium torulosum), 피티움 반테르포올리이(Pythium vanterpoolii), 피티움 미리오틸룸(Pythiummyriotylum), 피티움 페리일룸(Pythium periilum), 피티움 아리스토스포룸(Pythium aristosporum), 또는 피티움 아파니데르마툼(Pythium aphanidermatum)으로 이루어진 군에 속하는 병해, *말라시드는 병, *뿌리 부패증, *어린 식물의 경령(collar)부패증으로 구성된 군으로부터의 병해의 침해에 대하여 보호되는 것을 특징으로 하는 종자.The method according to claim 1 or 2, further comprising: * Pythium arrhenomanes, Pythium graminicola, Pythium torulosum, Pythium vanterpoolii, Disease belonging to the group consisting of Pythiummyriotylum, Pythium periilum, Pythium aristosporum, or Pythium aphanidermatum, * Malassid is a disease , * Root rot, * Seed characterized in that it is protected against invasion of the disease from the group consisting of collar rot of young plants. 제1 또는 2항에 있어서, 캅탄, 티람, 구아자틴, 옥신-구리 또는 메탈락실 뿐만 아니라 이미다클로프리드, 린단 및 엔도술판 등과같은 살곤충제로 이루어진 군으로부터 선택된 이차 활성 물질을 함유하는 것을 특징으로 하는 종자.The method according to claim 1 or 2, characterized in that it contains a secondary active substance selected from the group consisting of captanes, thirams, guazines, auxins-copper or metallaxyl as well as insecticides such as imidacloprid, lindane and endosulfane. strain. 제1 또는 2항에 있어서, 아스피린 또는 그의 염 및 에스테르 또는 살리실산 또는 그의 염 및 에스테르로 이루어진 군으로부터 선택된 이차활성 물질을 함유하는 것을 특징으로 하는 종자.The seed according to claim 1 or 2, which contains a secondary active substance selected from the group consisting of aspirin or salts and esters thereof or salicylic acid or salts and esters thereof. 제1 내지 9항중의 어느 한 항에 따른 종자의 발아로 부터 생성되는 것을 특징으로 하는 어린 식물.A young plant, which is produced from the germination of a seed according to any one of claims 1 to 9. 아인산 및 그의 염으로 이루어진 군을 포함하는 인 활성물질의 유효량을 상기 종자에 적용하는 것을 특징으로 하는 진균성 병해에 대하여, 종자 바람직하게는 외떡잎 식물의 종자를 보호하는 방법.A method for protecting the seed, preferably of the monocotyledonous plant, against fungal diseases characterized by applying an effective amount of a phosphorus active substance comprising a group consisting of phosphorous acid and salts thereof to the seed. *아인산 또는 그의 염으로 이루어진 군에서 선택된 하나 이상의 활성물질, *농경학적으로 수용 가능한 하나 이상의 비활성 부형제 및, *농경학적으로 수용 가능한 임의의 계면 활성제, *트리아졸 2-(4-클로로벤질리덴)-5,5-디메틸-1, -(1H-1,2,4-트리아졸-1-일메틸)-1-시클로펜탄올 이외의 이들 조성물의 여러 성분을 함유하는 것을 특징으로 하는 진균성 병해에 대하여 종자, 바람직하게는 외떡잎 식물의 종자를 보호하기 위한 살 진균성 조성물.At least one active substance selected from the group consisting of phosphorous acid or salts thereof, at least one agriculturally acceptable inert excipient, and any agriculturally acceptable surfactant, triazole 2- (4-chlorobenzylidene) Fungal diseases characterized by containing several components of these compositions other than -5,5-dimethyl-1,-(1H-1,2,4-triazol-1-ylmethyl) -1-cyclopentanol A fungicidal composition for protecting seed against seed, preferably seed of a monocotyledonous plant. 제12항에 있어서, 0.5 내지 95%의 인 형태의 활성물질을 함유하는 것을 특징으로 하는 조성물.13. A composition according to claim 12 which contains from 0.5 to 95% of the active substance in the form of phosphorus. 제12 또는 13항에 있어서, 조성물이 바람직하게는 수용액 또는 액체인 조성물.The composition according to claim 12 or 13, wherein the composition is preferably an aqueous solution or a liquid. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019940014506A 1993-06-23 1994-06-23 Seed treatment using phosphorous acid or one of its inflammations, and the seed so treated KR100353181B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9307866A FR2706736B1 (en) 1993-06-23 1993-06-23
FR9307866 1993-06-23

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KR950000003A true KR950000003A (en) 1995-01-03
KR100353181B1 KR100353181B1 (en) 2004-12-23

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CN (1) CN1051907C (en)
AT (1) AT406002B (en)
AU (1) AU679738B2 (en)
BE (1) BE1008436A5 (en)
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GR940100307A (en) 1995-02-28
ES2070792B1 (en) 1996-01-01
ITMI941312A0 (en) 1994-06-23
HRP940363A2 (en) 1996-12-31
RU2140728C1 (en) 1999-11-10
AU679738B2 (en) 1997-07-10
FR2706736B1 (en) 1995-08-25
PT101533B (en) 2000-01-31
GB9412469D0 (en) 1994-08-10
BR9401843A (en) 1995-05-02
SI9400260A (en) 1995-02-28
SE9402200L (en) 1994-12-24
KR100353181B1 (en) 2004-12-23
CN1098253A (en) 1995-02-08
TW292964B (en) 1996-12-11
CZ287051B6 (en) 2000-08-16
GB2279252A (en) 1995-01-04
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IE940516A1 (en) 1994-12-28
CA2126656A1 (en) 1994-12-24
PT101533A (en) 1995-03-31
HRP940363B1 (en) 2001-06-30
CO4340594A1 (en) 1996-07-30
DK74494A (en) 1994-12-24
ATA123494A (en) 1999-06-15
ES2070792A1 (en) 1995-06-01
PL303948A1 (en) 1995-01-09
RO113936B1 (en) 1998-12-30
LU88502A1 (en) 1996-02-01
IT1269941B (en) 1997-04-16
UA39171C2 (en) 2001-06-15
HU214299B (en) 1998-03-02
AU6484994A (en) 1995-01-05
FR2706736A1 (en) 1994-12-30
DE4422025B4 (en) 2008-01-31
IL110068A (en) 2005-11-20
IE80905B1 (en) 1999-06-16
SI9400260B (en) 2001-12-31
BE1008436A5 (en) 1996-05-07
SE9402200D0 (en) 1994-06-22
GB2279252B (en) 1997-10-15
JPH0759411A (en) 1995-03-07
CH688601A5 (en) 1997-12-15
SK75994A3 (en) 1995-01-12
SK283983B6 (en) 2004-06-08
NL9401039A (en) 1995-01-16
HU9401897D0 (en) 1994-09-28
NZ260826A (en) 1996-02-27
IL110068A0 (en) 1994-10-07
ITMI941312A1 (en) 1995-12-23

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