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KR930017491A - Bactericidal Compositions for Industrial Use - Google Patents

Bactericidal Compositions for Industrial Use Download PDF

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Publication number
KR930017491A
KR930017491A KR1019930001628A KR930001628A KR930017491A KR 930017491 A KR930017491 A KR 930017491A KR 1019930001628 A KR1019930001628 A KR 1019930001628A KR 930001628 A KR930001628 A KR 930001628A KR 930017491 A KR930017491 A KR 930017491A
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South Korea
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composition
group
isothiazolin
methyl
water
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KR1019930001628A
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Korean (ko)
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KR100250787B1 (en
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유따까 스네미
다이끼 구사까
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모리따 가쓰라
다께다야꾸힝고오교 가부시끼가이샤
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Publication of KR930017491A publication Critical patent/KR930017491A/en
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Publication of KR100250787B1 publication Critical patent/KR100250787B1/en

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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
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • 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
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

본 발명은 이소티아졸론 화합물, 브롬산 또는 요오드산의 알칼리 금속염 및 물을 함유하는 산업적 용도용 살균조성물에 관한 것이다. 살균조성물중의 이소티아졸론 화합물은 장기간 동안 안정하게 유지될 수 있다.The present invention relates to a sterilizing composition for industrial use containing isothiazolone compounds, alkali metal salts of bromic acid or iodic acid and water. The isothiazolone compound in the bactericidal composition can remain stable for a long time.

Description

산업적 용도를 위한 살균 조성물Bactericidal Compositions for Industrial Use

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

Claims (18)

이소티아졸론 화합물, 브롬산 또는 요오드산의 알칼리 금속염 및 물을 함유함을 특징으로 하는 산업적 용도용 살균 조성물.A sterilizing composition for industrial use, which comprises an isothiazolone compound, an alkali metal salt of bromic acid or iodic acid and water. 제1항에 있어서, 이소티아졸론 화합물이 하기 일반식(Ⅰ)의 화합물 또는 하기 일반식(Ⅱ)의 화합물인 조성물:The composition of claim 1, wherein the isothiazolone compound is a compound of formula (I) or a compound of formula (II) (상기식에서, Y는 수소원자 또는 임의로 치환된 탄화수기를 나타내고; X1및X2는 각각 수소원자, 할로겐원자 또는 알킬기를 나타내고, 고리 A는 임의로 치환된 벤젠을 나타낸다.(Wherein Y represents a hydrogen atom or an optionally substituted hydrocarbon group; X 1 and X 2 each represent a hydrogen atom, a halogen atom or an alkyl group, and ring A represents an optionally substituted benzene). 제2항에 있어서, 임으로 치환된 탄화수소기가 (ⅰ)C1~10알킬기, (ⅱ)C2~6알케닐기. (ⅲ)C2~6알키닐기, (ⅳ)C3~10시클로알킬기 또는 (ⅴ)C6~14아릴기이고, 이들 각각은 히드록실기, 할로겐원자, 시아노기, 아미노기, 카르복실기, C1~4알콕시기, C6~10아릴옥시기, C1~4알킬티오기 및 C6~10아릴티오기 및 C6~19아릴티오기로 구성된 군으로부터 선택된 1내지 5개의 환제로 치환될 수 있는 조성물.The hydrocarbon group according to claim 2, wherein the optionally substituted hydrocarbon group is (i) C 1-10 alkyl group, (ii) C 2-6 alkenyl group. (Ⅲ) C 2 ~ 6 alkynyl group, (ⅳ) C 3 ~ 10 cycloalkyl group, or (ⅴ) C 6 ~ 14 aryl group, each of which is a hydroxyl group, a halogen atom, a cyano group, an amino group, a carboxyl group, C 1 to 4 alkoxy groups, C 6 - 10 aryloxy group, C 1 - 4 alkylthio groups and C 6 ~ 10 arylthio, and C 6 ~ 19 arylthio group which may be substituted with 1 to 5 pill selected from the group consisting of Composition. 제2항에 있어서, 알킬기가 C1~6알킬기인 조성물.The composition of claim 2 wherein the alkyl group is a C 1-6 alkyl group. 제2항에 있어서, 임의로 치환된 벤젠이 히드록실기, 할로겐원자, 시아노기, 아미노기, 카르복실기, C1~4알킬기 및 C1~4알콕시기로 구성된 군으로부터 선택된 1 내지 4개의 치환체로 치환될 수 있는 벤젠을 나타내는 조성물.The optionally substituted benzene may be substituted with 1 to 4 substituents selected from the group consisting of hydroxyl group, halogen atom, cyano group, amino group, carboxyl group, C 1-4 alkyl group and C 1-4 alkoxy group. Composition representing benzene. 제1항에 있어서, 이소티아졸론 화합물이 2-메틸-4-이소티아졸린-3-온 및/또는 5-클로로-2-메틸-4-이소티아졸린-3-온인 조성물.The composition of claim 1 wherein the isothiazolone compound is 2-methyl-4-isothiazolin-3-one and / or 5-chloro-2-methyl-4-isothiazolin-3-one. 제6항에 있어서, 2-메틸-4-이소티아졸린-3-온 대 5-클로로-2-메틸-4-이소티아졸린-3-온의 중량비가 1:5 내지 20인 조성물.The composition of claim 6 wherein the weight ratio of 2-methyl-4-isothiazolin-3-one to 5-chloro-2-methyl-4-isothiazolin-3-one is from 1: 5 to 20. 제1항에 있어서, 알킬리 금속염이 리튬, 나트륨, 칼륨 또는 루비늄 염인 조성물.The composition of claim 1 wherein the alkyl metal salt is a lithium, sodium, potassium or rubinium salt. 제1항에 있어서, 브롬산의 알칼리 금속염이 포타슘 브로메이트인 조성물.The composition of claim 1 wherein the alkali metal salt of bromic acid is potassium bromate. 제1항에 있어서, 수용성 글리콜계 용매를 함유하는 조성물.The composition of claim 1 containing a water soluble glycol solvent. 제10항에 있어서, 수용성 글리콜계 용매가 에틸렌 글리콜, 프로필렌 글리콜 또는 디프로필렌 글리콜인 조성물.The composition of claim 10 wherein the water soluble glycol solvent is ethylene glycol, propylene glycol or dipropylene glycol. 제1항에 있어서, 이소티아졸론 화합물 대 브롬산 또는 요오드산의 알칼리 금속염의 중량비가 1:0.02 내지 0.5인 조성물.The composition of claim 1 wherein the weight ratio of the isothiazolone compound to the alkali metal salt of bromic acid or iodic acid is from 1: 0.02 to 0.5. 제1항에 있어서, 이소티아졸론 화합물 대 물의 중량비가 1:5 내지 30인 조성물.The composition of claim 1 wherein the weight ratio of isothiazolone compound to water is from 1: 5 to 30. 제10항에 있어서, 물 대 수용성 글리콜계 용매의 중량비가 1:0.1 내지 10인 조성물.The composition of claim 10 wherein the weight ratio of water to water soluble glycol solvent is from 1: 0.1 to 10. 제1항에 있어서, 이소티아졸론 화합물 0.1 내지 10중량%를 함유하는 조성물.The composition of claim 1 containing from 0.1 to 10% by weight of isothiazolone compound. 제1항에 있어서, 2-메틸-4-이소티아졸린-3-온, 5-클로로-2-메틸-4-이소티아졸린-3-온, 포타슘 브로메이트, 물 및 에틸렌 글리콜을 함유하는 조성물.The composition of claim 1 containing 2-methyl-4-isothiazolin-3-one, 5-chloro-2-methyl-4-isothiazolin-3-one, potassium bromate, water and ethylene glycol . 제1항에 있어서, 라텍스 유액용 살균조성물인 조성물.The composition of claim 1 which is a sterile composition for latex emulsion. 이소티아졸론 화합물, 브롬산 또는 요오드산의 알칼리 금속염 및 물을 혼합하는 것을 특징으로 하는 이소티아졸론 화합물의 안정화방법Method for stabilizing an isothiazolone compound characterized by mixing an isothiazolone compound, an alkali metal salt of bromic acid or iodic acid and water ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019930001628A 1992-02-10 1993-02-06 Bactericidal Compositions for Industrial Use KR100250787B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2398892 1992-02-10
JP92-23988 1992-02-10

Publications (2)

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KR930017491A true KR930017491A (en) 1993-09-20
KR100250787B1 KR100250787B1 (en) 2000-04-01

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KR1019930001628A KR100250787B1 (en) 1992-02-10 1993-02-06 Bactericidal Compositions for Industrial Use

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KR100250787B1 (en) 2000-04-01

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