KR930019619A - 아미도 퍼옥시카르복실산 - Google Patents

아미도 퍼옥시카르복실산 Download PDF

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Publication number
KR930019619A
KR930019619A KR1019930004926A KR930004926A KR930019619A KR 930019619 A KR930019619 A KR 930019619A KR 1019930004926 A KR1019930004926 A KR 1019930004926A KR 930004926 A KR930004926 A KR 930004926A KR 930019619 A KR930019619 A KR 930019619A
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group
groups
alkylene
piccarboxybenzoyl
arylene
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KR1019930004926A
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린 쿠프 자네트
윌리암 릴리 험프리스 로버트
알란 마디손 스테펜
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제이. 더블류. 하이넨
유니레버 엔브이
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Application filed by 제이. 더블류. 하이넨, 유니레버 엔브이 filed Critical 제이. 더블류. 하이넨
Publication of KR930019619A publication Critical patent/KR930019619A/ko

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C409/00Peroxy compounds
    • C07C409/40Peroxy compounds containing nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182Radicals derived from carboxylic acids
    • C07D295/192Radicals derived from carboxylic acids from aromatic carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3945Organic per-compounds

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Detergent Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

본 발명은 다음과 같은 식을 가지는 아미도 피옥시산에 관한 것이다.
[이 식에서, R은알킬렌,시클로알킬렌,아릴렌기 및 이러한 기의 혼합체로 구성되는 군으로부터 선택되며, R1및 R2는 각각 H,알킬,아릴기 및와 두개의 질소와 함께고리를 형성할 수 있는 기로 구성되는 군으로부터 선택되고,알킬렌,시클로알킬렌 및아릴렌기로 구성되는 군으로부터 선택되는데 이때가 아릴렌기이고, n' 및 m'가 각각 제로인 경우 R은

Description

아미도 퍼옥시카르복실산
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (9)

  1. 다음과 같은 식을 가지는 아미도 퍼옥시산.
    [이식에서 R은알킬렌,시클로알킬렌,아릴렌기 및 이러한 기의 혼합체로 구성되는 군으로부터 선택되며, R1및 R2는 각각 H,알킬,아릴기 및와 두개의 질소와 함께고리를 형성할 수 있는 기로 구성되는 군으로부터 선택되고,알킬렌,시클로알킬렌 및아릴렌기로 구성되는 군으로부터 선택되는데 이때가 아릴렌기이고, n' 및 m'가 각각 제로인 경우 R은알킬렌이 아닌 다른기이다. n 및 n'는 각각 그 합이 1이 되도록 선택되는 정수이며, m 및 m'는 각각 그 합이 1이 되도록 선택되는 정수이고, M은 H, 알칼리 금속, 알칼리토 금속, 알칸올암모늄 양이온 및 기 및 이들의 혼합체로 구성되는 군으로부터 선택된다.
  2. 제1항에 있어서, 다음과 같은 구조체로 구성되는 군으로부터 선택되는 구조체를 가지는 피옥시산.
  3. 제1항에 있어서, 다음과 같은 화합물로부터 선택되는 퍼옥시산.
    N,N'-디(4-피카르복시벤조일)-1,4-부탄디아민,N,N'-디(4-피카르복시벤조일)-1,2-페닐렌디아민, N,N'-숙시노일-디(4-피카르복시)아닐린, N,N'-디(4-피카르복시벤조일)에틸렌디아민, N,N'-디(4-피카르복시벤조일)피페라진, N,N'-디(4-피카르복시벤조일)-1,4-디아미노시클로헥산, N,N'-디(4-피카르복시벤조일)-1,4-페닐디아민, N,N'-디(피카르복시아디포일)페닐렌디아민, N,N'-디(피카르복시아디포일)에틸렌디아민, 및 N,N'-디(4-피카르복시아닐린)테레프탈레이트.
  4. 제1항에 있어서, 40℃에서의 과산화물 반감기가 10일이상인 것을 하는 피옥시산.
  5. 제4항에 있어서, 40℃에서의 과산화물 반감기가 30일이상인 것을 하는 피옥시산.
  6. 제1항에 있어서, 100℃이상의 자기-가열 개시온도(self-heating onset temperature)를 가지는 것을 특징으로 하는 피옥시산.
  7. 제6항에 있어서, 약 120℃-200℃의 자가-가열 개시온도를 가지는 것을 특징으로 하는 피옥시산.
  8. 오염을 제거하는데 효과적인 양의 다음가 같은 구조식을 가지는 아미도 피옥시산을 기질에 적용시키는 단계를 포함하는 것을 특징으로 하는, 기질을 표백시키는 방법.
    [이식에서, R은알킬렌,시클로알킬렌,아릴렌기 및 이러한 기의 혼합체로 구성되는 군으로부터 선택되며, R1및 R2는 각각 H,알킬,아릴기 및와 두개의 질소와 함께고리를 형성할수 있는 기로 구성되는 군으로부터 선택되고,알킬렌,시클로알킬렌 및아릴렌기로 구성되는 군으로부터 선택되는데 이때가 아릴렌기이고 n' 및 m'가 각각 제로인 경우 R은알킬렌이 아닌 다른기이다. n 및 n'는 각각 그 합이 1이 되도록 선택되는 정수이며, m 및 m'는 각각 그 합이 1이 되도록 선택되는 정수이고, M은 H, 알칼리금속, 알칼리토금속, 암모늄, 알칸올암모늄 양이온 및 기 및 이들의 혼합체로 구성되는 군으로 부터 선택된다.]
  9. 다음과 같은 성분을 함유하는 세정제 조성물.
    i) 1-40중량%의 제1항의 아미도 피옥시산. ii) 1-50중량%의 계면활성제. iii) 1-40중량%의 pH-점프 시스템.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019930004926A 1992-03-31 1993-03-29 아미도 퍼옥시카르복실산 KR930019619A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US07/860,849 US5268003A (en) 1992-03-31 1992-03-31 Stable amido peroxycarboxylic acids for bleaching
US860849 1992-03-31

Publications (1)

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KR930019619A true KR930019619A (ko) 1993-10-18

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US (1) US5268003A (ko)
EP (1) EP0564251B1 (ko)
JP (1) JPH06100531A (ko)
KR (1) KR930019619A (ko)
CN (1) CN1078719A (ko)
AU (1) AU651926B2 (ko)
BR (1) BR9301372A (ko)
CA (1) CA2092862A1 (ko)
DE (1) DE69300436T2 (ko)
ES (1) ES2078801T3 (ko)
MX (1) MX9301751A (ko)
ZA (1) ZA932318B (ko)

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CA2092862A1 (en) 1993-10-01
US5268003A (en) 1993-12-07
JPH06100531A (ja) 1994-04-12
BR9301372A (pt) 1993-10-13
ES2078801T3 (es) 1995-12-16
CN1078719A (zh) 1993-11-24
ZA932318B (en) 1994-09-30
EP0564251B1 (en) 1995-09-06
DE69300436T2 (de) 1996-02-29
DE69300436D1 (de) 1995-10-12
EP0564251A3 (en) 1993-10-27
AU3549493A (en) 1993-10-07
MX9301751A (es) 1993-10-01
AU651926B2 (en) 1994-08-04
EP0564251A2 (en) 1993-10-06

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