KR870007227A - 온도에 안전한 액체 조성물 - Google Patents

온도에 안전한 액체 조성물 Download PDF

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KR870007227A
KR870007227A KR870000065A KR870000065A KR870007227A KR 870007227 A KR870007227 A KR 870007227A KR 870000065 A KR870000065 A KR 870000065A KR 870000065 A KR870000065 A KR 870000065A KR 870007227 A KR870007227 A KR 870007227A
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phenylenediamine
dinitro
composition
group
phenyl
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KR870000065A
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KR910004552B1 (ko
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에취·잰시스 엘머
이·스토트 폴
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아이·제이·크라코워
유니로얄 케미컬 컴퍼니 인코퍼레이티드
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/32—Compounds containing nitrogen bound to oxygen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
    • C07C205/26—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups and being further substituted by halogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
    • C07C205/20—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C07C205/21—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to carbon atoms of six-membered aromatic rings having nitro groups and hydroxy groups bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C205/23—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to carbon atoms of six-membered aromatic rings having nitro groups and hydroxy groups bound to carbon atoms of the same non-condensed six-membered aromatic ring having two nitro groups bound to the ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00—Purification; Separation; Use of additives
    • C07C7/20—Use of additives, e.g. for stabilisation

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Analytical Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Water Supply & Treatment (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Anti-Oxidant Or Stabilizer Compositions (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

내용 없음

Description

온도에 안전한 액체 조성물
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (17)

  1. 방향족 탄화수소 용매에 용해된 하기 일반식의 디니트로 페놀로 구성되며 :
    (여기서 R 및 R1중의 하나는 니트로이며 다른 것은 수소, 염소 및 C1-C8알킬로 구성되어 있는 군으로 부터 선택된다)
    상기 용매내에 용해된 디니트로 페놀의 양이, 페닐렌 디아민이 존재하지 않을 경우에 상기 용매내에 용해될 수 있는 디니트로 페닐의 양보다 클 정도로 충분한 양의 하기 일반식의 페닐렌디아민을 더 포함하여 구성되는 엑체 조성물.
    (여기서 R2및 R3는, 수소, C1-C12알킬, 페닐 및 C1-C|8알킬로 치환된 페닐로 구성되어 있는 군으로부터 각각 독립적으로 선택된다)
  2. 제1항에 있어서, 디니트로 페놀이 2,6-디니트로-P-크레졸, 4,6-디니트로-0-크레졸, 2,6-디니트로-P-이소프로필 페놀, 4,6-디니트로-0-이소프로필페놀 및 4,6-디니트로-0-sec-부틸페놀로 구성되어 있는 군으로 부터 선택된 조성물.
  3. 제1항에 있어서, 페닐렌디아민이 N-페닐-N′-이소프로필-P-페닐렌디아민, N-레닐-N′-(1,3-디메틸부틸)-P-페닐렌디아민, N-페닐-N′-(1,3-디메틸펜틸)-P-페닐렌디아민, N,N′-디이소프로필-P-페닐렌디아민, N,N′-디-sec-부틸-P-페닐렌디아민 및 N,N′-비스(1,4-디메틸펜틸)-P-페닐렌디아민으로 구성되어 있는 군으로 부터 선택된 조성물.
  4. 제1항에 있어서, 방향족 탄화수소 용매가 벤젠, 톨루엔, 크실렌, 에틸벤젠, 스티렌, 비닐톨루엔, 디비닐벤젠 및 알파-메틸스티렌으로 구성되어 있는 군으로 부터 선택된 조성물.
  5. 제4항에 있어서, 방향족 탄화수소가 스티렌 및 에틸벤젠으로 구성되어 있는 군으로 선택된 조성물.
  6. 제1항에 있어서, 디니트로페놀+페닐렌디아민:방향족 탄화수소 용매의 중량비가 약 1:4-약 2:1인 조성물.
  7. 제1항에 있어서, 디니트로페놀:페닐렌디아민의 중량비가 약 2:3-3:2인 조성물.
  8. 하기 A,B,C로 구성되는 저온 안정성 액체 조성물.
    A) 하기 일반식의 디니트로페놀:
    여기서, R 및 R1중의 하나는 니트로이며 다른 것은 수소, 염소 및 C1-C8알킬로 구성되어 있는 군으로 부터 선택된다;
    B) 하기 일반식의 페닐렌디아민 :
    여기서 R2및 R3는 수소, C1-C12알킬, 페닐 및 C1-C|8알킬로 치환된 페닐로 구성되어 있는 군으로 부터 각각 독립적으로 선택된다 ; 및
    C) 방향족 탄화수소 용매 ; 여기서 성분 A:성분 B는 약 1:9-약 9:1 ; 및 여기서 성분 A+성분 B:성분 C는 최소한 약 1:10
  9. 제8항에 있어서, 디니트로페놀이 2,6-디니트로-P-크레줄, 4,6-디니트로-0-클레졸, 2,6-디니트로-P-이소프로필페놀, 4,6-디니트로-0-이소프로필레놀 및 4,6-디니트로-0-sec-부틸페놀로 구성되어 있는 군으로 부터 선택된 조성물.
  10. 제8항에 있어서, 페닐렌디아민이 N-페닐-N′-이소프로필-P-페닐렌디아민, N-페닐-N′-(1,3-디메틸부틸)-P-페닐렌디아민, N-페닐-N′-(1,3-디메틸펜틸)-P-페닐렌디아민, N,N′-디이소프로필-P-페닐렌디아민, N,N′-디-sec-부틸-P-페닐렌디아민 및 N,N′-비스(1,4-디메틸펜틸)-P-페닐렌디아민으로 구성되어 있는 군으로 부터 선택된 조성물.
  11. 제8항에 있어서, 방향족 탄화수소 용매가 벤젠, 톨루엔, 크실렌, 에틸벤젠, 스티렌, 비닐톨루엔, 디비닐벤젠 및 알파-메틸스티렌으로 구성되어 있는 군으로 부터 선택된 조성물.
  12. 제8항에 있어서, 방향족 탄화수소가 스티렌 및 에틸벤젠으로 구성되어 있는 군으로 부터 선택된 조성물.
  13. 제8항에 있어서, 디니트로페놀+페닐렌디아민:방향족 탄화수소 용매의 중량비가 약 1:4-약 2:1인 조성물.
  14. 제8항에 있어서, 디니트로페놀:페닐렌디아민의 중량비가 약 2:3-3:2인 조성물.
  15. 제8항에 있어서, 디니트로페놀이 2,6-디니트로-P-크레졸, 4,6-디니트로-0-클레졸, 2,6-디니트로-P-이소프로필페놀, 4,6-디니트로-0-이소프로필페놀 및 4,6-디니트로-0-sec-부틸페놀로 구성되어 있는 군으로 부터 선택되고, 페닐렌디아민이 N-페닐-N′-이소프로필-P-페닐렌디아민, N-페닐-N′-(1,3-디메틸부틸)-P-페닐렌디아민, N-페닐-N′-(1,3-디메틸펜틸)-P-페닐렌디아민, N,N′-디이소프로필-P-페닐렌디아민, N,N′- 디-sec-부틸-P-페닐렌디아민 및 N,N′-비스(1,4-디메틸펜틸)-P-페닐렌디아민으로 구성되어 있는 군으로 구성되어 있는 군으로 부터 선택되고 방향족 탄화수소 용매가 벤젠, 톨루엔, 크실렌, 에틸벤젠, 스티렌, 비닐톨루엔, 디비닐벤젠 및 알파-메틸스티렌으로 구성되어 있는 군으로 부터 선택된 조성물.
  16. 제15항에 있어서, 디니트로페놀+페닐렌디아민 : 방향족 탄화수소 용매의 중량비가 약 1:4-약 2:1인 조성물.
  17. 제15항에 있어서, 디니트로페놀:페닐렌디아민의 중량비가 약 2:3-3:2인 조성물.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019870000065A 1986-01-09 1987-01-08 온도에 안정한 액체 조성물 KR910004552B1 (ko)

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Application Number Priority Date Filing Date Title
US817324 1986-01-09
US06/817,324 US4664845A (en) 1986-01-09 1986-01-09 Phenylenediamine solubilizer for dinitrophenol in aromatic solvent

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KR870007227A true KR870007227A (ko) 1987-08-17
KR910004552B1 KR910004552B1 (ko) 1991-07-06

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EP (1) EP0234671B1 (ko)
JP (1) JPH01152146A (ko)
KR (1) KR910004552B1 (ko)
CN (1) CN1004139B (ko)
AR (1) AR245096A1 (ko)
AT (1) ATE63534T1 (ko)
AU (1) AU595571B2 (ko)
BR (1) BR8700050A (ko)
CA (1) CA1275168C (ko)
DE (1) DE3770019D1 (ko)
DK (1) DK11387A (ko)
ES (1) ES2022880B3 (ko)
FI (1) FI84906C (ko)
IN (1) IN166453B (ko)
MX (1) MX165080B (ko)
PT (1) PT84086B (ko)
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ZA8769B (en) 1987-08-26
IN166453B (ko) 1990-05-12
PT84086A (en) 1987-02-01
DK11387D0 (da) 1987-01-09
EP0234671B1 (en) 1991-05-15
FI84906C (fi) 1992-02-10
PT84086B (pt) 1989-02-28
CN1004139B (zh) 1989-05-10
BR8700050A (pt) 1987-12-01
AR245096A1 (es) 1993-12-30
CN87100819A (zh) 1987-09-23
US4664845A (en) 1987-05-12
AU595571B2 (en) 1990-04-05
ATE63534T1 (de) 1991-06-15
KR910004552B1 (ko) 1991-07-06
FI84906B (fi) 1991-10-31
CA1275168C (en) 1990-10-16
EP0234671A1 (en) 1987-09-02
FI870071A0 (fi) 1987-01-08
DE3770019D1 (de) 1991-06-20
FI870071A (fi) 1987-07-10
AU6717787A (en) 1987-07-16
JPH0588699B2 (ko) 1993-12-24
ES2022880B3 (es) 1991-12-16
JPH01152146A (ja) 1989-06-14
DK11387A (da) 1987-07-10
MX165080B (es) 1992-10-21

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