KR950704451A - 미네랄 오일에 대한 표지 시약으로서의 아닐린(anilines as marking agents for mineral oils) - Google Patents
미네랄 오일에 대한 표지 시약으로서의 아닐린(anilines as marking agents for mineral oils) Download PDFInfo
- Publication number
- KR950704451A KR950704451A KR1019950702020A KR19950702020A KR950704451A KR 950704451 A KR950704451 A KR 950704451A KR 1019950702020 A KR1019950702020 A KR 1019950702020A KR 19950702020 A KR19950702020 A KR 19950702020A KR 950704451 A KR950704451 A KR 950704451A
- Authority
- KR
- South Korea
- Prior art keywords
- substituted
- unsubstituted
- alkyl
- hydrogen
- alkenyl
- Prior art date
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- 239000002480 mineral oil Substances 0.000 title claims abstract 8
- 239000003550 marker Substances 0.000 title claims abstract 3
- 150000001448 anilines Chemical class 0.000 title 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims abstract 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 16
- 239000001257 hydrogen Substances 0.000 claims abstract 14
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 14
- 125000000217 alkyl group Chemical group 0.000 claims abstract 7
- 235000010446 mineral oil Nutrition 0.000 claims abstract 7
- -1 nitro, formyl Chemical group 0.000 claims abstract 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract 4
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract 3
- 125000000524 functional group Chemical group 0.000 claims abstract 3
- 125000005842 heteroatom Chemical group 0.000 claims abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 2
- 239000012954 diazonium Substances 0.000 claims 4
- 150000001989 diazonium salts Chemical class 0.000 claims 4
- 239000008346 aqueous phase Substances 0.000 claims 2
- 239000007864 aqueous solution Substances 0.000 claims 2
- 239000000987 azo dye Substances 0.000 claims 2
- 239000000872 buffer Substances 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 229950003476 aminothiazole Drugs 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 claims 1
- 125000005605 benzo group Chemical group 0.000 claims 1
- 239000007853 buffer solution Substances 0.000 claims 1
- 125000001033 ether group Chemical group 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- GLQWRXYOTXRDNH-UHFFFAOYSA-N thiophen-2-amine Chemical compound NC1=CC=CS1 GLQWRXYOTXRDNH-UHFFFAOYSA-N 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- TVEXGJYMHHTVKP-UHFFFAOYSA-N 6-oxabicyclo[3.2.1]oct-3-en-7-one Chemical compound C1C2C(=O)OC1C=CC2 TVEXGJYMHHTVKP-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000004450 alkenylene group Chemical class 0.000 abstract 1
- 125000005137 alkenylsulfonyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
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- C07D295/04—Heterocyclic 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 with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic 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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
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- G01—MEASURING; TESTING
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- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/26—Oils; Viscous liquids; Paints; Inks
- G01N33/28—Oils, i.e. hydrocarbon liquids
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Abstract
하기 일반식(I)의 아닐린은 미네랄 오일의 마커로서 사용되며, 상기 아닐린은 미네랄 오닐 내에서 검출된다.
상기 식에서, R1및 R2는 서로 독립적으로 수소원자, 치환되거나 치환되지 않고 각 작용기에 1 내지 3개의 산소원자 또는 알킬아미노로 차단된 알킬 치환되거나 치환되지 않은 페닐이거나, 또는 R1및 R2가 질소원자와 함께 다른 헤테로 원자를 더 포함할 수 있는 5원 또는 6원 포화 헤테로시클릭 라디칼이거나, R1이 치환되지 않거나 치환된 수소이거나 치환되지 않거나 치환된 아미노이며, R3및 R7는 서로 독립적으로 수소, 치환되거나 치환되지 않은 알킬, 알케닐, 시아노, 니트로, 포르밀, 치환되거나 치환되지 않은 C2-C4-알칼오일, 포르밀 아미노, 치환되거나 치환되지 않은 C2-C4-알카노일아미노, 벤조일아미노이거나, R2와 함께 치환되지 않거나 메틸기로 일치환 내지 삼치환된 알킬렌이거나 또는 치환되지 않거나 페닐-치환된 알케닐렌이며, R4는 수소, 치환되거나 치환되지 않은 알킬, 알케닐, 시아노, 니트로이며, R5및 R6는 각각 수소, 치환되거나 치환된지 않은 알킬, 알케닐, 치환되거나 치환되지 않은 페닐, 니트로, 아실아미노, 치환되거나 치환되지 않은 히드록실, 치환되거나 치환되지 않은 술파모일, 알킬-, 알케닐- 또는 아릴술포닐, 아실 또는 치환되거나 치환되지 않은 카르복실이며, 라디칼 R3, R5또는 R7중 적어도 하나가 수소이다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (7)
- 미네랄 오일을 마크하기 위하여, 마커로서, 하기 일반식(I)의 아닐린을 사용하는 방법.상기식에서, R1및 R2는 서로 독립적으로 수소원자, 치환되거나 치환되지 않고 각 작용기에 1 내지 3개의 산소원자 또는 C1-C4-알킬아미노로 차단된 C3-C18-알킬 또는 치환되거나 치환되지 않은 페닐이거나, 또는 R1및 R2가 질소원자와 함께 다른 헤테로 원자를 더 포함할 수 있는 5원 또는 6원 포화 헤테로시클릭 라디칼이거나, 또는 일반식 OL1또는 NL1L2의 라디칼로서, L1및 L2는 서로 독립적으로 수소, 치환되거나 치환되지 않은 C1-C18-알킬, C3-C18-알케닐 또는 치환되거나 치환되지 않은 페닐이며, R3및 R7는 서로 독립적으로 수소, 치환되거나 치환되지 않은 C1-C18-알킬, C2-C18-알케닐, 시아노, 니트로, 포르밀, 치환되거나 치환되지 않은 C2-C18-알케닐, 시아노, 니트로, 포르밀, 치환되거나 치환되지 않은 C2-C4-알칸오일아미노, 벤조일아미노이거나 또는 일반식 OL1, CH2COOL1, NL1L2, SL1또는 SO2NL1L2로서, L1및 L2가 각각 상기의 의미를 가지거나 R2와 함께 치환되지 않거나 메틸기로 일치환 내지 삼치환되는 C2- 또는 C3-알킬렌이거나 또는 치환되지 않거나 페닐-치환된 C2-또는 C3-알킬렌이며, R4는 수소, 치환되거나 치환되지 않은 C1-C18-알킬, C2-C18-알케닐, 시아노, 니트로, 또는 일반식 OL1, NL1L2, COOL1또는 SO2NL1L2의 라디칼이며, L1및 L2는 각각 상기한 바와 같으며, R5및 R6는 각 수소, 치환되거나 치환되지 않은 C1-C18알킬, C2-C18-알케닐, 치환되거나 치환되지 않은 페닐, 니트로, 포르밀아미노, 치환되거나 치환되지 않은 C2-C4-알카노일아미노, 벤조일아미노 또는 일반식 OL1, NL1L2, SO2NL1L2, SO2L3, COL1또는 COOL1의 라디칼로서, L1및 L2가 각각 상기와 같으며, L3는 치환되거나 치환되지 않은 C1-C18알킬, C2-C18-알케닐 또는 치환되지 않거나 치환된 페닐이며, 라디칼 R3, R5, 또는 R7중 적어도 하나가 수소이다.
- 제1항에 있어서, R1및 R2가 서로 독립적으로 수소원자, 치환되거나 치환되지 않고 각 작용기에 1 내지 3개의 산소원자 또는 C1-C4-알킬아미노로 차단된 C3-C18-알킬 또는 치환되거나 치환되지 않은 페닐이거나, 또는 R1및 R2가 질소원자와 함께 다른 헤테로 원자를 더 포함할 수 있는 5원 또는 6원 포화 헤테로시클릭 라디칼이며, R3및 R7는 서로 독립적으로 수소, C1-C4-알콕시이거나 또는 R2와 함께 메틸에 의해 일치환 내지 삼치환되는 1,3-프로필렌이며, R4및 R5는 1, 각각 수소이며, R6는 수소, C1-C4-알킬, C1-C4-알콕시, C1-C4-알카노일-아미노 또는 벤조일아미노인 것을 특징으로 하는 사용방법.
- 제1항에 있어서, R1및 R2각각 수소 또는 C1-C4알킬기이거나 또는 라디칼 R1및 R2중 최소한 하나가 수산기로 치환되고 C2-C15-알킬이며, 1 내지 3개의 C3-C4-알킬 아미노기 또는 에테르 작용기내에 1 내지 3개의 산소원자로 차단되는 C2-C15-알킬기인 것을 특징으로 하는 사용방법.
- 제1항에 따른 일반식(I)의 하나 이상 아닐린을 포함하는 미네랄 오일.
- 일반식(I)의 아닐린이 수성 매질에 의해 미네랄 오일을 처리하여 추출하고 버퍼 용액의 존재 또는 부재하에서 수성상에서 아미노아크라퀴논, 아미노파프탈렌, 아닐린, 아미노티오펜, 아미노티아졸 또는 아미노벤조이소티아졸류로 부터의 아민으로 부터 유도된 디아조늄염과 결합시켜, 아조염료를 형성하면서 추출하는 것을 특징으로 하는 미네날 오일에서 제1항에 따른 일반식(I)의 아닐린의 존재를 검출하는 방법.
- 제5항에 있어서, 일반식(I)의 아닐린이 디아조늄염의 산성 수용액으로 미네랄 오일을 처리하여 추출하며, 버퍼의 존재 또는 부재하에서 디아조늄염과 결합시켜, 아조 염료를 형성하면서 추출되는 것을 특징으로 하는 방법.
- 제5항에 있어서, 일반식(I)의 아닐린의 수용액으로 미네랄 오일을 처리하여 추출하며, 버퍼의 존재 또는 부재하에 수성상에서 기질에 고체 상태로 존재하는 디아조늄염과 결합하는 것을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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-
1992
- 1992-11-19 DE DE4238994A patent/DE4238994A1/de not_active Withdrawn
-
1993
- 1993-11-09 PL PL93309043A patent/PL177657B1/pl unknown
- 1993-11-09 DK DK94900118.4T patent/DK0669968T3/da active
- 1993-11-09 AU AU54647/94A patent/AU676517B2/en not_active Ceased
- 1993-11-09 ES ES94900118T patent/ES2098117T3/es not_active Expired - Lifetime
- 1993-11-09 AT AT94900118T patent/ATE148734T1/de not_active IP Right Cessation
- 1993-11-09 DE DE59305417T patent/DE59305417D1/de not_active Expired - Lifetime
- 1993-11-09 EP EP94900118A patent/EP0669968B1/de not_active Expired - Lifetime
- 1993-11-09 KR KR1019950702020A patent/KR100278235B1/ko not_active IP Right Cessation
- 1993-11-09 US US08/424,497 patent/US5627077A/en not_active Expired - Fee Related
- 1993-11-09 HU HU9501467A patent/HU215462B/hu not_active IP Right Cessation
- 1993-11-09 WO PCT/EP1993/003133 patent/WO1994011466A1/de not_active Application Discontinuation
- 1993-11-09 CZ CZ951307A patent/CZ130795A3/cs unknown
- 1993-11-09 CA CA002149747A patent/CA2149747A1/en not_active Abandoned
- 1993-11-09 JP JP6511701A patent/JPH08505647A/ja not_active Ceased
- 1993-11-12 IL IL107592A patent/IL107592A/xx not_active IP Right Cessation
- 1993-11-17 MX MX9307195A patent/MX9307195A/es not_active IP Right Cessation
- 1993-11-17 TR TR01064/93A patent/TR28259A/xx unknown
- 1993-11-18 PH PH47286A patent/PH31584A/en unknown
- 1993-11-18 ZA ZA938611A patent/ZA938611B/xx unknown
- 1993-11-19 CN CN93121269A patent/CN1045101C/zh not_active Expired - Fee Related
-
1995
- 1995-05-18 FI FI952423A patent/FI952423A0/fi unknown
-
1997
- 1997-04-15 GR GR970400808T patent/GR3023146T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
FI952423A (fi) | 1995-05-18 |
GR3023146T3 (en) | 1997-07-30 |
US5627077A (en) | 1997-05-06 |
DK0669968T3 (da) | 1997-04-28 |
JPH08505647A (ja) | 1996-06-18 |
HU9501467D0 (en) | 1995-07-28 |
EP0669968B1 (de) | 1997-02-05 |
FI952423A0 (fi) | 1995-05-18 |
PL309043A1 (en) | 1995-09-18 |
CZ130795A3 (en) | 1995-11-15 |
HU215462B (hu) | 1999-01-28 |
PH31584A (en) | 1998-11-03 |
EP0669968A1 (de) | 1995-09-06 |
MX9307195A (es) | 1994-07-29 |
CN1045101C (zh) | 1999-09-15 |
TR28259A (tr) | 1996-03-28 |
WO1994011466A1 (de) | 1994-05-26 |
IL107592A (en) | 1997-03-18 |
AU5464794A (en) | 1994-06-08 |
DE4238994A1 (de) | 1994-05-26 |
ATE148734T1 (de) | 1997-02-15 |
CA2149747A1 (en) | 1994-05-26 |
ES2098117T3 (es) | 1997-04-16 |
CN1092098A (zh) | 1994-09-14 |
IL107592A0 (en) | 1994-02-27 |
AU676517B2 (en) | 1997-03-13 |
DE59305417D1 (de) | 1997-03-20 |
ZA938611B (en) | 1995-05-18 |
PL177657B1 (pl) | 1999-12-31 |
KR100278235B1 (ko) | 2001-03-02 |
HUT72016A (en) | 1996-03-28 |
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