AR059897A1 - Uso de ftalocianinas sustituidas con arilo o alquiloxi como marcadores de liquidos - Google Patents

Uso de ftalocianinas sustituidas con arilo o alquiloxi como marcadores de liquidos

Info

Publication number
AR059897A1
AR059897A1 ARP070101035A ARP070101035A AR059897A1 AR 059897 A1 AR059897 A1 AR 059897A1 AR P070101035 A ARP070101035 A AR P070101035A AR P070101035 A ARP070101035 A AR P070101035A AR 059897 A1 AR059897 A1 AR 059897A1
Authority
AR
Argentina
Prior art keywords
different
same
substituted
alkyl
halogen
Prior art date
Application number
ARP070101035A
Other languages
English (en)
Inventor
C Vamvakaris
T Gessner
S Ebert
R Sens
M Konemann
W Ahlers
Original Assignee
Basf Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Basf Ag filed Critical Basf Ag
Publication of AR059897A1 publication Critical patent/AR059897A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/49Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/54Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/49Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/50Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
    • C07C255/51Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings containing at least two cyano groups bound to the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/22Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B47/00Porphines; Azaporphines
    • C09B47/04Phthalocyanines abbreviation: Pc
    • C09B47/06Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide
    • C09B47/067Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide from phthalodinitriles naphthalenedinitriles, aromatic dinitriles prepared in situ, hydrogenated phthalodinitrile
    • C09B47/0675Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide from phthalodinitriles naphthalenedinitriles, aromatic dinitriles prepared in situ, hydrogenated phthalodinitrile having oxygen or sulfur linked directly to the skeleton
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/003Marking, e.g. coloration by addition of pigments
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/52Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
    • C10M133/58Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M159/00Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12Reaction products
    • C10M159/18Complexes with metals
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M171/00Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
    • C10M171/007Coloured or dyes-containing lubricant compositions
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/56Ring systems containing bridged rings
    • C07C2603/58Ring systems containing bridged rings containing three rings
    • C07C2603/70Ring systems containing bridged rings containing three rings containing only six-membered rings
    • C07C2603/74Adamantanes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C10M2215/227Phthalocyanines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/09Complexes with metals
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/42Flashing oils or marking oils

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Lubricants (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Indole Compounds (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
  • Luminescent Compositions (AREA)

Abstract

También reivindica líquido que comprende una o varias ftalocianinas, proceso para identificar líquidos, ftalocianinas, ftalonitrilo, iminoaminisoindolina. Son apropiados como marcadores de líquidos, en especial aceites minerales. Reivindicacion 1: El uso de ftalocianinas de la formula (1) como marcadores de líquidos en donde los símbolos e índices en la formula (1) tienen las siguientes definiciones: M es dos veces hidrogeno, dos veces litio, magnesio, cinc, cobre, níquel, VO, TiO, AlCl, AlOCOCH3, AlOCOCF3, SiCl2 o Si(OH)2; m es 1, 2, 3 o 4; n es igual o diferente y es 0, 1, 2, 3 o 4; r es igual o diferente y es 0, 1, 2, 3 o 4; m+r es 1, 2,3 o 4; n+r es 0, 1, 2, 3 o 4; R es igual o diferente y escomo en los grupos de formulas (2), R1 es igual o diferente y es H, halogeno o R2, R2 es igual o diferente y es alquilo C1-18, cicloalquilo C4-8, alquenilo C2-12 , arilo C6-10, aralquilo C7-20 o alquinilo C2-12, en donde los radicales arilo no están sustituidos o están sustituidos con uno o varios halogeno, ciano, nitro, hidroxilo, amino, alquilo C1-20 que está opcionalmente interrumpido por 1 a 4 átomos de oxígeno en funcion éter, alcoxi C1-20, alquil C1-20-amino o dialquil C1-20-amino; R3 es igual o diferente y es R1, o dos radicales R3 o un radical R1 y un radical R3 forman juntos otro sistema de anillos; R4, R5, R6 son iguales o diferentes y son cada uno H, halogeno, CH3 o C2H5; Y1, Y2, Y3, Y4, Y5, Y6 son iguales o diferentes y son cada uno alquileno C1-4 que no está sustituido o que está sustituido con uno o varios átomos de halogeno; s es 0, 1, 2, 3, 4, 5 o 6; y t es 0, 1, 2, 3.
ARP070101035A 2006-03-15 2007-03-14 Uso de ftalocianinas sustituidas con arilo o alquiloxi como marcadores de liquidos AR059897A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP06111161 2006-03-15

Publications (1)

Publication Number Publication Date
AR059897A1 true AR059897A1 (es) 2008-05-07

Family

ID=38132225

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP070101035A AR059897A1 (es) 2006-03-15 2007-03-14 Uso de ftalocianinas sustituidas con arilo o alquiloxi como marcadores de liquidos

Country Status (17)

Country Link
US (1) US20090189086A1 (es)
EP (1) EP1996549A1 (es)
JP (1) JP2009530427A (es)
KR (1) KR20090008228A (es)
CN (1) CN101421236A (es)
AR (1) AR059897A1 (es)
AU (1) AU2007224512A1 (es)
BR (1) BRPI0708886A2 (es)
CA (1) CA2646205A1 (es)
EA (1) EA200801986A1 (es)
MX (1) MX2008011631A (es)
NO (1) NO20083763L (es)
PE (1) PE20071287A1 (es)
TW (1) TW200745131A (es)
UA (1) UA88747C2 (es)
WO (1) WO2007104685A1 (es)
ZA (1) ZA200808721B (es)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010531056A (ja) * 2007-06-22 2010-09-16 ビーエーエスエフ ソシエタス・ヨーロピア N,n’−ビス(1,1−ジヒドロペルフルオロ−c3−c5−アルキル)ペリレン−3,4:9,10−テトラカルボン酸ジイミドの使用
KR101580338B1 (ko) 2007-08-17 2015-12-23 바스프 에스이 할로겐-함유 페릴렌테트라카르복실산 유도체 및 이의 용도
AR069242A1 (es) * 2007-11-09 2010-01-06 Basf Se Polialcanolamidas alcoxiladas
US8318653B2 (en) * 2007-11-09 2012-11-27 Basf Se Amphiphilic water-soluble alkoxylated polyalkyleneimines having an inner polyethylene oxide block and an outer polypropylene oxide block
AU2010252080A1 (en) * 2009-05-26 2011-11-17 Basf Se Use of phthalocyanine compounds with aryl or hetaryl substituents in organic solar cells
CN101580506B (zh) * 2009-05-26 2012-11-07 福建师范大学 1-3代芳醚树枝状酞菁配合物及其聚合物纳米粒子
JP2011094127A (ja) * 2009-09-29 2011-05-12 Nippon Shokubai Co Ltd 熱線吸収材
US9995681B2 (en) 2010-09-28 2018-06-12 Authentix, Inc. Determining the quantity of a taggant in a liquid sample
JP5790546B2 (ja) * 2012-03-07 2015-10-07 コニカミノルタ株式会社 光電変換素子用色素、光電変換素子及びその製造方法
US9068147B2 (en) 2012-05-11 2015-06-30 Basf Se Quaternized polyethylenimines with a high quaternization degree
CN104614132A (zh) * 2015-02-05 2015-05-13 广西柳工机械股份有限公司 工程机械整机润滑油泄漏检测方法
JP6548221B2 (ja) * 2015-02-12 2019-07-24 株式会社日本触媒 フタロシアニン化合物
WO2017019337A1 (en) 2015-07-24 2017-02-02 Authentix, Inc. Determining the quantity of a taggant in a liquid sample
KR101816232B1 (ko) 2015-10-16 2018-01-08 삼성에스디아이 주식회사 신규한 화합물, 이를 포함하는 감광성 수지 조성물 및 컬러필터
CN106243115B (zh) * 2016-07-28 2018-03-30 北京化工大学 含金刚烷结构的双核金属酞菁催化剂及其制备方法
KR102061244B1 (ko) 2017-05-17 2019-12-31 삼성에스디아이 주식회사 감광성 수지 조성물, 이를 이용하여 제조된 감광성 수지막 및 컬러필터
US10705018B2 (en) 2017-12-28 2020-07-07 Authentix, Inc. Fluorescence based global fuel analysis method
CN109959626B (zh) * 2019-04-08 2022-05-03 天津农学院 一种定量总脂含量的分光光度法及应用
CN110951071B (zh) * 2019-12-11 2022-05-13 南通北风橡塑制品有限公司 一种酞菁金属盐改性多元醇及其制备方法和应用
CN114136943B (zh) * 2021-11-30 2024-01-05 厦门大学 一种以空壳酞菁为分子探针测定锂离子的荧光分析法
WO2023241950A1 (en) 2022-06-13 2023-12-21 Basf Se Mixtures of compounds having improved solubility for use as markers
CN116858827B (zh) * 2023-07-25 2023-12-19 河北科技大学 一种冷库用肉制品新鲜度荧光指示标签纸及其制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX9304188A (es) * 1992-07-23 1994-03-31 Basf Ag Uso de compuestos absorbentes y/o fluorescentes enla region infrarroja como marcadores para liquidos.
US5525516B1 (en) * 1994-09-30 1999-11-09 Eastman Chem Co Method for tagging petroleum products
JP3366508B2 (ja) * 1995-09-13 2003-01-14 山本化成株式会社 フタロニトリル化合物の製造方法
DE19721399A1 (de) * 1997-05-22 1998-11-26 Basf Ag Phthalocyanine und ihre Verwendung als Markierungsmittel
DE102004003791A1 (de) * 2004-01-23 2005-08-11 Basf Ag Verwendung von Phthalocyaninen als Markierungsstoffe für Flüssigkeiten

Also Published As

Publication number Publication date
EP1996549A1 (de) 2008-12-03
CN101421236A (zh) 2009-04-29
MX2008011631A (es) 2008-09-22
ZA200808721B (en) 2009-12-30
PE20071287A1 (es) 2008-02-11
NO20083763L (no) 2008-10-14
BRPI0708886A2 (pt) 2011-06-14
EA200801986A1 (ru) 2009-02-27
US20090189086A1 (en) 2009-07-30
TW200745131A (en) 2007-12-16
UA88747C2 (ru) 2009-11-10
WO2007104685A1 (de) 2007-09-20
JP2009530427A (ja) 2009-08-27
CA2646205A1 (en) 2007-09-20
KR20090008228A (ko) 2009-01-21
AU2007224512A1 (en) 2007-09-20

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