ES2079735T3 - Procedimiento para la obtencion de colorantes azoicos acetalizados. - Google Patents

Procedimiento para la obtencion de colorantes azoicos acetalizados.

Info

Publication number
ES2079735T3
ES2079735T3 ES92109350T ES92109350T ES2079735T3 ES 2079735 T3 ES2079735 T3 ES 2079735T3 ES 92109350 T ES92109350 T ES 92109350T ES 92109350 T ES92109350 T ES 92109350T ES 2079735 T3 ES2079735 T3 ES 2079735T3
Authority
ES
Spain
Prior art keywords
acetalized
procedure
obtaining
vinyl
azo
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES92109350T
Other languages
English (en)
Spanish (es)
Inventor
Guenter Dr Hansen
Georg Zeidler
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
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 SE filed Critical BASF SE
Application granted granted Critical
Publication of ES2079735T3 publication Critical patent/ES2079735T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C09B31/00Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/003Marking, e.g. coloration by addition of pigments
    • 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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/06Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
    • C09B29/08Amino benzenes
    • C09B29/0805Amino benzenes free of acid groups
    • C09B29/0807Amino benzenes free of acid groups characterised by the amino group
    • C09B29/0809Amino benzenes free of acid groups characterised by the amino group substituted amino group
    • C09B29/0811Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino
    • C09B29/0813Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino substituted by OH, O-C(=X)-R, O-C(=X)-X-R, O-R (X being O,S,NR; R being hydrocarbonyl)
    • 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
    • C09B31/00Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
    • C09B31/02Disazo dyes
    • C09B31/04Disazo dyes from a coupling component "C" containing a directive amino group
    • C09B31/043Amino-benzenes
    • 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
    • C09B43/00Preparation of azo dyes from other azo compounds
    • C09B43/28Preparation of azo dyes from other azo compounds by etherification of hydroxyl groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)
ES92109350T 1991-06-20 1992-06-03 Procedimiento para la obtencion de colorantes azoicos acetalizados. Expired - Lifetime ES2079735T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4120363A DE4120363C1 (enExample) 1991-06-20 1991-06-20

Publications (1)

Publication Number Publication Date
ES2079735T3 true ES2079735T3 (es) 1996-01-16

Family

ID=6434366

Family Applications (1)

Application Number Title Priority Date Filing Date
ES92109350T Expired - Lifetime ES2079735T3 (es) 1991-06-20 1992-06-03 Procedimiento para la obtencion de colorantes azoicos acetalizados.

Country Status (7)

Country Link
US (1) US5247071A (enExample)
EP (1) EP0519270B1 (enExample)
JP (1) JPH05194866A (enExample)
KR (1) KR100196106B1 (enExample)
CA (1) CA2071434C (enExample)
DE (2) DE4120363C1 (enExample)
ES (1) ES2079735T3 (enExample)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4343823A1 (de) * 1993-12-22 1995-06-29 Basf Ag Verwendung von Azofarbstoffen zum Markieren von Kohlenwasserstoffen sowie neue Azofarbstoffe
JP2009528417A (ja) * 2006-03-01 2009-08-06 ビーエーエスエフ ソシエタス・ヨーロピア 液体用の標識剤としてのリレンの使用
CN106634016B (zh) * 2016-12-10 2018-10-09 遵义师范学院 一种溶剂黄124的合成方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3244753A (en) * 1966-04-05 Process f-or manufacture cf acetals
US4011209A (en) * 1970-06-17 1977-03-08 Aziende Colori Nazionali Affini Acna S.P.A. Organic solvent-soluble azo dyes
NL7108044A (enExample) * 1970-06-17 1971-12-21
DE3627461A1 (de) * 1986-08-13 1988-02-25 Basf Ag Farbstoffmischungen

Also Published As

Publication number Publication date
CA2071434A1 (en) 1992-12-21
CA2071434C (en) 2002-09-03
EP0519270A3 (en) 1993-07-21
US5247071A (en) 1993-09-21
DE59204554D1 (de) 1996-01-18
EP0519270A2 (de) 1992-12-23
KR100196106B1 (ko) 1999-06-15
KR930000617A (ko) 1993-01-15
JPH05194866A (ja) 1993-08-03
DE4120363C1 (enExample) 1992-07-02
EP0519270B1 (de) 1995-12-06

Similar Documents

Publication Publication Date Title
Oliveira et al. Cocoa shell for the production of endoglucanase by Penicillium roqueforti ATCC 10110 in solid state fermentation and biochemical properties
AR025163A1 (es) Un procedimiento para preparar olefinas, un sistema catalizador soportado, el uso de un compuesto catalizador del grupo 15 que contiene hafnio y el uso deun sistema catalizador que comprende un compuesto catalizador
PT1100999E (pt) Processo para instalacao de cabos de dados
Helmchen et al. Functional groups at concave sites: Asymmetric diels-alder synthesis with almost complete (lewis-acid catalyzed) or high (uncatalyzed) stereoselectivity
Smiley Phenylene-and toluenediamines
BR0115108A (pt) Aparelho de transmissão de dados e aparelho de recepção de dados
EP1243572A4 (en) PROCESS FOR THE PREPARATION OF CYCLOHEXANOL
MX168547B (es) Procedimiento para la preparacion de colorantes azo
Arwidsson et al. Properties of ethyl cellulose films for extended release. Part 2. Influence of plasticizer content and coalescence conditions when using aqueous dispersions
Soltys et al. Human serum albumin. I. On the relationship of fatty acid and bilirubin binding sites and the nature of fatty acid allosteric effects—a monoanionic spin label study
Vora et al. Production of detergent olefins and linear alkylbenzenes
NO914991L (no) Avansert epoksyharpiks, samt fremgangsmaate for fremstilling av en slik i vanndispersjon
ES2186226T3 (es) Nuevo procedimiento para preparar una cetoimina.
Roy et al. Pharmacological evaluation of Enhydra fluctuans aerial parts for central nervous system depressant activity
Litvic et al. Ammonium carbamate; mild, selective and efficient ammonia source for preparation of beta-amino-alpha, beta-unsaturated esters at room temperature
DE68913863D1 (de) Anschlagen einer Presshülse an die Isolation eines isolierten Kabels.
KR860000071A (ko) 생약제제의 제조방법
CA2071434A1 (en) Preparation of acetalized azo dyes
Sakai et al. Effects of constituents of Paeony root on the mutagenicity of benzo (a) pyrene.
Takagi et al. Tyrosinase inhibitors from the pericarp of Jatoba (Hymenaea courbaril L.)
ES2175759T3 (es) Procedimiento y dispositivo para medir los parametros del eco en lineas telefonicas.
Mazeaud et al. Excretion and catabolism of catecholamines in fish. Part II. Catabolites
TWI337096B (enExample)
Li et al. Preparation of Highly Active Cr~ 2O~ 3-SiO~ 2 Catalyst by Sol-Gel Method for Ethylbenzene Dehydrogenation in the Presence of CO~ 2
Moller et al. P (III)-ACRIDINE DERIVATIVES AS BUILDING-BLOCKS FOR THE SOLID-PHASE SYNTHESIS OF NON-RADIOACTIVELY LABELED OLIGONUCLEOTIDES

Legal Events

Date Code Title Description
FG2A Definitive protection

Ref document number: 519270

Country of ref document: ES