GB1306092A - - Google Patents
Info
- Publication number
 - GB1306092A GB1306092A GB1851870A GB1851870A GB1306092A GB 1306092 A GB1306092 A GB 1306092A GB 1851870 A GB1851870 A GB 1851870A GB 1851870 A GB1851870 A GB 1851870A GB 1306092 A GB1306092 A GB 1306092A
 - Authority
 - GB
 - United Kingdom
 - Prior art keywords
 - treating
 - inert polar
 - organic solvent
 - water
 - polar organic
 - 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
 
Links
- 239000000975 dye Substances 0.000 abstract 4
 - 239000003495 polar organic solvent Substances 0.000 abstract 4
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
 - YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
 - QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 2
 - QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 2
 - 239000002253 acid Substances 0.000 abstract 2
 - 150000007513 acids Chemical class 0.000 abstract 2
 - 150000004982 aromatic amines Chemical class 0.000 abstract 2
 - 238000010533 azeotropic distillation Methods 0.000 abstract 2
 - 150000001555 benzenes Chemical class 0.000 abstract 2
 - QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 abstract 2
 - 238000001035 drying Methods 0.000 abstract 2
 - 238000001914 filtration Methods 0.000 abstract 2
 - LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 abstract 2
 - 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
 - 150000003142 primary aromatic amines Chemical class 0.000 abstract 2
 - 229910021653 sulphate ion Inorganic materials 0.000 abstract 2
 - 235000011149 sulphuric acid Nutrition 0.000 abstract 2
 - 239000001117 sulphuric acid Substances 0.000 abstract 2
 - AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 abstract 2
 - WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 abstract 1
 - OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 abstract 1
 - CDULGHZNHURECF-UHFFFAOYSA-N 2,3-dimethylaniline 2,4-dimethylaniline 2,5-dimethylaniline 2,6-dimethylaniline 3,4-dimethylaniline 3,5-dimethylaniline Chemical class CC1=CC=C(N)C(C)=C1.CC1=CC=C(C)C(N)=C1.CC1=CC(C)=CC(N)=C1.CC1=CC=C(N)C=C1C.CC1=CC=CC(N)=C1C.CC1=CC=CC(C)=C1N CDULGHZNHURECF-UHFFFAOYSA-N 0.000 abstract 1
 - XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
 - 230000001464 adherent effect Effects 0.000 abstract 1
 - 125000003545 alkoxy group Chemical group 0.000 abstract 1
 - 125000005907 alkyl ester group Chemical group 0.000 abstract 1
 - 125000000217 alkyl group Chemical group 0.000 abstract 1
 - 150000001412 amines Chemical class 0.000 abstract 1
 - 150000001448 anilines Chemical class 0.000 abstract 1
 - 229950005499 carbon tetrachloride Drugs 0.000 abstract 1
 - HJMZMZRCABDKKV-UHFFFAOYSA-N carbonocyanidic acid Chemical compound OC(=O)C#N HJMZMZRCABDKKV-UHFFFAOYSA-N 0.000 abstract 1
 - MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 abstract 1
 - 229940117389 dichlorobenzene Drugs 0.000 abstract 1
 - 238000007865 diluting Methods 0.000 abstract 1
 - 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
 - 125000005843 halogen group Chemical group 0.000 abstract 1
 - 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
 - 150000002825 nitriles Chemical class 0.000 abstract 1
 - PWXJULSLLONQHY-UHFFFAOYSA-N phenylcarbamic acid Chemical compound OC(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-N 0.000 abstract 1
 - 239000002798 polar solvent Substances 0.000 abstract 1
 - 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 1
 - 239000000725 suspension Substances 0.000 abstract 1
 - VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 1
 - 150000004992 toluidines Chemical class 0.000 abstract 1
 - 150000003672 ureas Chemical group 0.000 abstract 1
 
Classifications
- 
        
- C—CHEMISTRY; METALLURGY
 - C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
 - C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
 - C09B11/00—Diaryl- or thriarylmethane dyes
 - C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
 - C09B11/10—Amino derivatives of triarylmethanes
 - C09B11/12—Amino derivatives of triarylmethanes without any OH group bound to an aryl nucleus
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Organic Chemistry (AREA)
 - Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| DE19691919724 DE1919724C (de) | 1969-04-18 | Verfahren zur Herstellung hochreiner Monosulfonsäuren von Triphenylmethanfarbstoffen | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| GB1306092A true GB1306092A (forum.php) | 1973-02-07 | 
Family
ID=5731583
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| GB1851870A Expired GB1306092A (forum.php) | 1969-04-18 | 1970-04-17 | 
Country Status (8)
| Country | Link | 
|---|---|
| US (1) | US3671553A (forum.php) | 
| JP (1) | JPS496367B1 (forum.php) | 
| BE (1) | BE749217A (forum.php) | 
| CH (1) | CH534716A (forum.php) | 
| CS (2) | CS170147B2 (forum.php) | 
| FR (1) | FR2045482A5 (forum.php) | 
| GB (1) | GB1306092A (forum.php) | 
| RO (1) | RO57330A (forum.php) | 
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| DE2555747A1 (de) * | 1975-12-11 | 1977-06-16 | Bayer Ag | Verfahren zur gewinnung von triarylmethanfarbstoffen | 
| JPS5299469A (en) * | 1976-02-18 | 1977-08-20 | Hitachi Ltd | Clothing dryer | 
| DE3108720A1 (de) * | 1981-03-07 | 1982-09-16 | Basf Ag, 6700 Ludwigshafen | Triaminotriarylmethanfarbstoffe | 
| US4678613A (en) * | 1981-12-09 | 1987-07-07 | Pmc Specialties Group, Inc. | Process for the purification of triphenylmethane compounds | 
| US4448446A (en) * | 1981-12-09 | 1984-05-15 | The Sherwin-Williams Company | Process for the purification of triphenylmethane compounds and pressure sensitive copysheet containing same | 
| US4944806A (en) * | 1987-12-28 | 1990-07-31 | Basf Corporation | Rigmentary salt of a triphenylmethane compound and process for making same | 
| DE4134079C2 (de) * | 1990-11-14 | 1998-09-17 | Clariant Gmbh | Pigmentpräparation, Verfahren zu ihrer Herstellung und ihre Verwendung | 
| US5125975A (en) * | 1991-06-25 | 1992-06-30 | Anand Sharangpani | Purification of opal and opal oleate to remove aniline | 
| DE4444472A1 (de) * | 1994-12-14 | 1996-06-20 | Hoechst Ag | Verfahren zur Herstellung von Triphenylmethanfarbmitteln | 
| DE19927835A1 (de) | 1999-06-18 | 2000-12-21 | Clariant Gmbh | Verwendung von verbesserten Cyanpigmenten in elektrophotographischen Tonern und Entwicklern, Pulverlacken und Ink-Jet-Tinten | 
| US6653390B1 (en) | 2000-04-08 | 2003-11-25 | Basf Corporation | Triphenylmethane dyes for water-based compositions | 
| DE10054344A1 (de) | 2000-11-02 | 2002-05-29 | Clariant Gmbh | Verwendung von gecoateten Pigmentgranulaten in elektrophotographischen Tonern und Entwicklern, Pulverlacken und Ink-Jet-Tinten | 
| DE10251394A1 (de) * | 2002-11-05 | 2004-05-13 | Clariant Gmbh | Blaues Farbmittel mit besonders hoher Reinheit und positiver triboelektrischer Steuerwirkung | 
| US7442481B2 (en) | 2004-04-27 | 2008-10-28 | Xsys Print Solutions Us Llc | Charge control agent | 
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US538215A (en) * | 1895-04-23 | Traugott sandmeyer | 
- 
        1970
        
- 1970-04-13 US US28153A patent/US3671553A/en not_active Expired - Lifetime
 - 1970-04-14 RO RO63089A patent/RO57330A/ro unknown
 - 1970-04-15 CH CH560570A patent/CH534716A/de not_active IP Right Cessation
 - 1970-04-17 CS CS3659*A patent/CS170147B2/cs unknown
 - 1970-04-17 GB GB1851870A patent/GB1306092A/en not_active Expired
 - 1970-04-17 CS CS2640A patent/CS170146B2/cs unknown
 - 1970-04-18 JP JP45032688A patent/JPS496367B1/ja active Pending
 - 1970-04-20 FR FR7014201A patent/FR2045482A5/fr not_active Expired
 - 1970-04-20 BE BE749217D patent/BE749217A/xx unknown
 
 
Also Published As
| Publication number | Publication date | 
|---|---|
| RO57330A (forum.php) | 1975-01-15 | 
| CH534716A (de) | 1973-03-15 | 
| US3671553A (en) | 1972-06-20 | 
| CS170147B2 (forum.php) | 1976-08-27 | 
| JPS496367B1 (forum.php) | 1974-02-14 | 
| CS170146B2 (forum.php) | 1976-08-27 | 
| BE749217A (fr) | 1970-10-20 | 
| FR2045482A5 (forum.php) | 1971-02-26 | 
| DE1919724A1 (de) | 1970-11-05 | 
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Legal Events
| Date | Code | Title | Description | 
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |