BE638512A - - Google Patents

Info

Publication number: BE638512A
Authority: BE; Belgium
Prior art keywords: coupling; compound; parts; diamino; acetylamino
Prior art date: 1963-10-28

Application number

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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.)

1963-10-28

Publication of BE638512A publication Critical patent/BE638512A/fr

Links

238000005859 coupling reaction Methods 0.000 claims description 13
230000008878 coupling Effects 0.000 claims description 12
238000010168 coupling process Methods 0.000 claims description 12
150000001875 compounds Chemical class 0.000 claims description 11
238000000034 method Methods 0.000 claims description 11
125000001424 substituent group Chemical group 0.000 claims description 7
-1 azo compound Chemical class 0.000 claims description 4
239000004305 biphenyl Substances 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
229920005989 resin Polymers 0.000 claims description 4
239000011347 resin Substances 0.000 claims description 4
239000004033 plastic Substances 0.000 claims description 3
229920003023 plastic Polymers 0.000 claims description 3
239000004753 textile Substances 0.000 claims description 3
239000004215 Carbon black (E152) Substances 0.000 claims description 2
125000000217 alkyl group Chemical class 0.000 claims description 2
238000004040 coloring Methods 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
241000569446 Teyl Species 0.000 claims 1
235000021028 berry Nutrition 0.000 claims 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims 1
239000000126 substance Substances 0.000 claims 1
239000000243 solution Substances 0.000 description 12
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
239000000203 mixture Substances 0.000 description 8
239000000975 dye Substances 0.000 description 7
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 6
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 5
229910052794 bromium Inorganic materials 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
238000001914 filtration Methods 0.000 description 5
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
229960000583 acetic acid Drugs 0.000 description 4
239000012362 glacial acetic acid Substances 0.000 description 4
230000005012 migration Effects 0.000 description 4
238000013508 migration Methods 0.000 description 4
239000000049 pigment Substances 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
238000004061 bleaching Methods 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
235000010288 sodium nitrite Nutrition 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
238000005406 washing Methods 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
239000003086 colorant Substances 0.000 description 2
230000027326 copulation Effects 0.000 description 2
WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
239000000463 material Substances 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
229920000915 polyvinyl chloride Polymers 0.000 description 2
239000004800 polyvinyl chloride Substances 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
239000001632 sodium acetate Substances 0.000 description 2
235000017281 sodium acetate Nutrition 0.000 description 2
239000007787 solid Substances 0.000 description 2
ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
239000001856 Ethyl cellulose Substances 0.000 description 1
241001024304 Mino Species 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
241000282320 Panthera leo Species 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
239000012670 alkaline solution Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
239000001058 brown pigment Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
238000005108 dry cleaning Methods 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
235000019325 ethyl cellulose Nutrition 0.000 description 1
229920001249 ethyl cellulose Polymers 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
235000003642 hunger Nutrition 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
239000005060 rubber Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
230000037351 starvation Effects 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000001043 yellow dye Substances 0.000 description 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/08—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/08—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
- C09B35/10—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type
- C09B35/105—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type from two coupling components with reactive methylene groups

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Coloring (AREA)

BE638512D 1963-10-28 BE638512A (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR952029A FR84594E (fr)	1963-10-28	1963-10-28	Colorants disazoïques, leur fabrication et leurs applications

Publications (1)

Publication Number	Publication Date
BE638512A true BE638512A (es)

Family

ID=8815339

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE638512D BE638512A (es)	1963-10-28

Country Status (2)

Country	Link
BE (1)	BE638512A (es)
FR (1)	FR84594E (es)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1289931B (de) *	1964-02-22	1969-02-27	Hoechst Ag	Farbstoffgemisch aus wasserunloeslichen Disazofarbstoffen sowie Verfahren zur Herstellung dieser wasserunloeslichen Disazofarbstoffe

0
- BE BE638512D patent/BE638512A/fr unknown
1963
- 1963-10-28 FR FR952029A patent/FR84594E/fr not_active Expired

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1289931B (de) *	1964-02-22	1969-02-27	Hoechst Ag	Farbstoffgemisch aus wasserunloeslichen Disazofarbstoffen sowie Verfahren zur Herstellung dieser wasserunloeslichen Disazofarbstoffe

Also Published As

Publication number	Publication date
FR84594E (fr)	1965-03-05

Publication	Publication Date	Title
DE68920293T2 (de)	1995-05-24	Heterocyclische Dispersionsfarbstoffverbindungen, ihre Herstellung und ihre Verwendung zum Färben oder Bedrucken hydrophober Fasern.
JPS6261617B2 (es)	1987-12-22
DE2353987A1 (de)	1975-04-30	Verfahren zur isolierung leichtloeslicher basischer oxazin- und phenazinfarbstoffe
FR2695937A1 (fr)	1994-03-25	Compositions aqueuses de colorants solubles dans des solvants.
BE638512A (es)
EP0837107B1 (de)	2001-09-12	Verfahren zur Herstellung von Dioxazin-Verbindungen
DE1242775C2 (de)	1973-10-18	Verfahren zur herstellung von wasserunloeslichen disazofarbstoffen
DE1569750A1 (de)	1971-01-21	Verfahren zur Herstellung basischer Farbstoffe
CA1054756A (fr)	1979-05-22	Solution concentree de phosphate de colorant de la serie des auramines
DE865926C (de)	1953-02-05	Verfahren zur Herstellung von wasserloeslichen Farbstoffen der Phthalocyaninreihe
EP1038923A2 (de)	2000-09-27	Verfahren zur Herstellung von Dioxazin-Verbindungen
FR2519014A1 (fr)	1983-07-01	Nouveaux melanges de colorants de dispersion, leur preparation et leur utilisation
FR2630453A1 (fr)	1989-10-27	Nouveaux composes heterocycliques, leur preparation et leur utilisation comme colorants
US3098081A (en)	1963-07-16	Process for purifying triphenyl methane dyes
BE710460A (es)	1968-06-17
US251500A (en)	1881-12-27	Adolph baetee
BE571892A (es)
US1877948A (en)	1932-09-20	Vat dyestttets op the n-dihydbo i
DE855144C (de)	1952-11-10	Verfahren zur Herstellung von Kuepenfarbstoffen
DE1544409C (de)		Verfahren zur Herstellung von Monoazofarbstoffen
DE1644382C (de)	1972-10-12	Verfahren zur Herstellung von Disazofarbstoffen sowie zum Färben oder Bedrucken von Kunststoffmaterial oder Papier
DE631241C (de)	1936-06-16	Verfahren zur Herstellung von Kuepenfarbstoffen
DE837278C (de)	1952-04-21	Verfahren zur Herstellung von sauren Farbstoffen der Anthrachinonreihe
BE636085A (es)
EP0015563A1 (de)	1980-09-17	Verfahren zur Herstellung von farbstarken, brillanten, lasierenden Pigmentformen des Bromisoviolanthrons

BE638512A - - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (1)

Publications (1)

Family

ID=8815339

Family Applications (1)

Country Status (2)

Cited By (1)

Cited By (1)

Also Published As

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