DE893699C - Verfahren zur Herstellung von o,o'-Dioxyazo- bzw. -azomethinfarbstoffen bzw. ihren Kupferkomplexverbindungen - Google Patents

Verfahren zur Herstellung von o,o'-Dioxyazo- bzw. -azomethinfarbstoffen bzw. ihren Kupferkomplexverbindungen

Info

Publication number: DE893699C
Authority: DE; Germany
Prior art keywords: parts; copper; dioxyazo; azomethine dyes; complex compounds
Prior art date: 1951-07-27
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

Application number

DEB16051A

Other languages

German (de)

English (en)

Inventor

Otto Dr Kaufmann

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.)

1951-07-27

Filing date

1951-07-27

Publication date

1953-10-19

Priority to NL84796D priority Critical patent/NL84796C/xx

Priority to NLAANVRAGE7111880,B priority patent/NL170847B/xx

1951-07-27 Application filed by BASF SE filed Critical BASF SE

1951-07-27 Priority to DEB16051A priority patent/DE893699C/de

1953-10-19 Application granted granted Critical

1953-10-19 Publication of DE893699C publication Critical patent/DE893699C/de

Status Expired legal-status Critical Current

Links

239000000975 dye Substances 0.000 title claims description 31
-1 copper complex compounds Chemical class 0.000 title claims description 20
238000000034 method Methods 0.000 title claims description 11
230000008569 process Effects 0.000 title claims description 7
238000004519 manufacturing process Methods 0.000 title claims description 3
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 18
229910052802 copper Inorganic materials 0.000 claims description 8
239000010949 copper Substances 0.000 claims description 8
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
150000001879 copper Chemical class 0.000 claims description 6
239000001301 oxygen Substances 0.000 claims description 6
229910052760 oxygen Inorganic materials 0.000 claims description 6
150000004053 quinones Chemical class 0.000 claims description 5
230000002378 acidificating effect Effects 0.000 claims description 4
239000011541 reaction mixture Substances 0.000 claims description 4
230000007935 neutral effect Effects 0.000 claims description 3
238000006243 chemical reaction Methods 0.000 claims description 2
230000009467 reduction Effects 0.000 claims description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
150000001875 compounds Chemical class 0.000 description 10
239000000203 mixture Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000002253 acid Substances 0.000 description 7
229910000365 copper sulfate Inorganic materials 0.000 description 7
ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 7
MMNWSHJJPDXKCH-UHFFFAOYSA-N 9,10-dioxoanthracene-2-sulfonic acid Chemical compound C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 MMNWSHJJPDXKCH-UHFFFAOYSA-N 0.000 description 6
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 6
239000001632 sodium acetate Substances 0.000 description 6
235000017281 sodium acetate Nutrition 0.000 description 6
238000001816 cooling Methods 0.000 description 5
238000003756 stirring Methods 0.000 description 5
210000002268 wool Anatomy 0.000 description 4
SJEBAWHUJDUKQK-UHFFFAOYSA-N 2-ethylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3C(=O)C2=C1 SJEBAWHUJDUKQK-UHFFFAOYSA-N 0.000 description 3
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
229910052804 chromium Inorganic materials 0.000 description 3
239000011651 chromium Substances 0.000 description 3
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 3
230000003647 oxidation Effects 0.000 description 3
238000007254 oxidation reaction Methods 0.000 description 3
238000005185 salting out Methods 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 2
230000008878 coupling Effects 0.000 description 2
238000010168 coupling process Methods 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
239000010985 leather Substances 0.000 description 2
UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
239000007800 oxidant agent Substances 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
235000005811 Viola adunca Nutrition 0.000 description 1
240000009038 Viola odorata Species 0.000 description 1
235000013487 Viola odorata Nutrition 0.000 description 1
235000002254 Viola papilionacea Nutrition 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
229940092714 benzenesulfonic acid Drugs 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000000969 carrier Substances 0.000 description 1
230000008859 change Effects 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000007599 discharging Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
230000009972 noncorrosive effect Effects 0.000 description 1
150000004967 organic peroxy acids Chemical class 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
230000002040 relaxant effect Effects 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
238000010626 work up procedure Methods 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/01—Complex metal compounds of azo dyes characterised by the method of metallisation
- 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/06—Preparation of azo dyes from other azo compounds by oxidation
- 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
- C09B55/00—Azomethine dyes

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DEB16051A 1951-07-27 1951-07-27 Verfahren zur Herstellung von o,o'-Dioxyazo- bzw. -azomethinfarbstoffen bzw. ihren Kupferkomplexverbindungen Expired DE893699C (de)

Priority Applications (3)

Application Number	Priority Date	Filing Date	Title
NL84796D NL84796C (2)	1951-07-27
NLAANVRAGE7111880,B NL170847B (nl)	1951-07-27		Werkwijze ter bereiding van 5-cyclohexadeceen-1-on, en werkwijze ter bereiding van een reukstofcompositie.
DEB16051A DE893699C (de)	1951-07-27	1951-07-27	Verfahren zur Herstellung von o,o'-Dioxyazo- bzw. -azomethinfarbstoffen bzw. ihren Kupferkomplexverbindungen

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DEB16051A DE893699C (de)	1951-07-27	1951-07-27	Verfahren zur Herstellung von o,o'-Dioxyazo- bzw. -azomethinfarbstoffen bzw. ihren Kupferkomplexverbindungen

Publications (1)

Publication Number	Publication Date
DE893699C true DE893699C (de)	1953-10-19

Family

ID=6958743

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DEB16051A Expired DE893699C (de)	1951-07-27	1951-07-27	Verfahren zur Herstellung von o,o'-Dioxyazo- bzw. -azomethinfarbstoffen bzw. ihren Kupferkomplexverbindungen

Country Status (2)

Country	Link
DE (1)	DE893699C (2)
NL (2)	NL170847B (2)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3024239A (en) *	1958-06-11	1962-03-06	Ciba Ltd	Process for the manufacture of quinacridones from 6:13-dihydroquinacridones

0
- NL NL84796D patent/NL84796C/xx active
- NL NLAANVRAGE7111880,B patent/NL170847B/xx unknown
1951
- 1951-07-27 DE DEB16051A patent/DE893699C/de not_active Expired

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3024239A (en) *	1958-06-11	1962-03-06	Ciba Ltd	Process for the manufacture of quinacridones from 6:13-dihydroquinacridones

Also Published As

Publication number	Publication date
NL170847B (nl)
NL84796C (2)

Publication	Publication Date	Title
DE893699C (de)	1953-10-19	Verfahren zur Herstellung von o,o'-Dioxyazo- bzw. -azomethinfarbstoffen bzw. ihren Kupferkomplexverbindungen
CH413168A (de)	1966-05-15	Verfahren zur Herstellung von wasserunlöslichen Disazofarbstoffen
DE889196C (de)	1953-09-07	Verfahren zur Herstellung von o, o'-Dioxyazo- bzw. -azomethinfarb-stoffen bzw. ihrenKupferkomplexverbindungen
DE848979C (de)	1952-09-11	Verfahren zur Herstellung chromhaltiger Monoazofarbstoffe
DE807289C (de)	1951-06-28	Verfahren zur Herstellung von kupferhaltigen o, o-Dioxyazofarbstoffen
DE964975C (de)	1957-05-29	Verfahren zur Herstellung von Monoazofarbstoffen
DE888907C (de)	1953-09-07	Verfahren zur Herstellung von Azofarbstoffen
DE97106C (2)
DE1927211C3 (de)	1977-03-03	Verfahren zur Herstellung von Oxydationsfarbstoffen und deren Verwendung
DE656380C (de)	1938-02-07	Verfahren zur Herstellung von Leukoestern von Farbstoffen der Anthrachinonreihe
DE870149C (de)	1953-03-12	Verfahren zur Herstellung von Kupferkomplexverbindungen von aromatischen o, o'-Dioxyazomethinen
DE371258C (de)	1923-03-13	Verfahren zur Darstellung roter schwefelhaltiger Kuepenfarbstoffe
AT109699B (de)	1928-05-25	Verfahren zur Darstellung von Farbstoffen der Anthracenreihe.
CH310248A (de)	1955-10-15	Verfahren zur Herstellung eines metallhaltigen Monoazofarbstoffes.
CH286352A (de)	1952-10-15	Verfahren zur Herstellung eines chromhaltigen Monoazofarbstoffes.
CH308779A (de)	1955-07-31	Verfahren zur Herstellung eines metallhaltigen Azofarbstoffes.
CH286351A (de)	1952-10-15	Verfahren zur Herstellung eines chromhaltigen Monoazofarbstoffes.
CH286355A (de)	1952-10-15	Verfahren zur Herstellung eines chromhaltigen Monoazofarbstoffes.
CH286356A (de)	1952-10-15	Verfahren zur Herstellung eines chromhaltigen Monoazofarbstoffes.
DE1964148A1 (de)	1970-07-23	Chromhaltige Komplexfarbstoffe und Verfahren zur Herstellung derselben
CH290297A (de)	1953-04-30	Verfahren zur Herstellung eines metallhaltigen Monoazofarbstoffes.
CH312571A (de)	1956-01-15	Verfahren zur Herstellung eines metallhaltigen Monoazofarbstoffes
DE1011100B (de)	1957-06-27	Verfahren zur Herstellung von Monoazofarbstoffen bzw. deren Metallkomplexverbindungen
CH286354A (de)	1952-10-15	Verfahren zur Herstellung eines chromhaltigen Monoazofarbstoffes.
CH267264A (de)	1950-03-15	Verfahren zur Herstellung eines chromhaltigen Farbstoffes.

DE893699C - Verfahren zur Herstellung von o,o'-Dioxyazo- bzw. -azomethinfarbstoffen bzw. ihren Kupferkomplexverbindungen - Google Patents

Info

Links

Classifications

Landscapes

Priority Applications (3)

Applications Claiming Priority (1)

Publications (1)

Family

ID=6958743

Family Applications (1)

Country Status (2)

Cited By (1)

Cited By (1)

Also Published As

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