DE2155106A1 - Neue Nitrodiphenylamine, deren Herstellung und Verwendung - Google Patents

Neue Nitrodiphenylamine, deren Herstellung und Verwendung

Info

Publication number: DE2155106A1
Authority: DE; Germany
Prior art keywords: sulfonic acid; parts; chloro; acid; hydrogen
Prior art date: 1970-11-06
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.): Pending

Application number

DE19712155106

Other languages

German (de)

English (en)

Inventor

Christian Dr. Binningen Zickendraht (Schweiz)

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.)

Novartis AG

Original Assignee

Ciba Geigy 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.)

1970-11-06

Filing date

1971-11-05

Publication date

1972-05-10

1971-11-05 Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG

1972-05-10 Publication of DE2155106A1 publication Critical patent/DE2155106A1/de

Status Pending legal-status Critical Current

Links

AYLBVKUPVXVTSO-UHFFFAOYSA-N n,n-diphenylnitramide Chemical class C=1C=CC=CC=1N([N+](=O)[O-])C1=CC=CC=C1 AYLBVKUPVXVTSO-UHFFFAOYSA-N 0.000 title claims 5
238000004519 manufacturing process Methods 0.000 title description 2
239000000975 dye Substances 0.000 claims description 14
229910052739 hydrogen Inorganic materials 0.000 claims description 11
239000001257 hydrogen Substances 0.000 claims description 11
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 9
229910052736 halogen Inorganic materials 0.000 claims description 6
150000002367 halogens Chemical class 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 5
125000004093 cyano group Chemical group *C#N 0.000 claims description 3
238000004043 dyeing Methods 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
150000002431 hydrogen Chemical class 0.000 claims 1
125000000565 sulfonamide group Chemical group 0.000 claims 1
RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 14
-1 alkoxy radical Chemical class 0.000 description 13
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 10
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
238000000034 method Methods 0.000 description 8
239000002253 acid Substances 0.000 description 7
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 6
239000007859 condensation product Substances 0.000 description 5
238000001816 cooling Methods 0.000 description 5
238000009987 spinning Methods 0.000 description 5
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
229910021529 ammonia Inorganic materials 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
239000000460 chlorine Chemical group 0.000 description 4
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
238000009833 condensation Methods 0.000 description 4
230000005494 condensation Effects 0.000 description 4
239000000203 mixture Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000007858 starting material Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
229910052801 chlorine Chemical group 0.000 description 3
GABQKHQNXWNJJJ-UHFFFAOYSA-N diphenylcarbamic acid Chemical class C=1C=CC=CC=1N(C(=O)O)C1=CC=CC=C1 GABQKHQNXWNJJJ-UHFFFAOYSA-N 0.000 description 3
235000019441 ethanol Nutrition 0.000 description 3
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
239000004305 biphenyl Substances 0.000 description 2
235000010290 biphenyl Nutrition 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
238000004040 coloring Methods 0.000 description 2
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
229910000029 sodium carbonate Inorganic materials 0.000 description 2
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical group NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 2
229940124530 sulfonamide Drugs 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 2
KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
PXBFMLJZNCDSMP-UHFFFAOYSA-N 2-Aminobenzamide Chemical compound NC(=O)C1=CC=CC=C1N PXBFMLJZNCDSMP-UHFFFAOYSA-N 0.000 description 1
KFKCKBPFUJOIQG-UHFFFAOYSA-N 4-chloro-3-nitro-n-propan-2-ylbenzenesulfonamide Chemical compound CC(C)NS(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 KFKCKBPFUJOIQG-UHFFFAOYSA-N 0.000 description 1
XBLPHYSLHRGMNW-UHFFFAOYSA-N 4-chloro-3-nitrobenzonitrile Chemical compound [O-][N+](=O)C1=CC(C#N)=CC=C1Cl XBLPHYSLHRGMNW-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
VYZAHLCBVHPDDF-UHFFFAOYSA-N Dinitrochlorobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 VYZAHLCBVHPDDF-UHFFFAOYSA-N 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
102100039939 Growth/differentiation factor 8 Human genes 0.000 description 1
108050006583 Growth/differentiation factor 8 Proteins 0.000 description 1
DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
229920000297 Rayon Polymers 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
241000219315 Spinacia Species 0.000 description 1
235000009337 Spinacia oleracea Nutrition 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
229940040526 anhydrous sodium acetate Drugs 0.000 description 1
125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
229920003086 cellulose ether Polymers 0.000 description 1
239000012320 chlorinating reagent Substances 0.000 description 1
238000005660 chlorination reaction Methods 0.000 description 1
XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000004821 distillation Methods 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
230000002140 halogenating effect Effects 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
239000011707 mineral Substances 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
229920005615 natural polymer Polymers 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000000047 product Substances 0.000 description 1
XUWVIABDWDTJRZ-UHFFFAOYSA-N propan-2-ylazanide Chemical compound CC(C)[NH-] XUWVIABDWDTJRZ-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
150000004992 toluidines Chemical class 0.000 description 1
239000001993 wax 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
- C09B51/00—Nitro or nitroso dyes

Landscapes

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

DE19712155106 1970-11-06 1971-11-05 Neue Nitrodiphenylamine, deren Herstellung und Verwendung Pending DE2155106A1 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1647470A CH541608A (de)	1970-11-06	1970-11-06	Verfahren zur Herstellung von Nitrodiphenylaminen und deren Verwendung

Publications (1)

Publication Number	Publication Date
DE2155106A1 true DE2155106A1 (de)	1972-05-10

Family

ID=4417692

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19712155106 Pending DE2155106A1 (de)	1970-11-06	1971-11-05	Neue Nitrodiphenylamine, deren Herstellung und Verwendung

Country Status (8)

Country	Link
BE (1)	BE774961A (2)
CA (1)	CA967151A (2)
CH (1)	CH541608A (2)
DE (1)	DE2155106A1 (2)
FR (1)	FR2113616A5 (2)
GB (1)	GB1371378A (2)
IT (1)	IT946042B (2)
NL (1)	NL7115291A (2)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2000041505A3 (en) *	1999-01-13	2000-10-19	Warner Lambert Co	Anthranilic acid derivatives

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DOP2003000556A (es)	2002-01-23	2003-10-31	Warner Lambert Co	Esteres hidroxamato de acido n-(4-fenil-sustituido)-antranilico.
CA2473545A1 (en)	2002-01-23	2003-07-31	Warner-Lambert Company Llc	N-(4-substituted phenyl)-anthranilic acid hydroxamate esters
GB0723794D0 (en)	2007-12-05	2008-01-16	Lectus Therapeutics Ltd	Potassium ion channel modulators and uses thereof

1970
- 1970-11-06 CH CH1647470A patent/CH541608A/de not_active IP Right Cessation
1971
- 1971-10-26 CA CA126,078A patent/CA967151A/en not_active Expired
- 1971-11-04 GB GB5139171A patent/GB1371378A/en not_active Expired
- 1971-11-05 DE DE19712155106 patent/DE2155106A1/de active Pending
- 1971-11-05 NL NL7115291A patent/NL7115291A/xx unknown
- 1971-11-05 FR FR7139745A patent/FR2113616A5/fr not_active Expired
- 1971-11-05 IT IT3074571A patent/IT946042B/it active
- 1971-11-05 BE BE774961A patent/BE774961A/xx unknown

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2000041505A3 (en) *	1999-01-13	2000-10-19	Warner Lambert Co	Anthranilic acid derivatives

Also Published As

Publication number	Publication date
GB1371378A (en)	1974-10-23
CH541608A (de)	1973-09-15
NL7115291A (2)	1972-05-09
FR2113616A5 (2)	1972-06-23
IT946042B (it)	1973-05-21
CA967151A (en)	1975-05-06
BE774961A (fr)	1972-05-05

Publication	Publication Date	Title
DE2004487C3 (de)	1979-12-06	Wasserlösliche Azofarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung
DE963265C (de)	1957-05-02	Verfahren zur Herstellung von Anthrachinonfarbstoffen
DE1189669B (de)	1965-03-25	Verfahren zur Herstellung von Anthrachinonfarbstoffen
DE1148341B (de)	1963-05-09	Verfahren zur Herstellung von Farbstoffen
DE1644370A1 (de)	1970-07-30	Verfahren zur Herstellung in Wasser schwer loeslicher Farbstoffe
DE2155106A1 (de)	1972-05-10	Neue Nitrodiphenylamine, deren Herstellung und Verwendung
DE2510045A1 (de)	1975-09-11	Marineblaue monoazo-dispersionsfarbstoffe
DE2902485A1 (de)	1979-07-26	6/7-halogen-anthrachinonverbindungen, deren herstellung und verwendung
DE959669C (de)	1957-03-07	Verfahren zur Herstellung von Nitrofarbstoffen
DE751345C (de)	1952-11-10	Verfahren zur Herstellung von sauren Farbstoffen der Anthrachinonreihe
DE709632C (de)	1941-08-22	Verfahren zur Herstellung von Nitrofarbstoffen
DE1267360B (de)	1968-05-02	Verfahren zur Herstellung von Anthrachinonfarbstoffen
DE2203093C3 (de)	1977-02-10	N-(Aminobe nzoyl) -aminoarylsulfonsäuren, deren AlkaHsalze, Verfahren zur Herstellung dieser Verbindungen und Ihre Verwendung
DE2244061C3 (de)	1975-03-20	Wasserlösliche Reaktivfarbstoffe der Anthrachinonreihe und Verfahren zu deren Herstellung
DE745169C (de)	1944-02-28	Verfahren zur Herstellung eines sauren Anthrachinonfarbstoffs
DE1644551C2 (de)	1973-07-19	Verfahren zur Herstellung von sauren Anthrachinonfarbstoffen
DE941381C (de)	1956-04-12	Verfahren zur Herstellung von Kuepenfarbstoffen
DE1769108C (de)	1973-04-19	Saure Anthrachinonfarbstoffe, ihre Herstellung und Verwendung
DE2023632C3 (de)	1975-07-10	Basische Anthrachinonfarbstoffe, ihre Herstellung und Verwendung
AT226855B (de)	1963-04-10	Verfahren zur Herstellung neuer basischer Hydrazonfarbstoffe
DE1769612A1 (de)	1971-07-01	Anthrachinonfarbstoffe
DE1802562A1 (de)	1969-06-04	Neue Acridonfarbstoffe,deren Herstellung und Verwendung
DE1173602B (de)	1964-07-09	Verfahren zur Herstellung von Anthrachinonfarbstoffen
DE1644626A1 (de)	1971-05-13	Anthrachinonfarbstoffe
CH323916A (de)	1957-08-31	Verfahren zur Herstellung neuer Nitrofarbstoffe

DE2155106A1 - Neue Nitrodiphenylamine, deren Herstellung und Verwendung - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (1)

Publications (1)

Family

ID=4417692

Family Applications (1)

Country Status (8)

Cited By (1)

Families Citing this family (3)

Cited By (1)

Also Published As

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