DE276956C - - Google Patents
Info
- Publication number
 - DE276956C DE276956C DENDAT276956D DE276956DA DE276956C DE 276956 C DE276956 C DE 276956C DE NDAT276956 D DENDAT276956 D DE NDAT276956D DE 276956D A DE276956D A DE 276956DA DE 276956 C DE276956 C DE 276956C
 - Authority
 - DE
 - Germany
 - Prior art keywords
 - dye
 - naphthalene
 - dicarboximides
 - red
 - treated
 - 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.)
 - Active
 
Links
- 239000000975 dye Substances 0.000 claims description 15
 - -1 Naphthalene dicarboximides Chemical class 0.000 claims description 6
 - UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 5
 - 239000003513 alkali Substances 0.000 claims description 3
 - 239000003518 caustics Substances 0.000 claims description 3
 - 125000005462 imide group Chemical group 0.000 claims description 3
 - 239000000984 vat dye Substances 0.000 claims description 2
 - 238000000034 method Methods 0.000 claims 2
 - 238000012986 modification Methods 0.000 claims 2
 - 230000004048 modification Effects 0.000 claims 2
 - 239000000835 fiber Substances 0.000 claims 1
 - 150000002790 naphthalenes Chemical class 0.000 claims 1
 - ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 3
 - HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
 - VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 3
 - QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
 - IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
 - BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
 - 230000015572 biosynthetic process Effects 0.000 description 2
 - 239000000155 melt Substances 0.000 description 2
 - 239000000243 solution Substances 0.000 description 2
 - YATFILGBMGSWTE-UHFFFAOYSA-N 2-ethylbenzo[de]isoquinoline-1,3-dione Chemical compound C1=CC(C(N(CC)C2=O)=O)=C3C2=CC=CC3=C1 YATFILGBMGSWTE-UHFFFAOYSA-N 0.000 description 1
 - HWWBUBSEWUZCOC-UHFFFAOYSA-N 2-phenylbenzo[de]isoquinoline-1,3-dione Chemical compound O=C1C(C=23)=CC=CC3=CC=CC=2C(=O)N1C1=CC=CC=C1 HWWBUBSEWUZCOC-UHFFFAOYSA-N 0.000 description 1
 - 229920000742 Cotton Polymers 0.000 description 1
 - 206010012735 Diarrhoea Diseases 0.000 description 1
 - 241000854350 Enicospilus group Species 0.000 description 1
 - WLLGXSLBOPFWQV-UHFFFAOYSA-N MGK 264 Chemical compound C1=CC2CC1C1C2C(=O)N(CC(CC)CCCC)C1=O WLLGXSLBOPFWQV-UHFFFAOYSA-N 0.000 description 1
 - KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
 - 229960000583 acetic acid Drugs 0.000 description 1
 - 239000012670 alkaline solution Substances 0.000 description 1
 - 125000002877 alkyl aryl group Chemical group 0.000 description 1
 - 125000000217 alkyl group Chemical group 0.000 description 1
 - 125000003118 aryl group Chemical group 0.000 description 1
 - 239000003795 chemical substances by application 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
 - 239000012362 glacial acetic acid Substances 0.000 description 1
 - 238000010438 heat treatment Methods 0.000 description 1
 - 238000004519 manufacturing process Methods 0.000 description 1
 - JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical compound COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 1
 - 230000001035 methylating effect Effects 0.000 description 1
 - 230000007935 neutral effect Effects 0.000 description 1
 - 229910052757 nitrogen Inorganic materials 0.000 description 1
 - 229940045681 other alkylating agent in atc Drugs 0.000 description 1
 - 150000002923 oximes Chemical class 0.000 description 1
 - 229940072033 potash Drugs 0.000 description 1
 - BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
 - 235000015320 potassium carbonate Nutrition 0.000 description 1
 - 239000000843 powder Substances 0.000 description 1
 - 239000011541 reaction mixture Substances 0.000 description 1
 - RCTGMCJBQGBLKT-PAMTUDGESA-N scarlet red Chemical compound CC1=CC=CC=C1\N=N\C(C=C1C)=CC=C1\N=N\C1=C(O)C=CC2=CC=CC=C12 RCTGMCJBQGBLKT-PAMTUDGESA-N 0.000 description 1
 - 229960005369 scarlet red Drugs 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
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
 - C09B43/00—Preparation of azo dyes from other azo compounds
 - C09B43/11—Preparation of azo dyes from other azo compounds by introducing hydrocarbon radicals or substituted hydrocarbon radicals on primary or secondary amino groups
 
 - 
        
- 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
 - C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
 - C09B5/62—Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Organic Chemistry (AREA)
 - Indole Compounds (AREA)
 - Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| DE276956C true DE276956C (forum.php) | 
Family
ID=533104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| DENDAT276956D Active DE276956C (forum.php) | 
Country Status (1)
| Country | Link | 
|---|---|
| DE (1) | DE276956C (forum.php) | 
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| DE1138876B (de) * | 1959-12-17 | 1962-10-31 | Hoechst Ag | Verfahren zur Herstellung von Fluoreszenzfarbstoffen | 
| WO1998006786A1 (de) * | 1996-08-09 | 1998-02-19 | Basf Aktiengesellschaft | Verfahren zur herstellung von n,n'-dialkylperylen-3,4,9,10-tetracarbonsäurediimiden | 
| US6747428B1 (en) | 1999-11-12 | 2004-06-08 | Lg Electronics Inc. | Device and method for controlling supply of current and static capacitance to compressor | 
| US7393956B2 (en) | 2002-04-25 | 2008-07-01 | Basf Aktiengesellschaft | Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides | 
- 
        0
        
- DE DENDAT276956D patent/DE276956C/de active Active
 
 
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| DE1138876B (de) * | 1959-12-17 | 1962-10-31 | Hoechst Ag | Verfahren zur Herstellung von Fluoreszenzfarbstoffen | 
| WO1998006786A1 (de) * | 1996-08-09 | 1998-02-19 | Basf Aktiengesellschaft | Verfahren zur herstellung von n,n'-dialkylperylen-3,4,9,10-tetracarbonsäurediimiden | 
| US6084099A (en) * | 1996-08-09 | 2000-07-04 | Basf Aktiengesellschaft | Preparation of N,N'-dialkylperylene-3,4,9,10-tetracarboxylic acid diimides | 
| US6747428B1 (en) | 1999-11-12 | 2004-06-08 | Lg Electronics Inc. | Device and method for controlling supply of current and static capacitance to compressor | 
| US7393956B2 (en) | 2002-04-25 | 2008-07-01 | Basf Aktiengesellschaft | Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides | 
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