US4562247A
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Disazo compounds containing a 6-acetoacetamide-1-naphthol-3-sulfonic derivative as coupling component
Assignee: BASF Corp
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Filing: 1984-05-29
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Granted: 1985-12-31
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Expires: 2004-05-29
Abstract
Abstract There are described azo compounds of the formula <IMAGE> wherein D1 and D2 are each the radical of a diazo component, R is C1-C4-alkyl or C1-C4alkyl substituted by C1-C4-alkoxy or halogen or is phenyl or phenyl substituted by C1-C4-alkyl, halogen or C1-C4 alkoxy, and Y is a basic or cationic group. These azo compounds can be used as dyes for dyeing and printing natural and synthetic, cationically dyeing substrates, particularly textile materials and paper.
Inventors
- 👤 Visvanathan Ramanathan
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-30 00:17
CPC Classifications
D; D21; D21H; D21H21/00; D21H21/14; D21H21/28; C; C09; C09B; C09B33/00; C09B33/02; C09B33/08; C09B33/10; C09B44/00; C09B44/02
Claims Analysis
Total Claims: 7
Claim 1
Independent Claim
99 words
An azo compound of the formula ##STR50## wherein D 1 and D 2 independently of one another are each the radical of a diazo component, R is C 1 -C 4 -alkyl or C 1 -C 4 alkyl substituted by C 1 -C 4 -alkoxy or halogen or is phenyl or phenyl substituted by C 1 -C 4 -alkyl, halogen or C 1 -C 4 alkoxy, and Y is a basic or cationic group, with the proviso that the number of basic or cationic Y groups is equal to or greater than the number of SO 3 H groups.
Claim 2
Dependent Claim
99 words
An azo compound of the formula ##STR50## wherein D 1 and D 2 independently of one another are each the radical of a diazo component, R is C 1 -C 4 -alkyl or C 1 -C 4 alkyl substituted by C 1 -C 4 -alkoxy or halogen or is phenyl or phenyl substituted by C 1 -C 4 -alkyl, halogen or C 1 -C 4 alkoxy, and Y is a basic or cationic group, with the proviso that the number of basic or cationic Y groups is equal to or greater than the number of SO 3 H groups.
Claim 3
Dependent Claim
24 words
An azo compound of claim 1, wherein D 1 and D 2 independently of one another are each a benzene, naphthalene or heterocyclic radical.
Claim 4
Dependent Claim
15 words
An azo compound of claim 1, wherein R is unsubstituted C 1 -C 4 -alkyl.
Claim 5
Dependent Claim
10 words
An azo compound of claim 1, wherein R is methyl.
Claim 6
Dependent Claim
177 words
An azo compound of claim 1 wherein Y is a basic group of the formula ##STR51## wherein T 1 and T 2 independently of one another are each hydrogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkyl substituted by hydroxyl, C 1 -C 4 -alkoxy, or --N.sup.⊕ T 7 T 8 T 9 , or T 1 +T 2 with the inclusion of the nitrogen atom form a heterocyclic pyrrolidine, piperidine, morpholine or piperazine ring, and wherein T 7 , T 8 and T 9 independently of each other are each C 1 -C 4 -alkyl, or C 1 -C 4 -alkyl substituted by phenyl, C 1 -C 4 -alkylphenyl, hydroxyl, halogen, CN, --NT 1 T 2 or T 7 , T 8 , and T 9 complete a nitrogen-containing heterocyclic ring selected from the group consisting of pyridinium, pyridinium substituted by methyl, hydroxyl, amino, COOH and CN, 1,4-diazobicyclo[2,2,0]octyl and 1,4-diazobicyclo[2,2,0]octyl substituted by C 1 -C 4 -alkyl in the 4-position, or T 7 and T 8 are C 5 or C 6 -cycloalkyl.
Claim 7
Dependent Claim
161 words
An azo compound of claim 1, wherein Y is a cationic group of the formula ##STR52## wherein T 3 and T 4 independently of one another are each C 1 -C 4 -alkyl or cycloalkyl, T 5 and T 6 independently of one another are each hydrogen, C 1 -C 4 -alkyl or cycloalkyl, T 7 , T 8 , and T 9 independently of each other are each C 1 -C 4 -alkyl, or C 1 -C 4 -alkyl substituted by phenyl, C 1 -C 4 -alkylphenyl, hydroxyl, halogen, CN, --NT 1 T 2 or --N.sup.⊕ T 7 T 8 T 9 , or T 7 , T 8 , and T 9 complete a nitrogen-containing heterocyclic ring selected from the group consisting of pyridinium, pyridinium substituted by methyl, hydroxyl, amino, COOH and CN, 1,4-diazobicyclo[2,2,0]octyl and 1,4-diazobicyclo[2,2,0]octyl substituted by C 1 -C 4 -alkyl in the 4-position, or T 7 and T 8 are C 5 or C 6 cycloalkyl.
References Cited (Backward Citations)
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| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1988-12-30 | 1989-07-01 | 1989-12-31 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1992-12-30 | 1993-07-01 | 1993-12-31 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1996-12-30 | 1997-07-01 | 1997-12-31 | $7700.00 | Window Closed / Lapsed |