GB858183A - Water-soluble azo dyestuffs containing acryloylamino groups - Google Patents
Water-soluble azo dyestuffs containing acryloylamino groupsInfo
- Publication number
- GB858183A GB858183A GB40106/58A GB4010658A GB858183A GB 858183 A GB858183 A GB 858183A GB 40106/58 A GB40106/58 A GB 40106/58A GB 4010658 A GB4010658 A GB 4010658A GB 858183 A GB858183 A GB 858183A
- Authority
- GB
- United Kingdom
- Prior art keywords
- groups
- amino
- dyes
- group
- alkyl
- 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.)
- Expired
Links
- -1 acryloylamino groups Chemical group 0.000 title abstract 4
- 239000000975 dye Substances 0.000 abstract 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 5
- 238000010168 coupling process Methods 0.000 abstract 4
- 125000003277 amino group Chemical group 0.000 abstract 3
- 230000008878 coupling Effects 0.000 abstract 3
- 238000005859 coupling reaction Methods 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 3
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 3
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 238000004043 dyeing Methods 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 abstract 2
- ZSQSHCAGSCBOAE-UHFFFAOYSA-N 1-(3,4-diaminophenyl)prop-2-en-1-one Chemical compound NC1=C(C=C(C=C1)C(C=C)=O)N ZSQSHCAGSCBOAE-UHFFFAOYSA-N 0.000 abstract 1
- FYXJXUMICYGRKV-UHFFFAOYSA-N 2-[(2-amino-5-nitrophenyl)methylsulfonylmethyl]-4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1CS(=O)(=O)CC1=CC([N+]([O-])=O)=CC=C1N FYXJXUMICYGRKV-UHFFFAOYSA-N 0.000 abstract 1
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 abstract 1
- MBMUXWIDJGGEEX-UHFFFAOYSA-N 4-methylphenol N-phenylprop-2-enamide Chemical compound OC=1C=CC(=CC1)C.C(C=C)(=O)NC1=CC=CC=C1 MBMUXWIDJGGEEX-UHFFFAOYSA-N 0.000 abstract 1
- DSBIJCMXAIKKKI-UHFFFAOYSA-N 5-nitro-o-toluidine Chemical compound CC1=CC=C([N+]([O-])=O)C=C1N DSBIJCMXAIKKKI-UHFFFAOYSA-N 0.000 abstract 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000001476 alcoholic effect Effects 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 abstract 1
- 239000000987 azo dye Substances 0.000 abstract 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 abstract 1
- 229950011260 betanaphthol Drugs 0.000 abstract 1
- 125000002843 carboxylic acid group Chemical group 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- HLVXFWDLRHCZEI-UHFFFAOYSA-N chromotropic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(O)=CC(S(O)(=O)=O)=CC2=C1 HLVXFWDLRHCZEI-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000010408 film Substances 0.000 abstract 1
- 239000011888 foil Substances 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000010985 leather Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- CHMBIJAOCISYEW-UHFFFAOYSA-N n-(4-aminophenyl)acetamide Chemical compound CC(=O)NC1=CC=C(N)C=C1 CHMBIJAOCISYEW-UHFFFAOYSA-N 0.000 abstract 1
- WNVPACYPJUPHON-UHFFFAOYSA-N n-(4-aminophenyl)prop-2-enamide Chemical compound NC1=CC=C(NC(=O)C=C)C=C1 WNVPACYPJUPHON-UHFFFAOYSA-N 0.000 abstract 1
- 150000002790 naphthalenes Chemical class 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 229920002994 synthetic fiber Polymers 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/465—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an acryloyl group, a quaternised or non-quaternised aminoalkyl carbonyl group or a (—N)n—CO—A—O—X or (—N)n—CO—A—Hal group, wherein A is an alkylene or alkylidene group, X is hydrogen or an acyl radical of an organic or inorganic acid, Hal is a halogen atom, and n is 0 or 1
- C09B62/47—Azo dyes
-
- 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
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
- C09B43/124—Preparation of azo dyes from other azo compounds by acylation of amino groups with monocarboxylic acids, carbamic esters or halides, mono- isocyanates, or haloformic acid esters
- C09B43/128—Aliphatic, cycloaliphatic or araliphatic acids
-
- 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/465—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an acryloyl group, a quaternised or non-quaternised aminoalkyl carbonyl group or a (—N)n—CO—A—O—X or (—N)n—CO—A—Hal group, wherein A is an alkylene or alkylidene group, X is hydrogen or an acyl radical of an organic or inorganic acid, Hal is a halogen atom, and n is 0 or 1
- C09B62/47—Azo dyes
- C09B62/473—Monoazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB47131A DE1211346B (de) | 1957-12-13 | 1957-12-13 | Verfahren zur Herstellung wasserloeslicher Azofarbstoffe |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB858183A true GB858183A (en) | 1961-01-11 |
Family
ID=6968151
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB40106/58A Expired GB858183A (en) | 1957-12-13 | 1958-12-12 | Water-soluble azo dyestuffs containing acryloylamino groups |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE573862A (enrdf_load_stackoverflow) |
| CH (2) | CH374436A (enrdf_load_stackoverflow) |
| DE (1) | DE1211346B (enrdf_load_stackoverflow) |
| FR (1) | FR1228834A (enrdf_load_stackoverflow) |
| GB (1) | GB858183A (enrdf_load_stackoverflow) |
| NL (1) | NL234181A (enrdf_load_stackoverflow) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3208992A (en) * | 1962-01-10 | 1965-09-28 | Ici Ltd | Acryloylamino benzene monoazo dyestuffs |
| DE1225322B (de) * | 1962-01-10 | 1966-09-22 | Ici Ltd | Verfahren zur Herstellung von Azofarbstoffen |
| US3364186A (en) * | 1960-05-20 | 1968-01-16 | Basf Ag | Colored terpolymers prepared from (1) dyes, (2) monomers containing crosslinkable groups, and (3) ethylenic unsaturated monomers |
| US3413280A (en) * | 1961-12-29 | 1968-11-26 | Ciba Ltd | Monoazo dyestuffs |
| US3974271A (en) * | 1972-08-19 | 1976-08-10 | Beecham Group Limited | Lipstick containing 8-amino-2-(azo-benzene-4-sulphonic acid)-1-naphthol-3,6-disulphonic acid or an edible salt thereof |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3142669A (en) * | 1960-12-12 | 1964-07-28 | Crompton & Knowles Corp | Monoazo dyes |
| IT1310320B1 (it) | 1999-01-11 | 2002-02-13 | Comprex S P A | Perfezionamenti alle strutture portanti dei mobili componibili. |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1180079B (de) | 1957-03-01 | 1964-10-22 | Cassella Farbwerke Mainkur Ag | Verfahren zur Herstellung von wasserloeslichen, Cellulose echt faerbenden Farbstoffen |
| DE1089095B (de) | 1957-03-06 | 1960-09-15 | Ciba Geigy | Verfahren zur Herstellung von Farbstoffen |
| DE1089097B (de) | 1957-09-27 | 1960-09-15 | Ciba Geigy | Verfahren zur Herstellung organischer Farbstoffe |
| DE1110347B (de) | 1957-11-01 | 1961-07-06 | Ciba Geigy | Verfahren zur Herstellung von nicht metallisierbaren Azofarbstoffen |
-
0
- BE BE573862D patent/BE573862A/xx unknown
-
1957
- 1957-12-13 DE DEB47131A patent/DE1211346B/de active Pending
-
1958
- 1958-12-04 CH CH6693258A patent/CH374436A/de unknown
- 1958-12-04 CH CH1542363A patent/CH379667A/de unknown
- 1958-12-12 GB GB40106/58A patent/GB858183A/en not_active Expired
- 1958-12-12 FR FR781472A patent/FR1228834A/fr not_active Expired
- 1958-12-12 NL NL234181A patent/NL234181A/xx unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3364186A (en) * | 1960-05-20 | 1968-01-16 | Basf Ag | Colored terpolymers prepared from (1) dyes, (2) monomers containing crosslinkable groups, and (3) ethylenic unsaturated monomers |
| US3413280A (en) * | 1961-12-29 | 1968-11-26 | Ciba Ltd | Monoazo dyestuffs |
| US3208992A (en) * | 1962-01-10 | 1965-09-28 | Ici Ltd | Acryloylamino benzene monoazo dyestuffs |
| DE1225322B (de) * | 1962-01-10 | 1966-09-22 | Ici Ltd | Verfahren zur Herstellung von Azofarbstoffen |
| US3974271A (en) * | 1972-08-19 | 1976-08-10 | Beecham Group Limited | Lipstick containing 8-amino-2-(azo-benzene-4-sulphonic acid)-1-naphthol-3,6-disulphonic acid or an edible salt thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| NL234181A (enrdf_load_stackoverflow) | 1964-01-27 |
| DE1211346B (de) | 1966-02-24 |
| CH374436A (de) | 1964-01-15 |
| FR1228834A (fr) | 1960-09-02 |
| CH379667A (de) | 1964-07-15 |
| BE573862A (enrdf_load_stackoverflow) |
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