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| SECTION C CHEMISTRY; METALLURGY |
| C 09 | DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS |
| C 09 B | ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES; MORDANTS; LAKES (fermentation or enzyme-using processes to synthesise a desired chemical compound C12P) |
6/ | 00 | Anthracene dyes not provided for above [2] |
7/ | 00 | Indigoid dyes |
7/ | 02 | . | Bis-indole indigos |
7/ | 04 | . | . | Halogenation thereof |
7/ | 06 | . | Indone-thionaphthene indigos |
7/ | 08 | . | Other indole-indigos |
7/ | 10 | . | Bis-thionaphthene indigos |
7/ | 12 | . | Other thionaphthene indigos |
9/ | 00 | Esters or ester-salts of leuco compounds of vat dyestuffs |
9/ | 02 | . | of anthracene dyes |
9/ | 04 | . | of indigoid dyes |
11/ | 00 | Diaryl- or triarylmethane dyes |
11/ | 02 | . | derived from diarylmethanes |
11/ | 04 | . | derived from triarylmethanes |
11/ | 06 | . | . | Hydroxy derivatives of triarylmethanes in which at least one OH group is bound to an aryl nucleus |
11/ | 08 | . | . | . | Phthaleins |
11/ | 10 | . | . | Amino derivatives of triarylmethanes |
11/ | 12 | . | . | . | without any OH group bound to an aryl nucleus |
11/ | 14 | . | . | . | . | Preparation from aromatic aldehydes, aromatic carboxylic acids or derivatives thereof, and aromatic amines |
11/ | 16 | . | . | . | . | Preparation from diarylketones or diarylcarbinols |
11/ | 18 | . | . | . | . | Preparation by oxidation |
11/ | 20 | . | . | . | . | Preparation from other triarylmethane derivatives |
11/ | 22 | . | . | . | containing OH groups bound to an aryl nucleus |
11/ | 24 | . | . | . | Phthaleins containing amino groups |
11/ | 26 | . | . | Triarylmethane dyes in which at least one of the aromatic nuclei is heterocyclic |
11/ | 28 | . | Pyronines |
13/ | 00 | Oxyketone dyes |
13/ | 02 | . | of the naphthalene series, e.g. naphthazarin |
13/ | 04 | . | of the pyrene series |
13/ | 06 | . | of the acetophenone series |
| Acridine, azine, oxazine, or thiazine dyes |
15/ | 00 | Acridine dyes |
17/ | 00 | Azine dyes |
17/ | 02 | . | of the benzene series |
17/ | 04 | . | of the naphthalene series |
17/ | 06 | . | Fluorindine or its derivatives |
19/ | 00 | Oxazine dyes |
19/ | 02 | . | Bisoxazines prepared from amino quinones |
21/ | 00 | Thiazine dyes |
| Quinoline or polymethine dyes |
23/ | 00 | Methine or polymethine dyes, e.g. cyanine dyes |
23/ | 01 | . | characterised by the methine chain [3] |
23/ | 02 | . | . | containing an odd number of |
23/ | 04 | . | . | . | one |
23/ | 06 | . | . | . | three |
23/ | 08 | . | . | . | more than three |
23/ | 10 | . | . | containing an even number of |
23/ | 12 | . | the polymethine chain being branched |
23/ | 14 | . | Styryl dyes |
23/ | 16 | . | the polymethine chain containing hetero atoms |
25/ | 00 | Quinophthalones |
26/ | 00 | Hydrazone dyes; Triazene dyes [3] |
26/ | 02 | . | Hydrazone dyes (hydrazone-azo dyes C09B 56/18) [3] |
26/ | 04 | . | . | cationic [3] |
26/ | 06 | . | Triazene dyes (triazene-azo dyes C09B 56/20) [3] |
| Azo dyes |
| Note |
| In groups C09B 27/00 to C09B 46/00, arrows in the formulae of the various types of azo dyes indicate which part of an azo dye, prepared by diazotising and coupling, is derived from the diazo component and which part is derived from the coupling component. The arrow is pointing to the part derived from the coupling component. [4] |
27/ | 00 | Preparations in which the azo group is formed in any way other than by diazotising and coupling |
27/ | 06 | . | Tartrazines [3] |
29/ | 00 | Monoazo dyes prepared by diazotising and coupling |
29/ | 01 | . | characterised by the diazo component [3] |
29/ | 02 | . | . | from diazotised o-amino-hydroxy compounds [3] |
29/ | 03 | . | . | from diazotised o-amino carboxylic acids or o-amino-sulfonic acids [3] |
29/ | 033 | . | . | from diazotised amines containing a heterocyclic ring [3] |
29/ | 036 | . | . | . | the heterocyclic ring containing only nitrogen as hetero atoms [3] |
29/ | 039 | . | . | . | the heterocyclic ring containing nitrogen and sulfur as hetero atoms [3] |
29/ | 042 | . | . | . | . | the hetero ring being a thiazole ring [3] |
29/ | 045 | . | . | . | . | . | Benzothiazoles [3] |
29/ | 048 | . | . | . | . | the hetero ring being a thiadiazole ring [3] |
29/ | 06 | . | from coupling components containing amino as the only directing group |
29/ | 08 | . | . | Amino benzenes |
29/ | 085 | . | . | . | coupled with diazotised anilines [3] |
29/ | 09 | . | . | . | coupled with diazotised amines containing heterocyclic rings [3] |
29/ | 095 | . | . | Amino naphthalenes [3] |
29/ | 10 | . | from coupling components containing hydroxy as the only directing group |
29/ | 12 | . | . | of the benzene series |
29/ | 14 | . | . | . | Hydroxy carboxylic acids |
29/ | 15 | . | . | of the naphthalene series [3] |
29/ | 16 | . | . | . | Naphthol-sulfonic acids [3] |
29/ | 18 | . | . | ortho-Hydroxy carbonamides |
29/ | 20 | . | . | . | of the naphthalene series |
29/ | 22 | . | . | . | of heterocyclic compounds |
29/ | 24 | . | from coupling components containing both hydroxy and amino directing groups |
29/ | 26 | . | . | Amino phenols |
29/ | 28 | . | . | Amino naphthols |
29/ | 30 | . | . | . | Amino naphtholsulfonic acid |
29/ | 32 | . | from coupling components containing a reactive methylene group |
29/ | 33 | . | . | Aceto- or benzoyl-acetylarylides [3] |
29/ | 34 | . | from other coupling components |
29/ | 36 | . | . | from heterocyclic compounds |
29/ | 40 | . | . | . | containing a five-membered ring with one nitrogen atom as the only ring hetero atom [3] |
29/ | 42 | . | . | . | containing a six-membered ring with one nitrogen atom as the only ring hetero atom [3] |
29/ | 44 | . | . | . | . | Quinolines or hydrogenated quinolines [3] |
29/ | 46 | . | . | . | 1,2-Diazoles or hydrogenated 1,2-diazoles [3] |
29/ | 48 | . | . | . | . | Amino-1,2-diazoles [3] |
29/ | 50 | . | . | . | . | 1,2-Diazolones [3] |
29/ | 52 | . | . | . | Diazines [3] |
| | C09B 31/00 - C09B 35/64 |