IPC 6 English version  C09-C09B00562
    C09B 6/00 - C09B 29/52 >> 
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 C 12 P)

Notes

(1)

In this subclass, in the absence of an indication to the contrary, a compound is classified in the last appropriate place.

(2)

Processes using enzymes or micro-organisms in order to:

(i)

liberate, separate or purify a pre-existing compound or composition, or to

(ii)

treat textiles or clean solid surfaces of materials

are further classified in subclass C 12 S. [5]


Anthracene dyes

1/

00

Dyes with an anthracene nucleus not condensed with any other ring

1/

02

Hydroxy anthraquinones; Ethers or esters thereof

1/

04

. . 

Preparation by synthesis of the nucleus

1/

06

. . 

Preparation from starting materials already containing the anthracene nucleus

1/

08

. . . 

Dyes containing only OH groups

1/

10

. . . 

Dyes containing halogen

1/

12

. . . 

Dyes containing sulfonic acid groups

1/

14

. . . 

Dyes containing ether groups

1/

16

Amino anthraquinones

1/

18

. . 

Preparation by synthesis of the nucleus

1/

20

. . 

Preparation from starting materials already containing the anthracene nucleus

1/

22

. . . 

Dyes with unsubstituted amino groups

1/

24

. . . . 

sulfonated

1/

26

. . . 

Dyes with amino groups substituted by hydrocarbon radicals

1/

28

. . . . 

substituted by alkyl, aralkyl, or cyclo-alkyl groups

1/

30

. . . . . 

sulfonated

1/

32

. . . . 

substituted by aryl groups (anthrimides C 09 B 1/48)

1/

34

. . . . . 

sulfonated

1/

36

. . . 

Dyes with acylated amino groups

1/

38

. . . . 

Urea or thiourea derivatives

1/

40

. . . . 

the acyl groups being residues of an aliphatic or araliphatic carboxylic acid

1/

42

. . . . 

the acyl groups being residues of an aromatic carboxylic acid

1/

43

. . . . . 

Dicarboxylic acids [3]

1/

44

. . . . 

the acyl groups being residues of a heterocyclic carboxylic acid

1/

46

. . . . 

the acyl groups being residues of cyanuric acid or an analogous heterocyclic compound

1/

467

. . . . . 

attached to two or more anthraquinone rings [3]

1/

473

. . . . 

the acyl groups being residues of a sulfonic acid [3]

1/

48

. . . 

Anthrimides

1/

50

Amino-hydroxy anthraquinones; Ethers or esters thereof

1/

503

. . 

unsubstituted amino-hydroxy anthraquinone [2]

1/

51

. . 

N-substituted amino-hydroxy anthraquinone [2]

1/

514

. . . 

N-aryl derivatives (N-aralkyl derivatives C 09 B 1/515) [2]

1/

515

. . . 

N-alkyl, N-aralkyl, or N-cycloalkyl derivatives [2]

1/

516

. . . 

N-acylated derivatives [2]

1/

52

. . 

sulfonated

1/

54

. . 

etherified

1/

56

Mercapto-anthraquinones

1/

58

. . 

with mercapto groups substituted by aliphatic, cycloaliphatic, araliphatic or aryl radicals [3]

1/

60

. . . 

substituted by aliphatic, cycloaliphatic or araliphatic radicals [3]

1/

62

. . 

with mercapto groups substituted by a heterocyclic ring [3]

3/

00

Dyes with anthracene nucleus condensed with one or more carbocyclic rings

3/

02

Benzanthrones

3/

04

. . 

Preparation by synthesis of the nucleus

3/

06

. . 

Preparation from starting materials already containing the benzanthrone nucleus

3/

08

. . . 

by halogenation

3/

10

. . . 

Amino derivatives

3/

12

. . 

Dibenzanthronyls

3/

14

Perylene derivatives

3/

16

. . 

Preparation by synthesis of the nucleus

3/

18

. . 

Preparation from starting materials already containing the perylene nucleus

3/

20

. . . 

by halogenation

3/

22

Dibenzanthrones; Isodibenzanthrones

3/

24

. . 

Preparation by synthesis of the nucleus

3/

26

. . . 

from dibenzanthronyls

3/

28

. . . 

from perylene derivatives

3/

30

. . 

Preparation from starting materials already containing the dibenzanthrone or isodibenzanthrone nucleus

3/

32

. . . 

by halogenation

3/

34

. . . 

by oxidation

3/

36

. . . 

by etherification of hydroxy compounds

3/

38

. . . 

by introduction of hydrocarbon or acyl residues into amino groups

3/

40

Pyranthrones

3/

42

. . 

Preparation by synthesis of the nucleus

3/

44

. . 

Preparation from starting materials already containing the pyranthrone nucleus

3/

46

. . . 

by halogenation

3/

48

. . . 

Amino derivatives

3/

50

Dibenzopyrenequinones

3/

52

. . 

Preparation by synthesis of the nucleus

3/

54

. . 

Preparation from starting materials already containing the dibenzopyrenequinone nucleus

3/

56

. . . 

Amino derivatives

3/

58

Benzanthraquinones

3/

60

Anthanthrones

3/

62

. . 

Preparation by synthesis of the nucleus

3/

64

. . 

Preparation from starting materials already containing the anthanthrone nucleus

3/

66

. . . 

by halogenation

3/

68

. . . 

Amino derivatives

3/

70

Benzo-, naphtho-, or anthra-dianthrones

3/

72

. . 

Preparation by synthesis of the nucleus

3/

74

. . 

Preparation from starting materials already containing the benzo-, naphtho-, or anthra-dianthrone nucleus

3/

76

. . . 

by halogenation

3/

78

Other dyes in which the anthracene nucleus is condensed with one or more carbocyclic rings

3/

80

. . 

Preparation by synthesis of the nucleus

3/

82

. . 

Preparation from starting materials already containing the condensed anthracene nucleus

5/

00

Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings

5/

02

the heterocyclic ring being condensed in peri position

5/

04

. . 

Pyrazolanthrones

5/

06

. . . 

Benzanthronyl-pyrazolanthrone condensation products

5/

08

. . . 

Dipyrazolanthrones

5/

10

. . 

Isothiazolanthrones; Isoxazolanthrones; Isoselenazolanthrones

5/

12

. . 

Thiophenanthrones

5/

14

. . 

Benz-azabenzanthrones (anthrapyridones)

5/

16

. . 

Benz-diazabenzanthrones, e.g. anthrapyrimidones

5/

18

. . 

Coeroxene; Coerthiene; Coeramidene; Derivatives thereof

5/

20

. . 

Flavanthrones

5/

22

. . . 

Preparation from starting materials already containing the flavanthrone nucleus

5/

24

the heterocyclic ring(s) being condensed with an anthraquinone nucleus in 1-2 or 2-3 position

5/

26

. . 

Carbazoles of the anthracene series

5/

28

. . . 

Anthrimide carbazoles

5/

30

. . 

1.2 azoles of the anthracene series

5/

32

. . 

1.3 azoles of the anthracene series

5/

34

. . 

Anthraquinone acridones or thioxanthones

5/

36

. . . 

Amino acridones

5/

38

. . . 

Compounds containing acridone and carbazole rings

5/

40

. . . 

Condensation products of benzanthronyl-amino anthraquinones

5/

42

. . 

Pyridino anthraquinones

5/

44

. . 

Azines of the anthracene series

5/

46

. . . 

Para-diazines

5/

48

. . . . 

Bis-anthraquinonediazines (indanthrone)

5/

50

. . . . . 

Preparation by alkaline melting of 2-amino anthraquinones

5/

52

. . . . . 

Preparation by condensation of 1.2-halogeno-amino anthraquinones

5/

54

. . . . . 

Preparation from 2-amino anthrahydroquinones

5/

56

. . . . . 

Preparation from starting materials already containing the indanthrene nucleus

5/

58

. . . . . . 

by halogenation

5/

60

. . . 

Thiazines; Oxazines

5/

62

Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
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