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O

H3 C

OH2

HO

 

 

 

 

H3 C

S O

N N

N

N

Acid Red 114

O

 

 

C

 

 

 

NaO2 S

SO2 Na

NH

OH

H3 CO

OCH3

2

 

 

 

Direct Blue 15

 

N N

N N

NaO2 S

 

SO2 Na

NaO2 S

 

NH

CH3 O

OCH3

 

2

 

 

Direct Violet 32

 

N N

N N

 

 

 

 

SO2 Na

 

 

OH

CH3 O

OCH3

Direct Blue 8

 

N N

N N

 

 

 

 

SO2 Na

 

OH

OH

CH3 O

OCH3

Direct Blue 10

 

N N

N N

 

 

 

NaO2 S

 

 

NaO2 S

NH2 OH

C

SO2 Na

OH

C

SO2 Na

OH

C

SO2 Na

OH OH

C

SO2 Na

SO2 Na

(continued overleaf )

1209

TABLE 8. (continued)

Common

 

 

Chemical

 

 

name

 

 

structure

 

 

OH

OH

OH2

OH2

 

OH OH

Direct Blue 25

N N

N N

 

NaO2 S

SO2 Na

SO2 Na

SO2 Na

H3 C

NH2 H3 C

CH3

 

COOH2

Direct Orange 6

N N

N N

OH

NaO2 S

NH2

 

 

 

 

 

 

OH2

OH2

HO

 

C3 H2 O

N N

N N

 

Direct Red 39

 

 

 

 

 

 

 

 

NaO2 S

 

 

 

 

 

 

SO2 Na

NaO2 S

NH2

O

O

NH2

SO2 Na

 

N N

N N

 

Direct Red 46

 

 

 

 

 

NaO S

 

 

 

 

SO2 Na

2

 

 

 

 

 

Miscellaneous Azo Dyes

 

 

 

 

 

 

 

 

CH3 HO

 

 

Sudan 2

H3 C

N N

 

 

 

 

 

 

 

Metabolic activationa

C

C

C

C

C

1210

Acid Alizarin Red B

Acid Alizarin Violet N

Ponceau 3R

(Acid Dye, C.I.16155)

Eriochrome Blue

Black B

Thiodiphenyl-4,40 - diazo-bis-salicyclic Acid

N O

O HO

N N

 

OH HO

 

N N

NaO2 S

 

 

 

CH3

HO

H3 C

N

N

H3 C

 

 

 

OH

 

NaO2 S

N

N

HO

N N

S

COOH

SO2 Na

C

SO2 Na

C

SO2 Na

C

SO2 Na

OH

 

 

C

N N

OH

š

 

COOH

 

a C, metabolic activation required; , no metabolic activation is required, i.e. a direct mutagen. Reproduced with permission from Reference 106.

1211

1212

H. K. Chagger and A. Williams

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