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3.3- dichlorobenzidine

Used in the production of yellow and red pigments for the printing ink, textile, paper, paint, rubber, plastic, and related industries [Pg.223]

Toxicology. 3,3 -Dichlorobenzidine (DCB) is carcinogenic in several animal species. [Pg.223]

The acute LD50 of DCB in rats has been estimated to be 7100mg/kg for the free base and 3800mg/kg for the dihydrochloride salt. Considering these high LD50 values, acute lethality in man after oral exposure is not expected to be very likely.  [Pg.223]

Dermatitis was cited as the only verified health problem encountered by workers in contact with DCB at a DCB manufacturing plant. Applied to the skin of rabbits DCB dihydrochloride caused no discernable reaction instilled in the rabbit eye 20 mg (as 0.1 ml of 20% corn oil suspension) produced erythema, pus, and corneal opacity. No effects were reported when 100 mg of the free base was placed in rabbit eyes. [Pg.223]

Existing animal data shows that DCB induces tumors at a variety of sites in several animal species.  [Pg.224]


One area which requires special comment is a study (13) which showed that certain diaryUde pigments processed ia polymers above 200°C and particularly above 240°C decompose to give off 3,3 -dichlorobenzidine, an animal carciaogen. As a consequence diaryUde pigments (not, however, condensation disazo pigments) are not recommended for use ia any appHcations where they might be exposed to temperatures exceeding 200°C. [Pg.37]

Orthotolidine and its salts Dianisidine and its salts Dichlorobenzidine and its salts In manufacture, formation or use of these substances... [Pg.117]

Dichloro-1 -nitroethane o-Dichlorobenzene p-Dichlorobenzene 3,3 -Dichlorobenzidine Dichlorodifluoromethane (Refrigerant 12)... [Pg.366]

Dibromoethane, 51 Dibutylamine, 51 Dibutylaminoethanol, 51 Di-tert-butyl-p-cresol, 51 Dibutyl phosphate, 51 Dibutyl phthalate (DBF), 51 Dicamba, 51 Dichloroacetic acid, 51 Dichlorobenzenes, 51 3,3 -Dichlorobenzidine and its salts, 52... [Pg.329]

Mere alteration of the strnctnre of the contaminant by biotransformation may not necessarily be acceptable. For example, although anaerobic dechlorination of PCBs is desirable, microbial redaction of 3,3 -dichlorobenzidine, which is an intermediate in the manufacture of dyes, produced benzidine that is both more toxic and more snsceptible to dissemination in the aqnatic phase (Nyman et al. 1997). [Pg.601]

Nyman MC, AK Nyman, LS Lee, LF Nies, ER Blatchley (1997) 3,3 -Dichlorobenzidine transformation processes in natural sediments. Environ Sci Technol 31 1068-1073. [Pg.617]

Emissions of dichlorobenzidine, chloroaniline, cuprous chloride and more during pigment production (17-20%)... [Pg.214]

Burton, D.J. and D.J. Fisher. 1990. Acute toxicity of cadmium, copper, zinc, ammonia, 3,3 -dichlorobenzidine, 2,6-dichloro-4-nitroaniline, methylene chloride, and 2,4,6-trichlorophenol to juvenile grass shrimp and killifish. Bull. Environ. Contam. Toxicol. 44 776-783. [Pg.728]


See other pages where 3.3- dichlorobenzidine is mentioned: [Pg.222]    [Pg.2211]    [Pg.93]    [Pg.93]    [Pg.101]    [Pg.156]    [Pg.375]    [Pg.60]    [Pg.215]    [Pg.52]    [Pg.128]    [Pg.67]    [Pg.82]    [Pg.241]    [Pg.249]    [Pg.122]    [Pg.122]    [Pg.130]    [Pg.375]    [Pg.666]    [Pg.612]    [Pg.61]    [Pg.194]    [Pg.215]    [Pg.99]    [Pg.121]    [Pg.133]    [Pg.385]    [Pg.89]    [Pg.248]    [Pg.256]    [Pg.15]    [Pg.213]    [Pg.263]    [Pg.39]    [Pg.58]    [Pg.58]    [Pg.63]    [Pg.183]    [Pg.225]   
See also in sourсe #XX -- [ Pg.61 , Pg.194 ]

See also in sourсe #XX -- [ Pg.15 ]




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3,3 -Dichlorobenzidine (and its

3,3’-Dichlorobenzidine and its salts

3.3- Dichlorobenzidine, concentration

Dichlorobenzidine base

Dichlorobenzidine base 3,3 -Dichloro-4,4 -diaminobiphenyl

Dichlorobenzidine base 3,3 -Dichlorobiphenyl-4,4 -diamine

Dichlorobenzidine pigment production

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