journal article·2007-02

Synthesis and mutagenic properties of direct dyes from 4,4′‐diamino‐p‐terphenyl and 4,4′‐diamino‐p‐quaterphenyl

Jinlong Wang, Harold S Freeman, Larry D Claxton

Coloration Technology· Volume 123· Issue 1
Publisher page

Abstract

Disazo direct dyes were synthesised using bis‐diazotisation and coupling reactions involving 4,4′‐diamino‐p‐terphenyl and 4,4′‐diamino‐p‐quaterphenyl. The formation of the target dyes was confirmed by electrospray mass spectrometry and their mutagenicity was examined in the Salmonella microsome assay using TA98 and TA100. While most of these dyes were clearly non‐mutagenic, results from the Prival modification of the standard assay showed that Congo Red and its homologue derived from 4,4′‐diamino‐p‐terphenyl were clearly mutagenic.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: bioluminescence and chemiluminescence research · Dyeing and Modifying Textile Fibers · Dye analysis and toxicity

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (14)

Show source-provided references
1. Zollinger H · 1991
2. Woodward H E · 1972
3. Stead C V · 1990
4. Information Notice No. 6. German Ban of Use of Certain Azo Compounds in some Consumer Goods (Basel: ETAD 1998).
5. RPowell MMuray CChenandALee Report: Survey of the Manufacture Import and Uses for Benzidine Related Substances and Related Dyes and Pigments(1979).
6. Freeman H S · Chemtech · 1991 · 21 · 438
7. 10.1016/S0143-7208(02)00010-410.1016/S0143-7208(02)00010-4 ↗
8. 10.1111/j.1478-4408.2006.00058.x10.1111/j.1478-4408.2006.00058.x ↗
9. AATCC Technical Manual 75(2000)23 88 364 366 373.
10. 10.1016/0165-1161(83)90010-910.1016/0165-1161(83)90010-9 ↗
11. 10.1016/0165-1218(95)90093-410.1016/0165-1218(95)90093-4 ↗
12. 10.1016/0165-1161(82)90008-510.1016/0165-1161(82)90008-5 ↗
13. 10.1016/S0143-7208(00)00063-210.1016/S0143-7208(00)00063-2 ↗
14. Field F H · Adv. Mass Spectrom. · 1986 · 10 · 271