Product Name :
2,6-Dichloro-p-phenylenediamine (CAS 609-20-1)
Synonym :
2,6-dichlorobenzene-1,4-diamine; 2,6-Dichloro-1,4-phenylenediamine
Application :
2,6-Dichloro-p-phenylenediamine is a useful biochemical for proteomics research
CAS:
609-20-1
Purity:
Molecular Weight:
177.03
Formula :
C6H6Cl2N2
Physical state:
Solid
solubility :
Shipping Condition :
Store at room temperature
Melting point:
122-127° C
SMILES:
C1=C(C=C(C(=C1Cl)N)Cl)N
References:
:Chemical carcinogenicity: can it be predicted from knowledge of mutagenicity and allergic contact dermatitis? | Rosenkranz, HS. and Karol, MH. 1999. 1-BOC-3-trifluoromethyl-piperidin-4-one site Mutat Res. Azido-PEG4-alcohol site 431: 81-91. PMID: 10656488Carcinogenesis Bioassay of 2,6-Dichloro-p-Phenylenediamine (CAS No. 609-20-1) in F344 Rats and B6C3F1 Mice (Feed Study). | ,. 1982. Natl Toxicol Program Tech Rep Ser. 219: 1-121. PMID: 12778217Microbial transformation of aniline derivatives: regioselective biotransformation and detoxification of 2-phenylenediamine by Bacillus cereus strain PDa-1. | Takenaka, S., et al. 2006. J Biosci Bioeng. 102: 21-7. PMID: 16952832Performance of 133 compounds in the lambda prophage induction endpoint of the Microscreen assay and a comparison with S. typhimurium mutagenicity and rodent carcinogenicity assays. | Rossman, TG., et al. 1991. Mutat Res. 260: 349-67. PMID: 1831244Significant differences in the structural basis of the induction of sister chromatid exchanges and chromosomal aberrations in Chinese hamster ovary cells. | Rosenkranz, HS., et al. 1990. Environ Mol Mutagen. 16: 149-77. PMID: 2209572Pancreatic hepatocytes associated with chronic 2,6-dichloro-p-phenylenediamine administration in Fischer 344 rats. | McDonald, MM. and Boorman, GA. 1989. Toxicol Pathol. 17: 1-6. PMID: 2665028Reductive transformation of nitroaromatic compounds by Pd nanoparticles on nitrogen-doped carbon (Pd@NC) biosynthesized using Pantoea sp. IMH. | Liu, W., et al. 2019. J Hazard Mater. 366: 338-345. PMID: 30530026Exploring relationships between mutagenic and carcinogenic potencies. | Piegorsch, WW. and Hoel, DG. 1988. Mutat Res. 196: 161-75. PMID: 3419441Chemical enhancement of SA7 virus transformation of hamster embryo cells: evaluation by interlaboratory testing of diverse chemicals. | Hatch, GG., et al. 1986. Environ Mutagen. 8: 515-31. PMID: 37321942,6-Dichloro-p-phenylenediamine: comparative disposition in male and female rats and mice. | Ioannou, YM. and Matthews, HB. 1985. J Toxicol Environ Health. 16: 285-97. PMID: 4078934Comparison of results from mouse bone marrow chromosome aberration and micronucleus tests. | Shelby, MD. and Witt, KL. 1995. Environ Mol Mutagen. 25: 302-13. PMID: 7607185Assessing the predictiveness of the Syrian hamster embryo cell transformation assay for determining the rodent carcinogenic potential of single ring aromatic/nitroaromatic amine compounds. | Kerckaert, GA., et al. 1998. Toxicol Sci. 41: 189-97. PMID: 9520355Mouse-specific carcinogens: an assessment of hazard and significance for validation of short-term carcinogenicity bioassays in transgenic mice. | Battershill, JM. and Fielder, RJ. 1998. Hum Exp Toxicol. 17: 193-205. PMID: 9617631
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