| Identification | Back Directory | [Name]
octasodium 7,7'-[(2,2'-disulphonato[1,1'-biphenyl]-4,4'-diyl)bis[imino(6-chloro-1,3,5-triazine-4,2-diyl)imino[2-(carbamoylamino)]-4,1-phenylene]azo]]bis(naphthalene-1,3,6-trisulphonate) | [CAS]
68133-40-4 | [Synonyms]
ZGGSNAKRSFXFON-AJRZDRFTSA-N
1,3,6-naphthalenetrisulfonic acid, 7,7'-[(2,2'-disulfo[1,1'-biphenyl]-4,4'-diyl
4,4'-Bis[[6-chloro-4-[[3-ureido-4-[(3,6,8-trissulfo-2-naphtyl)azo]phenyl]amino]-1,3,5-triazine-2-yl]amino]-1,1'-biphenyl-2,2'-disulfonic acid octasodium salt
1,3,6-Naphthalenetrisulfonic acid, 7,7-(2,2-disulfo1,1-biphenyl-4,4-diyl)bisimino(6-chloro-1,3,5-triazine-4,2-diyl)imino2-(aminocarbonyl)amino-4,1-phenyleneazobis-, octasodium salt
7,7'-[(2,2'-Disulfo-1,1'-biphenyl-4,4'-diyl)bis[imino(6-chloro-1,3,5-triazine-4,2-diyl)imino[2-(carbamoylamino)-4,1-phenylene]azo]]bis(1,3,6-naphthalenetrisulfonic acid)octasodium salt
octasodium 7,7'-[(2,2'-disulphonato[1,1'-biphenyl]-4,4'-diyl)bis[imino(6-chloro-1,3,5-triazine-4,2-diyl)imino[2-(carbamoylamino)]-4,1-phenylene]azo]]bis(naphthalene-1,3,6-trisulphonate)
7,7'-((2,2'-Disulfo(1,1'-biphenyl)-4,4'-diyl)bis(imino(6-chloro-1,3,5-triazine-4,2- diyl)imino(2-((aminocarbonyl)amino)-4,1-phenylene)azo))bis-1,3,6-naphthalenetrisulfonic acid, octasodium salt | [EINECS(EC#)]
268-684-5 | [Molecular Formula]
C52H39Cl2N18NaO26S8 | [MOL File]
68133-40-4.mol | [Molecular Weight]
1682.35 |
| Chemical Properties | Back Directory | [density ]
1.805[at 20℃] | [Water Solubility ]
58.25g/L at 20℃ | [LogP]
-1.598 at 20℃ | [EPA Substance Registry System]
1,3,6-Naphthalenetrisulfonic acid, 7,7'-[(2,2'-disulfo[1,1'-biphenyl]-4,4'-diyl)bis[imino(6-chloro-1,3,5-triazine-4,2-diyl)imino[2-[(aminocarbonyl)amino]-4,1-phenylene]azo]]bis-, octasodium salt (68133-40-4) |
| Hazard Information | Back Directory | [Uses]
Procion Yellow H-E 4R is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes are also widely used in traditional fields such as textile dyeing, as well as in emerging fields such as functional textile processing, food pigments and dye-sensitized solar cells. | [Flammability and Explosibility]
Nonflammable | [References]
[1] Sultana M, et al. A review on experimental chemically modified activated carbon to enhance dye and heavy metals adsorption[J]. Cleaner engineering and technology, 2022, 6: 100382. |
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