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642-59-1

642-59-1 Structure

642-59-1 Structure
IdentificationBack Directory
[Name]

3-hydroxy-4-[(4-sulphonaphthyl)azo]naphthalene-2,7-disulphonic acid
[CAS]

642-59-1
[Synonyms]

IRPXADUBAQAOKL-QURGRASLSA-N
2-Hydroxy-(1,1'-azobisnaphthalene)-3,4',6-trisulfonic acid
3'-Hydroxy[1,4'-azobisnaphthalene]-2',4,7'-trisulfonic acid
3-Hydroxy-4-(4-sulfo-1-naphtylazo)-2,7-naphthalenedisulfonic acid
3-Hydroxy-4-[(4-sulfo-1-naphtyl)azo]naphthalene-2,7-disulfonic acid
3-hydroxy-4-[(4-sulphonaphthyl)azo]naphthalene-2,7-disulphonic acid
2,7-Naphthalenedisulfonic acid, 3-hydroxy-4-[2-(4-sulfo-1-naphthalenyl)diazenyl]-
[EINECS(EC#)]

211-385-1
[Molecular Formula]

C20H14N2O10S3
[MDL Number]

MFCD00004076
[MOL File]

642-59-1.mol
[Molecular Weight]

538.53
Safety DataBack Directory
[HS Code ]

2927000090
Hazard InformationBack Directory
[Uses]

Amaranth free acid (Acid Red 27 free acid; Azorubin S free acid; FD & C Red Dye No. 2 free acid) 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.
[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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