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reactive red 2

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Reactive Red 2 is a synthetic azo dye used in various applications, including dyeing textiles, leather, and paper. Its synthesis involves diazotization of 4-aminoazobenzene-3,4'-disulfonic acid followed by coupling with 1-amino-8-naphthol-3,6-disulfonic acid. The dye exhibits strong reddish-brown color and is known to be mutagenic in some studies. Due to its widespread use and potential environmental and health concerns, Reactive Red 2 has been studied extensively for its toxicity, bioaccumulation, and degradation pathways. Its importance lies in understanding its environmental fate and potential risks to human health.'

reactive red 2: inhibitor of ecto-nucleotidase and P(2y)-selective purinoceptor antagonist; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

procion red MX-5B : A 2,4-dichloro-1,3,5-triazine with a multi-substituted napthalen-1-ylamino substituent at the 6-position. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID28781
CHEBI ID53726
SCHEMBL ID3654363
SCHEMBL ID6808069
MeSH IDM0258994

Synonyms (45)

Synonym
chemictive brilliant red 5b
mikacion brilliant red 5bs
procion brilliant red 5bs
procion brilliant red mx 5b
cerven reaktivni 2 [czech]
brilliant red 5skh
5-((4,6-dichloro-1,3,5-triazin-2-yl)amino)-4-hydroxy-3-(phenylazo)-2,7-naphthalenedisulfonic acid, disodium salt
reactive brilliant red 5skh
2,7-naphthalenedisulfonic acid, 4-((4,6-dichloro-1,3,5-triazin-2-yl)amino)-5-hydroxy-6-(phenylazo)-, disodium salt
procion brilliant red m 5b
disodium 5-((4,6-dichloro-1,3,5-triazin-2-yl)amino)-4-hydroxy-3-(phenylazo)naphthalene-2,7-disulphonate
2,7-naphthalenedisulfonic acid, 5-((4,6-dichloro-1,3,5-triazin-2-yl)amino)-4-hydroxy-3-(phenylazo)-, disodium salt
ostazin brilliant red s 5b
procion red mx 5b
c.i. reactive red 2
2,7-naphthalenedisulfonic acid, 5-((4,6-dichloro-s-triazin-2-yl)amino)-4-hydroxy-3-(phenylazo)-, disodium salt
einecs 241-776-2
procion(r) red mx-5b, dye content 40 %
reactive red 2
CHEBI:53726 ,
disodium 5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-[(e)-phenyldiazenyl]naphthalene-2,7-disulfonate
17804-49-8
procion red mx-5b
5-((4,6-dichloro-1,3,5-triazin-2-yl)amino)-4-hydroxy-3-(phenylazo)-2,7-naphthalenedisulfonic acid, sodium salt
106740-69-6
2,7-naphthalenedisulfonic acid, 5-((4,6-dichloro-1,3,5-triazin-2-yl)amino)-4-hydroxy-3-(phenylazo)-, sodium salt
2,7-naphthalenedisulfonic acid, 5-((4,6-dichloro-1,3,5-triazin-2-yl)amino)-4-hydroxy-3-(2-phenyldiazenyl)-, sodium salt (1:?)
cerven reaktivni 2
2,7-naphthalenedisulfonic acid, 5-((4,6-dichloro-1,3,5-triazin-2-yl)amino)-4-hydroxy-3-(2-phenyldiazenyl)-, sodium salt (1:2)
AKOS024319587
EPITOPE ID:116222
SCHEMBL3654363
SCHEMBL6808069
2,7-naphthalenedisulfonic acid, 5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-(phenylazo)-, sodium salt
disodium 5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-(phenylazo)naphthalene-2,7-disulphonate
W-110468
12226-03-8
disodium 5-[(4,6-dichloro-1,3,5-triazin-2(1h)-ylidene)amino]-4-oxo-3-(2-phenylhydrazinylidene)-3,4-dihydronaphthalene-2,7-disulfonate
DTXSID70924123
disodium;5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-phenyldiazenylnaphthalene-2,7-disulfonate
DTXSID10889666
2,7-naphthalenedisulfonic acid,5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-(phenylazo)-,disodium salt
disodium;(3z)-5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-oxo-3-(phenylhydrazinylidene)naphthalene-2,7-disulfonate
reactive red 2
reactivered2

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Based on the present findings, biodegradation was effective in the decolorization of the samples, but generated toxic metabolites, while biosorption was effective in both decolorization and reducing the toxicity of the solutions."( Comparative study of toxicity of azo dye Procion Red MX-5B following biosorption and biodegradation treatments with the fungi Aspergillus niger and Aspergillus terreus.
Almeida, EJ; Corso, CR, 2014
)
0.4

Dosage Studied

ExcerptRelevanceReference
" The use of high temperature may decrease or even take the place of the need for continuous redox mediator dosage in bioreactors, contrarily to the evident effect of those compounds on dye reduction under mesophilic conditions."( Azo dye reduction by mesophilic and thermophilic anaerobic consortia.
Cervantes, FJ; de Madrid, MP; Dos Santos, AB; Stams, AJ; van Lier, JB,
)
0.13
" The amount adsorbed increased with the CNTs dosage; however, the adsorption capacity initially increased with the CNTs dosage (<0."( Adsorption of reactive dye onto carbon nanotubes: equilibrium, kinetics and thermodynamics.
Wu, CH, 2007
)
0.34
"5-3g/l TiO2 was added, the effect of TiO2 dosage for RR2 decolorization was insignificant in the UV/TiO2/O3 system."( Decolorization of C.I. Reactive Red 2 by catalytic ozonation processes.
Chang, CL; Kuo, CY; Wu, CH, 2008
)
0.66
" The effects of pH and catalyst dosage were evaluated in O3/Mn(II), O3/Fe(II), O3/Fe(III), O3/Zn(II), O3/Co(II) and O3/Ni(II) systems."( Homogeneous catalytic ozonation of C.I. Reactive Red 2 by metallic ions in a bubble column reactor.
Chang, CL; Kuo, CY; Wu, CH, 2008
)
0.61
" Furthermore, the effects of calcination temperature, pH, RR2 concentration, and the TiO2/CNTs composite dosage on RR2 decolourization were determined simultaneously."( Synergistic effects between TiO2 and carbon nanotubes (CNTs) in a TiO2/CNTs system under visible light irradiation.
Chen, ST; Kuo, CY; Wu, CH,
)
0.13
" The use of immobilized RMs avoids the requirement of their continuous dosing in MFCs, which has been the main limitation for practical applications."( AQDS immobilized solid-phase redox mediators and their role during bioelectricity generation and RR2 decolorization in air-cathode single-chamber microbial fuel cells.
Logan, BE; Martinez, CM; Zhu, X, 2017
)
0.46
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (61)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (1.64)18.7374
1990's3 (4.92)18.2507
2000's25 (40.98)29.6817
2010's30 (49.18)24.3611
2020's2 (3.28)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 20.57

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index20.57 (24.57)
Research Supply Index4.17 (2.92)
Research Growth Index5.44 (4.65)
Search Engine Demand Index18.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (20.57)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other64 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]