Page last updated: 2024-11-06

reactive red 120 dye

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

Description

reactive red 120 dye: used in dye ligand chromatography; MF & structure unknown [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Reactive red 120 : A bis(azo) compound that consists of a benzene core having two (4-amino-6-chloro-1,3,5-triazin-2-yl)amino groups attached at positions 1 and 4 and which in turn have 5-hydroxy-6-[(2-sulfophenyl)diazenyl]-2,7-disulfonaphthalen-4-yl groups attached to their 4-amino functions. [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 CID73264
CHEMBL ID3596198
CHEBI ID63886
SCHEMBL ID13474896
MeSH IDM0125532

Synonyms (17)

Synonym
2,7-naphthalenedisulfonic acid, 4,4'-[1,4-phenylenebis[imino(6-chloro-1,3,5-triazine-4,2-diyl)imino]]bis[5-hydroxy-6-[(2-sulfophenyl)azo]-
reactive red 120
5-[[4-chloro-6-[4-[[4-chloro-6-[[8-hydroxy-3,6-disulfo-7-[(e)-(2-sulfophenyl)azo]-1-naphthyl]amino]-1,3,5-triazin-2-yl]amino]anilino]-1,3,5-triazin-2-yl]amino]-4-hydroxy-3-[(e)-(2-sulfophenyl)azo]naphthalene-2,7-disulfonic acid
61951-82-4
reactive red 120 dye
4,4'-(1,4-phenylenebis(imino(6-chloro-1,3,5-triazine-4,2-diyl)imino))bis(5-hydroxy-6-((2-sulphophenyl)azo)naphthalene-2,7-disulphonic acid)
triazine dye red a
c.i. reactive red 120
einecs 263-351-0
red a gel (amicon)
4,4'-{1,4-phenylenebis[imino(6-chloro-1,3,5-triazine-4,2-diyl)imino]}bis{5-hydroxy-6-[(2-sulfophenyl)diazenyl]naphthalene-2,7-disulfonic acid}
CHEBI:63886
SCHEMBL13474896
CHEMBL3596198
Q27132894
procion red h-e3b
DTXSID701335746

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Based on the results, the test item RR 120 could be classified as non-toxic to green alga, harmful to duck weed and Rainbow trout, toxic to water flea."( Acute Toxicity Assessment of Reactive Red 120 to Certain Aquatic Organisms.
Ayyappan, S; Chandrasehar, G; Chitrikha, T; Darsana, R; Deepa, V; Goparaju, A; Gowthami, Y, 2015
)
0.42
" PRACTITIONER POINTS: Current study is the first report on Pseudomonas guariconensis capable of degrading reactive dyes (Reactive Red 120) It was observed that the degradation potential was maximum when cells were immobilized with Ca-Ag biocarrier matrix Breakdown metabolism of Reactive Red 120 was derived through pathway prediction Employing immobilized bacteria in a packed bed column found to possess a prominent biosorption ability on the matrix enhancing the degradation process Toxic reactive dye was converted into nontoxic compounds, evidenced by phytotoxicity studies."( Biodegradation and biosorption of Reactive Red 120 dye by immobilized Pseudomonas guariconensis: Kinetic and toxicity study.
Osborne, JW; Reddy, S, 2020
)
0.84

Dosage Studied

ExcerptRelevanceReference
" In this experiment, comparison on the removal of reactive dye by photolysis using UV light alone, photocatalyst adsorption using TiO2 alone and photocatalysis using UV light with photocatalysts as well as the effect of experimental parameters such as the number of column employed, intensity of the light, pH and TiO2 dosage affecting the reaction efficiency of photocatalytic degradation of reactive dye in circular type reactor was examined."( Removal of reactive dye using UV/TiO2 in circular type reactor.
Choi, E; Gil, KI; Park, JH, 2003
)
0.32
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
dyenull
[role information is derived from 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]

Drug Classes (5)

ClassDescription
bis(azo) compoundAny azo compound containing two -N=N- groups.
azobenzenesAny member of the wide class of molecules that share the core azobenzene structure, comprising two phenyl rings linked by a N=N double bond, which may have different functional groups extending from the rings.
chloro-1,3,5-triazineA member of the class of 1,3,5-triazines that is 1,3,5-triazine substituted by at least one chloro group at unspecified position.
diamino-1,3,5-triazineAny member of the class of 1,3,5-triazines that consists of a 1,3,5-triazine skeleton substituted by two amino groups.
naphthalenesulfonic acid
[compound class information is derived from 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]

Research

Studies (59)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (10.17)18.7374
1990's8 (13.56)18.2507
2000's20 (33.90)29.6817
2010's21 (35.59)24.3611
2020's4 (6.78)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 29.86

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 Index29.86 (24.57)
Research Supply Index4.09 (2.92)
Research Growth Index4.82 (4.65)
Search Engine Demand Index35.06 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (29.86)

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%
Other59 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]