Page last updated: 2024-12-07

reactive yellow 2

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

Description

Reactive Yellow 2, also known as C.I. Reactive Yellow 14, is a synthetic dye commonly used in textile industries to impart bright yellow hues to fabrics. Its synthesis typically involves the reaction of a diazotized aromatic amine with a coupling component, followed by a reaction with a reactive group, such as a chloro-s-triazine or vinyl sulfone. The reactive group allows for the dye to covalently bond to the fabric fibers, resulting in a strong and durable color. However, concerns regarding the environmental impact and potential health risks associated with Reactive Yellow 2 have led to research efforts aimed at developing alternative dyes with improved safety profiles and reduced ecological footprints. This research includes exploring new synthetic pathways, investigating the degradation and bioaccumulation of the dye in the environment, and evaluating its potential toxicity to aquatic organisms. The importance of studying Reactive Yellow 2 stems from its widespread use in the textile industry, the potential hazards associated with its handling and disposal, and the need to develop safer and more sustainable dyeing technologies.'
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reactive yellow 2: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID92331
MeSH IDM0457113

Synonyms (8)

Synonym
cibacron brilliant yellow 3g-p
reactive yellow 2
trisodium 4-((4-chloro-6-((4-sulphonatophenyl)amino)-1,3,5-triazin-2-yl)amino)-2-((1-(2,5-dichloro-4-sulphonatophenyl)-4,5-dihydro-3-methyl-5-oxo-1h-pyrazol-4-yl)azo)benzenesulphonate
einecs 256-692-1
benzenesulfonic acid, 4-((4-chloro-6-((4-sulfophenyl)amino)-1,3,5-triazin-2-yl)amino)-2-((1-(2,5-dichloro-4-sulfophenyl)-4,5-dihydro-3-methyl-5-oxo-1h-pyrazol-4-yl)azo), trisodium salt
AKOS025310820
sodium (e)-2,5-dichloro-4-(4-((5-(4-chloro-6-(4-sulfonatophenylamino)-1,3,5-triazin-2-ylamino)-2-sulfonatophenyl)diazenyl)-5-hydroxy-3-methyl-1h-pyrazol-1-yl)benzenesulfonate
trisodium;2,5-dichloro-4-[4-[[5-[[4-chloro-6-(4-sulfonatoanilino)-1,3,5-triazin-2-yl]amino]-2-sulfonatophenyl]diazenyl]-5-methyl-3-oxo-1h-pyrazol-2-yl]benzenesulfonate

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" The decolorization rate increased as the catalyst dosage was increased."( Photocatalysis process to treat polluted water by azo dye Cibacron Brilliant Yellow 3G-P.
Bentahar, F; Fouzia, T; Rachida, R; Radia, D; Wahib, NM, 2022
)
0.72
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (50.00)29.6817
2010's3 (37.50)24.3611
2020's1 (12.50)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 17.54

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 Index17.54 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.56 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (17.54)

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%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]