Page last updated: 2024-12-05

disperse orange 3

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

Description

Disperse Orange 3, also known as C.I. Solvent Orange 7, is an azo dye widely used in the textile industry for dyeing synthetic fibers like polyester and nylon. It is typically synthesized through a diazotization and coupling reaction involving an aromatic amine and a diazonium salt. Disperse Orange 3 is known for its vibrant orange color and good lightfastness. It is often used in the production of clothing, carpets, and other textile materials. The compound is studied due to its potential environmental impacts, as its release into waterways can contribute to water pollution and harm aquatic life. Research focuses on developing sustainable alternatives and optimizing dyeing processes to minimize environmental impact.'

4-(4-nitrophenylazo)aniline : Azobenzene substituted at the phenyl 4-positions by an amino and a nitro group. [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 CID12896
CHEBI ID75648
SCHEMBL ID15922
MeSH IDM0122438

Synonyms (47)

Synonym
730-40-5
b7j3o076ot ,
c.i. disperse orange 3
unii-b7j3o076ot
benzenamine, 4-(2-(4-nitrophenyl)diazenyl)-
4-(4-nitrophenylazo)aniline
benzenamine, 4-[(4-nitrophenyl)azo]-
4-amino-4'-nitroazobenzene
disperse orange 3, dye content 90 %
do3 ,
4-((4-nitrophenyl)azo)aniline
ci 11005
disperse orange 3
benzenamine, 4-((4-nitrophenyl)azo)-
4-((4-nitrophenyl)azo)benzenamine
benzeneamine, 4-((nitrophenyl)azo)-
einecs 211-984-8
4-[(4-nitrophenyl)diazenyl]aniline
4-(2-(4-nitrophenyl)diazenyl)benzenamine
4-[(4-nitrophenyl)azo]benzenamine
4-(4-nitroazophenyl)aniline
CHEBI:75648
1-(4'-aminophenylazo)-4-nitrobenzene
4-((nitrophenyl)azo)benzeneamine
4-(4'-nitroazophenyl)anilin
4-[(4-nitrophenyl)azo]benzenamin
4-((4-nitrophenyl)diazenyl)aniline
AKOS015902549
70734-98-4
SCHEMBL15922
DTXSID7061061
UNBOSJFEZZJZLR-UHFFFAOYSA-N
T487 ,
UNBOSJFEZZJZLR-CCEZHUSRSA-N
benzenamine, 4-[2-(4-nitrophenyl)diazenyl]-
disperse orange 3 [inci]
4-(4'-nitrophenylazo)aniline
lowadene orange 3
AKOS028108375
disperse orange 3, analytical standard
mfcd00007856
(e)-4-((4-nitrophenyl)diazenyl)aniline
Q26840859
E79393
trans-4-((4-nitrophenyl)azo)aniline
Q27274464
AS-81858
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
dyenull
allergenA chemical compound, or part thereof, which causes the onset of an allergic reaction by interacting with any of the molecular pathways involved in an allergy.
[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 (2)

ClassDescription
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.
primary arylamineA primary amine formally derived from ammonia by replacing one hydrogen atom by an aryl group. R-NH2 where R is an aryl group.
[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 (16)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (6.25)18.7374
1990's2 (12.50)18.2507
2000's2 (12.50)29.6817
2010's9 (56.25)24.3611
2020's2 (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: 35.14

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 strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index35.14 (24.57)
Research Supply Index2.94 (2.92)
Research Growth Index5.10 (4.65)
Search Engine Demand Index43.27 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (35.14)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (5.88%)5.53%
Reviews1 (5.88%)6.00%
Case Studies2 (11.76%)4.05%
Observational0 (0.00%)0.25%
Other13 (76.47%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]