Disperse Red 60

Disperse Red 60
Names
	Other names 1-Amino-4-hydroxy-2-phenoxyanthraquinone; C.I. 60756 (Colour index numbers)
Identifiers
CAS Number	17418-58-5;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL3561744;
ChemSpider	26544;
ECHA InfoCard	100.037.659
EC Number	241-442-6;
PubChem CID	28531;
UNII	T4431S01IG;
CompTox Dashboard (EPA)	DTXSID2025210 ;
	InChI InChI=1S/C20H13NO4/c21-18-15(25-11-6-2-1-3-7-11)10-14(22)16-17(18)20(24)13-9-5-4-8-12(13)19(16)23/h1-10,22H,21H2 Key: MHXFWEJMQVIWDH-UHFFFAOYSA-N;
	SMILES C1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N;
Properties
Chemical formula	C20H13NO4
Molar mass	331.327 g·mol−1
Appearance	dark red solid
Density	1.44 g/cm3
Melting point	185 °C (365 °F; 458 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H317, H319
Precautionary statements	P261, P264, P272, P280, P302 P352, P305 P351 P338, P321, P333 P313, P337 P313, P363, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Disperse Red 60, or 1-amino-4-hydroxy-2-phenoxyanthraquinone, is a popular disperse dye of the anthraquinone family of dyes.^[1] It is a dark red solid that is insoluble in water but soluble in dichloromethane.^[2]

Because Disperse Red 60 is produced on a large scale, its disposal or degradation has received considerable attention.^[3]

References

^ Hamprecht, Rainer; Westerkamp, Aloys (2000). "Disperse Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a08_565. ISBN 3527306730.
^ Black, S. N.; Davey, R. J.; O'Mahoney, C. A.; Williams, D. J. (1992). "Structure of 1-amino-4-hydroxy-2-phenoxy-9,10-anthracenedione". Acta Crystallographica Section C Crystal Structure Communications. 48 (2): 321–323. doi:10.1107/S0108270191009381.
^ Xu, Xiang-Rong; Li, Hua-Bin; Wang, Wen-Hua; Gu, Ji-Dong (2004). "Degradation of dyes in aqueous solutions by the Fenton process". Chemosphere. 57 (7): 595–600. Bibcode:2004Chmsp..57..595X. doi:10.1016/j.chemosphere.2004.07.030. PMID 15488921.

[1] Hamprecht, Rainer; Westerkamp, Aloys (2000). "Disperse Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a08_565. ISBN 3527306730.

[2] Black, S. N.; Davey, R. J.; O'Mahoney, C. A.; Williams, D. J. (1992). "Structure of 1-amino-4-hydroxy-2-phenoxy-9,10-anthracenedione". Acta Crystallographica Section C Crystal Structure Communications. 48 (2): 321–323. doi:10.1107/S0108270191009381.

[3] Xu, Xiang-Rong; Li, Hua-Bin; Wang, Wen-Hua; Gu, Ji-Dong (2004). "Degradation of dyes in aqueous solutions by the Fenton process". Chemosphere. 57 (7): 595–600. Bibcode:2004Chmsp..57..595X. doi:10.1016/j.chemosphere.2004.07.030. PMID 15488921.

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