Disperse Red 60

Disperse Red 60
Names
	Other names 1-amino-4-hydroxy-2-phenoxy-9,10-anthracenedione
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 pictograms
GHS Signal word	Warning
GHS hazard statements	H317, H319
GHS precautionary statements	P261, P264, P272, P280, P302+352, P305+351+338, P321, P333+313, P337+313, 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 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.
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.

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

[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.