HTHQ Datasheet DC Chemicals
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Cat.No DC9960
Name HTHQ

Chemical Properties

CAS 148081-72-5
Formula C15H24O2
MW 236.3499
Storage 4°C for 1 year, -20°C for more than 2 years

Biological activity

Description CAS NO.:148081-72-5
Product Name:1-O-Hexyl-2,3,5-trimethylhydroquinone
Synonyms:Phenol,4-(hexyloxy)-2,3,6-trimethyl-;1-O-Hexyl-2,3,5-trimethylhydroquinone;1-O-n-hexyl-2,3,5-trimethylhydroquinone;3-Hydroxy-6-hexyloxy-1.2.4-trimethyl-benzol;4-Hexyloxy-2,3,6-trimethyl-phenol;DSSTox_CID_697;HTHQ;HTHQ-2,3,5;HX-1171;4-Hexyloxy-2,3,6-triMethylphenol;4-(Hexyloxy)-2,3,6-triMethyl-phenol;4-(Hexyloxy)-2,3,6-trimethylphenol;HX 1171;Phenol, 4-(hexyloxy)-2,3,6-trimethyl-;70BK60I8RP;C15H24O2;4-hexoxy-2,3,6-trimethylphenol;DSSTox_RID_75742;DSSTox_GSID_20697;BCP19301;Tox21_301245;DB1216
EINEC:7478
Molecular Formula:C15H24O2
Molecular Weight:236.3499
Target:
In Vivo
In Vitro
Kinase Assay
Cell Assay
Animal Administration

References

[1]. Hino T et al. HTHQ (1-O-hexyl-2,3,5-trimethylhydroquinone), an anti-lipid-peroxidative compound: its chemical and biochemical characterizations. Biochim Biophys Acta. 1998 Sep 16;1425(1):47-60. [2]. Hirose M et al. Inhibitory effects of 1-O-hexyl-2,3,5-trimethylhydroquinone (HTHQ), green tea catechins and other antioxidants on 2-amino-6-methyldipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1)-induced rat hepatocarcinogenesis and dose-dependent inhibition by HTHQ of lesion induction by Glu-P-1 or 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx). Carcinogenesis. 1995 Dec;16(12):3049-55. [3]. Jung YR et al. Inhibitory Effect of 1-O-Hexyl-2,3,5-Trimethylhydroquinone on Dimethylnitrosamine-induced Liver Fibrosis in Male SD Rats. Toxicol Res. 2010 Sep;26(3):193-201.
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