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方案
98%
表单
solid
mp
54-58 °C (lit.)
官能团
ketone
SMILES字符串
CC(C)(C)C1=CC(=O)C=CC1=O
InChI
1S/C10H12O2/c1-10(2,3)8-6-7(11)4-5-9(8)12/h4-6H,1-3H3
InChI key
NCCTVAJNFXYWTM-UHFFFAOYSA-N
一般描述
2-叔 -丁基-1,4-苯醌（TBQ、TBBQ、TBQ、BuBQ、BQ、 叔 -丁基- p -醌）是 1,4-苯醌衍生物。它是食品添加剂丁基羟基茴香醚 (BHA) 的主要代谢产物。据报道，TBQ 在人单核细胞白血病 U937 细胞中具有很强的细胞毒性。TBQ 是 2- 叔 -丁基对苯二酚 (TBHQ) 的氧化产物。研究证实 TBQ 诱导慢性粒细胞白血病 (CML) 细胞凋亡和细胞增殖抑制。研究发现，它与溶菌酶的结合相互作用现介于 BHA 和 TBHQ 之间。据报道，它是使用30% H2O2经过钛超氧催化氧化 2- 叔 -丁基苯酚水溶液合成的。TBQ 是 PLA-TBHQ 薄膜（聚乳酸）中 TBHQ 分解产生的主要新生化合物之一。
应用
2--叔 -丁基-1，4-苯醌可用于氮杂三恶烷 [8] 环烯的合成。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
W H Kalus et al.
Environmental health perspectives, 102(1), 96-99 (1994-01-01)
We examined t-butylhydroquinone (t-BHQ) and t-butylquinone (t-BuQ), two of the major microsomal metabolites of the synthetic antioxidant butylated hydroxyanisole (BHA), for their ability to react with the xenobiotic arylamines aniline and N-methylaniline. A number of substances were isolated by thin-layer
R Kahl et al.
Toxicology, 59(2), 179-194 (1989-12-01)
The synthetic antioxidant butylated hydroxyanisole (BHA) stimulates superoxide formation in rat liver microsomes up to 10-fold. This stimulation is prevented by the monooxygenase inhibitor metyrapone and does not occur when NADH is consumed instead of NADPH indicating that metabolic activation
2-tert-butyl-1, 4-benzoquinone Induces Apoptosis in Chronic Myeloid Leukemia Cells Resistant to Imatinib via Inducing Caspase-Dependent Bcr-Abl Downregulation.
Shi X, et al.
Medicinal Chemistry, 4, 784-790 (2014)
M Mizuno et al.
Mutation research, 176(2), 179-184 (1987-02-01)
The reaction products from butylated hydroxyanisole treated with nitrite under acidic conditions were investigated for mutagenic activity in Salmonella typhimurium his reversion assay and for DNA-damaging activity using H17 Rec+ (wild) and M45 Rec- (recombinationless) of Bacillus subtilis. The chloroform
C G Rogers et al.
Mutation research, 299(1), 9-18 (1993-03-01)
tert.-Butyl-p-quinone (TBQ), a major metabolite of the phenolic antioxidant tert.-butyl-4-hydroxyanisole (BHA), was examined for cytotoxic and genotoxic properties in an in vitro assay system with Chinese hamster V79 cells and in diploid strain D7 of Saccharomyces cerevisiae. TBQ was prepared
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