20021
3-叔丁基-4-羟基苯甲醚
≥98% (sum of isomers, GC), ≤10% 2-BHA basis (GC)
别名:
2-叔丁基-4-甲氧基苯酚, 3-BHA, BHA
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关于此项目
经验公式（希尔记法）:
C11H16O2
化学文摘社编号:
分子量:
180.24
Beilstein:
1867499
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
≥98% (sum of isomers, GC)
表单
solid
组成
2-BHA, ≤10% GC
3-BHA, ≥90% GC
杂质
≤1% 4-hydroxyanisole
灼烧残渣
≤0.05%
mp
48-63 °C
溶解性
ethanol: soluble 1 g/10 mL, clear, colorless to faint yellow or tan
SMILES字符串
COc1ccc(O)c(c1)C(C)(C)C
InChI
1S/C11H16O2/c1-11(2,3)9-7-8(13-4)5-6-10(9)12/h5-7,12H,1-4H3
InChI key
MRBKEAMVRSLQPH-UHFFFAOYSA-N
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一般描述
研究了 3--叔 -丁基-4-羟基苯甲醚在酞菁镍（作为电子媒介体）修饰的聚合物电极上的伏安行为 。
应用
- 调节间充质干细胞中的Smad信号通路：3-叔丁基-4-羟基苯甲醚通过调节Smad信号通路干扰C3H10T1/2间充质干细胞向褐色脂肪细胞的分化，揭示它在肥胖症和代谢综合征研究中的潜在应用(Wang et al., 2023)。
危险声明
预防措施声明
危险分类
Aquatic Chronic 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
C de la Fuente et al.
Talanta, 49(2), 441-452 (2008-10-31)
The voltammetric behaviour of the antioxidants 3-tert-butyl-4-hydroxyanisole (BHA) and tert-butylhydroquinone (TBHQ), at a polymer electrode modified with nickel phthalocyanine as electron mediator, is described, and an electroanalytical method for the determination of these antioxidants based on their electrochemical oxidation on
L K Lam et al.
Carcinogenesis, 12(12), 2311-2315 (1991-12-01)
Carcinogen-induced aberrant crypts (AC) of the colon are a precancerous state that leads to malignancy. The inhibition of AC formation by chemopreventive agents was evaluated in this study. Colon AC were induced by 1,2-dimethylhydrazine (DMH) in 3 weeks in CF1
Mengxiao Xie et al.
Journal of autoimmunity, 102, 96-113 (2019-05-28)
The subset of regulatory T (Treg) cells, with its specific transcription Foxp3, is a unique cell type for the maintenance of immune homeostasis by controlling effector T (Teff) cell responses. Although it is common that a defect in Treg cells
A Matsuoka et al.
Mutation research, 241(2), 125-132 (1990-06-01)
The mutagenicity of 3-tert-butyl-4-hydroxyanisole (BHA) and its metabolites was investigated in the reverse mutation assay using S. typhimurium strains and the chromosomal aberration test in vitro using a Chinese hamster fibroblast cell line, CHL. BHA, tert-butylhydroquinone (BHQ), tert-butylquinone (BQ) and
K Tajima et al.
Drug metabolism and disposition: the biological fate of chemicals, 20(6), 816-820 (1992-11-01)
3-Tert-butyl-4-hydroxyanisole (3-BHA) was metabolized in the presence of horseradish peroxidase and hydrogen peroxide to 2-tert-butyl-p-benzoquinone (TBQ), 2,3-epoxy-5-tert-butyl-1,4-benzoquinone (TBQ-epoxide), and two known dimers. The formation of TBQ from 3-BHA required both horseradish peroxidase and hydrogen peroxide. When 2.5 mM 3-BHA was
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