B1378
2,6-二- 叔-丁基-4-甲基苯酚
≥99.0% (GC), powder
别名:
2,6-二-叔丁基对甲酚, BHT, DBPC, 丁基化羟基甲苯, 丁基羟基甲苯
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关于此项目
线性分子式:
[(CH3)3C]2C6H2(CH3)OH
化学文摘社编号:
分子量:
220.35
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-881-4
Beilstein/REAXYS Number:
1911640
MDL number:
Assay:
≥99.0% (GC)
Form:
powder
vapor density
7.6 (vs air)
Quality Level
vapor pressure
<0.01 mmHg ( 20 °C)
assay
≥99.0% (GC)
form
powder
autoignition temp.
878 °F
bp
265 °C (lit.)
mp
69-73 °C (lit.)
solubility
ethanol: 100 mg/mL, vegetable oils: soluble
SMILES string
Cc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C
InChI
1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3
InChI key
NLZUEZXRPGMBCV-UHFFFAOYSA-N
Gene Information
human ... CAPN1(823)
rat ... Capn1(29153), Nos1(24598)
Application
- BHT及其过氧化物(BHTOOH)的热解特性：BHT具有优异的抗氧化性，在特定条件下分解为BHTOOH(S Dai, et al., 2024)。
- 低应力聚合物网络的松弛机制：BHT被用于聚合物网络，评估其对牙科复合树脂的机械性能和耐久性的影响(SH Lewis, et al., 2024)。
- 药品包装标签的相容性和安全性：研究发现标签中含有BHT，说明BHT因其稳定性广泛用于药品包装(C Fu, et al., 2023)。
Biochem/physiol Actions
二丁基羟基甲苯 (BHT) 是一种酚类抗氧化剂。它可以抑制脂类过氧化。它会导致小鼠肺部损伤以及促进肿瘤生长，这可能是由于 BHT 的代谢产物造成，即 6-叔丁基-2-[2′-(2′-羟基甲基)-丙基]-4-甲基苯酚。还报道了 BHT 的代谢产物会引起培养细胞中的 DNA 链断裂以及核小体间 DNA 断裂（细胞凋亡的典型特征）。向大鼠进行单次 BHT 腹腔注射（60mg/kg 体重）会引起肝、肾、心脏、脾、大脑和肺部的核 DNA 甲基转移酶活动的显著提高。用 BHT 孵育肺泡巨噬细胞可以显著降低 TNF-α 的含量，这可以解释该抗氧化剂缓解炎症的机理。用 BHT 预孵育经阿司匹林处理的血小板可以抑制由蛋白激酶 C 活化剂引起的分泌、聚集以及蛋白质磷酸化。BHT 还可抑制由黄曲霉素 B1 诱发的肝癌形成。
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signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
260.6 °F - open cup
flash_point_c
127 °C - open cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Nadja S Sieber-Ruckstuhl et al.
Scientific reports, 9(1), 6015-6015 (2019-04-14)
Glucocorticoids (GCs) are critical regulators of metabolic control in mammals and their aberrant function has been linked to several pathologies. GCs are widely used in human and veterinary clinical practice as potent anti-inflammatory and immune suppressive agents. Dyslipidaemia is a
A M Vijesh et al.
European journal of medicinal chemistry, 46(11), 5591-5597 (2011-10-05)
In the present study two new series of Hantzsch 1,4-dihydropyridine derivatives (1,4-DHPs) containing substituted pyrazole moiety (4a-f and 5a-f) were synthesized by the reaction of 3-aryl-1H-pyrazole-4-carbaldehydes with 1,3-dicarbonylcompounds (ethylacetoacetate and methylacetoacetate) and ammonium acetate. The newly synthesized compounds were characterized
Xiao-Juan Duan et al.
Journal of natural products, 70(7), 1210-1213 (2007-07-03)
Four new highly brominated and fully substituted mono- and bis-phenols, 1-(2,3,6-tribromo-4,5-dihydroxybenzyl)pyrrolidin-2-one (1), 1,2-bis(2,3,6-tribromo-4,5-dihydroxyphenyl)ethane (2), 6-(2,3,6-tribromo-4,5-dihydroxybenzyl)-2,5-dibromo-3,4-dihydroxybenzyl methyl ether (3), and 2,3,6-tribromo-4,5-dihydroxybenzyl methyl sulfone (4), were characterized from the marine red alga Symphyocladia latiuscula. In addition, five known bromophenols, bis(2,3,6-tribromo-4,5-dihydroxyphenyl)methane (5), bis(2,3,6-tribromo-4,5-dihydroxybenzyl)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| B1378-100G | 04061835521616 |
| B1378-1KG | 04061835555703 |
| B1378-500G | 04061835555710 |