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Merck
CN

220159

Sigma-Aldrich

2,3-二甲基-2-丁烯

≥99%

别名:

四甲基乙烯

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关于此项目

线性分子式:
(CH3)2C=C(CH3)2
化学文摘社编号:
分子量:
84.16
Beilstein:
1361357
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽压

215 mmHg ( 37.7 °C)

质量水平

方案

≥99%

表单

liquid

自燃温度

754 °F

折射率

n20/D 1.412 (lit.)

沸点

73 °C (lit.)

mp

−75 °C (lit.)

密度

0.708 g/mL at 25 °C (lit.)

储存温度

2-8°C

SMILES字符串

C\C(C)=C(\C)C

InChI

1S/C6H12/c1-5(2)6(3)4/h1-4H3

InChI key

WGLLSSPDPJPLOR-UHFFFAOYSA-N

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一般描述

2,3-二甲基-2-丁烯在黑暗中臭氧分解产生羟基自由基 。用流动管接口式紫外光电子能谱仪研究了臭氧与 2,3-二甲基-2-丁烯 (DMB) 的反应 。在 0°C 和-15°C 下,DMB 与四氟硼酸硫代阳离子自由基形成加合物

应用

2,3-二甲基-2-丁烯作为底物参与了 2-羟基-1,4-萘醌的光诱导分子转化

象形图

FlameHealth hazard

警示用语:

Danger

危险声明

预防措施声明

危险分类

Asp. Tox. 1 - Flam. Liq. 2

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

17.6 °F - closed cup

闪点(°C)

-8 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The Journal of Organic Chemistry, 58, 4614-4614 (1993)
Bing-Jun Zhao et al.
The Journal of organic chemistry, 71(10), 3737-3742 (2006-05-06)
Thianthrene cation radical tetrafluoroborate (Th*+ BF4-) has been found to add to 2,3-dimethyl-2-butene (DMB) at 0 degrees C and -15 degrees C. The adduct, 2,3-dimethyl-2,3-(5,10-thianthreniumdiyl)butane ditetrafluoroborate (12), was isolated at -15 degrees C, and its 1H NMR spectrum was recorded
Maryline Pflieger et al.
Environmental science & technology, 47(12), 6239-6246 (2013-05-15)
In order to investigate the heterogeneous oxidation kinetics of the herbicide terbuthylazine (TERB), a stable and reproducible generation system of "dark" hydroxyl radical in the gas phase was developed and optimized using a PTR-MS. TERB was adsorbed on silica particles
P Di Mascio et al.
Free radical biology & medicine, 12(6), 471-478 (1992-01-01)
Ultraweak chemiluminescence arising from lipoperoxidation has been attributed by several authors to the radiative deactivation of singlet oxygen and triplet carbonyl products. The latter emitters have been suggested to come from annihilation of RO. and ROO. radicals as well as
Bridgett E Coleman et al.
The journal of physical chemistry. A, 114(48), 12667-12674 (2010-11-17)
The matrix isolation technique, combined with infrared spectroscopy and twin jet codeposition, has been used to characterize intermediates formed during the ozonolysis of 2,3-dimethyl-2-butene (DMB). Absorptions of early intermediates in the twin jet experiments grew up to 200% upon annealing

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