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Merck

04365

Sigma-Aldrich

1-乙基-3-甲基咪唑四氟硼酸盐

≥97.0% (HPLC/T)

别名:

EMIMBF4

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About This Item

经验公式(希尔记法):
C6H11BF4N2
分子量:
197.97
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

≥97.0% (HPLC/T)

形狀

liquid

折射率

n20/D 1.41
n20/D 1.413 (lit.)

bp

>350 °C (lit.)

mp

15 °C (lit.)

密度

1.294 g/mL at 25 °C (lit.)

SMILES 字串

F[B-](F)(F)F.CCn1cc[n+](C)c1

InChI

1S/C6H11N2.BF4/c1-3-8-5-4-7(2)6-8;2-1(3,4)5/h4-6H,3H2,1-2H3;/q+1;-1

InChI 密鑰

CUNYTRQQXKCRTJ-UHFFFAOYSA-N

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一般說明

1-乙基-3-甲基咪唑四氟硼酸盐是一种室温离子液体 (RTIL)。

應用

可以使用1-乙基-3-甲基咪唑四氟硼酸盐作为反应介质,进行高苯丙氨酸酯的酶促拆分以形成对映体高苯丙氨酸。

其他說明

空气和水稳定性液体电解质 (m.p. 15°C)

象形圖

Exclamation markEnvironment

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral - Aquatic Chronic 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

235.4 °F - closed cup

閃點(°C)

113 °C - closed cup

個人防護裝備

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


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分析证书(COA)

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访问文档库

Enzymatic Reactions in Ionic Liquids
Aldrich Chemfiles, 5(6) null
Viscosity Measurements for Binary Mixtures of 1-Ethyl-3-Methylimidazolium Tetrafluoroborate with Acetonitrile, Ethylene Glycol, and Methanol
Fan, Xian-Heng, Yan-Ping Chen, and Chie-Shaan Su.
Journal of Solution Chemistry, 45.10, 1377-1390 (2016)
NMR evidence of hydrogen bonding in 1-ethyl-3-methylimidazolium-tetrafluoroborate room temperature ionic liquid
Huang, Jing-Fang, et al.
Inorgorganica Chimica Acta, 320.1, 7-11 (2001)
Densities and viscosities of binary liquid mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate with acetone, methyl ethyl ketone, and N-methyl-2-pyrrolidone
Fan, Xian-Heng, Yan-Ping Chen, and Chie-Shaan Su.
Journal of the Taiwan Institute of Chemical Engineers, 61, 117-123 (2016)
Flexible Asymmetric Supercapacitor Based on Structure?Optimized Mn3O4/Reduced Graphene Oxide Nanohybrid Paper with High Energy and Power Density
Hu, Yating, et al.
Advances in Functional Materials, 25.47, 7291-7299 (2015)

实验方案

One of the most popular lipase for synthetic use is the Candida antarctica lipase (CALB). CALB catalyzes the enantioselective acylation of 1-phenylethylamine with 4-pentenoic acid

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