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775061

Sigma-Aldrich

双(三甲基硅基)酰胺钾 溶液

greener alternative

1.0 M in 2-methyltetrahydrofuran

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别名:
六甲基二硅基胺基钾 溶液, 六甲基二硅氮烷 钾盐 溶液
线性分子式:
[(CH3)3Si]2NK
CAS号:
40949-94-8
分子量:
199.48
Beilstein:
4006754
MDL编号:
MFCD00010330
PubChem化学物质编号:
329767734
NACRES:
NA.22

蒸汽密度

3.2 (vs air)

质量水平

100

形式

liquid

环保替代产品特性

Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Inherently Safer Chemistry for Accident Prevention
Learn more about the Principles of Green Chemistry.

浓度

1.0 M in 2-methyltetrahydrofuran

密度

0.884 g/mL at 25 °C

环保替代产品分类

Aligned,

SMILES string

C[Si](C)(C)N([K])[Si](C)(C)C

InChI

1S/C6H18NSi2.K/c1-8(2,3)7-9(4,5)6;/h1-6H3;/q-1;+1

InChI key

IUBQJLUDMLPAGT-UHFFFAOYSA-N

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相关类别

一般描述

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product, 1.0 M in 2-methyltetrahydrofuran aligns with "Safer Solvents and Auxiliaries", "Use of Renewable Feedstocks" and "Inherently Safer Chemistry for Accident Prevention". Click here for more information.

应用

Strong organic base in greener solvent, 2-methyltetrahydrofuran (2-MeTHF).

2-Methyltetrahydrofuran (2-MeTHF): A Biomass-Derived Solvent with Broad Application in Organic Chemistry

包装

The 25 mL Sure/Seal™ bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

法律信息

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

警示用语：

Danger

危险声明

H225 - H302 - H314

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

补充剂危害

EUH014 - EUH019

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

12.2 °F

闪点(°C)

-11 °C

法规信息

危险化学品

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Hua Lu et al.
Journal of the American Chemical Society, 129(46), 14114-14115 (2007-10-30)
A Sebok et al.
Journal of chromatography. A, 1211(1-2), 104-112 (2008-10-14)
This paper presents a derivatization, mass fragmentation study relating to the most common six cholic acids, such as cholic, lithocholic, chenodeoxycholic, ursodeoxycholic, 3-hydroxy,7-ketocholanic and dehydrocholic acids, identified and quantified as pollutants in the aquatic environment at the first time. Derivatizations
Jerry Isaacson et al.
Angewandte Chemie (International ed. in English), 48(10), 1845-1848 (2009-01-29)
(-)-Dysibetaine has been synthesized in 11 steps from readily available L-malic acid (see scheme). The key step is a unique Ugi 4-center-3-component cyclization reaction, where an ester group acts as the carboxylic acid component. The use of 1,1,1,3,3,3-hexamethyldisilazane as an
Daniele Fabbri et al.
Environmental science & technology, 42(8), 2957-2963 (2008-05-24)
Using the pyrolysis-gas chromatography-mass spectrometry and off-line pyrolysis/silylation methods for lignites from three Miocene brown coal basins of Poland resulted in the characterization of many organic compounds, including dominant cellulose degradation products such as levoglucosan, 1,6-anhydro-beta-D-glucofuranose, and 1,4:3,6-dianhydroglucopyranose. Levoglucosan is
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