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重要文件

14755

Supelco

双(二甲基氨基)二甲基硅烷

for GC derivatization, LiChropur, ≥95.0% (GC)

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About This Item

線性公式:
[(CH3)2N]2Si(CH3)2
CAS號碼:
分子量::
146.31
Beilstein:
1736095
EC號碼:
MDL號碼:
分類程式碼代碼:
41116105
PubChem物質ID:
NACRES:
NA.22
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等級

derivatization grade ((GC derivatization))
for GC derivatization

品質等級

蒸汽密度

>1 (vs air)

蒸汽壓力

1 mmHg ( 20 °C)

化驗

≥95.0% (GC)

形狀

liquid

品質

LiChropur

反應適用性

reagent type: derivatization reagent
reaction type: Silylations

技術

gas chromatography (GC): suitable

折射率

n20/D 1.417 (lit.)
n20/D 1.418

bp

128-129 °C (lit.)

mp

−98 °C (lit.)

密度

0.809 g/mL at 25 °C (lit.)

SMILES 字串

CN(C)[Si](C)(C)N(C)C

InChI

1S/C6H18N2Si/c1-7(2)9(5,6)8(3)4/h1-6H3

InChI 密鑰

QULMGWCCKILBTO-UHFFFAOYSA-N

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應用

Bis(dimethylamino)-dimethyl silane was used to silanize pH-sensitive microelectrodes, used to measure the membrane potential in oocytes, in an experimental procedure aimed towards cloning and characterising human electrogenic Na+-cotransporter isoform (hhNBC).[1] It was also used for microelectrode measurements, in a study conducted to measure carbon dioxide transport through membranes.[2]

其他說明

类固醇的衍生化试剂:可通过 GC/氮-磷检测器分析 (二甲氨基)二甲基甲硅烷基衍生物[3];保护二醇、二胺等[4][5]

法律資訊

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

象形圖

FlameCorrosion

訊號詞

Danger

危險聲明

危險分類

Flam. Liq. 2 - Skin Corr. 1B

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

19.4 °F - closed cup

閃點(°C)

-7 °C - closed cup

個人防護裝備

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


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存取文件庫

Journal of Organometallic Chemistry, 294, 7-7 (1985)
Carbon dioxide transport through membranes.
Missner A
The Journal of Biological Chemistry, 283 (37), 25340-25347 (2008)
Cloning and characterization of a human electrogenic Na+-cotransporter isoform (hhNBC).
American Journal of Physiology. Cell Physiology, 276 (3), C576-C584 (1999)
R.H. Cragg et al.
Journal of Organometallic Chemistry, 289, 23-23 (1985)
C.F. Poole et al.
Journal of Chromatographic Science, 17, 115-115 (1979)

文章

Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs

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