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关于此项目
线性分子式:
[(CH3)2N]2Si(CH3)2
化学文摘社编号:
分子量:
146.31
UNSPSC Code:
41116105
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-200-1
Beilstein/REAXYS Number:
1736095
MDL number:
InChI key
QULMGWCCKILBTO-UHFFFAOYSA-N
InChI
1S/C6H18N2Si/c1-7(2)9(5,6)8(3)4/h1-6H3
SMILES string
CN(C)[Si](C)(C)N(C)C
grade
derivatization grade (GC derivatization)
vapor density
>1 (vs air)
vapor pressure
1 mmHg ( 20 °C)
assay
≥95.0% (GC)
form
liquid
quality
LiChropur™
reaction suitability
reagent type: derivatization reagent
reaction type: Silylations
technique(s)
gas chromatography (GC): suitable
refractive index
n20/D 1.417 (lit.), n20/D 1.418
bp
128-129 °C (lit.)
mp
−98 °C (lit.)
density
0.809 g/mL at 25 °C (lit.)
Quality Level
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Other Notes
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;保护二醇、二胺等
Application
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). It was also used for microelectrode measurements, in a study conducted to measure carbon dioxide transport through membranes.
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
19.4 °F - closed cup
flash_point_c
-7 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
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)
R.H. Cragg et al.
Journal of Organometallic Chemistry, 289, 23-23 (1985)
Cloning and characterization of a human electrogenic Na+-cotransporter isoform (hhNBC).
American Journal of Physiology. Cell Physiology, 276 (3), C576-C584 (1999)
C.F. Poole et al.
Journal of Chromatographic Science, 17, 115-115 (1979)
商品
Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs
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