InChI
1S/C8H21NOSi2.C6H12N2Si.C3H9ClSi/c1-8(9-11(2,3)4)10-12(5,6)7;1-9(2,3)8-5-4-7-6-8;1-5(2,3)4/h1-7H3;4-6H,1-3H3;1-3H3
InChI key
QSBHIAMPMUWWFU-UHFFFAOYSA-N
grade
derivatization grade (GC derivatization)
form
liquid
quality
LiChropur™
reaction suitability
reagent type: derivatization reagent
reaction type: Silylations
technique(s)
gas chromatography (GC): suitable
storage temp.
2-8°C
Quality Level
Application
Learn more in the Product Information
Other Notes
最有效的通用硅烷化试剂之一
N,O-Bis(trimethylsilyl)acetamide : chlorotrimethylsilane : 1-(trimethylsilyl)imidazole = 3:3:2 (v/v/v)
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
39.2 °F - closed cup
flash_point_c
4.0 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
J. Heberle et al.
Silylating Agents, 2nd ed. (1995)
Conversion of steroids to trimethylsilyl derivatives for gas phase analytical studies: reactions of silylating reagents.
E M Chambaz et al.
Analytical biochemistry, 30(1), 7-24 (1969-07-01)
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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