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CAS NO.18156-74-6
N-(Trimethylsilyl)imidazole Basic information |
Product Name: | N-(Trimethylsilyl)imidazole |
Synonyms: | 1-(Trimethylsily)imidazole;1-(trimethylsilyl)-1h-imidazol;1-(trimethylsilyl)-imidazol;1-Imidazolyltrimethylsilane;CT3600;Imidazole, 1-(trimethylsilyl)-;Imidazole, N-(trimethylsilyl)-;N-(Trimethylsilyl)imidazol |
CAS: | 18156-74-6 |
MF: | C6H12N2Si |
MW: | 140.26 |
EINECS: | 242-040-3 |
Product Categories: | Analytical Chemistry;GC Derivatizing Reagents;Si (Classes of Silicon Compounds);Silylation (GC Derivatizing Reagents);Silylimidazoles;Si-N Compounds;Trimethylsilylation (GC Derivatizing Reagents);Silicon Compounds (for Synthesis);Synthetic Organic Chemistry;Special Silanes;Amines;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Building Blocks;C3 to C8;Chemical Synthesis;Heterocyclic Building Blocks;Imidazoles;Silylation Reagents |
Mol File: | 18156-74-6.mol |
N-(Trimethylsilyl)imidazole Chemical Properties |
mp | -42 °C |
bp | 93-94 °C14 mm Hg(lit.) |
density | 0.957 g/mL at 20 °C |
refractive index |
n |
Fp | 42 °F |
storage temp. | 2-8°C |
Water Solubility | decomposes |
Sensitive | Moisture Sensitive |
BRN | 606148 |
CAS DataBase Reference | 18156-74-6(CAS DataBase Reference) |
NIST Chemistry Reference | 1h-Imidazole, 1-(trimethylsilyl)-(18156-74-6) |
EPA Substance Registry System | 1H-Imidazole, 1-(trimethylsilyl)-(18156-74-6) |
Safety Information |
Hazard Codes | F,Xi,C |
Risk Statements | 11-36/37/38-14-40-34-37-35-20/21/22 |
Safety Statements | 16-26-33-37/39-45-36/37/39 |
RIDADR | UN 1993 3/PG 2 |
WGK Germany | 3 |
RTECS | NI8700000 |
F | 10-21 |
TSCA | T |
HazardClass | 3 |
PackingGroup | II |
HS Code | 29332990 |
MSDS Information |
Provider | Language |
---|---|
N-(Trimethylsilyl)imidazole | English |
ACROS | English |
SigmaAldrich | English |
ALFA | English |
N-(Trimethylsilyl)imidazole Usage And Synthesis |
Chemical Properties | Colorless transparent liquid |
Usage | A general silylating agent, particularly for alcohols. An intermediate for the synthesis of imidazole derivatives. |
Usage | Silylating reagent for the protection of hydroxyl groups in the presence of amine functionalities.1 |
N-(Trimethylsilyl)imidazole Preparation Products And Raw materials |
N-(Trimethylsilyl)imidazole Basic information |
Product Name: | N-(Trimethylsilyl)imidazole |
Synonyms: | 1-(Trimethylsily)imidazole;1-(trimethylsilyl)-1h-imidazol;1-(trimethylsilyl)-imidazol;1-Imidazolyltrimethylsilane;CT3600;Imidazole, 1-(trimethylsilyl)-;Imidazole, N-(trimethylsilyl)-;N-(Trimethylsilyl)imidazol |
CAS: | 18156-74-6 |
MF: | C6H12N2Si |
MW: | 140.26 |
EINECS: | 242-040-3 |
Product Categories: | Analytical Chemistry;GC Derivatizing Reagents;Si (Classes of Silicon Compounds);Silylation (GC Derivatizing Reagents);Silylimidazoles;Si-N Compounds;Trimethylsilylation (GC Derivatizing Reagents);Silicon Compounds (for Synthesis);Synthetic Organic Chemistry;Special Silanes;Amines;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Building Blocks;C3 to C8;Chemical Synthesis;Heterocyclic Building Blocks;Imidazoles;Silylation Reagents |
Mol File: | 18156-74-6.mol |
N-(Trimethylsilyl)imidazole Chemical Properties |
mp | -42 °C |
bp | 93-94 °C14 mm Hg(lit.) |
density | 0.957 g/mL at 20 °C |
refractive index |
n |
Fp | 42 °F |
storage temp. | 2-8°C |
Water Solubility | decomposes |
Sensitive | Moisture Sensitive |
BRN | 606148 |
CAS DataBase Reference | 18156-74-6(CAS DataBase Reference) |
NIST Chemistry Reference | 1h-Imidazole, 1-(trimethylsilyl)-(18156-74-6) |
EPA Substance Registry System | 1H-Imidazole, 1-(trimethylsilyl)-(18156-74-6) |
Safety Information |
Hazard Codes | F,Xi,C |
Risk Statements | 11-36/37/38-14-40-34-37-35-20/21/22 |
Safety Statements | 16-26-33-37/39-45-36/37/39 |
RIDADR | UN 1993 3/PG 2 |
WGK Germany | 3 |
RTECS | NI8700000 |
F | 10-21 |
TSCA | T |
HazardClass | 3 |
PackingGroup | II |
HS Code | 29332990 |
MSDS Information |
Provider | Language |
---|---|
N-(Trimethylsilyl)imidazole | English |
ACROS | English |
SigmaAldrich | English |
ALFA | English |
N-(Trimethylsilyl)imidazole Usage And Synthesis |
Chemical Properties | Colorless transparent liquid |
Usage | A general silylating agent, particularly for alcohols. An intermediate for the synthesis of imidazole derivatives. |
Usage | Silylating reagent for the protection of hydroxyl groups in the presence of amine functionalities.1 |
N-(Trimethylsilyl)imidazole Preparation Products And Raw materials |