250236
1-(tert-Butyldimethylsilyl)imidazole
≥95%
Synonym(s):
TBDMSIM
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C9H18N2Si
CAS Number:
Molecular Weight:
182.34
Beilstein:
606695
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥95%
form
liquid
refractive index
n20/D 1.481 (lit.)
bp
53 °C/0.2 mmHg (lit.)
density
0.939 g/mL at 25 °C (lit.)
SMILES string
CC(C)(C)[Si](C)(C)n1ccnc1
InChI
1S/C9H18N2Si/c1-9(2,3)12(4,5)11-7-6-10-8-11/h6-8H,1-5H3
InChI key
VUENSYJCBOSTCS-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
1-(tert-Butyldimethylsilyl)imidazole is a reactive silylating agent.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
related product
Product No.
Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
210.2 °F - closed cup
Flash Point(C)
99 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
D C Landrum et al.
Journal of chromatography, 483, 21-32 (1989-12-08)
The use of gas-liquid chromatography and mass spectrometry with derivatizing agents that give stable derivatives and consistent fragmentation patterns allows for accurate identification of a variety of compounds. In this study either N-methyl-N-tert.-butyldimethylsilyltrifluoroacetamide or N-tert.-butyldimethylsilylimidazole were employed to derivatize a
P Bydal et al.
Steroids, 61(6), 349-353 (1996-06-01)
Five dehydrated compounds obtained from a tert-butyldimethylsilylchloride/imidazole or an aqueous hydrochloric acid treatment of 17 alpha-butyl-3-O-methyl estradiol in refluxing solvent were purified and characterized. Three compounds were obtained from a direct vicinal proton elimination, the two others from a vicinal
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
