Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

515876

Sigma-Aldrich

Imidazole trifluoromethanesulfonate salt

97%

Synonym(s):

Imidazolium triflate

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C3H4N2 · CHF3O3S
CAS Number:
29727-06-8
Molecular Weight:
218.15
MDL number:
MFCD00035430
UNSPSC Code:
12352005
eCl@ss:
39161001
PubChem Substance ID:
24873850
NACRES:
NA.22

Assay

97%

mp

189-193 °C (lit.)

functional group

fluoro
triflate

SMILES string

c1c[nH]cn1.OS(=O)(=O)C(F)(F)F

InChI

1S/C3H4N2.CHF3O3S/c1-2-5-3-4-1;2-1(3,4)8(5,6)7/h1-3H,(H,4,5);(H,5,6,7)

InChI key

JNJFONBBNLVENC-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

515876-25G:
515876-VAR:
515876-2G:
515876-BULK:
515876-5G:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000246896
0000244372
0000244372
0000246896
0000144436

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

S Iwai et al.
Nucleic acids research, 27(11), 2299-2303 (1999-05-15)
In the solid-phase synthesis of oligonucleotides containing the pyrimidine(6-4)pyrimidone photoproduct using a dinucleotide building block, considerable amounts of by-products were found as the chain length increased. The by-products were the major product when a 49mer was synthesized on a 40
Stéphane Bernier et al.
Bioorganic & medicinal chemistry, 13(1), 69-75 (2004-12-08)
Three nonhydrolyzable aspartyl adenylate analogs have been prepared and tested as inhibitors of E. coli aspartyl-tRNA synthetase. 5'-O-[N-(L-Aspartyl)sulfamoyl]adenosine is a potent competitive inhibitor (K(i) = 15 nM) whereas L-aspartol adenylate is a weaker inhibitor (K(i) = 45 microM) with respect

Questions

Reviews

No rating value

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