324787
2,2,2-Trifluoroethanesulfonyl chloride
99%
Synonym(s):
Tresyl chloride
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About This Item
Linear Formula:
CF3CH2SO2Cl
CAS Number:
Molecular Weight:
182.55
Beilstein:
1860983
EC Number:
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22
Assay
99%
form
liquid
refractive index
n20/D 1.388 (lit.)
bp
140-141 °C (lit.)
64-67 °C/45 mmHg (lit.)
density
1.651 g/mL at 25 °C (lit.)
functional group
fluoro
storage temp.
2-8°C
SMILES string
FC(F)(F)CS(Cl)(=O)=O
InChI
1S/C2H2ClF3O2S/c3-9(7,8)1-2(4,5)6/h1H2
InChI key
CXCHEKCRJQRVNG-UHFFFAOYSA-N
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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
161.6 °F - closed cup
Flash Point(C)
72 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Jie Mei et al.
Electrophoresis, 29(18), 3825-3833 (2008-08-30)
A novel covalent coupling method for coating of capillaries with liposomes has been developed, which includes three steps: (i) epoxy-diol coating, (ii) activation with 2,2,2-trifluoroethanesulfonyl chloride, and (iii) liposome coupling. The coating conditions, such as the reaction time and temperature
K I Allam et al.
Analytical biochemistry, 162(1), 171-177 (1987-04-01)
A stable T-2 hydrazide gel is prepared by activating T-2 toxin with tresyl chloride followed by coupling to agarose-adipic acid hydrazide. Utilized as an affinity chromatography column, this T-2 hydrazide gel purifies a monoclonal antibody for T-2 in high yield
K Nakamura et al.
Journal of chromatography, 510, 101-113 (1990-06-27)
A new activated support TSK gel Tresyl-5PW was evaluated for the coupling of antibodies, which was found to occur easily under mild conditions with high yields. Optimum coupling conditions were a 2-h reaction at 25 degrees C in 1 M
C F Mandenius et al.
Analytical biochemistry, 137(1), 106-114 (1984-02-01)
Two methods for the chemical binding of biomolecules to silicon surfaces are described. The first method utilizes an alkyl silane and a nucleophilic reagent to join the biomolecule to the silicon surface; the second method involves crosslinking with glutaraldehyde in
Markus Gantert et al.
Pharmaceutical research, 26(3), 529-538 (2008-11-19)
The challenge in developing liposomes to be used in active drug targeting is to design a method that can be used for modifying liposomal membranes that is applicable for a number of different specific ligands. In this study, the post
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