Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

28625

Sigma-Aldrich

Cyanuric fluoride

Synonym(s):

2,4,6-Trifluoro-1,3,5-triazine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C3F3N3
CAS Number:
Molecular Weight:
135.05
Beilstein/REAXYS Number:
124237
EC Number:
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:

SMILES string

Fc1nc(F)nc(F)n1

InChI

1S/C3F3N3/c4-1-7-2(5)9-3(6)8-1

InChI key

VMKJWLXVLHBJNK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Caution

can precipitate on storage

Other Notes

Modifies tyrosyl residues in proteins; Reagent used for the preparation of carboxylic fluorides

pictograms

Skull and crossbonesCorrosion

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Eye Dam. 1 - Skin Corr. 1A

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

[43] cyanuration.
M J Gorbunoff
Methods in enzymology, 25, 506-514 (1972-01-01)
Tyrosyl residues of two molecular forms of human urinary urokinase: their ionization mode characterized by spectrophotometric and CD titrations and reactivity with cyanuric fluoride in relation to enzymic activity.
N Miwa et al.
Biochemical and biophysical research communications, 108(3), 1136-1143 (1982-10-15)
M.J.S. Dewar et al.
The Journal of Organic Chemistry, 40, 1521-1521 (1975)
Julia Laskin et al.
Journal of the American Society for Mass Spectrometry, 28(7), 1304-1312 (2017-03-16)
Using mass-selected ion deposition combined with in situ infrared reflection absorption spectroscopy (IRRAS), we examined the reactive landing of gramicidin S and ubiquitin ions onto activated self-assembled monolayer (SAM) surfaces terminated with N-hydroxysuccinimidyl ester (NHS-SAM) and acyl fluoride (COF-SAM) groups.
Chemical reactivity of the tyrosyl residues in yeast hexokinase. Properties of the nitroenzyme.
G Coffe et al.
Biochimica et biophysica acta, 484(2), 322-335 (1977-10-13)

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