28620
Cyanuric chloride
purum, ≥98.0% (T)
Synonym(s):
2,4,6-Trichloro-1,3,5-triazine
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About This Item
Empirical Formula (Hill Notation):
C3Cl3N3
CAS Number:
Molecular Weight:
184.41
EC Number:
203-614-9
UNSPSC Code:
12352101
PubChem Substance ID:
Beilstein/REAXYS Number:
124246
MDL number:
vapor density
6.36 (vs air)
vapor pressure
0.8 mmHg ( 62.2 °C)
grade
purum
assay
≥98.0% (T)
bp
190 °C (lit.)
mp
145-147 °C
SMILES string
Clc1nc(Cl)nc(Cl)n1
InChI
1S/C3Cl3N3/c4-1-7-2(5)9-3(6)8-1
InChI key
MGNCLNQXLYJVJD-UHFFFAOYSA-N
Other Notes
Coupling agent in the immobilization of microorganisms and enzymes
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A - STOT SE 3
target_organs
Respiratory system
supp_hazards
Storage Class
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 1
flash_point_f
>392.0 °F - closed cup
flash_point_c
> 200 °C - closed cup
Regulatory Information
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W.J. Smith
Proc. Ann. Biochem. Eng. Symp., 6, 34-34 (1976)
J.L. Gainer et al.
Biotechnology and Bioengineering Symposium, 10, 35-35 (1980)
Chao Gao et al.
Chemical communications (Cambridge, England), 49(11), 1127-1129 (2013-01-04)
A series of novel triazinonide-bridged bisimidazolium pincers were easily synthesized by quaternization of functionalized N-phenylimidazoles with highly reactive cyanuric chloride under mild conditions. The pincer was proven to be a very efficient ligand for in situ Pd-catalyzed Suzuki-Miyaura reaction with