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Merck
CN

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:
108-77-0
Molecular Weight:
184.41
EC Number:
203-614-9
UNSPSC Code:
12352101
PubChem Substance ID:
24857235
Beilstein/REAXYS Number:
124246
MDL number:
MFCD00006046

Key Documents

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InChI key

MGNCLNQXLYJVJD-UHFFFAOYSA-N

InChI

1S/C3Cl3N3/c4-1-7-2(5)9-3(6)8-1

SMILES string

Clc1nc(Cl)nc(Cl)n1

vapor density

6.36 (vs air)

vapor pressure

0.8 mmHg ( 62.2 °C)

grade

purum

assay

≥98.0% (T)

bp

190 °C (lit.)

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Other Notes

Coupling agent in the immobilization of microorganisms and enzymes

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

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

EUH014

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)
Ravi Bhushan et al.
Journal of chromatography. A, 1217(41), 6382-6387 (2010-09-08)
Four dichloro-s-triazine (DCT) and five monochloro-s-triazine (MCT) chiral derivatizing reagents (CDRs) were synthesized by incorporating amino acid amide moieties as chiral auxiliaries in trichloro-s-triazine and its 6-methoxy derivative, respectively. Another MCT reagent was synthesized by substitution of two chlorine atoms
Xue Jiang et al.
Bioresource technology, 104, 473-479 (2011-11-25)
The influence of introduction of cyanuric chloride on glucose's yield (Y) in acid-catalyzed hydrolysis of microcrystalline cellulose (MCC) has been studied. The content of cyanuric chloride (C) in modified MCCs was determined by X-ray photoelectric spectroscopy. The chemical structures of
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
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