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Key Documents

690740

Sigma-Aldrich

Cyanuric chloride

Lonza quality, ≥99.5 % (w/w)

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
Beilstein/REAXYS Number:
124246
EC Number:
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:

vapor density

6.36 (vs air)

vapor pressure

0.8 mmHg ( 62.2 °C)

form

lumps

manufacturer/tradename

Lonza Ltd

concentration

≥99.5 % (w/w)

bp

190 °C (lit.)

mp

145-147 °C (lit.)
145.0-147.0 °C

storage temp.

2-8°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

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pictograms

Skull and crossbonesCorrosion

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

Storage Class

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 1

flash_point_f

>392.0 °F - closed cup

flash_point_c

> 200 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Morten Hansen et al.
Journal of biomedical materials research. Part A, 96(2), 372-383 (2010-12-21)
Standard cell culture plastic was surface modified by passive adsorption or covalent attachment of interleukin (IL)-4 and investigated for its ability to induce differentiation of human monocytes into mature dendritic cells, a process dose-dependently regulated by IL-4. Covalent attachment of
Yue Wang et al.
Analytical and bioanalytical chemistry, 399(3), 1151-1162 (2010-11-03)
Tyrosinase (TYR: EC 1.14.18.1) was covalently modified onto the surface of a cyanuric chloride-activated carbon felt (CF) from the mixed buffer solution of TYR and acridine orange (AO). The resulting TYR-immobilized CF (TYR/AO-CF) was used as a working electrode unit
Lijuan Song et al.
Analytica chimica acta, 703(2), 257-263 (2011-09-06)
A fast, simple and cost-effective one-pot labeling strategy coupled with capillary zone electrophoresis was developed for the complete separation of amino acid mixture. The strategy includes two steps of reactions: Cyanuric chloride was made to react first with 7-amino-1,3-naphthalenedisulfonic acid
Ravi Bhushan et al.
Journal of chromatography. A, 1217(49), 7669-7676 (2010-11-03)
A new series of chiral derivatizing reagents (CDRs) consisting of four dichloro-s-triazine reagents was synthesized by nucleophilic substitution of one chlorine atom in trichloro-s-triazine with amino acids, namely L-Leu, D-Phg, L-Val and L-Ala as chiral auxiliaries. Two other sets of
Ravi Bhushan et al.
Amino acids, 42(4), 1417-1423 (2011-02-05)
L-Ala-NH(2), L-Val-NH(2), L-Leu-NH(2), and D-Phg-NH(2) were used as chiral auxiliaries to synthesize four chiral derivatizing reagents (CDRs) of each of the three categories, viz., difluoro dinitro benzene (DFDNB) based chiral variants, and cyanuric chloride (CC) based monochloro-s-triazine reagents (MCTs) and

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