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Documentos Principais

690740

Sigma-Aldrich

Cyanuric chloride

Lonza quality, ≥99.5 % (w/w)

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C3Cl3N3
Número CAS:
Peso molecular:
184.41
Beilstein:
124246
Número CE:
Número MDL:
Código UNSPSC:
12352101
ID de substância PubChem:

densidade de vapor

6.36 (vs air)

pressão de vapor

0.8 mmHg ( 62.2 °C)

Formulário

lumps

fabricante/nome comercial

Lonza Ltd

concentração

≥99.5 % (w/w)

p.e.

190 °C (lit.)

pf

145-147 °C (lit.)
145.0-147.0 °C

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

Clc1nc(Cl)nc(Cl)n1

InChI

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

chave InChI

MGNCLNQXLYJVJD-UHFFFAOYSA-N

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Pictogramas

Skull and crossbonesCorrosion

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A - STOT SE 3

Órgãos-alvo

Respiratory system

Perigos de suplementos

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

>392.0 °F - closed cup

Ponto de fulgor (°C)

> 200 °C - closed cup

Equipamento de proteção individual

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
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
Ravi Bhushan et al.
Amino acids, 40(2), 403-409 (2010-06-19)
Two new chiral monochloro-s-triazines (MCT) were synthesized [viz N-(4-chloro-6-piperidinyl-[1,3,5]-triazine-2-yl)-L-leucine amide and N-(4-chloro-6-piperidinyl-[1,3,5]-triazine-2-yl)-L-leucine) (CDR 1 and 2, respectively)] by the nucleophilic displacement of chlorine atoms in s-triazine moiety. One of the Cl atoms was replaced with piperidine, and the second Cl
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

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