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Merck

268151

Sigma-Aldrich

Triethylamine hydrochloride

reagent grade, 98%

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About This Item

Fórmula lineal:
(C2H5)3N · HCl
Número de CAS:
Peso molecular:
137.65
Beilstein/REAXYS Number:
3906409
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

grade

reagent grade

assay

98%

mp

261 °C (dec.) (lit.)

SMILES string

Cl.CCN(CC)CC

InChI

1S/C6H15N.ClH/c1-4-7(5-2)6-3;/h4-6H2,1-3H3;1H

InChI key

ILWRPSCZWQJDMK-UHFFFAOYSA-N

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Referencia del producto
Descripción
Precios

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Eugenio Hardy et al.
Analytical biochemistry, 430(2), 203-213 (2012-09-11)
Nanoaggregates composed of selected glycoforms from Escherichia coli 055:B5 lipopolysaccharide (LPS) were prepared by combining sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis, zinc-imidazole reverse staining, zinc chelation after cutting gel slices, elution with either 0.5% triethylamine (TEA) or 0.4% to 0.5%
Samit Majumder et al.
Inorganic chemistry, 51(16), 8739-8749 (2012-08-09)
The work in the present investigation reports the syntheses, structures, steady state, and time-resolved photophysical properties of a tetraiminodiphenol macrocyclic ligand H(2)L and its eight dinuclear zinc(II) complexes and one cadmium(II) complex having composition [Zn(2)L(H(2)O)(2)](ClO(4))(2)·2CH(3)CN (1), [Zn(2)L(H(2)O)(2)](ClO(4))(2)·2dmf (2), [Zn(2)L(H(2)O)(2)](NO(3))(2)·2dmf (3)
A Guesmi et al.
Ultrasonics sonochemistry, 20(1), 571-579 (2012-06-09)
Cationization of cotton fabric was conferred by the sonicator reaction of cellulose with bromoacetyl bromide, followed by substitution of the terminal bromo groups by triethylamine. Experiments showed that the optimal volume of bromoacetyl bromide necessary to succeed the first stage
Małgorzata Jaworska et al.
Amino acids, 43(4), 1653-1661 (2012-02-22)
A new approach for the separation of 6-aminoquinolyl-carbamyl (AQC)-derivatized amino acids has been proposed. The chromatography used ion-pairing mechanism to increase the method selectivity. Mobile phase was based on triethylamine buffer containing N,N-dimethyloctylamine as a modifier. A number of factors
Sven Hansen et al.
ChemSusChem, 6(1), 92-101 (2012-11-14)
Water reduction systems that use a bis-cyclometalated Ir(III) photosensitiser (PS) along with homogeneous Pd complexes as a source of in-situ-formed colloidal Pd as the water reducing complex (WRC) and triethylamine (TEA) as the sacrificial electron donor were tested and characterised

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