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Merck

W424601

Sigma-Aldrich

Triethylamine

≥99.5%

Sinónimos:

N,N-Diethylethanamine

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About This Item

Fórmula lineal:
(C2H5)3N
Número de CAS:
Peso molecular:
101.19
Número de FEMA:
4246
Beilstein:
605283
Número CE:
Número MDL:
Código UNSPSC:
12352116
ID de la sustancia en PubChem:
Número Flavis:
11.023
NACRES:
NA.21

origen biológico

synthetic

Nivel de calidad

cumplimiento norm.

FDA 21 CFR 117

densidad de vapor

3.5 (vs air)

presión de vapor

51.75 mmHg ( 20 °C)

Ensayo

≥99.5%

Formulario

liquid

temp. de autoignición

593 °F

caducidad

5 yr

lim. expl.

8 %

índice de refracción

n20/D 1.401 (lit.)

pH

12.7 (15 °C, 100 g/L)

bp

88.8 °C (lit.)

mp

−115 °C (lit.)

densidad

0.726 g/mL at 25 °C (lit.)

aplicaciones

flavors and fragrances

Documentación

see Safety & Documentation for available documents

alérgeno alimentario

no known allergens

Organoléptico

fishy

cadena SMILES

CCN(CC)CC

InChI

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

Clave InChI

ZMANZCXQSJIPKH-UHFFFAOYSA-N

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Descripción general

Triethylamine may be used as a test volatile organic compound (VOC) in studies of the development of sensors for detecting VOCs.

Aplicación


  • Novel hybrid thiazoles, bis-thiazoles linked to azo-sulfamethoxazole: Synthesis, docking, and antimicrobial activity.: This study showcases the synthesis of hybrid thiazoles linked to azo-sulfamethoxazole, employing triethylamine in the reaction process, highlighting its role in antimicrobial applications (Salem et al., 2024).

  • Spirocyclic rhodamine B benzoisothiazole derivative: a multi-stimuli fluorescent switch manifesting ethanol-responsiveness, photo responsiveness, and acidochromism.: This research demonstrates a spirocyclic rhodamine derivative acting as a multi-stimuli-responsive fluorescent switch, where triethylamine plays a critical role in the synthesis process (Battula et al., 2023).

  • Para-Substituted Thiosemicarbazones as Cholinesterase Inhibitors: Synthesis, In Vitro Biological Evaluation, and In Silico Study.: This paper reports on the synthesis of para-substituted thiosemicarbazones where triethylamine is employed as a base, evaluating their potential as cholinesterase inhibitors (Khan et al., 2023).

  • Separation and purification of quinolyridine alkaloids from seeds of Thermopsis lanceolata R. Br. by conventional and pH-zone-refining counter-current chromatography.: This study involves the use of triethylamine in the pH-zone-refining counter-current chromatography technique to separate and purify specific alkaloids, illustrating its utility in advanced separation methodologies (Ning et al., 2023).

Cláusula de descargo de responsabilidad

For R&D or non-EU Food use. Not for retail sale.

Palabra de señalización

Danger

Clasificaciones de peligro

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

12.2 °F - closed cup

Punto de inflamabilidad (°C)

-11 °C - closed cup

Equipo de protección personal

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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