Merck
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T0886

Sigma-Aldrich

Triethylamine

≥99%

Sinónimos:
TEA, N,N-Diethylethanamine
Fórmula lineal:
(C2H5)3N
Número de CAS:
Peso molecular:
101.19
Beilstein:
605283
Número de EC:
Número MDL:
ID de la sustancia en PubChem:
NACRES:
NA.21

Nivel de calidad

200

densidad de vapor

3.5 (vs air)

presión de vapor

51.75 mmHg ( 20 °C)

ensayo

≥99%

temp. de autoignición

593 °F

caducidad

3 yr

lim. expl.

8 %

impurezas

≤0.5% water (Karl Fischer)

índice de refracción

n20/D 1.401 (lit.)

bp

88.8 °C (lit.)

mp

−115 °C (lit.)

densidad

0.726 g/mL at 25 °C (lit.)

SMILES string

CCN(CC)CC

InChI

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

InChI key

ZMANZCXQSJIPKH-UHFFFAOYSA-N

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Aplicación

Triethylamine has been used:
  • as a hydrogen donor for the polymerization of various monomers
  • to catalyze silanization
  • in the synthesis of the Cy3-Alexa647 heterodimer
  • in the synthesis of methacrylated solubilized decellularized cartilage

Envase

1 L in glass bottle
100, 4×100, 500 mL in glass bottle

Acciones bioquímicas o fisiológicas

Triethylamine is known to drive polymerization reaction. It acts as a source of carbon and nitrogen for bacterial cultures. Triethylamine is used in pesticides. Triethylamine can serve as an organic solvent.

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

WGK

WGK 1

Punto de inflamabilidad F

12.2 °F

Punto de inflamabilidad C

-11 °C

Equipo de protección personal

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

Certificado de Análisis

Introduzca el número de lote para buscar un certificado de análisis (COA).

Certificado de origen

Introduzca el número de lote para buscar un Certificado de origen (COO).

Wide-field in vivo background free imaging by selective magnetic modulation of nanodiamond fluorescence.
Sarkar SK, et al.
Biomedical Optics Express, 5(4), 1190-1202 (2014)
Effects of tissue processing on bioactivity of cartilage matrix-based hydrogels encapsulating osteoconductive particles.
Townsend JM, et al.
Biomedical Materials (Bristol, England), 13(3) (2018)
RESOLFT nanoscopy with photoswitchable organic fluorophores.
Kwon J, et al.
Scientific reports (2015)
States of Water Located in the Continuous Organic Phase of 1?Butyl?3?methylimidazolium Tetrafluoroborate/Triton X-100/Triethylamine Reverse Microemulsions
Na Li, et al.
ChemPhysChem (2007)
Synthesis and characterization of poly(vinylchloride) type macrophotoinitiator comprising side-chain thioxanthone via click chemistry
Akat H and Ozkan M
Express Polymer Letters, 5(4), 318?326-318?326 (2011)

Artículos

Greener Chemistry: Methods and Products for Amide Bond Formation

Amide bonds are ubiquitous in both nature and industrial applications. They are vital to the structure and function of biological macromolecules and polymers. The importance of this functionality has resulted in numerous approaches to its formation, ranging from stoichiometric activation of carboxylic acids to more recent advances in catalytic amide bond formation.

Heck Reaction Applications & Products

The Heck reaction is the palladium catalyzed cross-coupling reaction between alkenes and aryl or vinyl halides (or triflates) to afford substituted alkenes.

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