T0886

Sigma-Aldrich

Triethylamine

≥99%

Sinônimo(s):
TEA, N,N-Diethylethanamine
Fórmula linear:
(C2H5)3N
Número CAS:
Peso molecular:
101.19
Beilstein/REAXYS Number:
605283
Número EC:
Número MDL:
ID de substância PubChem:
NACRES:
NA.21

Nível de qualidade

200

densidade de vapor

3.5 (vs air)

pressão de vapor

51.75 mmHg ( 20 °C)

teor

≥99%

temperatura de autoignição

593 °F

prazo de validade

3 yr

Lim. expl.

8 %

Impurezas

≤0.5% water (Karl Fischer)

índice de refração

n20/D 1.401 (lit.)

pb

88.8 °C (lit.)

pf

−115 °C (lit.)

densidade

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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Aplicação

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

Embalagem

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

Ações bioquímicas/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.

Palavra indicadora

Danger

hazcat

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

Órgãos-alvo

Respiratory system

storage_class_code

3 - Flammable liquids

WGK Alemanha

WGK 1

Ponto de fulgor (ºF)

12.2 °F

Ponto de fulgor (ºC)

-11 °C

Equipamento de proteção individual

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

Certificado de análise

Certificado de origem

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)
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)
The biodegradation pathway of triethylamine and its biodegradation by immobilized Arthrobacter protophormiae cells
Cai T, et al.
Journal of Hazardous Materials, 186(1), 59-66 (2011)
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)
Artigos
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.
Leia mais
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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