T0886
Triethylamine
≥99%
Synonym(s):
TEA, N,N-Diethylethanamine
About This Item
Recommended Products
vapor density
3.5 (vs air)
Quality Level
vapor pressure
51.75 mmHg ( 20 °C)
assay
≥99%
autoignition temp.
593 °F
shelf life
3 yr
expl. lim.
8 %
impurities
≤0.5% water (Karl Fischer)
refractive index
n20/D 1.401 (lit.)
bp
88.8 °C (lit.)
mp
−115 °C (lit.)
density
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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Related Categories
Application
- 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
Biochem/physiol Actions
also commonly purchased with this product
suggested gloves for splash protection
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
target_organs
Respiratory system
wgk_germany
WGK 1
flash_point_f
closed cup
flash_point_c
closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Articles
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.
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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