Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

T0886

Sigma-Aldrich

Triethylamine

≥99%

Synonym(s):

TEA, N,N-Diethylethanamine

Sign Into View Organizational & Contract Pricing

Select a Size

50 MG
HUF 96,800.00

HUF 96,800.00


Please contact Customer Service for Availability

Request a Bulk Order

Select a Size

Change View
50 MG
HUF 96,800.00

About This Item

Linear Formula:
(C2H5)3N
CAS Number:
Molecular Weight:
101.19
Beilstein:
605283
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.21

Assay:
≥99%
bp:
88.8 °C (lit.)
vapor pressure:
51.75 mmHg ( 20 °C)

HUF 96,800.00


Please contact Customer Service for Availability

Request a Bulk Order

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.)

Looking for similar products? Visit Product Comparison Guide

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
9034090063290337
assay

≥99%

assay

≥99.5% (GC)

assay

≥99%

assay

≥99.5% (GC)

refractive index

n20/D 1.401 (lit.)

refractive index

n20/D 1.401 (lit.)

refractive index

n20/D 1.401 (lit.)

refractive index

n20/D 1.401 (lit.)

mp

−115 °C (lit.)

mp

−115 °C (lit.)

mp

−115 °C (lit.)

mp

−115 °C (lit.)

expl. lim.

8 %

expl. lim.

8 %

expl. lim.

8 %

expl. lim.

8 %

vapor pressure

51.75 mmHg ( 20 °C)

vapor pressure

51.75 mmHg ( 20 °C)

vapor pressure

51.75 mmHg ( 20 °C)

vapor pressure

51.75 mmHg ( 20 °C)

Application

Triethylamine has been used:
  • as a hydrogen donor for the polymerization of various monomers[1]
  • to catalyze silanization[2]
  • in the synthesis of the Cy3-Alexa647 heterodimer[3]
  • in the synthesis of methacrylated solubilized decellularized cartilage[4]

Biochem/physiol Actions

Triethylamine is known to drive polymerization reaction. It acts as a source of carbon and nitrogen for bacterial cultures. Triethylamine is used in pesticides.[5] Triethylamine can serve as an organic solvent.[6]

also commonly purchased with this product

suggested gloves for splash protection

Signal Word

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

12.2 °F - closed cup

Flash Point(C)

-11 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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)
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)

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service