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Safety Information

90337

Sigma-Aldrich

Triethylamine

for amino acid analysis, ≥99.5% (GC)

Synonym(s):

N,N-Diethylethanamine

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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.26

grade

for amino acid analysis

Quality Level

vapor density

3.5 (vs air)

vapor pressure

51.75 mmHg ( 20 °C)

Assay

≥99.5% (GC)

form

liquid

autoignition temp.

593 °F

shelf life

42 mo.

expl. lim.

8 %

impurities

≤0.1% water

refractive index

n20/D 1.401 (lit.)

pH

12.7 (15 °C, 100 g/L)

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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Application


  • Surface-grafted macromolecular nanowires with pedant fluorescein chromophores by dense non-aggregated nanoarchitectonics as versatile photoactive platforms.: This research demonstrates the use of triethylamine in the synthesis of surface-grafted macromolecular nanowires with fluorescein chromophores, presenting their applications as versatile photoactive platforms in biochemistry and materials science (Kuciel et al., 2024).

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

WGK

WGK 1

Flash Point(F)

12.2 °F

Flash Point(C)

-11 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

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Sumanta Kumar Padhi et al.
Inorganic chemistry, 51(15), 8091-8102 (2012-07-26)
Cyclometalated ruthenium complexes having C(^)N and N(^)C type coordinating ligands with NAD(+)/NADH function have been synthesized and characterized by spectroscopic methods. The variation of the coordinating position of σ-donating carbon atom leads to a drastic change in their properties. Both
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Fungal genetics and biology : FG & B, 81, 88-97 (2015-06-09)
The genome of the filamentous fungus, Aspergillus flavus, has been shown to harbor as many as 56 putative secondary metabolic gene clusters including the one responsible for production of the toxic and carcinogenic, polyketide synthase (PKS)-derived aflatoxins. Except for the

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