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90337

Sigma-Aldrich

Triethylamine

for amino acid analysis, ≥99.5% (GC)

Synonyma:

N,N-Diethylethanamine

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About This Item

Lineární vzorec:
(C2H5)3N
Číslo CAS:
121-44-8
Molekulová hmotnost:
101.19
Beilstein/REAXYS Number:
605283
EC Number:
204-469-4
MDL number:
MFCD00009051
UNSPSC Code:
12352116
PubChem Substance ID:
57653385
NACRES:
NA.26

grade

for amino acid analysis

Quality Level

200

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).

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

12.2 °F - closed cup

flash_point_c

-11 °C - closed cup

ppe

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

Osvědčení o analýze (COA)

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Triethylamine United States Pharmacopeia (USP) Reference Standard

USP

1683559

Triethylamine

Triethylamine hydrochloride suitable for HPLC, LiChropur™, 99.0-101.0% (AT)

Supelco

63961

Triethylamine hydrochloride

Phenyl isothiocyanate for HPLC derivatization, the detection of alcohols and amines, ≥99.0%

Sigma-Aldrich

78780

Phenyl isothiocyanate

Triethyl-d15-amine 98 atom % D, 98% (CP)

Sigma-Aldrich

448982

Triethyl-d15-amine

Triethylamine hydrochloride ≥99.0% (AT)

Sigma-Aldrich

90350

Triethylamine hydrochloride

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
Kai Morino et al.
Scientific reports, 5, 8953-8953 (2015-05-21)
Well-trained clinicians may be able to provide diagnosis and prognosis from very short biomarker series using information and experience gained from previous patients. Although mathematical methods can potentially help clinicians to predict the progression of diseases, there is no method
Hannah Coyle et al.
The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry, 23(4), 335-359 (2014-07-08)
The aim of this study was to assess the efficacy of cognitive training, specifically computerized cognitive training (CCT) and virtual reality cognitive training (VRCT), programs for individuals living with mild cognitive impairment (MCI) or dementia and therefore at high risk
André R Fajardo et al.
Biomacromolecules, 15(7), 2691-2700 (2014-05-27)
Despite a growing interest in amphiphilic polysaccharide-based diblock copolymers as functional polymeric drug delivery nanosystems, biologically relevant sulfated glycosaminoglycan systems were not yet investigated. Here, we report the synthesis and the self-assembly properties in water of chondroitin sulfate-b-poly(lactic acid) (CS-b-PLA(n)).
Jeffrey W Cary et al.
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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