W424601
Triethylamine
≥99.5%
Synonym(s):
N,N-Diethylethanamine
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About This Item
Linear Formula:
(C2H5)3N
CAS Number:
Molecular Weight:
101.19
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352116
FEMA Number:
4246
Flavis number:
11.023
EC Number:
204-469-4
MDL number:
Beilstein/REAXYS Number:
605283
Organoleptic:
fishy
Biological source:
synthetic
Food allergen:
no known allergens
biological source
synthetic
reg. compliance
FDA 21 CFR 117
vapor density
3.5 (vs air)
vapor pressure
51.75 mmHg ( 20 °C)
assay
≥99.5%
form
liquid
autoignition temp.
593 °F
shelf life
5 yr
expl. lim.
8 %
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.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
fishy
SMILES string
CCN(CC)CC
InChI
1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3
InChI key
ZMANZCXQSJIPKH-UHFFFAOYSA-N
General description
Triethylamine may be used as a test volatile organic compound (VOC) in studies of the development of sensors for detecting VOCs.
Application
- Novel hybrid thiazoles, bis-thiazoles linked to azo-sulfamethoxazole: Synthesis, docking, and antimicrobial activity.: This study showcases the synthesis of hybrid thiazoles linked to azo-sulfamethoxazole, employing triethylamine in the reaction process, highlighting its role in antimicrobial applications (Salem et al., 2024).
- Spirocyclic rhodamine B benzoisothiazole derivative: a multi-stimuli fluorescent switch manifesting ethanol-responsiveness, photo responsiveness, and acidochromism.: This research demonstrates a spirocyclic rhodamine derivative acting as a multi-stimuli-responsive fluorescent switch, where triethylamine plays a critical role in the synthesis process (Battula et al., 2023).
- Para-Substituted Thiosemicarbazones as Cholinesterase Inhibitors: Synthesis, In Vitro Biological Evaluation, and In Silico Study.: This paper reports on the synthesis of para-substituted thiosemicarbazones where triethylamine is employed as a base, evaluating their potential as cholinesterase inhibitors (Khan et al., 2023).
- Separation and purification of quinolyridine alkaloids from seeds of Thermopsis lanceolata R. Br. by conventional and pH-zone-refining counter-current chromatography.: This study involves the use of triethylamine in the pH-zone-refining counter-current chromatography technique to separate and purify specific alkaloids, illustrating its utility in advanced separation methodologies (Ning et al., 2023).
Disclaimer
For R&D or non-EU Food use. Not for retail sale.
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signalword
Danger
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
flash_point_f
12.2 °F - closed cup
flash_point_c
-11 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
Regulatory Information
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Porphyrins-based opto-electronic nose for volatile compounds detection.
Di Natale C, et al.
Sensors and Actuators B, Chemical, 65(1), 220-226 (2000)
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| W424601-1KG | 04061838249333 |
| W424601-20KG | 04061837540721 |
| W424601-SAMPLE | 04061838194091 |