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W424601

Triethylamine

≥99.5%

Sinónimos:

N,N-Diethylethanamine

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Fórmula lineal:
(C2H5)3N
Número CAS:
121-44-8
Peso molecular:
101.19
NACRES:
NA.21
PubChem Substance ID:
24901993
UNSPSC Code:
12352116
FEMA Number:
4246
Flavis number:
11.023
EC Number:
204-469-4
MDL number:
MFCD00009051
Beilstein/REAXYS Number:
605283
Organoleptic:
fishy
Biological source:
synthetic
Food allergen:
no known allergens
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biological source

synthetic

Quality Segment

300, 400

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

Clase de almacenamiento

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

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