W424601

Triethylamine

≥99.5%

• Synonym(s): N,N-Diethylethanamine
• Linear Formula: (C₂H₅)₃N
• CAS Number: 121-44-8
• Molecular Weight: 101.19
• FEMA Number: 4246
• Beilstein: 605283
• EC Number: 204-469-4
• MDL number: MFCD00009051
• UNSPSC Code: 12352116
• PubChem Substance ID: 24901993
• Flavis number: 11.023
• NACRES: NA.21

Properties

• biological source: synthetic
• Quality Level: 400
• 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

Description

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.

Safety Information

• Pictograms: GHS02,GHS06,GHS05
• Signal Word: Danger
• Hazard Statements: H225,H302,H311 + H331,H314,H335
• Precautionary Statements: P210 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• 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