W424601

Triéthylamine

≥99.5%

• Synonyme(s) : N,N-Diéthyléthanamine
• Formule linéaire : (C₂H₅)₃N
• Numéro CAS: 121-44-8
• Poids moléculaire : 101.19
• Numéro FEMA: 4246
• Numéro Beilstein : 605283
• Numéro CE : 204-469-4
• Numéro MDL: MFCD00009051
• Code UNSPSC : 12352116
• ID de substance PubChem : 24901993
• Numéro Flavis : 11.023
• Nomenclature NACRES : NA.21

Propriétés

• Source biologique: synthetic
• Niveau de qualité: 400
• Conformité réglementaire: FDA 21 CFR 117
• Densité de vapeur: 3.5 (vs air)
• Pression de vapeur: 51.75 mmHg ( 20 °C)
• Pureté: ≥99.5%
• Forme: liquid
• Température d'inflammation spontanée: 593 °F
• Durée de conservation: 5 yr
• Limite d'explosivité: 8 %
• Indice de réfraction: n20/D 1.401 (lit.)
• pH: 12.7 (15 °C, 100 g/L)
• Point d'ébullition: 88.8 °C (lit.)
• Pf: −115 °C (lit.)
• Densité: 0.726 g/mL at 25 °C (lit.)
• Application(s): flavors and fragrances
• Documentation: see Safety & Documentation for available documents
• Allergène alimentaire: no known allergens
• Propriétés organoleptiques: fishy
• Chaîne SMILES: CCN(CC)CC
• InChI: 1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3
• Clé InChI: ZMANZCXQSJIPKH-UHFFFAOYSA-N

Description

Description générale

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).

Clause de non-responsabilité

For R&D or non-EU Food use. Not for retail sale.

Informations sur la sécurité

• Pictogrammes: GHS02,GHS06,GHS05
• Mention d'avertissement: Danger
• Mentions de danger: H225,H302,H311 + H331,H314,H335
• Conseils de prudence: P210 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Classification des risques: Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
• Organes cibles: Respiratory system
• Code de la classe de stockage: 3 - Flammable liquids
• Classe de danger pour l'eau (WGK): WGK 1
• Point d'éclair (°F): 12.2 °F - closed cup
• Point d'éclair (°C): -11 °C - closed cup
• Équipement de protection individuelle: Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter