W424601

Triethylamin

≥99.5%

• Synonym(e): N,N-Diethylethanamin
• Lineare Formel: (C₂H₅)₃N
• CAS-Nummer: 121-44-8
• Molekulargewicht: 101.19
• FEMA-Nummer: 4246
• Beilstein: 605283
• EG-Nummer: 204-469-4
• MDL-Nummer: MFCD00009051
• UNSPSC-Code: 12352116
• PubChem Substanz-ID: 24901993
• Flavis-Nummer: 11.023
• NACRES: NA.21

Eigenschaften

• Biologische Quelle: synthetic
• Qualitätsniveau: 400
• Dampfdichte: 3.5 (vs air)
• Dampfdruck: 51.75 mmHg ( 20 °C)
• Assay: ≥99.5%
• Form: liquid
• Selbstzündungstemp.: 593 °F
• Haltbarkeit: 5 yr
• Expl.-Gr.: 8 %
• Brechungsindex: n20/D 1.401 (lit.)
• pH-Wert: 12.7 (15 °C, 100 g/L)
• bp: 88.8 °C (lit.)
• mp (Schmelzpunkt): −115 °C (lit.)
• Dichte: 0.726 g/mL at 25 °C (lit.)
• Anwendung(en): flavors and fragrances
• Dokumentation: see Safety & Documentation for available documents
• Nahrungsmittelallergen: no known allergens
• Organoleptisch: fishy
• SMILES String: CCN(CC)CC
• InChI: 1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3
• InChIKey: ZMANZCXQSJIPKH-UHFFFAOYSA-N

Beschreibung

Allgemeine Beschreibung

Triethylamine may be used as a test volatile organic compound (VOC) in studies of the development of sensors for detecting VOCs.

Anwendung

• 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).

Haftungsausschluss

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

Sicherheitshinweise

• Piktogramme: GHS02,GHS06,GHS05
• Signalwort: Danger
• H-Sätze: H225,H302,H311 + H331,H314,H335
• P-Sätze: P210 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Gefahreneinstufungen: Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
• Zielorgane: Respiratory system
• Lagerklassenschlüssel: 3 - Flammable liquids
• WGK: WGK 1
• Flammpunkt (°F): 12.2 °F - closed cup
• Flammpunkt (°C): -11 °C - closed cup
• Persönliche Schutzausrüstung: Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter