W424601
Trietilammina
≥99.5%
Sinonimo/i:
N,N-dietiletanammina
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W424601-SAMPLE
CHF 60.20
1 KG
CHF 106.00
20 KG
CHF 512.00
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Cambia visualizzazione
W424601-SAMPLE
CHF 60.20
1 KG
CHF 106.00
20 KG
CHF 512.00
About This Item
Formula condensata:
(C2H5)3N
Numero CAS:
Peso molecolare:
101.19
Numero FEMA:
4246
Beilstein:
605283
Numero CE:
Numero MDL:
Codice UNSPSC:
12352116
ID PubChem:
Numero Flavis:
11.023
NACRES:
NA.21
Prodotti consigliati
Origine biologica
synthetic
Conformità normativa
FDA 21 CFR 117
Densità del vapore
3.5 (vs air)
Tensione di vapore
51.75 mmHg ( 20 °C)
Saggio
≥99.5%
Stato
liquid
Temp. autoaccensione
593 °F
Durata
5 yr
Limite di esplosione
8 %
Indice di rifrazione
n20/D 1.401 (lit.)
pH
12.7 (15 °C, 100 g/L)
P. ebollizione
88.8 °C (lit.)
Punto di fusione
−115 °C (lit.)
Densità
0.726 g/mL at 25 °C (lit.)
applicazioni
flavors and fragrances
Documentazione
see Safety & Documentation for available documents
Allergene alimentare
no known allergens
Organolettico
fishy
Stringa SMILE
CCN(CC)CC
InChI
1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3
ZMANZCXQSJIPKH-UHFFFAOYSA-N
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Categorie correlate
Descrizione generale
Triethylamine may be used as a test volatile organic compound (VOC) in studies of the development of sensors for detecting VOCs.[1]
Applicazioni
- 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).
Esclusione di responsabilità
For R&D or non-EU Food use. Not for retail sale.
Avvertenze
Danger
Indicazioni di pericolo
Classi di pericolo
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
3 - Flammable liquids
Classe di pericolosità dell'acqua (WGK)
WGK 1
Punto d’infiammabilità (°F)
12.2 °F - closed cup
Punto d’infiammabilità (°C)
-11 °C - closed cup
Dispositivi di protezione individuale
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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