W424601
Trietilamina
≥99.5%
Sinônimo(s):
N,N-Dietiletanamina
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About This Item
Fórmula linear:
(C2H5)3N
Número CAS:
Peso molecular:
101.19
Número FEMA:
4246
Beilstein:
605283
Número CE:
Número MDL:
Código UNSPSC:
12352116
ID de substância PubChem:
Número de Flavis:
11.023
NACRES:
NA.21
Produtos recomendados
fonte biológica
synthetic
Nível de qualidade
conformidade reg.
FDA 21 CFR 117
densidade de vapor
3.5 (vs air)
pressão de vapor
51.75 mmHg ( 20 °C)
Ensaio
≥99.5%
forma
liquid
temperatura de autoignição
593 °F
prazo de validade
5 yr
Lim. expl.
8 %
índice de refração
n20/D 1.401 (lit.)
pH
12.7 (15 °C, 100 g/L)
pb
88.8 °C (lit.)
pf
−115 °C (lit.)
densidade
0.726 g/mL at 25 °C (lit.)
aplicação(ões)
flavors and fragrances
Documentação
see Safety & Documentation for available documents
alérgeno alimentar
no known allergens
Organoléptico
fishy
cadeia de caracteres SMILES
CCN(CC)CC
InChI
1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3
chave InChI
ZMANZCXQSJIPKH-UHFFFAOYSA-N
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Categorias relacionadas
Descrição geral
Triethylamine may be used as a test volatile organic compound (VOC) in studies of the development of sensors for detecting VOCs.
Aplicação
- 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).
Exoneração de responsabilidade
For R&D or non-EU Food use. Not for retail sale.
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
3 - Flammable liquids
Classe de risco de água (WGK)
WGK 1
Ponto de fulgor (°F)
12.2 °F - closed cup
Ponto de fulgor (°C)
-11 °C - closed cup
Equipamento de proteção individual
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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