W424601
Triethylamine
≥99.5%
동의어(들):
N,N-Diethylethanamine
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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
(C2H5)3N
CAS 번호:
Molecular Weight:
101.19
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352116
FEMA Number:
4246
Flavis number:
11.023
EC Number:
204-469-4
MDL number:
Beilstein/REAXYS Number:
605283
Organoleptic:
fishy
Biological source:
synthetic
Food allergen:
no known allergens
biological source
synthetic
reg. compliance
FDA 21 CFR 117
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
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.
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Danger
target_organs
Respiratory system
저장 등급
3 - Flammable liquids
flash_point_f
12.2 °F - closed cup
flash_point_c
-11 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3