Triethylamine

ALDRICH/W424601 - ≥99.5%

Synonym: N,N-Diethylethanamine

CAS Number: 121-44-8
Empirical Formula (Hill Notation): C₆H₁₅N
Molecular Weight: 101.19
EC Number: 204-469-4
MDL Number: MFCD00009051
Linear Formula: (C₂H₅)₃N
Product Type: Chemical

Catalog Number	PKG Qty.	Price


45-W424601-SAMPLE	1 each	$56.20 1/EA	Add To Favorites
45-W424601-1KG	1 kg	$118.00 1/EA	Add To Favorites
45-W424601-20KG	20 kg	$573.00 1/EA	Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

application(s)	flavors and fragrances
assay	≥99.5%
autoignition temp.	593 °F
biological source	synthetic
bp	88.8 °C (lit.)
density	0.726 g/mL at 25 °C (lit.)
documentation	see Safety & Documentation for available documents
expl. lim.	8 %
food allergen	no known allergens
form	liquid
InChI	1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3
InChI key	ZMANZCXQSJIPKH-UHFFFAOYSA-N
mp	−115 °C (lit.)
organoleptic	fishy
pH	12.7 (15 °C, 100 g/L)
Quality Level	300
	400
refractive index	n20/D 1.401 (lit.)
reg. compliance	FDA 21 CFR 117
shelf life	5 yr
SMILES string	CCN(CC)CC
vapor density	3.5 (vs air)
vapor pressure	51.75 mmHg ( 20 °C)

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.
General description:	Triethylamine may be used as a test volatile organic compound (VOC) in studies of the development of sensors for detecting VOCs.
Packaging:	1 kg in glass bottle
Packaging:	20 kg in composite drum

Symbol	GHS02,GHS05,GHS06
Signal word	Danger
Hazard statements	H225 - H302 - H311 + H331 - H314 - H335
Precautionary statements	P210 - P280 - P301 + P330 + P331 - P303 + P361 + P353 - P304 + P340 + P311 - P305 + P351 + P338 + P310
Hazard Codes	F,C
Risk Statements	11-20/21/22-35
Safety Statements	3-16-26-29-36/37/39-45-61
RIDADR	UN1296 - class 3 - PG 2 - Triethylamine
WGK Germany	WGK 1
Flash Point(F)	12.2 °F
Flash Point(C)	-11 °C

Purity	≥99.5%
bp	88.8 °C (lit.)
mp	−115 °C (lit.)
Density	0.726 g/mL at 25 °C (lit.)
Refractive Index	n20/D 1.401 (lit.)
FEMA Number	4246
UNSPSC	12352116

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