Sodium ethoxide

SIAL/156248 - 95%

Synonym: Sodium ethylate

CAS Number: 141-52-6
Empirical Formula (Hill Notation): C₂H₅NaO
Molecular Weight: 68.05
MDL Number: MFCD00012417
Linear Formula: CH₃CH₂ONa
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-156248-5G	5 g	$53.50 1/EA		Add To Favorites
45-156248-100G	100 g	$72.10 1/EA		Add To Favorites
45-156248-500G	500 g	$129.00 1/EA		Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

assay	95%
form	powder
InChI	1S/C2H5O.Na/c1-2-3;/h2H2,1H3;/q-1;+1
InChI key	QDRKDTQENPPHOJ-UHFFFAOYSA-N
Quality Level	200
SMILES string	[Na+].CC[O-]
vapor density	1.6 (vs air)
vapor pressure	<0.1 mmHg ( 20 °C)

Application:	Organic solvent fractionation in lignin depolymerization: A study focused on enhancing the monophenolic yield of lignin depolymerization using a dualistic aprotic solvent system, employing sodium ethoxide for effective organic solvent fractionation. This approach underscores the versatility of sodium ethoxide in complex organic synthesis and biomass processing (Xu et al., 2024 ). Solid-state self-quenching-resistant sulfur dots: Research on sulfur dots utilized a solvent-type passivation strategy to control solid-state self-quenching-resistant behavior, where sodium ethoxide played a crucial role in the synthesis process. This study illustrates sodium ethoxides utility in advanced materials synthesis, particularly for optoelectronic applications (Wu et al., 2022 ). Synthesis of corrosion inhibitors: Sodium ethoxide was used in the efficient synthesis of 6,7-Dihydro-5H-cyclopenta[b]pyridine-3-carbonitrile compounds, demonstrating its applicability as a base in the synthesis of corrosion inhibitors for steel alloys. This application combines computational and practical approaches to highlight sodium ethoxide′s role in materials science and corrosion prevention (Abd El-Lateef et al., 2022 ). Colon-targeted drug delivery systems: The design and synthesis of Thieno[2,3-b]pyridines-chitosan nanocomposites for colon targeting employed sodium ethoxide. This research showcases sodium ethoxides application in the preparation of targeted drug delivery systems, focusing on enhancing the efficacy and specificity of pharmaceutical treatments (Mansour et al., 2020 ). Synthesis of antimicrobial compounds: Sodium ethoxide was integral in the synthesis of novel bis-alpha,beta-unsaturated ketones and nicotinonitrile derivatives, aimed at antimicrobial applications. This study highlights the compound′s critical role in the development of new antimicrobial agents, demonstrating its utility in medicinal chemistry (Altalbawy, 2013 ).
General description:	Sodium ethoxide (Sodium ethylate) is a sodium alkoxide. It has been synthesized by reacting sodium with ethanol. It undergoes decomposition in the presence of water to afford ethanol and sodium hydroxide. It is widely employed as a strong base in organic synthesis studies.
Packaging:	5, 100, 500 g in steel can

Symbol	GHS02,GHS05
Signal word	Danger
Hazard statements	H228 - H251 - H314
Precautionary statements	P210 - P235 - P260 - P280 - P303 + P361 + P353 - P305 + P351 + P338
RIDADR	UN 3095 4.2(8) / PGI
WGK Germany	WGK 1
Flash Point(F)	86.0 °F - closed cup
Flash Point(C)	30 °C - closed cup
Supplemental Hazard Statements	EUH014

Purity	95%
UNSPSC	12352100

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