156248

Sodium ethoxide

95%

Manufacturer: Sigma Aldrich

CAS Number: 141-52-6

Synonym(S): Sodium ethylate

Select a Size

Pack Size SKU Availability Price
5 G 156248-5-G In Stock ₹ 2,630.48
100 G 156248-100-G In Stock ₹ 3,204.20
500 G 156248-500-G In Stock ₹ 5,260.95

156248 - 5 G

₹ 2,630.48

In Stock

Quantity

1

Base Price: ₹ 2,630.48

GST (18%): ₹ 473.486

Total Price: ₹ 3,103.966

vapor density

1.6 (vs air)

Quality Level

200

vapor pressure

<0.1 mmHg ( 20 °C)

Assay

95%

form

powder

SMILES string

[Na+].CC[O-]

InChI

1S/C2H5O.Na/c1-2-3;/h2H2,1H3;/q-1;+1

InChI key

QDRKDTQENPPHOJ-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
71210
Sodium ethoxide
Sigma Aldrich ₹ 2,024.28 - ₹ 5,574.88
230553
Sodium ethoxide solution
Sigma Aldrich ₹ 1,710.35 - ₹ 6,999.98

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Description

  • 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.[1]
  • 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).

SAFETY INFORMATION

Pictograms

GHS02,GHS05

Signal Word

Danger

Hazard Statements

H228,H251,H314

Precautionary Statements

P210 - P235 - P260 - P280 - P303 + P361 + P353 - P305 + P351 + P338

Hazard Classifications

Flam. Sol. 1 - Self-heat. 1 - Skin Corr. 1A

Supplementary Hazards

EUH014

WGK

WGK 1

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Quality Level:
200

vapor pressure:
<0.1 mmHg ( 20 °C)

Assay:
95%

form:
powder

SMILES string:
[Na+].CC[O-]

InChI:
1S/C2H5O.Na/c1-2-3;/h2H2,1H3;/q-1;+1

InChI key:
QDRKDTQENPPHOJ-UHFFFAOYSA-N

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[Na+].C[O-]

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1S/CH3O.Na/c1-2;/h1H3;/q-1;+1

InChI key:
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SMILES string:
N.OC=O

InChI:
1S/CH2O2.H3N/c2-1-3;/h1H,(H,2,3);1H3

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VZTDIZULWFCMLS-UHFFFAOYSA-N

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Clc1ccc2C(=O)c3ccccc3C(=O)c2c1

InChI:
1S/C14H7ClO2/c15-8-5-6-11-12(7-8)14(17)10-4-2-1-3-9(10)13(11)16/h1-7H

InChI key:
FPKCTSIVDAWGFA-UHFFFAOYSA-N