230553
Sodium ethoxide solution
21 wt. % in ethanol
Synonym(s):
Sodium ethylate
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About This Item
Linear Formula:
CH3CH2ONa
CAS Number:
Molecular Weight:
68.05
Beilstein:
3593646
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
form:
liquid
Recommended Products
form
liquid
Quality Level
concentration
21 wt. % in ethanol
refractive index
n20/D 1.385
density
0.868 g/mL at 25 °C
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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General description
Sodium ethoxide is an alkoxide salt mainly used as a strong base in organic reactions such as deprotonation, dehydration and dehalogenation.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Self-heat. 1 - Skin Corr. 1A - STOT SE 2
Target Organs
Eyes,Central nervous system
Supplementary Hazards
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 1
Flash Point(F)
48.2 °F - closed cup
Flash Point(C)
9 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Sodium Ethoxide
Whitaker KS and Whitaker DT
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2001)
Emad A Jaffar Al-Mulla et al.
Journal of oleo science, 58(9), 467-471 (2009-08-06)
N,N'-Carbonyl difatty amides (CDFAs) have been synthesized from palm oil using sodium ethoxide as catalyst. Ethyl fatty esters (EFEs) were produced as a by-product as well as glycerol. The synthesis was carried out by reflux palm oil and urea in
E S H El Ashry et al.
Nucleosides, nucleotides & nucleic acids, 26(5), 437-451 (2007-06-21)
Regioselective alkylation of 5-(3-chlorobenzo[b]thien-2-yl)-4H-1,2,4-triazole (1) with hydroxy alkylating agents 2, 3, 13, and the 2,3-O-isopropylidene-1-O-(p-tolylsulfonyl)-glycerol (10) afforded the corresponding S-alkylated derivatives 6, 7, 11, and 14 under both conventional and microwave irradiation conditions; bentonite as a solid support gave better
Franklin R Tay et al.
Journal of endodontics, 31(8), 593-598 (2005-07-27)
Polycaprolactone, a thermoplastic aliphatic polyester, is reportedly susceptible to both alkaline and enzymatic hydrolyzes. This screening study examined the susceptibility of Resilon, a polycaprolactone-based root filling composite, to alkaline hydrolysis. There were 15-mm diameter disks of Resilon and Obtura gutta-percha
N C Luu et al.
Chemical research in toxicology, 13(7), 610-615 (2000-07-18)
Glutathione conjugate formation plays important roles in the detoxification and bioactivation of xenobiotics. A range of nephrotoxic haloalkenes undergo bioactivation that involves glutathione and cysteine S-conjugate formation. The cysteine S-conjugates thus formed may undergo cysteine conjugate beta-lyase-catalyzed biotransformation to form
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