28-2650
Sodium ethoxide
SAJ first grade, ≥95.0%
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:
12352300
PubChem Substance ID:
grade
SAJ first grade
vapor density
1.6 (vs air)
vapor pressure
<0.1 mmHg ( 20 °C)
Assay
≥95.0%
form
solid
availability
available only in Japan
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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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Sol. 1 - Self-heat. 1 - Skin Corr. 1A
Supplementary Hazards
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 1
Flash Point(F)
86.0 °F - closed cup
Flash Point(C)
30 °C - closed cup
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C Mazzitelli et al.
Journal of dental research, 87(2), 186-190 (2008-01-26)
The chemo-mechanical surface treatment of fiber posts increases their bonding properties. The combined use of atomic force and confocal microscopy allows for the assessment and quantification of the changes on surface roughness that justify this behavior. Quartz fiber posts were
Wisam H Hoidy et al.
Journal of oleo science, 59(5), 229-233 (2010-05-01)
Difatty acyl thiourea (DFAT), which has biological activities as antibiotics and antifungal, has been synthesized from palm oil and thiourea using sodium ethoxide as catalyst. Ethyl fatty ester (EFE) and glycerol were produced as by-products. The synthesis was carried out
On the preparation of optically active phenyl-p-tolyl-methanesulphonic acid and its racemisation by sodium ethoxide.
E E PEDERSEN et al.
Acta chemica Scandinavica, 2(8), 651-656 (1948-01-01)
Frank Derosa et al.
The Journal of organic chemistry, 73(3), 1139-1142 (2008-01-11)
Despite over a century of reports to the contrary, sodium methoxide has been found to react with nitric oxide (NO). The reaction, whose final organic product is sodium formate, is postulated to occur via an intermediate O-bound diazeniumdiolate [CH3O-N(O)=NO-] that
Ali Reza Harifi-Mood et al.
Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques, 7(1), 88-91 (2004-05-18)
Variable-Temperature Kinetics has been used to obtain the rate constants of the reaction at various temperatures during one kinetic run. Pseudo-first-order rate constants for the transesterification of procaine with aliphatic alcohols ethanol, n-propanol and tert-butanol were obtained by the fluorescence
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