Sigma Aldrich 259527 1,2-Dimethoxyethane anhydrous, 99.5%, inhibitor-free 100 mL
Category
Brand
Stock Code
LB.SA.259527-100ML
Kısa Bilgi
Synonym(s): DME, mono-Glyme, Dimethylglycol, Ethylene glycol dimethyl ether, Monoglyme Linear Formula: CH3OCH2CH2OCH3 CAS Number: 110-71-4 Molecular Weight: 90.12 Beilstein: 1209237 EC Number: 203-794-9 MDL number: MFCD00008502 PubChem Substance ID: 57648156 NACRES: NA.21
| Sigma Aldrich 259527 1,2-Dimethoxyethane anhydrous, 99.5%, inhibitor-free 100 mL |
|
Synonym(s): DME, mono-Glyme, Dimethylglycol, Ethylene glycol dimethyl ether, Monoglyme
Linear Formula: CH3OCH2CH2OCH3
CAS Number: 110-71-4
Molecular Weight: 90.12
Beilstein: 1209237
EC Number: 203-794-9
MDL number: MFCD00008502
PubChem Substance ID: 57648156
NACRES: NA.21 |
|
PROPERTIES
grade anhydrous
Quality Level 100
vapor density 3.1 (20 °C, vs air)
vapor pressure 48 mmHg ( 20 °C)
Assay 99.5%
form liquid
autoignition temp. 396 °F
expl. lim. 10.4 %
impurities <0.003% water, <0.005% water (100 mL pkg)
evapn. residue <0.0005%
refractive index n20/D 1.379 (lit.)
pH 7
bp 85 °C (lit.)
mp −58 °C (lit.)
density 0.867 g/mL at 25 °C (lit.)
SMILES string COCCOC
InChI 1S/C4H10O2/c1-5-3-4-6-2/h3-4H2,1-2H3
InChI key XTHFKEDIFFGKHM-UHFFFAOYSA-N
DESCRIPTION
Application
1,2-Dimethoxyethane may be used as a solvent in the following processes:
- Synthesis of cyclic amines from amino alcohols via direct cyclodehydration.[1]
- Stereoselective synthesis of trans-1,2-disubstituted alkenes from 1-phenyl-1H-tetrazol-5-yl sulfones and aldehydes in the presence of potassium or sodium hexamethyldisilazide.[2]
- Synthesis of adamantylideneadamantane from 2-adamantanone via reductive coupling.[3] |
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