09-1625
1,2-Dimethoxyethane
SAJ first grade, ≥99.0%
Synonym(s):
mono-Glyme, Dimethylglycol, Ethylene glycol dimethyl ether, Monoglyme
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About This Item
Linear Formula:
CH3OCH2CH2OCH3
CAS Number:
Molecular Weight:
90.12
EC Number:
203-794-9
UNSPSC Code:
12352112
Beilstein/REAXYS Number:
1209237
MDL number:
PubChem Substance ID:
grade
SAJ first grade
vapor density
3.1 (20 °C, vs air)
vapor pressure
48 mmHg ( 20 °C)
assay
≥99.0%
form
liquid
autoignition temp.
396 °F
expl. lim.
10.4 %
availability
available only in Japan
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
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Flam. Liq. 2 - Repr. 1B - Skin Irrit. 2
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
41.0 °F - closed cup
flash_point_c
5 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Guangmin Zhou et al.
Nature communications, 6, 7760-7760 (2015-07-18)
Lithium-sulphur batteries with a high theoretical energy density are regarded as promising energy storage devices for electric vehicles and large-scale electricity storage. However, the low active material utilization, low sulphur loading and poor cycling stability restrict their practical applications. Herein
Peter A Campochiaro et al.
Ophthalmology, 122(3), 545-554 (2014-12-03)
AKB-9778 is a small-molecule competitive inhibitor of vascular endothelial-protein tyrosine phosphatase (VE-PTP) that promotes Tie2 activation and reduces vascular leakage and neovascularization in mouse models. The purpose of this study was to test the safety, tolerability, pharmacokinetics, and biological activity
Andrew Martins et al.
Organic letters, 12(22), 5186-5188 (2010-10-19)
A palladium-catalyzed crossed biaryl coupling/reduction sequence enables the formation of meta-substituted biaryls via solvent-mediated arylpalladium(II) reduction. Isotope labeling studies determined that the decomposition of 1,2-dimethoxyethane (DME) is indeed involved in the reductive process.