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307432

Sigma-Aldrich

1,2-Dimethoxyethane

suitable for HPLC, 99.9%, inhibitor-free

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Synonym(s):
mono-Glyme, Dimethylglycol, Ethylene glycol dimethyl ether, Monoglyme
Linear Formula:
CH3OCH2CH2OCH3
CAS Number:
Molecular Weight:
90.12
Beilstein:
1209237
EC Number:
MDL number:
UNSPSC Code:
12190000
PubChem Substance ID:
NACRES:
NA.21

vapor density

3.1 (20 °C, vs air)

Quality Level

vapor pressure

48 mmHg ( 20 °C)

Assay

99.9%

form

liquid

autoignition temp.

396 °F

purified by

glass distillation

expl. lim.

10.4 %

technique(s)

HPLC: suitable

impurities

<0.030% water

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.)

λ

H2O reference

UV absorption

λ: 220 nm Amax: 1.00
λ: 250 nm Amax: 0.20
λ: 300 nm Amax: 0.03
λ: 350-400 nm Amax: 0.01

application(s)

food and beverages

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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General description

This solvent is glass distilled, submicron filtered and subjected to rigorous specification testing to provide lot-to-lot consistency.

Application

Designed for use with HPLC instrumentation and organic synthesis applications.

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Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Flam. Liq. 2 - Repr. 1B - Skin Irrit. 2

Supplementary Hazards

WGK

WGK 1

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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NMR Chemical Shifts of Common Laboratory Solvents as Trace Impurities.
Hugo E. Gottlieb et al.
The Journal of organic chemistry, 62(21), 7512-7515 (2001-10-24)
Theoretical study of cation/ether complexes: Alkali metal cations with 1, 2-dimethoxyethane and 12-crown-4.
Hill SE, et al.
The Journal of Physical Chemistry A, 102(21), 3813-3819 (1998)
The catalytic Pauson-Khand reaction promoted by a small amount of 1, 2-dimethoxyethane or water.
Sugihara T and Yamaguchi M.
Synlett, 12, 1384-1386 (1998)
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.
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

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