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2-Ethoxyethanol

analytical standard

Synonym(s):

Ethyl glycol, Ethylene glycol monoethyl ether

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About This Item

Linear Formula:
C2H5OCH2CH2OH
CAS Number:
Molecular Weight:
90.12
Beilstein:
1098271
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor density

3.1 (vs air)

vapor pressure

3.8 mmHg ( 20 °C)

Assay

≥99.8% (GC)

autoignition temp.

460 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

14 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.407 (lit.)
n20/D 1.408

bp

135 °C (lit.)

mp

−90 °C (lit.)

density

0.93 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

CCOCCO

InChI

1S/C4H10O2/c1-2-6-4-3-5/h5H,2-4H2,1H3

InChI key

ZNQVEEAIQZEUHB-UHFFFAOYSA-N

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General description

2-Ethoxyethanol is an organic compound, widely used as a component or solvent for nitrocellulose and in a variety of dyes, inks, cleaning agents, resins, paints, varnishes, etc. It is also used for increasing the stability of emulsions.

Application

2-Ethoxyethanol may be used as an extraction solvent for the quantification and analysis of algal lipids from algae samples using normal-phase high performance liquid chromatography(HPLC) coupled in parallel to an evaporative light scattering detector (ELSD) and quadrupole mass spectrometer(QMS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 3 - Repr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

104.0 °F - closed cup

Flash Point(C)

40 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Extraction of algal lipids and their analysis by HPLC and mass spectrometry
Jones J, et al.
Journal of the American Oil Chemists' Society, 89(8), 1371-1381 (2012)
I A Adedara et al.
Andrologia, 45(2), 111-119 (2012-06-20)
Endocrine disrupting chemicals cause reproductive dysfunction by interacting with intricate regulation and cellular processes involve in spermatogenesis. This study investigated the probable mechanism of action of ethylene glycol monoethyl ether (EGEE) as an antiandrogenic compound as well as the effects
Douglas J Fort et al.
Drug and chemical toxicology, 25(3), 293-308 (2002-08-14)
Currently, no standardized and well-validated alternative models exist for screening for progesterone-responsive endocrine disrupting chemicals (EDCs). Because of this, a rapid assay for evaluating progestin/antiprogestin activity using Xenopus oocyte germinal vesicle breakdown (GVBD) as a model was evaluated. Five compounds
Gargi Bagchi et al.
International journal of andrology, 31(2), 269-274 (2008-01-09)
Methoxyacetic acid (MAA), the active biological oxidation product of the industrial solvent ethylene glycol monomethyl ether (EGME), causes acute toxicity in several species including humans. MAA primarily affects tissues with rapidly dividing cells and high rates of energy metabolism, including
Chang Yong Yoon et al.
The Journal of veterinary medical science, 65(2), 207-212 (2003-03-26)
The effects of ethylene glycol monoethyl ether (EGEE) on testicular cell populations in rats were investigated by a flow cytometric method. Rats were administered by gavage with EGEE at the various doses of 0 (saline alone), 100, 200, 400, and

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