260428
3-Ethoxy-1,2-propanediol
98%
Synonym(s):
3-Ethoxypropane-1,2-diol, Glycerol 1-ethyl ether
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
C2H5OCH2CH(OH)CH2OH
CAS Number:
Molecular Weight:
120.15
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
Assay
98%
form
liquid
refractive index
n20/D 1.441 (lit.)
bp
222 °C (lit.)
density
1.063 g/mL at 25 °C (lit.)
SMILES string
CCOCC(O)CO
InChI
1S/C5H12O3/c1-2-8-4-5(7)3-6/h5-7H,2-4H2,1H3
InChI key
LOSWWGJGSSQDKH-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
3-Ethoxy-1,2-propanediol (also known as glycerol α-ethyl ether) is primarily used as a solvent in various industries, including pharmaceuticals, cosmetics, and coatings. It can also be used as a substrate in the synthesis of cyclic phosphates for use in flame retardants.
Application
3-Ethoxy-1,2-propanediol (EGE) can be used as a crosslinking agent in the development of poly(glycidol) hydrogels for use in various biomedical applications such as tissue engineering and drug delivery. It is also used as a potential component in a bio-based solvent system for dissolving or processing nitrocellulose.
3-Ethoxy-1,2-propanediol can be used as:
3-Ethoxy-1,2-propanediol can be used as:
- An analyte protector in gas chromatographic analysis of pesticides.
- An acceptor substrate in glycosylation reaction by sucrose phosphorylase.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Steven J Lehotay et al.
Journal of agricultural and food chemistry, 68(5), 1468-1479 (2020-01-17)
In this study, sample processing of bulk commodities using an efficient one-step comminution procedure with liquid nitrogen (LN2) was devised and assessed in the analysis of pesticide residues in fruits and vegetables. LN2 was added to the fresh samples from
Lucia Ivorra et al.
Chemosphere, 235, 662-669 (2019-07-06)
Uptake and depuration kinetics of 4,4'-dichlorobenzophenone (main metabolite of dicofol) in the edible clam Meretrix meretrix were evaluated through a mesocosm experiment. M. meretrix was exposed to different dicofol concentrations (environmental concentration, D1 = 50 ng/L; supra-environmental concentration, D2 = 500 ng/L) for 15 days, followed by
Michelangelo Anastassiades et al.
Journal of chromatography. A, 1015(1-2), 163-184 (2003-10-23)
A common problem in gas chromatography (GC) applications is the analyte losses and/or peak tailing due to undesired interactions with active sites in the inlet and column. Analytes that give poor peak shapes or degrade have higher detection limits, are
Jian Du et al.
Scientific reports, 6, 38355-38355 (2016-12-08)
The presence of pesticides in human milk (HM) is of great concern due to the potential health effects for the breastfed infant. To determine the relationships between HM pesticides and infant growth and development, a longitudinal study was conducted. HM
Lijun Han et al.
Journal of agricultural and food chemistry, 66(20), 4986-4996 (2017-11-15)
In this study, analytical results were compared when using different approaches to bulk food sample comminution, consisting of a vertical chopper (Blixer) at room temperature and dry ice cryogenic conditions, followed by further subsample processing (20 g) using liquid nitrogen
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service