Skip to Content
MilliporeSigma
All Photos(1)

Documents

325260

Sigma-Aldrich

Methyl glycolate

98%

Synonym(s):

Hydroxyacetic acid methyl ester, Methyl 2-hydroxyacetate, Methyl 2-hydroxyethanoate, Methyl hydroxyacetate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
HOCH2CO2CH3
CAS Number:
Molecular Weight:
90.08
Beilstein:
1699571
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

3.12 (vs air)

vapor pressure

17 mmHg ( 52 °C)

Assay

98%

form

liquid

refractive index

n20/D 1.417 (lit.)

bp

149-151 °C (lit.)

density

1.167 g/mL at 25 °C (lit.)

SMILES string

COC(=O)CO

InChI

1S/C3H6O3/c1-6-3(5)2-4/h4H,2H2,1H3

InChI key

GSJFXBNYJCXDGI-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Synthesis of methyl glycolate from the carbonylation of HCHO using heteropoly acids (HPAs) as catalysts, followed by esterification with methanol was reported. Size-selective vibrational spectroscopy of methyl glycolate clusters was reported.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

152.6 °F - closed cup

Flash Point(C)

67 °C - closed cup

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.

Visit the Document Library

Size-selective vibrational spectroscopy of methyl glycolate clusters: comparison with ragout-jet FTIR spectroscopy.
Farnik M, et al.
Physical Chemistry Chemical Physics, 6(19), 4614-4620 (2004)
Highly effective synthesis of methyl glycolate with heteropolyacids as catalysts.
Sun Y, et al.
Catalysis Communications, 10(5), 678-681 (2009)
Jong-Ryul Park et al.
Biointerphases, 16(1), 011001-011001 (2021-01-07)
Poly(2-alkyl-2-oxazoline) (PAOx) hydrogels are tailorable synthetic materials with demonstrated biomedical applications, thanks to their excellent biocompatibility and tunable properties. However, their use as injectable hydrogels is challenging as it requires invasive surgical procedures to insert the formed hydrogel into the

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