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Merck
CN

325260

Methyl glycolate

98%

Synonym(s):

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

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About This Item

Linear Formula:
HOCH2CO2CH3
CAS Number:
Molecular Weight:
90.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-502-7
Beilstein/REAXYS Number:
1699571
MDL number:
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Product Name

Methyl glycolate, 98%

InChI key

GSJFXBNYJCXDGI-UHFFFAOYSA-N

InChI

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

SMILES string

COC(=O)CO

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.)

functional group

ester
hydroxyl

Quality Level

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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

10 - Combustible liquids

wgk

WGK 3

flash_point_f

152.6 °F - closed cup

flash_point_c

67 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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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

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