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Sigma-Aldrich

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:
96-35-5
Molecular Weight:
90.08
Beilstein/REAXYS Number:
1699571
EC Number:
202-502-7
MDL number:
MFCD00004667
UNSPSC Code:
12352100
PubChem Substance ID:
24859497
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

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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_germany

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)

Certificates of Analysis (COA)

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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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