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Methyl glycolate - ≥96%, high purity , CAS No.96-35-5

    Grade & Purity:
  • ≥96%
In stock
Item Number
M670438
Grouped product items
SKU Size
Availability
Price Qty
M670438-5g
5g
2
$9.90
M670438-25g
25g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$11.90
M670438-100g
100g
2
$19.90
M670438-500g
500g
2
$59.90

Basic Description

Synonyms Glycolic acid methyl ester | Methyl hydroxyacetate
Specifications & Purity ≥96%
Shipped In Normal
Product 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.

Methyl glycolate is a chemical reagent used in the synthesis of taxol and rapamycin. It is used in leather tanning and textile dyeing. It acts as a flavoring agent, preservative in food processing, in water treatment industries and as chemical intermediates. Further, it is used in emulsion polymers, ink and paint additive to improve flow properties and impart gloss. It plays an important role in producing triisopropylsilanyloxy-acetic acid methyl ester using imidazole as reagent.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Carboxylic acid derivatives
Intermediate Tree Nodes Carboxylic acid esters
Direct Parent Methyl esters
Alternative Parents Monocarboxylic acids and derivatives  Primary alcohols  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Methyl ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as methyl esters. These are organic compounds containing a carboxyl group that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=H or organyl group and R'=methyl group.
External Descriptors Not available

Names and Identifiers

IUPAC Name methyl 2-hydroxyacetate
INCHI InChI=1S/C3H6O3/c1-6-3(5)2-4/h4H,2H2,1H3
InChIKey GSJFXBNYJCXDGI-UHFFFAOYSA-N
Smiles COC(=O)CO
Isomeric SMILES COC(=O)CO
WGK Germany 3
Molecular Weight 90.08
Beilstein 1699571
Reaxy-Rn 1699571
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1699571&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot Number Certificate Type Date Item
H2407189 Certificate of Analysis Aug 14, 2024 M670438
H2407190 Certificate of Analysis Aug 14, 2024 M670438
H2407191 Certificate of Analysis Aug 14, 2024 M670438
H2407192 Certificate of Analysis Aug 14, 2024 M670438
H2407193 Certificate of Analysis Aug 14, 2024 M670438
H2407194 Certificate of Analysis Aug 14, 2024 M670438
H2407195 Certificate of Analysis Aug 14, 2024 M670438
H2407196 Certificate of Analysis Aug 14, 2024 M670438
H2407197 Certificate of Analysis Aug 14, 2024 M670438

Chemical and Physical Properties

Solubility Miscible with water.
Refractive Index 1.417
Flash Point(°F) 152.6 °F
Flash Point(°C) 67 °C
Boil Point(°C) 149-151°C
Molecular Weight 90.080 g/mol
XLogP3 -0.500
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 2
Exact Mass 90.0317 Da
Monoisotopic Mass 90.0317 Da
Topological Polar Surface Area 46.500 Ų
Heavy Atom Count 6
Formal Charge 0
Complexity 50.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Yao Jian, Gui Lun, Yin Shaocheng.  (2021)  A novel esterase from a soil metagenomic library displaying a broad substrate range.  AMB Express,  11  (1): (1-10). 
2. Xilei Lu, Lixin Wang, Xiuyang Lu.  (2018)  Catalytic conversion of sugars to methyl lactate over Mg-MOF-74 in near-critical methanol solutions.  CATALYSIS COMMUNICATIONS,  110  (23). 
3. Shengqiang Zhou, Tianliang Lu, Lipeng Zhou, Xiaomei Yang.  (2025)  Au@Snβ zeolite as stable and active catalyst for the conversion of glycerol to methyl lactate.  JOURNAL OF CATALYSIS,  442  (115913). 

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