Skip to Content
Merck
All Photos(1)

Documents

294632

Sigma-Aldrich

Methyl dimethoxyacetate

97%

Synonym(s):

Glyoxylic acid methyl ester dimethyl acetal

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CH3O)2CHCOOCH3
CAS Number:
89-91-8
Molecular Weight:
134.13
Beilstein:
1757582
EC Number:
201-950-0
MDL number:
MFCD00008484
UNSPSC Code:
12352100
PubChem Substance ID:
24857724
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.405 (lit.)

bp

67 °C/18 mmHg (lit.)

density

1.096 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

COC(OC)C(=O)OC

InChI

1S/C5H10O4/c1-7-4(6)5(8-2)9-3/h5H,1-3H3

InChI key

NZTCVGHPDWAALP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Methyl dimethoxyacetate has been used:
  • in Claisen acylation of active hydrogen compounds
  • in preparation of 3, 9-disubstituted 2,4,8,10-tetroxaspiro [5.5] undecane
  • as Lithium enolate precursor
  • as acylating reagent for cycloalkanone enolates and amino alcohols

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

Tetrahedron, 46, 6799-6799 (1990)
P J Connolly et al.
Journal of medicinal chemistry, 36(23), 3674-3685 (1993-11-12)
Compounds comprising a series of 7-[2-(4-fluorophenyl)-4,5,6,7-tetrahydro-2H-indazol-3-yl]-3,5- dihydroxy-6-heptenoic acid sodium salts (18) were synthesized and tested for their ability to inhibit HMG-CoA reductase in a partially purified enzyme preparation and cholesterol biosynthesis from acetate in cultured HEP-G2 cells. Changing the size
Synthetic Communications, 23, 1003-1003 (1993)
Some 3, 9-Dicarboxylic Acids of 2, 4, 8, 10-Tetroxaspiro [5.5] undecane.
CLEMENTS JB and RICE LM.
The Journal of Organic Chemistry, 24(12), 1958-1961 (1959)
Studies in Mixed Ester Condensations. IV. Acylations with Methyl Dimethoxyacetate1.
Royals EE and Robinson AG.
Journal of the American Chemical Society, 78(16), 4161-4164 (1956)

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