Skip to Content
Merck

128422

mono-Ethyl fumarate

95%

Synonym(s):

Fumaric acid monoethyl ester, Monoethyl fumarate

Slide 1 of 1
Sign In to View Organizational & Contract Pricing.

Select a Size

25 G

₪394.00

₪394.00

Please contact Customer Service for Availability
Request a Bulk Order

About This Item

Linear Formula:
C2H5OCOCH=CHCOOH
CAS Number:
2459-05-4
Molecular Weight:
144.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847858
EC Number:
219-544-7
Beilstein/REAXYS Number:
1723588
MDL number:
MFCD00002699

Key Documents

View All Documentation

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

mono-Ethyl fumarate, 95%

InChI key

XLYMOEINVGRTEX-ONEGZZNKSA-N

InChI

1S/C6H8O4/c1-2-10-6(9)4-3-5(7)8/h3-4H,2H2,1H3,(H,7,8)/b4-3+

SMILES string

CCOC(=O)\C=C\C(O)=O

assay

95%

form

solid

bp

147 °C/16 mmHg (lit.)

mp

66-68 °C (lit.)

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
651419M47353A26403
mono-Ethyl fumarate 95%

Sigma-Aldrich

128422

mono-Ethyl fumarate

mono-Methyl fumarate 97%

Sigma-Aldrich

651419

mono-Methyl fumarate

mono-Methyl glutarate 95%

Sigma-Aldrich

M47353

mono-Methyl glutarate

mono-Methyl adipate 99%

Sigma-Aldrich

A26403

mono-Methyl adipate

assay

95%

assay

97%

assay

95%

assay

99%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

solid

form

solid

form

liquid

form

liquid

mp

66-68 °C (lit.)

mp

144-145 °C (lit.)

mp

-

mp

7-9 °C (lit.)

bp

147 °C/16 mmHg (lit.)

bp

-

bp

150-151 °C/10 mmHg (lit.)

bp

162 °C/10 mmHg (lit.)

Application

mono-Ethyl fumarate (fumaric acid monoethyl ester, monoethyl fumarate) was used in the preparation of photo-crosslinkable macromers[1]. It was also used to synthesize Ugi/intramolecular Diels-Alder (IMDA) cycloaddition products[2].

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 1

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
WXBF1884V
BCCC0427
BCCB2532
BCBV5828
BCBR7587V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Janine Jansen et al.
Acta biomaterialia, 8(10), 3652-3659 (2012-06-19)
Photo-crosslinked networks were prepared from fumaric acid monoethyl ester-functionalized poly(D,L-lactic acid) oligomers and N-vinyl-2-pyrrolidone. Two model proteins, lysozyme and albumin, were incorporated into the network films as solid particles and their release behavior was studied. By varying the NVP content
Janine Jansen et al.
Biomacromolecules, 10(2), 214-220 (2008-12-19)
Polymer networks were prepared by photocross-linking fumaric acid monoethyl ester (FAME) functionalized, three-armed poly(D,L-lactide) oligomers using N-vinyl-2-pyrrolidone (NVP) as diluent and comonomer. The use of NVP together with FAME-functionalized oligomers resulted in copolymerization at high rates, and networks with gel
J Z Hu et al.
Solid state nuclear magnetic resonance, 6(1), 85-94 (1996-02-01)
The 1H magic-angle spinning (MAS) spectrum for a typical powdered solid is composed of a high resolution component and a broadline component. The high resolution component can be well isolated from the broadline component by the Hahn echo sequence with
Treatment of recurrent aphthous stomatitis with fumaric acid esters.
Emmanuella Guenova et al.
Archives of dermatology, 147(3), 282-284 (2011-03-23)
K Paulvannan
The Journal of organic chemistry, 69(4), 1207-1214 (2004-02-14)
An efficient approach to rigid tricyclic nitrogen heterocycles via sequential and tandem Ugi/intramolecular Diels-Alder (IMDA) cycloaddition of pyrrole is described. The one-pot Ugi four-component condensation (4CC) reaction was used as the key transformation to prepare trienes with a carboxamide substituent
View All Related Papers

Questions

Reviews

No rating value

Active Filters

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