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128422

Sigma-Aldrich

mono-Ethyl fumarate

95%

Sinonimo/i:

Fumaric acid monoethyl ester, Monoethyl fumarate

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25 G
CHF 64.30

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25 G
CHF 64.30

About This Item

Formula condensata:
C2H5OCOCH=CHCOOH
Numero CAS:
2459-05-4
Peso molecolare:
144.13
Beilstein:
1723588
Numero CE:
219-544-7
Numero MDL:
MFCD00002699
Codice UNSPSC:
12352100
ID PubChem:
24847858
NACRES:
NA.22

CHF 64.30

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Livello qualitativo

100

Saggio

95%

Stato

solid

P. ebollizione

147 °C/16 mmHg (lit.)

Punto di fusione

66-68 °C (lit.)

Stringa SMILE

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

InChI

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

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Applicazioni

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].

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H317,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
WXBF1884V
BCCC0427
BCCB2532
BCBV5828
BCBR7587V

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M Vandermeeren et al.
Biochemical and biophysical research communications, 234(1), 19-23 (1997-05-08)
Most studies on the antipsoriatic mode of action of dimethylfumarate focused on its antiproliferative effects in keratinocytes. Because inflammatory skin diseases are associated with an upregulation of endothelial cell adhesion molecules and because the presence of inflammatory cells in dermis
P J Altmeyer et al.
Journal of the American Academy of Dermatology, 30(6), 977-981 (1994-06-01)
Psoriasis vulgaris may benefit from treatment with fumaric acid and/or its derivatives; however, because different preparations have been used, results have been contradictory and difficult to interpret. The purpose of this clinical trial was to evaluate the therapeutic value of
Dirk W Grijpma et al.
Biomaterials, 26(16), 2795-2802 (2004-12-18)
Biodegradable polymer networks were prepared from fumaric acid derivatives of oligomeric esters. Photo-crosslinkable macromers were prepared by reacting star-shaped hydroxyl-group terminated lactide, epsilon-caprolactone and trimethylene carbonate based oligomers and fumaric acid monoethyl ester in the presence of N,N-dicyclohexylcarbodiimide and 4-dimethylamino
U Mrowietz et al.
The British journal of dermatology, 141(3), 424-429 (1999-12-03)
Fumaric acid ester (FAE) therapy has proved to be safe and effective in patients with severe psoriasis vulgaris. This treatment was introduced nearly 30 years ago, but is only now gaining renewed interest among dermatologists. FAE therapy is licensed in
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
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