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151386

Sigma-Aldrich

Fumarylchlorid

95%

Synonym(e):

(2E)-2-Butenedioyl dichloride, Fumaric acid chloride, Fumaric acid dichloride, Fumaric dichloride, Fumaroyl dichloride, Fumaryl dichloride

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About This Item

Lineare Formel:
ClCOCH=CHCOCl
CAS-Nummer:
627-63-4
Molekulargewicht:
152.96
Beilstein:
1721342
EG-Nummer:
211-005-4
MDL-Nummer:
MFCD00000733
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24849125
NACRES:
NA.22

Qualitätsniveau

200

Assay

95%

Form

liquid

Brechungsindex

n20/D 1.499 (lit.)

bp

161-164 °C (lit.)

Dichte

1.415 g/mL at 25 °C (lit.)

Funktionelle Gruppe

acyl chloride

Lagertemp.

2-8°C

SMILES String

ClC(=O)\C=C\C(Cl)=O

InChI

1S/C4H2Cl2O2/c5-3(7)1-2-4(6)8/h1-2H/b2-1+

InChIKey

ZLYYJUJDFKGVKB-OWOJBTEDSA-N

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Allgemeine Beschreibung

The photodissociation dynamics of fumaryl chloride was studied.

Anwendung

Fumaryl chloride was used in the preparation of high molecular weight poly(propylene fumarate).

Piktogramme

CorrosionExclamation mark
GHS05,GHS07

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

170.6 °F - closed cup

Flammpunkt (°C)

77 °C - closed cup

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
STBL3164
STBK9964
BCCJ2936
BCCH3085
BCCG3172

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Sigma-Aldrich

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Seyed Amin Mirmohammadi et al.
Materials science & engineering. C, Materials for biological applications, 68, 530-539 (2016-08-16)
Hydroxyl functionalized nano-sized POSS or ethyleneglycol as diol monomers was incorporated to hydroxyl-terminated polybutadiene (HTPBD) chain in the presence of fumaryl chloride as extender. Blue light photocrosslinking system based on camphorquinone (photoinitiator) and dimethylaminoethyl methacrylate (accelerator) was applied to cure
Monali Kawade et al.
The journal of physical chemistry. A, 115(9), 1538-1546 (2011-02-17)
The photodissociation dynamics of fumaryl chloride (ClCO-CH═CH-COCl) has been studied in a supersonic molecular beam around 235 nm using resonance enhanced multiphoton ionization (REMPI) time-of-flight (TOF) technique by detecting the nascent state of the primary chlorine atom. A single laser
Elham Shamirzaei Jeshvaghani et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 106(6), 2371-2383 (2017-11-24)
With regard to flexibility and strength properties requirements of soft biological tissue, elastomeric materials could be more beneficial in soft tissue engineering applications. The present work investigates the use of an elastic polymer, (polycaprolactone fumarate [PCLF]), for fabricating an electrospun
S J Peter et al.
Journal of biomaterials science. Polymer edition, 10(3), 363-373 (1999-04-03)
To synthesize high molecular weight poly(propylene fumarate) (PPF), fumaryl chloride and propylene glycol were reacted in the presence of potassium carbonate, which serves as a proton scavenger. Transesterification of the resulting low molecular weight oligomer led to a polymer with
Sepideh Koosehgol et al.
Materials science & engineering. C, Materials for biological applications, 79, 66-75 (2017-06-21)
In the present study, polyethylene glycol fumarate (PEGF) was synthesized as a component of blend solutions via polycondensation polymerization and characterized by different tests in order to determine its functional groups and its physical properties included melting and crystallization temperature
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