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151386

Fumaryl chloride

Name: Fumaryl chloride
Brand: ALDRICH

95%

Synonym(s):

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

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About This Item

Linear Formula:

ClCOCH=CHCOCl

CAS Number:

627-63-4

Molecular Weight:

152.96

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24849125

EC Number:

211-005-4

Beilstein/REAXYS Number:

1721342

MDL number:

MFCD00000733

Assay:

95%

Form:

liquid

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Properties

Quality Level

200

assay

95%

form

liquid

refractive index

n20/D 1.499 (lit.)

bp

161-164 °C (lit.)

density

1.415 g/mL at 25 °C (lit.)

functional group

acyl chloride

storage temp.

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+

InChI key

ZLYYJUJDFKGVKB-OWOJBTEDSA-N

Description

General description

The photodissociation dynamics of fumaryl chloride was studied.

Application

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

pictograms

GHS05,GHS07

signalword

Danger

hcodes

H302 + H312,H314

pcodes

P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P362 + P364

Hazard Classifications

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

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

170.6 °F - closed cup

flash_point_c

77 °C - closed cup

ppe

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

Regulatory Information

危险化学品

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Preparation and characterization of in situ chitosan/polyethylene glycol fumarate/thymol hydrogel as an effective wound dressing.

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

Fabrication, characterization, and biocompatibility assessment of a novel elastomeric nanofibrous scaffold: A potential scaffold for soft tissue engineering.

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

Synthesis of poly(propylene fumarate) by acylation of propylene glycol in the presence of a proton scavenger.

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

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Global Trade Item Number

SKU	GTIN
151386-5G	04061837375729
151386-25G	04061837375712
151386-100G	04061838739162