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03761

Fumaric acid

Name: Fumaric acid
Brand: SIAL

≥99.5%, fine crystals, tested according to USP/NF

Synonym(s):

(2E)-2-Butenedioic acid, trans-Butenedioic acid, Acidum fumaricum

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About This Item

Linear Formula:

HOOCCH=CHCOOH

CAS Number:

110-17-8

Molecular Weight:

116.07

NACRES:

NA.21

PubChem Substance ID:

329747799

eCl@ss:

39021709

UNSPSC Code:

12352100

EC Number:

203-743-0

MDL number:

MFCD00002700

Beilstein/REAXYS Number:

605763

Assay:

≥99.5%

Form:

fine crystals, powder

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Properties

Product Name

Fumaric acid, tested according to USP/NF

agency

tested according to USP/NF

Quality Level

200

vapor pressure

1.7 mmHg ( 165 °C)

assay

≥99.5%

form

fine crystals, powder

autoignition temp.

1364 °F

expl. lim.

40 %

mp

298-300 °C (subl.) (lit.)

application(s)

pharmaceutical (small molecule)

functional group

carboxylic acid

SMILES string

OC(=O)\C=C\C(O)=O

InChI

1S/C4H4O4/c5-3(6)1-2-4(7)8/h1-2H,(H,5,6)(H,7,8)/b2-1+

InChI key

VZCYOOQTPOCHFL-OWOJBTEDSA-N

Description

General description

Fumaric acid or trans-butenedioic acid, is crystalline compound that occurs widely in nature.

Application

Fumaric acid may be used in the preparation of L-Lysine-fumaric acid crystals.

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pictograms

GHS07

signalword

Warning

hcodes

H319

pcodes

P264 - P280 - P305 + P351 + P338 - P337 + P313

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

flash_point_f

523.4 °F

flash_point_c

273 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

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UV-curable methacrylated/fumaric acid modified epoxy as a potential support for enzyme immobilization.

Kahraman MV, et al.

Reactive functional Polymers, 67(2), 97-103 (2007)

Propionate precursors and other metabolic intermediates as possible alternative electron acceptors to methanogenesis in ruminal fermentation in vitro.

C J Newbold et al.

The British journal of nutrition, 94(1), 27-35 (2005-08-24)

Fifteen potential precursors of propionate were tested for their ability to decrease CH4 production by ruminal fluid in vitro. Sodium acrylate and sodium fumarate produced the most consistent effects in batch cultures, with 50 % of the added precursors being

Vibrational spectra and second harmonic generation in molecular complexes of L-lysine with L-tartaric, D, L-malic, acetic, arsenous, and fumaric acids.

Marchewka MK, et al.

Crystal Growth & Design, 3(4), 587-592 (2003)

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Global Trade Item Number

SKU	GTIN
03761-500G	04061838627834