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Fumaric Acid CAS 110-17-8

Appearance: White odorless powder or crystalline solid particles
Purity (base on C4H4O4) %: 99.50~100.50 (dry basis)
Heavy metal (base on Pb) PPM: ≤ 10
Water content %: ≤ 0.5
Melting range oC: 286~302
Arsenic (base on As) PPM: ≤ 3
Residue on ignition %: ≤ 0.1
Maleic acid %: ≤ 0.1
Chroma (in 5% ethanol) #: ≤ 15

  • 110-17-8
  • MOSINTER
  • 110-17-8
Product Description

Payment & Shipping Terms

Supply Capacity

Payment Terms:

T/T, WU

Production Capacity:

5000MT/year

Min. Order:

1 KG

Packing:

according to the customer's requirements 

Means of Transport:

Ocean, Air, Land

Delivery Date:

7 days

 

 Fumaric Acid

CAS: 110-17-8

Item

Index

Appearance

White odorless   powder or crystalline solid particles

Purity (base on   C4H4O4) %

99.50~100.50   (dry basis)

Heavy metal   (base on Pb) PPM

≤ 10

Arsenic (base on   As)  PPM

≤ 3

Water   content  %

≤ 0.5

Melting range oC

286~302

Residue on   ignition %

≤ 0.1

Chroma (in 5%   ethanol) #

≤ 15

Maleic acid %

≤ 0.1

 

Fumaric acid or trans-butenedioic acid is the chemical compound with the formula HO2CCH=CHCO2H. This white crystalline compound is one of twoisomeric unsaturated dicarboxylic acids, the other being maleic acid. In fumaric acid the carboxylic acid groups are trans (E) and in maleic acid they are cis (Z). Fumaric acid has a fruit-like taste. The salts and esters are known as fumarates. Dimethyl fumarate significantly reduces disability progression in multiple sclerosis.

Chemistry

Fumaric acid was first prepared from succinic acid. A traditional synthesis involves oxidation of furfural (from the processing of maize) usingchlorate in the presence of a vanadium-based catalyst. Currently, industrial synthesis of fumaric acid is mostly based on catalytic isomerisationof maleic acid in aqueous solutions at low pH. Maleic acid is accessible in large volumes as a hydrolysis product of maleic anhydride, produced by catalytic oxidation of benzene or butane.

The chemical properties of fumaric acid can be anticipated from its component functional groups. This weak acid forms a diester, it undergoes additions across the double bond, and it is an excellent dienophile.

 


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