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Fumaric Acid, CAS: 110-17-8, Mf: C4h4o4 manufacturer / supplier in China, offering Fumaric Acid CAS: 110-17-8 Mf: C4h4o4 Food Grade, Sodium Hypophosphite Monohydrate CAS: 10039-56-2 Mf: H2nao2p· H2O Grade: Top Quality, Pharmaceutical Raw Material Methylamine Hydrochloride / Methylamine HCl CAS 593-51-1 and so on.

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Supplier Homepage Product acids Fumaric Acid CAS: 110-17-8 Mf: C4h4o4 Food Grade

Fumaric Acid CAS: 110-17-8 Mf: C4h4o4 Food Grade

FOB Price: Get Latest Price
Min. Order: 25 Tons
Production Capacity: 5000tons/Per Month
Transport Package: Follow Client′s Requirement
Payment Terms: L/C, T/T, Western Union, Money Gram
Basic Info
  • Model NO.: CAS: 110-17-8
  • Classification: Food Additives
  • Appearance: Colourless Liquid with an Amine Odour
  • Nw: 116.07
  • Specification: food grade
  • Efficacy: Feed Preservatives
  • Type: Fumaric Acid
  • Color: Colorless
  • Trademark: customized
  • Origin: China
Product Description
Fumaric acid Basic information
Product Name:Fumaric acid
Synonyms:(2E)-2-Butenedioic acid;(e)-2-butenedioicaci;(e)-butenedioicaci;(E)-HO2CCH=CHCO2H;1,2-Ethenedicarboxylic acid, trans-;1,2-Ethylenedicarboxylic acid, (E);1,2-ethylenedicarboxylicacid;1,2-ethylenedicarboxylicacid,(e)
Product Categories:INORGANIC & ORGANIC CHEMICALS;FOOD ADDITIVES;Intermediates;Food & Feed ADDITIVES;Substrates;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Alphabetical Listings;E-F;Flavors and Fragrances;Companion Products and ReagentsCancer Research;Chemopreventive Agents;Insect Platform;Multidrug Resistance;Phase II Enzyme Inducers;Phase II Enzyme InducersCancer Research;Serum-free Media;Food & Flavor Additives;Aliphatics;Building Blocks;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks;Allium cepa (Onion);Nutrition Research;Panax ginseng;Phytochemicals by Plant (Food/Spice/Herb);reagent;standard substance;Food additive and acidulant;CONSTRUCTION
Mol File:110-17-8.mol
Fumaric acid Chemical Properties
mp 298-300 °C (subl.)(lit.)
density 1.62
vapor pressure 1.7 mm Hg ( 165 °C)
FEMA 2488
Fp 230 °C
Water Solubility 0.63 g/100 mL (25 ºC)
Merck 14,4287
BRN 605763
Stability:Stable at room temperature. Decomposes at around 230 C. Incompatible with strong oxidizing agents, bases, reducing agents. Combustible.
Fumaric acid Usage And Synthesis
Chemical Propertieswhite powder or colourless crystals
UsageOccurs in many plants. Essential to vegetable and tissue respiration. Used as an antioxidant.
General DescriptionA colorless crystalline solid. The primary hazard is the threat to the environment. Immediate steps should be taken to limit spread to the environment. Combustible, though may be difficult to ignite. Used to make paints and plastics, in food processing and preservation, and for other uses.
Air & Water ReactionsSlightly soluble in water.
Reactivity ProfileFumaric acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt.. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions. Partial carbonization and formation of maleic anhydride occur at 446° F (open vessel).
Health HazardInhalation of dust may cause respiratory irritation. Compound is non-toxic when ingested. Prolonged contact with eyes or skin may cause irritation.
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