110-17-8

  • Product Name:Fumaric acid
  • Molecular Formula:C4H4O4
  • Purity:99%
  • Molecular Weight:116.073
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Product Details;

CasNo: 110-17-8

Molecular Formula: C4H4O4

Appearance: white powder or colourless crystals

Factory Sells Best Quality Fumaric acid 110-17-8 with GMP standards

  • Molecular Formula:C4H4O4
  • Molecular Weight:116.073
  • Appearance/Colour:white powder or colourless crystals 
  • Melting Point:295-300 ºC 
  • Boiling Point:355.5°Cat760mmHg 
  • Flash Point:230 ºC 
  • PSA:74.60000 
  • Density:1.499 g/cm3 
  • LogP:-0.28820 

Fumaric acid(Cas 110-17-8) Usage

Chemical Description

Fumaric acid is used to transform the bases into salts.

Use Description

Fumaric acid, a specific chemical compound, serves diverse roles in various fields. In the food industry, it acts as a food additive and acidulant, enhancing the flavor and preserving the quality of various products. In the pharmaceutical sector, it plays a crucial role as an ingredient in the formulation of medications, particularly in controlled-release drug delivery systems. Moreover, in the field of polymer science, fumaric acid is used in the production of biodegradable plastics and resins, contributing to the development of more sustainable materials. Its applications in food, pharmaceuticals, and polymers underscore its significance in improving taste, enabling drug delivery, and promoting environmental sustainability within these distinct fields.

Industrial Applications and Production

Fumaric acid, also known as trans-1,2-ethylenedicarboxylic acid, is extensively used in various industries including food, chemicals, agriculture, and pharmaceuticals. Its multifunctional structure, featuring a carbon-carbon double bond and two carboxylic acid groups, allows for easy esterification and polymerization, making it a key chemical feedstock for producing paper resins, unsaturated polyester resins, alkyd resins, plasticizers, and other industrial products. Additionally, its non-toxic nature and unique flavor have led to its widespread use as a food acidulant and beverage ingredient.

Synthesis Methods

Fumaric acid is primarily synthesized through the isomerization of maleic acid, typically catalyzed by mineral acids, peroxy compounds, or thiourea. This petrochemical method, while yielding high production rates, often involves high temperatures, leading to the formation of by-products and significant energy consumption. Alternatively, microbial fermentation processes have gained attention due to their sustainability and environmentally friendly characteristics, offering a potential alternative to petrochemical synthesis.

Uses in Various Industries

Fumaric acid finds applications in diverse industries, including food, medicine, and construction. It is used for native chitosan modification and as an active material in antioxidant, antibacterial, and antiviral reagents. It is also recognized as one of the "top 12" chemical building blocks due to its wide-ranging applications and importance in industrial processes.

Biological Functions

Fumaric acid is a component of the tricarboxylic acid (TCA) cycle and plays a role in metabolic pathways in various organisms. Some lactobacilli utilize the TCA cycle in the direction of reductive reactions, metabolizing fumarate to malic acid or succinic acid. Additionally, fumaric acid and its salts are commonly used in terrestrial animal feeds.

Use in Wine Production

Fumaric acid is permitted as an additive for wine acidification and inhibition of malolactic fermentation (MLF). It can effectively inhibit MLF in red wines at specific concentrations, improving microbiological stability and freshness while allowing for the reduction of SO2 levels. Tastings have shown that fumaric acid enhances acidity and body in wines, making it a valuable technological additive in winemaking.

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

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Paragraph 0028-0076, (2021/06/22)

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110-17-8 Process route

(E)-4-(4-nitrophenoxy)-4-oxobut-2-enoic acid

(E)-4-(4-nitrophenoxy)-4-oxobut-2-enoic acid

4-nitro-phenol
100-02-7,78813-13-5,89830-32-0

4-nitro-phenol

(2E)-but-2-enedioic acid
110-17-8,26099-09-2

(2E)-but-2-enedioic acid

Conditions
Conditions Yield
With pH=5.1 buffer; polypeptide MN-42; In acetonitrile; at 16.9 ℃; Rate constant; other polypetides vith var. amino acids sequences;
With acetate buffer; JNIIHR polypeptide; In acetonitrile; at 16.85 ℃; pH=5.1; Further Variations:; Reagents; Kinetics;
With AcAPLEPEYPGDNATPEQMHQYAHQLRRYINMLCONH2; In acetate buffer; at 16.85 ℃; pH=4.1; Further Variations:; pH-values; Reagents; Kinetics;
water
7732-18-5

water

thiourea
17356-08-0

thiourea

CYANAMID
420-04-2

CYANAMID

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

(2E)-but-2-enedioic acid
110-17-8,26099-09-2

(2E)-but-2-enedioic acid

Conditions
Conditions Yield

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