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5873-57-4

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5873-57-4 Usage

Description

SODIUM HYDROGEN FUMARATE, also known as an organic sodium salt, is a compound derived from fumaric acid where one of the carboxy groups has been replaced by a sodium ion. This substitution results in a unique chemical structure that offers various applications across different industries.

Uses

Used in Pharmaceutical Industry:
SODIUM HYDROGEN FUMARATE is used as a pharmaceutical agent for its potential therapeutic properties. It is known to exhibit anti-inflammatory, antioxidant, and immunomodulatory effects, making it a promising candidate for the treatment of various medical conditions.
Used in Food Industry:
SODIUM HYDROGEN FUMARATE is used as a preservative and acidity regulator in the food industry. Its ability to maintain an acidic environment helps prevent the growth of microorganisms, thereby extending the shelf life of food products.
Used in Cosmetics Industry:
SODIUM HYDROGEN FUMARATE is used as a skin conditioning agent in the cosmetics industry. Its antioxidant and anti-inflammatory properties contribute to the development of skincare products that promote skin health and address various skin concerns.
Used in Chemical Industry:
SODIUM HYDROGEN FUMARATE is used as a raw material in the chemical industry for the synthesis of various compounds and materials. Its unique chemical structure allows it to be a versatile building block in the production of different chemicals and additives.
Used in Agricultural Industry:
SODIUM HYDROGEN FUMARATE is used as a fertilizer additive in the agricultural industry. Its ability to improve soil structure and promote plant growth makes it a valuable component in the development of advanced fertilizer formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 5873-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5873-57:
(6*5)+(5*8)+(4*7)+(3*3)+(2*5)+(1*7)=124
124 % 10 = 4
So 5873-57-4 is a valid CAS Registry Number.

5873-57-4 Well-known Company Product Price

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  • Alfa Aesar

  • (B24683)  Sodium hydrogen fumarate, 98%   

  • 5873-57-4

  • 50g

  • 140.0CNY

  • Detail
  • Alfa Aesar

  • (B24683)  Sodium hydrogen fumarate, 98%   

  • 5873-57-4

  • 250g

  • 514.0CNY

  • Detail

5873-57-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name SODIUM HYDROGEN FUMARATE

1.2 Other means of identification

Product number -
Other names Sodium fumarate (monobasic)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5873-57-4 SDS

5873-57-4Relevant articles and documents

Tuning of the double-well potential of short strong hydrogen bonds by ionic interactions in alkali metal hydrodicarboxylates

Ananyev,Bushmarinov,Ushakov,Aitkulova,Lyssenko

, p. 97495 - 97502 (2015)

Short strong hydrogen bonds within crystals of sodium and potassium hydrofumarates were investigated by means of high-resolution and multitemperature X-ray diffraction studies. Various parameters, including geometry data, displacement parameters and cation-anion interaction energy, are considered to discuss hydrogen atom disorder. The influence of cation-anion interactions, being mainly electrostatic in nature, on the H-bond peculiarities is discussed. Equations interlinking the distance and energy of metal-oxygen interactions are introduced for carboxylates of sodium and potassium.

Chemical process

-

, (2008/06/13)

There is disclosed herein improved processes for the preparation of ether carboxylates by reacting in an alkaline reaction medium the salts of maleic acid and a carboxylic or polycarboxylic acid having a reactive hydroxyl group on a non-carbonyl carbon atom in the presence of a calcium ion catalyst wherein unreacted acid salts are recovered from the reaction medium by lowering the pH of the reaction medium to a range of from about 4 to about 6. The precipitated salts are recycled to the synthesis reaction to prepare additional amounts of product.

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