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Monosodium fumarate, a chemical compound derived from fumaric acid and sodium, is widely recognized for its preservative and stabilizing properties. It is known for its ability to inhibit the growth of bacteria and fungi, thereby extending the shelf life of various products. Its versatility makes it a valuable component in the food, pharmaceutical, and animal feed industries.

7704-73-6

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7704-73-6 Usage

Uses

Used in the Food Industry:
Monosodium fumarate is used as a food additive and preservative for its ability to inhibit bacterial and fungal growth, enhancing the safety and quality of processed and packaged foods.
Used in the Pharmaceutical Industry:
In the pharmaceutical sector, monosodium fumarate serves as a stabilizer and buffer in various medications, ensuring the efficacy and safety of the products.
Used in Animal Feed Production:
Monosodium fumarate is used as a nutritional enhancer and stabilizer in animal feeds, improving the feed's nutritional content and stability, which in turn supports the health and well-being of animals.

Check Digit Verification of cas no

The CAS Registry Mumber 7704-73-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7704-73:
(6*7)+(5*7)+(4*0)+(3*4)+(2*7)+(1*3)=106
106 % 10 = 6
So 7704-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H4O4.2Na/c5-3(6)1-2-4(7)8;;/h1-2H,(H,5,6)(H,7,8);;/q;2*+1/p-2/b2-1+;;

7704-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,(E)-but-2-enedioic acid

1.2 Other means of identification

Product number -
Other names Sodium 2-butenedioate,(E)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food Additives: ACIDITY_REGULATOR; FLAVOUR_ENHANCER
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:7704-73-6 SDS

7704-73-6Upstream product

7704-73-6Relevant academic research and scientific papers

Study of corrosion and scale inhibition of polyepoxysuccinic acid derivative

Liu, Xinhua,Wang, Wenjing,Tong, Xinjia,Ding, Yunfei,Zhao, Xinqiang,Su, Hong

, p. 7716 - 7720 (2015/02/02)

Polyepoxysuccinic acid derivative was synthesized from L-cysteine and polyepoxysuccinic acid a condensation polymer formed by cyclization and polymerization with maleic anhydride. The structure of polyepoxysuccinic acid derivative was characterized by means of FTIR and 13C NMR. The scale inhibition and corrosion inhibition performances of polyepoxysuccinic acid derivative were studied. Scale inhibition and corrosion mechanisms were analyzed by means of SEM. The scale inhibition rate of polyepoxysuccinic acid derivative can reach 98.9 % under Ca2+ 400 mg L-1, HCO3- 800 mg L-1, polyepoxysuccinic acid derivative 8 mg L-1. Polyepoxysuccinic acid derivative is better than polyepoxysuccinic acid in corrosion inhibition performance and the corrosion inhibition rate can reach 65.14 % at 40 °C in dynamic experiment. SEM showed that the calcium carbonate crystal lattice was distorted completely from calcite to vaterite by using polyepoxysuccinic acid derivative. The surface of the test piece has dense protective adsorption film layer when it was immersed in solution with polyepoxysuccinic acid derivative.

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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