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Aspartic acid, homopolymer is a biodegradable and non-toxic polymer composed of repeating units of aspartic acid, a non-essential amino acid naturally occurring in the human body. It is recognized for its environmentally friendly properties, being easily biodegradable and not accumulating in the environment. Additionally, it is considered safe for consumption and has been approved for use in various food and pharmaceutical products.

39444-67-2

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39444-67-2 Usage

Uses

Used in Food Industry:
Aspartic acid, homopolymer is used as a thickening agent and stabilizer in food products. Its ability to improve the texture and consistency of food items contributes to better product quality and consumer satisfaction.
Used in Pharmaceutical Industry:
Aspartic acid, homopolymer is used as a drug delivery system in pharmaceutical applications. Its biodegradable and non-toxic nature makes it a suitable carrier for various medications, enhancing their efficacy and safety.
Used in Environmental Applications:
Aspartic acid, homopolymer is utilized for its environmentally friendly properties, as it is easily biodegradable and does not contribute to environmental pollution. This makes it a preferred choice for industries seeking eco-friendly alternatives to traditional materials.

Check Digit Verification of cas no

The CAS Registry Mumber 39444-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,4,4 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39444-67:
(7*3)+(6*9)+(5*4)+(4*4)+(3*4)+(2*6)+(1*7)=142
142 % 10 = 2
So 39444-67-2 is a valid CAS Registry Number.

39444-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diazanium,(Z)-but-2-enedioate

1.2 Other means of identification

Product number -
Other names 2-Butenedioic acid (2Z)-,ammonium salt (1:?),homopolymer

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:39444-67-2 SDS

39444-67-2Downstream Products

39444-67-2Relevant academic research and scientific papers

Preparation method of organic metal salt additive (by machine translation)

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Paragraph 0011; 0023, (2020/06/02)

The organic metal salt additive, prepared by mixing :(1), washing, with short-chain organic acid as acid source, and then mixing, with the resulting solution of Step ;(2) to obtain the high-purity organic metal salt additive, has the advantages (1) as follows, The organic metal salt additive is relatively high in crystal form structure and high in purity, and has good industrial application prospects, through mixing, of an iron source or a calcium source, or a, zinc source with a high-purity, organic metal salt additive agent in an aqueous solution with, a wide,price. product source. (by machine translation)

METHOD FOR PREPARING AMMONIUM SALTS OF FUMARIC OR SUCCINIC ACID

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Page/Page column 2, (2012/06/01)

An improved process for preparing ammonium salts from fumaric or succinic acid, is described. The method consists of neutralizing the corresponding acid carbonate or ammonium bicarbonate at a molar stoichiometric or greater than the stoichiometric ratio of 4-5% in a saturated aqueous solution of the synthesized salt at a temperature not exceeding 40° C., followed by separation of the product and drying at a temperature not exceeding 70° C. After separation of the ammonium salts, the filtrate can be re-used. Isolation of the product is usually carried out by cooling the reaction mixture to a temperature of 15-18C°. The product comes out in almost crystalline form. Saturated aqueous solution of the synthesized salt is formed by the interaction of carbonate or ammonium bicarbonate with the appropriate acid at a temperature not exceeding 40° C. It is possible to obtain cleaner salt concentration weighing more than 99% and not yielding lower than 98%. The method allows for an increase in the yield of targeted products and ensures their consistent high quality due to their formation in crystalline form.

PROCESSES FOR PRODUCING NH4+ -OOC-R-COOH COMPOUNDS FROM FERMENTATION BROTHS CONTAINING NH4+ -OOC-R-COO-NH4+COMPOUNDS AND/OR HOOC-R-COOH COMPOUND ACIDS, AND CONVERSION OF NH4+ -OOC-R-COOH COMPOUNDS TO HOOC-R-COOH COMPOUND ACIDS

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Page/Page column 31, (2011/11/13)

A process for making a NH4+ OOC-R-COOH compound from a clarified NH4+ OOC- R-COO' NH4+ compound-containing fermentation broth includes (a) distilling the broth to form an overhead that includes water and ammonia, and a liquid bottoms that includes a NH4+ OOC~R~COOH compound, at least some of a NH4+ QOC-R-COO" NH4+ compound, and at least about 20 wt% water; (b) cooling the bottoms to a temperature sufficient to cause the bottoms to separate into a NH4+ OOC-R~C00' NH4+ compound-containing liquid portion in contact with a NH4+ OOC-R-COOH compoond-containing solid portion that is substantially free of the NH4+ OOC-R-COO" NH4+compound; (c) separating the solid portion from the liquid portion; and (d) recovering the solid portion.

Opening of the Furan Ring in 5-Azido-2-furaldehyde

Povazanec, Frantisek,Kovac, Jaroslav,Hesek, Dusan

, p. 150 - 154 (2007/10/02)

Fission of the furan ring in 5-azido-2-furaldehyde is described. α-Furylnitrene, formed from α-azido furan derivatives, is stabilized by the furan ring fission.Transformation of the intermediate to quinoxaline and pyrazole derivatives is also studied.

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