Ammonium itaconate
From Wikipedia, the free encyclopedia
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| IUPAC name
diazanium;2-methylidenebutanedioate
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C5H12N2O4 | |
| Molar mass | 164.161 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Ammonium itaconate is a chemical compound with the chemical formula C5H12N2O4.This is an organic ammonium salt of itaconic acid.[1] [2]
Synthesis
[edit ]The compound is synthesized through neutralization reactions between itaconic acid and ammonia or ammonium hydroxide.[3]
Uses
[edit ]Itaconic acid derivatives, including ammonium salts, serve as precursors for polymers, adhesives, and biofuels. For example, itaconate-based polymers are used to produce superabsorbents and synthetic rubbers.[4] [5]
References
[edit ]- ^ Greenwich, University of (1997). Biotechnological Innovations in Chemical Synthesis. Butterworth-Heinemann. p. 140. ISBN 978-0-7506-0561-8 . Retrieved 31 March 2025.
- ^ Washington University Studies. Washington University. 1915. p. 115. Retrieved 31 March 2025.
- ^ Gupta, Satyaranjan Das (1 May 2002). "The Double Auric Iodides of Substituted Ammonium Bases". ACS Publications . 36 (4): 747. doi:10.1021/ja02181a014 . Retrieved 31 March 2025.
- ^ Cui, Chuansheng; Wang, Chengguo; Zhao, Yaqi (2006). "Acrylonitrile/ammonium itaconate aqueous deposited copolymerization" . Journal of Applied Polymer Science . 102 (1): 904–908. doi:10.1002/app.24376. ISSN 1097-4628 . Retrieved 31 March 2025.
- ^ Ge, He-yi; Liu, Jian-jun; Chen, Juan; Wang, Cheng-guo (1 April 2007). "Texture and Properties of Acrylonitrile–Ammonium Itaconate Copolymer Precursor Fibers and Carbon Fibers" . Journal of Polymer Research. 14 (2): 91–97. doi:10.1007/s10965-006-9085-3. ISSN 1572-8935 . Retrieved 31 March 2025.