409464
Zinc acrylate
98%
Synonyme(s) :
Acrylic acid zinc salt
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About This Item
Formule linéaire :
(H2C=CHCO2)2Zn
Numéro CAS:
Poids moléculaire :
207.50
Numéro CE :
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23
Produits recommandés
Essai
98%
Forme
powder
Pf
240-244 °C (lit.)
Chaîne SMILES
C=CC(=O)O[Zn]OC(=O)C=C
InChI
1S/2C3H4O2.Zn/c2*1-2-3(4)5;/h2*2H,1H2,(H,4,5);/q;;+2/p-2
Clé InChI
XKMZOFXGLBYJLS-UHFFFAOYSA-L
Catégories apparentées
Description générale
Zincacrylate is a compound that belongs to the class of acrylate polymers, whichare known for their versatile applications in various fields, including biomedicine.In the biomedical field, zinc acrylate is primarily recognized for its use indental materials, drug delivery systems, and tissue engineering. In dental applications, zinc acrylate is often used in dental adhesives and restorative materials dueto its excellent bonding properties and biocompatibility.
Application
Zinc acrylate can be used as a:
- A monomer in the development of zinc oxide (ZnO) thin films via photopolymerization reaction. ZnO thin films exhibit favorable characteristics for use in optoelectronic devices, such as sensors, light-emitting diodes (LEDs), and photovoltaic cells. The incorporation of zinc acrylate allows for tunable properties, making these films versatile for various applications in the field of electronics and photonics.
- A key component in the formulation of gelatin/poly(zinc acrylate) hydrogel stent. Zinc acrylate incorporated into the gelatin-based hydrogel to enhance its mechanical properties contributing to its performance and suitability for use in medical applications.
- A monomer used in the synthesis of fluorescent resins through the incorporation of coumarin acid structures. The resultant fluorescent zinc acrylate resins exhibit improved antifouling properties, which are crucial for applications in marine environments.
- A monomer in the development of a poly zinc acrylate (PZA) coating that enhances the performance and stability of zinc anodes in aqueous Zn metal batteries, contributing to their high reversibility and longevity.
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Dam. 1
Code de la classe de stockage
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Chemical communications (Cambridge, England), 49(26), 2643-2645 (2013-02-23)
Chemi-enzymatic synthesis of ribavirin acrylate and subsequent RAFT co-polymerization with acrylic acid afforded a formulation of a broad spectrum antiviral drug which avoids accumulation in erythrocytes, the origin of the main side effect of ribavirin. In cultured macrophages the macromolecular
M Drozd et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 105, 135-148 (2013-01-10)
The X-ray and vibrational spectroscopic analysis of a new molecular complex of guanidine and acrylic acid are reported. The crystal of C(NH(2))(2)(NH)(*)CH(2)=CHCOOH belongs to Pna2(1) space group of orthorhombic system with Z=4, a=9.9242(34) Å, b, c=8.3951(14) Å. In the crystal
Liang Hu et al.
Chemical communications (Cambridge, England), 49(26), 2649-2651 (2013-02-22)
We present the hysteresis of the response of the poly(N-isopropylacrylamide)-co-acrylic acid microgel-based etalons to solution temperature and pH changes. We find that the optical hysteresis of the etalon can be controlled using various solution ionic strengths and/or counterions, as well
Mehmet Cinar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 104, 428-436 (2013-01-01)
The optimized geometrical structure, vibrational and electronic transitions, chemical shifts and non-linear optical properties of ethyl trans-alfa-cyano-3-indole-acrylate (C(14)H(12)N(2)O(2)) compound were presented in this study. The ground state geometrical structure and vibrational wavenumbers were carried out by using density functional (DFT/B3LYP)
Xiaobei Wang et al.
Macromolecular bioscience, 12(11), 1575-1582 (2012-10-09)
Comb-shaped glycopolymer/peptide bioconjugates are constructed by grafting reduced glutathione (GSH) onto acrylate-functional block glycocopolymers via thiol-ene click chemistry. In aqueous solution, the glycopolymer/GSH bioconjugate self-assembles to sugar-installed spherical micelles. The size of micelles decreases with increasing pH, demonstrating pH-responsive character.
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