Online Database of Chemicals from Around the World

Imidazole-epichlorohydrin copolymer
[CAS# 68797-57-9]

List of Suppliers
Wuhan Jadechem Chemicals Co., Ltd. China Inquire  
+86 (27) 8355-2071
info@jadechem-intl.com
jhc0005@jadechem.com
Chemical manufacturer since 2000
chemBlink standard supplier since 2007
Langfang GreatAp Chemicals Co., Ltd. China Inquire  
+86 (316) 209-8955
+86 18630626679
sales@grechembld.com
QQ chat
Chemical manufacturer since 2001
chemBlink standard supplier since 2012
Wuhan Surfachem New Material Co., Ltd. China Inquire  
+86 (27) 8393-7661
sale@surfachem.com.cn
Chemical distributor since 2018
chemBlink standard supplier since 2018
Saian Chemical (shanghai) Co., Ltd. China Inquire  
+86 18633110822
teresa.liu@saianchem.com
QQ chat
WeChat: 18633110822
Chemical distributor since 2018
chemBlink standard supplier since 2025
Complete supplier list of Imidazole-epichlorohydrin copolymer
Identification
Classification Catalysts and additives >> Polymer
Name Imidazole-epichlorohydrin copolymer
Synonyms RaluPlate IME; RaluPlate MOME
CAS Registry Number 68797-57-9
EC Number 614-729-2
SMILES ClCC1CO1.c1c[nH]cn1
Safety Data
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Acute toxicityAcute Tox.4H312
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute toxicityAcute Tox.4H302
Acute hazardous to the aquatic environmentAquatic Acute1H400
up Discovory and Applicatios
Imidazole-epichlorohydrin copolymer is a synthetic polymer formed by the reaction of imidazole, a heterocyclic organic compound, with epichlorohydrin, an epoxy compound. This copolymer is commonly used in various industrial and biomedical applications due to its unique properties, which include high chemical stability, water solubility, and the ability to form cross-linked structures.

The synthesis of imidazole-epichlorohydrin copolymer typically involves the reaction of imidazole with epichlorohydrin in the presence of a base, such as sodium hydroxide (NaOH). This reaction leads to the formation of the polymer through a process known as nucleophilic substitution, where the hydroxyl group of epichlorohydrin reacts with the nitrogen atom of imidazole, forming a covalent bond and creating the polymer backbone. The reaction can be carried out under controlled conditions to achieve the desired molecular weight and structure of the copolymer.

One of the key characteristics of imidazole-epichlorohydrin copolymer is its ability to form a cross-linked network when exposed to certain chemical agents or physical conditions. This cross-linking enhances the polymer's stability and strength, making it suitable for use in various applications where durability and resistance to chemical degradation are required. The imidazole groups in the polymer provide a high degree of chemical reactivity, allowing for further modification or functionalization of the polymer structure.

In the biomedical field, imidazole-epichlorohydrin copolymer is used in drug delivery systems, particularly in the design of hydrogels. The copolymer's water-soluble nature and its ability to form networks make it an ideal candidate for controlled drug release applications. The polymer can encapsulate therapeutic agents and release them gradually in response to changes in environmental conditions, such as pH or temperature. This property is particularly useful for targeted drug delivery, where the release of the drug can be controlled to match the needs of the patient.

In addition to its use in drug delivery systems, imidazole-epichlorohydrin copolymer is employed in various other biomedical applications, such as wound dressings and tissue engineering. Its biocompatibility and ability to form hydrogels make it suitable for applications where moisture retention and support for tissue regeneration are important.

The copolymer is also used in water treatment and purification processes. Its functional groups can interact with various contaminants, allowing the polymer to remove impurities from water. This makes it useful in the development of filtration systems, where the copolymer can act as a selective adsorbent for certain types of pollutants, including heavy metals or organic compounds.

Imidazole-epichlorohydrin copolymer also finds applications in the textile industry. Its ability to form films and coatings makes it suitable for use in the production of fabrics with specific properties, such as water resistance or antimicrobial activity. The copolymer can be applied to textiles as a coating, providing enhanced durability and functionality to the fabric.

In addition to its industrial and biomedical applications, imidazole-epichlorohydrin copolymer has potential use in catalysis and sensors. The imidazole groups in the polymer structure can act as active sites for catalysis, enabling the polymer to be used in various chemical reactions. Furthermore, the copolymer can be designed to interact with specific analytes, making it useful in the development of sensors for detecting gases or chemicals in the environment.

Despite its many beneficial properties, imidazole-epichlorohydrin copolymer must be handled with care, especially in its raw form. Epichlorohydrin, a component of the copolymer, is a toxic and potentially carcinogenic substance. Proper safety protocols should be followed during the synthesis and handling of the copolymer to minimize exposure to harmful chemicals.

In conclusion, imidazole-epichlorohydrin copolymer is a versatile material with a wide range of applications in industries such as medicine, water treatment, textiles, and catalysis. Its ability to form cross-linked networks and respond to environmental stimuli makes it a valuable material for controlled drug release, tissue engineering, and various other applications. However, care must be taken in its handling and synthesis to ensure safety due to the toxic nature of one of its components, epichlorohydrin.
Market Analysis Reports
List of Reports Available for Imidazole-epichlorohydrin copolymer
Related Products
1H-Imidazole-1-carboxaldehyde  Imidazole-2-carboxaldehyde  Imidazole-4-carboxamide  1H-Imidazole-4-carboxylic acid  1H-Imidazole-2-carboxylic acid  1H-Imidazole-2-carboxylic acid methyl ester  1H-Imidazole-4-carboxylic acid methyl ester monohydrochloride  1H-Imidazole-1,2-diamine  4,5-Imidazoledicarboxylic acid  1H-Imidazole-4,5-dimethanol  1H-Imidazole-1-ethanamine  1H-Imidazole-1-ethanamine monohydrochloride  Imidazole hydrochloride  Imidazole hydroiodide  Imidazole ketone erastin  L-beta-Imidazolelactic acid  1H-Imidazole-4-methanamine dihydrochloride  1H-Imidazole-2-methanol  Imidazole-4-methanol  4-Imidazolemethanol hydrochloride