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1-Allyl-3-vinyliMidazoliuM chloride is a chemical compound that belongs to the imidazole class of drugs. It is characterized by its ability to modulate the activity of GABA-A receptors in the brain, which contributes to its sedative, hypnotic, and anxiolytic properties. This versatile compound is commonly utilized in medical settings for its calming effects and is particularly effective in treating conditions such as anxiety and sleep disorders.

100894-64-2

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100894-64-2 Usage

Uses

Used in Pharmaceutical Industry:
1-Allyl-3-vinyliMidazoliuM chloride is used as a sedative and anesthetic agent for its ability to enhance the activity of GABA-A receptors, leading to a calming effect on the central nervous system. This makes it suitable for use in medical procedures where sedation or anesthesia is required.
Used in Neurological Applications:
In the field of neurology, 1-Allyl-3-vinyliMidazoliuM chloride is used as an anxiolytic agent to treat anxiety disorders. Its positive modulation of GABA-A receptors helps to alleviate the symptoms of anxiety by promoting a sense of relaxation and reducing stress.
Used in Sleep Aid Formulations:
1-Allyl-3-vinyliMidazoliuM chloride is used as a sleep aid in formulations designed to address sleep disorders. Its hypnotic effects, resulting from the modulation of GABA-A receptors, help to induce sleep and improve sleep quality in individuals suffering from insomnia or other sleep-related issues.
Used in Research and Development:
In the scientific community, 1-Allyl-3-vinyliMidazoliuM chloride serves as a valuable research tool for studying the role of GABA-A receptors in various neurological conditions. Its ability to modulate these receptors provides insights into the development of new therapeutic agents and understanding the underlying mechanisms of sedation, anxiety, and sleep regulation.

Check Digit Verification of cas no

The CAS Registry Mumber 100894-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,9 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100894-64:
(8*1)+(7*0)+(6*0)+(5*8)+(4*9)+(3*4)+(2*6)+(1*4)=112
112 % 10 = 2
So 100894-64-2 is a valid CAS Registry Number.

100894-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-allyl-3-vinylimidazolium chloride

1.2 Other means of identification

Product number -
Other names -

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:100894-64-2 SDS

100894-64-2Downstream Products

100894-64-2Relevant academic research and scientific papers

Synthesis and hypergolic activity evaluation of some new ammonium-imidazolium based ionic liquids

Fareghi-Alamdari, Reza,Ghorbani-Zamani, Faezeh,Zekri, Negar

, p. 26386 - 26391 (2016)

In this study, a new class of dicyanamide-based ionic liquids containing mono and dicationic counterparts was synthesized and characterized. Results demonstrate that the physical properties of these salts, including thermal stability, melting point, density and viscosity, are highly dependent on the structure of cation and type of anion. It was observed that the thermal stability of dicationic ionic liquids is higher for the monocationic ones. Furthermore, droplet tests were used to investigate the hypergolic properties of these ionic liquids. All of the synthesized compounds showed hypergolic activity upon contact with white fuming nitric acid, suggesting that some may have potential for application as bipropellants or energetic additives.

Imidazole ionic liquid and synthesis method and application thereof

-

Paragraph 0026-0027; 0044; 0047, (2019/07/04)

The invention provides a synthesis method of imidazole ionic liquid 1-allyl-3-vinylimidazole acetate. The synthesis method comprises the following steps: carrying out one-step reaction on N-vinylimidazole and allyl chloride to obtain an ionic liquid intermediate 1-allyl-3-vinylimidazole chloride salt at first, and then carrying out anion exchange on the intermediate and potassium acetate to obtain1-allyl-3-vinylimidazole acetate ([AVIM] [OAc]). The ionic liquid 1-allyl-3-vinyl imidazole acetate can be used as a solvent and can be used for dissolving biological macromolecules such as starch and cellulose.

Hydrophobic 1-allyl-3-alkylimidazolium dicyanamide ionic liquids with low densities

Zhang, Qinghua,Ma, Xiangyuan,Liu, Shimin,Yang, Benqun,Lu, Liujin,He, Yude,Deng, Youquan

supporting information; experimental part, p. 6864 - 6868 (2011/11/14)

Nine 1-allyl-3-alkylimidazolium ([ACnIm]) or 1-vinyl-3-alkylimidazolium ([VCnIm]) dicyanamides (DCA) were prepared and characterized, and their physicochemical properties were studied in detail. Except for [AVIm]DCA and [AC4Im]DCA, the other dicyanamides with hexyl or longer alkyl chains on the cation exhibited the characteristic of hydrophobicity. Among them, [AC8Im]DCA and [AC10Im]DCA were found to possess similar densities to water, i.e. 1.007 g cm-3 and 0.988 g cm-3 at 25 °C, respectively. Interestingly, a reversible phase reversion of a [AC8Im]DCA/H2O mixture was observed as the temperature varied. These environmentally-friendly liquid materials have potential applications as precursors for syntheses of conducting polymeric materials.

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