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3-Decyl-1-methyl-1H-imidazolium nitrate is a versatile ionic liquid belonging to the imidazolium family, characterized by a long decyl chain attached to the imidazolium ring. This unique structure endows it with distinctive solubility and chemical properties, making it a valuable component in a range of applications across chemical, industrial, and biomedical fields.

1057409-91-2

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1057409-91-2 Usage

Uses

Used in Chemical and Industrial Applications:
3-Decyl-1-methyl-1H-imidazolium nitrate is used as a solvent, electrolyte, or catalyst in various chemical processes and industrial applications. Its unique properties, such as low melting point, high thermal stability, and non-flammability, make it an ideal candidate for tasks requiring a stable and efficient medium.
Used in Organic Synthesis:
In the field of organic synthesis, 3-Decyl-1-methyl-1H-imidazolium nitrate is employed as a green solvent, offering an environmentally friendly alternative to traditional volatile organic compounds. Its ability to dissolve a wide range of organic compounds and its tunable properties through structural modifications make it a promising choice for various chemical reactions.
Used in Electrochemistry:
3-Decyl-1-methyl-1H-imidazolium nitrate is utilized as an electrolyte in electrochemical processes, such as batteries and fuel cells. Its high ionic conductivity and wide electrochemical window contribute to improved performance and stability in these applications.
Used in Material Science:
In material science, 3-Decyl-1-methyl-1H-imidazolium nitrate is used as a component in the development of new materials with tailored properties. Its ability to form self-assembled structures and its compatibility with various materials make it a valuable building block for creating innovative materials with applications in areas such as sensors, coatings, and nanotechnology.
Used in Biomedical Research:
3-Decyl-1-methyl-1H-imidazolium nitrate has attracted attention in biomedical research due to its potential antimicrobial and anticancer properties. Its ability to disrupt bacterial cell membranes and inhibit the growth of cancer cells makes it a subject of interest for the development of new therapeutic agents and antimicrobial strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 1057409-91-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,7,4,0 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1057409-91:
(9*1)+(8*0)+(7*5)+(6*7)+(5*4)+(4*0)+(3*9)+(2*9)+(1*1)=152
152 % 10 = 2
So 1057409-91-2 is a valid CAS Registry Number.

1057409-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Decyl-1-Methyl-1H-Imidazolium Nitrate

1.2 Other means of identification

Product number -
Other names 1-Decyl-3-methyl-1H-imidazol-3-ium nitrate

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:1057409-91-2 SDS

1057409-91-2Downstream Products

1057409-91-2Relevant articles and documents

Anion effects on ionogel formation in N,N′-dialkylimidazolium-based ionic liquids

Firestone, Millicent A.,Rickert, Paul G.,Seifert, S?nke,Dietz, Mark L.

, p. 3991 - 3998 (2004)

Addition of an appropriate concentration of water to either 1-decyl-3-methylimidazolium bromide or its nitrate analog is shown to trigger the self-assembly of the ionic liquid (IL) and the concomitant formation of gel ( ionogel ) phases adopting a rich variety of structural motifs. Infrared and 1H nuclear magnetic resonance studies indicate that water addition disrupts hydrogen bonding between the imidazolium ring and the IL anion, and that gelation involves the partial replacement of these bonds with H-bonds between the anion and water. Using small angle X-ray scattering, the relationship of the water content and the nature of the IL anion to the mesoscopic structure of the ionogels has been determined. Of particular note is the observation that by adjustment of the ionogel composition (water content or anion), near-monodomain materials can be formed with either lamellar, 2-D hexagonal or 3-D cubic structures with tunable lattice dimensions.

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