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33529-02-1

  • Product Name1-decyl-1H-imidazole
  • Molecular FormulaC13H24 N2
  • Molecular Weight208.347
  • Purity99%
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Product Details

Quick Details

  • CasNo: 33529-02-1
  • Molecular Formula: C13H24 N2
  • Purity: 99%

Cost-effective and customizable 1-decyl-1H-imidazole 33529-02-1 factory

  • Molecular Formula:C13H24 N2
  • Molecular Weight:208.347
  • Vapor Pressure:0.000257mmHg at 25°C 
  • Boiling Point:333.9°Cat760mmHg 
  • PKA:7.09±0.10(Predicted) 
  • Flash Point:155.7°C 
  • PSA:17.82000 
  • Density:0.91g/cm3 
  • LogP:4.02380 

1-decyl-1H-imidazole(Cas 33529-02-1) Usage

General Description

1-Decyl-1H-Imidazole is a chemical compound belonging to the class of organic compounds known as imidazoles. This type of compounds contains an imidazole ring, which is an unsaturated five-member ring structure with two nitrogen atoms and three carbon atoms. Imidazoles are regarded as fundamental units of various natural products and pharmaceuticals. The 1-Decyl-1H-Imidazole, specifically, is typically used in commercial applications and industrial products. However, detailed safety and toxicity information regarding its prolonged usage remain undisclosed due to limited studies.

InChI:InChI=1/C13H24N2/c1-2-3-4-5-6-7-8-9-11-15-12-10-14-13-15/h10,12-13H,2-9,11H2,1H3

33529-02-1 Relevant articles

Imidazolium-based zwitterionic surfactants: Characterization of normal and reverse micelles and stabilization of nanoparticles

Souza, Franciane D.,Souza, Bruno S.,Tondo, Daniel W.,Leopoldino, Elder C.,Fiedler, Haidi D.,Nome, Faruk

, p. 3587 - 3595 (2015)

This paper presents the physicochemical ...

Ordered, microphase-separated, noncharged-charged diblock copolymers via the sequential ATRP of styrene and styrenic imidazolium monomers

Shi, Zhangxing,Newell, Brian S.,Bailey, Travis S.,Gin, Douglas L.

, p. 6664 - 6671 (2014)

A series of imidazolium-based noncharged...

Synthesis of a novel alkylimidazolium iodide containing an amide group for electrolyte of dye-sensitized solar cells

Jeon, Seung-Hwan,Priya, A.R. Sathiya,Kang, Eun-Ji,Kim, Kang-Jin

, p. 5652 - 5658 (2010)

A novel alkylimidazolium iodide containi...

Influence of dlutaraldehyde cross-linking modes on the recyclability of immobilized lipase b from candida antarctica for transesterification of soy bean oil

Modenez, Iago A.,Sastre, Diego E.,Moares, Fernando C.,Marques Netto, Caterina G.C.

, (2018)

Lipase B from Candida antarctica (CAL-B)...

Crystallographic and spectroscopic analysis of 9,10-bis-alkyl imidazolium anthracene hexatungstate supramolecular complexes

Annapareddy, Gayatri,Mubeena, Shaik,N, Meghana,Sarma, Monima

, (2021)

This article describes the ionic and sup...

A Remarkable Fluorescence Quenching Based Amplification in ATP Detection through Signal Transduction in Self-Assembled Multivalent Aggregates

Biswas, Rakesh,Naskar, Sumit,Ghosh, Surya,Das, Mousumi,Banerjee, Supratim

supporting information, p. 13595 - 13600 (2020/10/06)

Signal transduction is essential for the...

Inhibition of bacterial growth and galactosyltransferase activity of WbwC by α, ω-bis(3-alkyl-1H-imidazolium)alkane salts: Effect of varying carbon content

Brockhausen, Inka,Kocev, Alexander,Kong, Xianqi,Melamed, Jacob,Szarek, Walter A.,Vlahakis, Jason Z.,Wang, Shuo,Xu, Yaozu

, (2020/04/21)

A series of compounds was designed and s...

Synthesis and Antibacterial Evaluation of Bis-thiazolium, Bis-imidazolium, and Bis-triazolium Derivatives

Thomas, Beno?t,Duval, Rapha?l E.,Fontanay, Stéphane,Varbanov, Mihayl,Boisbrun, Michel

supporting information, p. 1232 - 1237 (2019/06/13)

Given the worldwide spread of bacterial ...

33529-02-1 Process route

1H-imidazole
288-32-4

1H-imidazole

1-bromo dodecane
112-29-8

1-bromo dodecane

1-decylimidazole
33529-02-1

1-decylimidazole

Conditions
Conditions Yield
With sodium hydroxide; In tetrahydrofuran; for 72h; Reflux;
98%
With tetrabutylammomium bromide; potassium carbonate; potassium hydroxide; at 50 ℃; Temperature; Microwave irradiation;
94%
With sodium hydroxide; In dimethyl sulfoxide; at 20 - 25 ℃; Inert atmosphere;
88.3%
1H-imidazole; With sodium hydride; In tetrahydrofuran; mineral oil; at 0 ℃; for 0.5h; Inert atmosphere;
1-bromo dodecane; In tetrahydrofuran; mineral oil; at 20 ℃; Inert atmosphere;
86%
With propan-1-ol; sodium; Heating;
85%
1H-imidazole; With potassium hydroxide; In dimethyl sulfoxide; at 20 ℃; for 2h;
1-bromo dodecane; In dimethyl sulfoxide; for 4h;
81.2%
With potassium hydroxide; In methanol; water; at 90 ℃; for 4h;
80%
1H-imidazole; With sodium hydroxide; In dimethyl sulfoxide; at 20 ℃; for 1.5h;
1-bromo dodecane; In dimethyl sulfoxide; at 20 ℃;
76%
With potassium carbonate; In acetone; for 24h; Reflux;
75%
With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 12h; Inert atmosphere;
71%
With sodium hydroxide; tetrabutylammomium bromide; In toluene; at 60 - 80 ℃; for 3h;
70%
With sodium hydroxide; tetraethylammonium iodide; In toluene; for 10h; Reflux;
64%
With tetraethylammonium iodide; sodium hydroxide; In toluene; for 10h; Reflux;
64%
With tetraethylammonium iodide; sodium hydroxide; In toluene; for 10h; Reflux;
64%
With sodium hydroxide; tetraethylammonium iodide; In toluene; Heating;
63%
With 1.) K; Yield given. Multistep reaction; 1) THF, reflux, 2.) THF, reflux, 16 h;
With sodium hydride; In tetrahydrofuran; for 24h; Heating;
With potassium hydroxide; potassium carbonate; tetrabutylammomium bromide; for 0.0333333h; microwave irradiation;
1H-imidazole; With sodium hydroxide; In tetrahydrofuran; at 60 ℃; for 1h;
1-bromo dodecane; In tetrahydrofuran; at 60 ℃;
1H-imidazole; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 1h;
1-bromo dodecane; With tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; at 20 ℃; for 24h; Inert atmosphere;
With potassium carbonate; In acetone; Reflux;
1H-imidazole; 1-bromo dodecane; In tetrahydrofuran; at 20 ℃; for 48h;
With sodium hydroxide; In tetrahydrofuran; for 12h;
1H-imidazole; With sodium methylate; In methanol;
1-bromo dodecane; In methanol; at 65 ℃; for 6h;
1H-imidazole; With potassium hydroxide; In dimethyl sulfoxide; at 20 ℃; for 0.5h;
1-bromo dodecane; In dimethyl sulfoxide; at 18 ℃;
1H-imidazole; With sodium methylate; for 8h;
1-bromo dodecane; In ethanol; for 48h;
1H-imidazole; With sodium hydride; In 1,4-dioxane; at 90 ℃; for 2h;
1-bromo dodecane; In 1,4-dioxane; at 90 ℃; for 48h;
1H-imidazole; With potassium hydroxide; In dimethyl sulfoxide;
1-bromo dodecane; In dimethyl sulfoxide; at 18 ℃; for 2h;
With potassium carbonate; potassium hydroxide; In acetonitrile; at 80 ℃; for 16h;
With tetraethylammonium iodide; sodium hydroxide; In toluene; for 10h; Reflux;
1H-imidazole; With sodium; In ethanol; for 2h; Reflux; Inert atmosphere;
1-bromo dodecane; In ethanol; for 2h; Reflux; Inert atmosphere;
With sodium hydroxide; In dimethyl sulfoxide; at 20 ℃;
1H-imidazole
288-32-4

1H-imidazole

1-Bromononane
693-58-3

1-Bromononane

1-decylimidazole
33529-02-1

1-decylimidazole

Conditions
Conditions Yield
With potassium carbonate; In acetone; Reflux;
70%

33529-02-1 Upstream products

  • 288-32-4
    288-32-4

    1H-imidazole

  • 1002-69-3
    1002-69-3

    decyl chloride

  • 112-29-8
    112-29-8

    1-bromo dodecane

  • 2050-77-3
    2050-77-3

    Iododecane

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