8.18839
Tetra-n-butylammonium bromide
より環境に優しい選択肢
for synthesis
別名:
Tetra-n-butylammonium bromide, TBAB
ログインで組織・契約価格をご覧ください。
サイズを選択してください
表示を変更する
この商品について
化学式:
(CH3CH2CH2CH2)4NBr
CAS番号:
分子量:
322.37
UNSPSC Code:
12352107
EC Index Number:
216-699-2
NACRES:
NA.22
MDL number:
Quality Segment
form
crystals
greener alternative product characteristics
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
mp
100-103 °C
solubility
600 g/L
density
1.15 g/cm3
bulk density
700 kg/m3
greener alternative category
storage temp.
2-30°C
SMILES string
[Br-].[N+](CCCC)(CCCC)(CCCC)CCCC
InChI
1S/C16H36N.BrH/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H/q+1;/p-1
InChI key
JRMUNVKIHCOMHV-UHFFFAOYSA-M
General description
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalysis. Click here for more information.
Application
- Cobalt-based MOF Nanoribbons: Tetra-n-butylammonium bromide is utilized in the synthesis of cobalt-based metal-organic framework (MOF) nanoribbons, which are applied for the cycloaddition of carbon dioxide to epoxides. This process is crucial for carbon capture and utilization, demonstrating the compound′s role in green chemistry solutions (Ullah et al., 2022).
- Phosphate Removal: In environmental applications, Tetra-n-butylammonium bromide is incorporated into polyacrylonitrile composite nanofibers to enhance the removal of phosphate from water, showcasing its utility in water treatment technologies (Wang et al., 2021).
- Iron(III) Spin-crossover Compounds: This quaternary ammonium salt is used in the synthesis of a rare octacoordinated mononuclear iron(III) compound with spin-crossover properties. This application is significant in materials science, particularly in the development of magnetic materials and sensors (Hao et al., 2020).
- Protein Extraction Technologies: Its application extends to the enrichment and extraction of hydrophobic proteins using fluoroalcohol-induced coacervates. This technique is vital for biochemical research and the pharmaceutical industry, where efficient isolation and purification of proteins are essential (Koolivand et al., 2018).
Analysis Note
Assay (argentometric): ≥ 99.0 %
Identity (IR): passes test
Identity (IR): passes test
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2
保管分類
11 - Combustible Solids
wgk
WGK 3
