56776
Trihexyltetradecylphosphonium dicyanamide
≥95% (qNMR)
Synonym(s):
Tetradecyltrihexylphosphonium dicyanamide
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About This Item
Linear Formula:
[CH3(CH2)5]3P[N(CN)2](CH2)13CH3
CAS Number:
Molecular Weight:
549.90
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
≥95% (qNMR)
density
0.90 g/mL at 20 °C (lit.)
functional group
amine
phosphine
SMILES string
N#C[N-]C#N.CCCCCCCCCCCCCC[P+](CCCCCC)(CCCCCC)CCCCCC
InChI
1S/C32H68P.C2N3/c1-5-9-13-17-18-19-20-21-22-23-24-28-32-33(29-25-14-10-6-2,30-26-15-11-7-3)31-27-16-12-8-4;3-1-5-2-4/h5-32H2,1-4H3;/q+1;-1
InChI key
DOMOOBQQQGXLGU-UHFFFAOYSA-N
Application
Trihexyltetradecylphosphonium dicyanamide is an ionic liquid that can be used:
- As an extraction solvent for the separation of organic compounds.
- In the experiment to study the solubility of carbon dioxide and binary gas mixtures in ionic liquids.
- To prepare hybrid ionogels having electrochemical applications.
- As a solvent for the extraction of aromatics from pyrolytic sugars.
Caution
may become slightly turbid on storage
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Solubility of CO2/CH4 gas mixtures in ionic liquids
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Application of trihexyltetradecylphosphonium dicyanamide ionic liquid for various types of separations problems: Activity coefficients at infinite dilution measurements utilizing GLC method
Kabane B and Redhi GG
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Journal of Materials Chemistry, 21(24), 8687-8693 (2011)
Xiaohua Li et al.
Bioresource technology, 216, 12-18 (2016-05-24)
Fermentative bioethanol production from pyrolytic sugars was improved via aromatics removal by liquid-liquid extraction. As solvents, the ionic liquid (IL) trihexyltetradecylphosphonium dicyanamide (P666,14[N(CN)2]) and ethyl acetate (EA) were compared. Two pyrolytic sugar solutions were created from acid-leached and untreated pinewood
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