Chemistry:7-Methyl-1,5,7-triazabicyclo(4.4.0)dec-5-ene
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dec-5-ene.svg)
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| Names | |
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| Preferred IUPAC name
1-Methyl-2,3,4,6,7,8-hexahydro-1H-pyrimido[1,2-a]pyrimidine | |
| Other names
mTBD; 7-Methyl-TBD; 7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene; 1,3,4,6,7,8-Hexahydro-1-methyl-2H-pyrimido[1,2-a]pyrimidine
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C8H15N3 | |
| Molar mass | 153.225 g/mol |
| Appearance | clear liquid[2] |
| Density | 1063.35 kg/m3[2] |
| Melting point | 17[2] °C (63 °F; 290 K) |
| Boiling point | 263[2] °C (505 °F; 536 K) |
| Thermal conductivity | 0.144 W/m/K[2] |
Refractive index (nD)
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1.5357[2] |
| Viscosity | 7.1 cP[2] |
| Hazards | |
| GHS pictograms | 
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| GHS Signal word | Danger |
| H314 | |
| P260, P264, P280, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P405, P501 | |
| Thermochemistry | |
Heat capacity (C)
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1.75 J/g/K[2] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 (what is   ?)
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| Infobox references | |
7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (mTBD) is a bicyclic strong guanidine base (pKa = 25.43 in CH3CN and pKa = 17.9 in THF).[3] mTBD, like 1,5,7-triazabicyclo[4.4.0]dec-5-ene and other guanidine super bases, can be used as a catalyst in a variety of chemical reactions.[4] It also reacts with CO2,[5] which could make it useful for carbon capture and storage.[6]
When brought into contact with some acids, mTBD reacts to form an ionic liquid. Some of these ionic liquids can dissolve cellulose.[7]
References
- ↑ 7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene at PubChem
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 Baird, Zachariah Steven; Dahlberg, Artur; Uusi-Kyyny, Petri; Osmanbegovic, Nahla; Witos, Joanna; Helminen, Jussi; Cederkrantz, Daniel; Hyväri, Paulus et al. (2019). "Physical properties of 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (mTBD)". International Journal of Thermophysics 40 (71): 1. doi:10.1007/s10765-019-2540-2. Bibcode: 2019IJT....40...71B.
- ↑ Ishikawa, T. (2009). Superbases for Organic Synthesis: Guanidines, Amidines, Phosphazenes and Related Organocatalysts. John Wiley & Sons. ISBN 9780470740866.
- ↑ Simoni, D.; Rondanin, R.; Morini, M.; Baruchello, R.; Invidiata, F. P. (2000). "1,5,7- Triazabicyclo[4.4.0]Dec-1-Ene (TBD), 7-Methyl-TBD (MTBD) and the PolymerSupported TBD (P-TBD): Three Efficient Catalysts for the Nitroaldol (Henry) Reaction and for the Addition of Dialkyl Phosphites to Unsaturated Systems". Tetrahedron Lett. 41 (10): 1607–1610. doi:10.1016/S0040-4039(99)02340-0.
- ↑ Villiers, Claude; Dognon, Jean-Pierre; Pollet, Rodolphe; Thuéry, Pierre; Ephritikhine, Michel (3 May 2010). "An Isolated CO2 Adduct of a Nitrogen Base: Crystal and Electronic Structures". Angewandte Chemie International Edition 49 (20): 3465–3468. doi:10.1002/anie.201001035. PMID 20358577.
- ↑ Yang, Z.-Z.; Zhao, Y.-N.; He, L.-N. (2011). "CO2 Chemistry: Task-Specific Ionic Liquids for CO2 Capture/ Activation and Subsequent Conversion". RSC Adv. 1 (4): 545–567. doi:10.1039/C1RA00307K. Bibcode: 2011RSCAd...1..545Y.
- ↑ Parviainen, A.; King, A. W. T.; Mutikainen, I.; Hummel, M.; Selg, C.; Hauru, L. K. J.; Sixta, H.; Kilpeläinen, I. (2013). "Predicting Cellulose Solvating Capabilities of Acid–Base Conjugate Ionic Liquids". ChemSusChem 6 (11): 2161–2169. doi:10.1002/cssc.201300143. PMID 24106149. Bibcode: 2013ChSCh...6.2161P.
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