Molecule:100505: Difference between revisions
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{{Molecule | {{Molecule | ||
|abbrev=TEA | |abbrev=TEA | ||
|trivialname= | |trivialname=TRIETHYLAMINE | ||
|cid=8471 | |cid=8471 | ||
|iupacName= | |iupacName=N,N-diethylethanamine | ||
|molecularMass=101.120449483 | |molecularMass=101.120449483 | ||
|molecularFormula=C<sub>6</sub>H<sub>15</sub>N | |molecularFormula=C<sub>6</sub>H<sub>15</sub>N | ||
|logP=1.4 | |logP=1.4 | ||
|synonyms= | |synonyms=TRIETHYLAMINE$N,N-Diethylethanamine$Ethanamine, N,N-diethyl-$(Diethylamino)ethane$Triethylamin$triethyl amine$Triaethylamin$Trietilamina$N,N,N-Triethylamine$NEt3$trietylamine$tri-ethyl amine$UNII-VOU728O6AY$(C2H5)3N$MFCD00009051$N,N-diethyl-ethanamine$VOU728O6AY$CHEBI:35026$Diethylaminoethane$Triethylamine, >=99.5%$Triaethylamin [German]$Trietilamina [Italian]$CCRIS 4881$HSDB 896$Et3N$TEN [Base]$EINECS 204-469-4$UN1296$triehtylamine$triehylamine$trieihylamine$triethlyamine$triethyamine$TRIETHYLAMINE 100ML$triethylamme$triethylarnine$Thethylamine$Triethlamine$triethyIamine$Triethylannine$tri-ethylamine$triehyl amine$triethyl amin$triethylam ine$triethylami-ne$triethylamine-$trietyl amine$tri ethyl amine$triethyl- amine$AI3-15425$Green Tea 95%$N, N-diethylethanamine$Green Tea PE 50%$Green Tea PE 90%$N,N,N-Triethylamine #$triethylamine, 99.5%$Triethylamine, >=99%$Triethylamine [UN1296] [Flammable liquid]$DSSTox_CID_4366$EC 204-469-4$N(Et)3$DSSTox_RID_77381$NCIOpen2_006503$DSSTox_GSID_24366$BIDD:ER0331$Triethylamine (Reagent Grade)$Triethylamine, LR, >=99%$(CH3CH2)3N$CHEMBL284057$N(CH2CH3)3$Green Tea Extract (50/30)$Green Tea Extract (90/40)$DTXSID3024366$Triethylamine, HPLC, 99.6%$Triethylamine, p.a., 99.0%$Green Tea Extract 50% Material$Triethylamine, analytical standard$ADAL1185352$BCP07310$N(C2H5)3$Triethylamine, for synthesis, 99%$ZINC1242720$Tox21_200873$Triethylamine, 99.7%, extra pure$GREEN TEA Powder & Powder Extract$STL282722$AKOS000119998$Triethylamine, purum, >=99% (GC)$Triethylamine, ZerO2(TM), >=99%$ZINC112977393$UN 1296$NCGC00248857-01$NCGC00258427-01$Triethylamine 100 microg/mL in Methanol$CAS-121-44-8$Triethylamine, BioUltra, >=99.5% (GC)$Triethylamine, SAJ first grade, >=98.0%$FT-0688146$T0424$Triethylamine 100 microg/mL in Acetonitrile$Triethylamine [UN1296] [Flammable liquid]$Triethylamine, trace metals grade, 99.99%$Triethylamine, SAJ special grade, >=98.0%$Triethylamine, puriss. p.a., >=99.5% (GC)$Q139199$J-004499$J-525077$F0001-0344$Triethylamine, for amino acid analysis, >=99.5% (GC)$Z137796018$Triethylamine, for protein sequence analysis, ampule, >=99.5% (GC)$Triethylamine, United States Pharmacopeia (USP) Reference Standard | ||
|cas=121-44-8 | |cas=121-44-8 | ||
|hasVendors=true | |hasVendors=true | ||
Revision as of 17:01, 3 May 2024
| Properties | |
|---|---|
| CID | 8471 |
| CAS | 121-44-8 |
| IUPAC-Name | N,N-diethylethanamine |
| Abbreviation | TEA |
| Trivialname | TRIETHYLAMINE |
| Exact mass | 101.120449483 |
| Molecular formula | C6H15N |
| LogP | 1.4 |
| Has vendors | true |
| Molecular role | n/a |
| Synonyms | TRIETHYLAMINE, N,N-Diethylethanamine, Ethanamine, N,N-diethyl-, (Diethylamino)ethane, Triethylamin, triethyl amine, Triaethylamin, Trietilamina, N,N,N-Triethylamine, NEt3, trietylamine, tri-ethyl amine, UNII-VOU728O6AY, (C2H5)3N, MFCD00009051, N,N-diethyl-ethanamine, VOU728O6AY, CHEBI:35026, Diethylaminoethane, Triethylamine, >=99.5%, [[Synonym::Triaethylamin [German]]], [[Synonym::Trietilamina [Italian]]], CCRIS 4881, HSDB 896, Et3N, [[Synonym::TEN [Base]]], EINECS 204-469-4, UN1296, triehtylamine, triehylamine, trieihylamine, triethlyamine, triethyamine, TRIETHYLAMINE 100ML, triethylamme, triethylarnine, Thethylamine, Triethlamine, triethyIamine, Triethylannine, tri-ethylamine, triehyl amine, triethyl amin, triethylam ine, triethylami-ne, triethylamine-, trietyl amine, tri ethyl amine, triethyl- amine, AI3-15425, Green Tea 95%, N, N-diethylethanamine, Green Tea PE 50%, Green Tea PE 90%, N,N,N-Triethylamine #, triethylamine, 99.5%, Triethylamine, >=99%, [[Synonym::Triethylamine [UN1296] [Flammable liquid]]], DSSTox_CID_4366, EC 204-469-4, N(Et)3, DSSTox_RID_77381, NCIOpen2_006503, DSSTox_GSID_24366, BIDD:ER0331, Triethylamine (Reagent Grade), Triethylamine, LR, >=99%, (CH3CH2)3N, CHEMBL284057, N(CH2CH3)3, Green Tea Extract (50/30), Green Tea Extract (90/40), DTXSID3024366, Triethylamine, HPLC, 99.6%, Triethylamine, p.a., 99.0%, Green Tea Extract 50% Material, Triethylamine, analytical standard, ADAL1185352, BCP07310, N(C2H5)3, Triethylamine, for synthesis, 99%, ZINC1242720, Tox21_200873, Triethylamine, 99.7%, extra pure, GREEN TEA Powder & Powder Extract, STL282722, AKOS000119998, Triethylamine, purum, >=99% (GC), Triethylamine, ZerO2(TM), >=99%, ZINC112977393, UN 1296, NCGC00248857-01, NCGC00258427-01, Triethylamine 100 microg/mL in Methanol, CAS-121-44-8, Triethylamine, BioUltra, >=99.5% (GC), Triethylamine, SAJ first grade, >=98.0%, FT-0688146, T0424, Triethylamine 100 microg/mL in Acetonitrile, [[Synonym::Triethylamine [UN1296] [Flammable liquid]]], Triethylamine, trace metals grade, 99.99%, Triethylamine, SAJ special grade, >=98.0%, Triethylamine, puriss. p.a., >=99.5% (GC), Q139199, J-004499, J-525077, F0001-0344, Triethylamine, for amino acid analysis, >=99.5% (GC), Z137796018, Triethylamine, for protein sequence analysis, ampule, >=99.5% (GC), Triethylamine, United States Pharmacopeia (USP) Reference Standard |
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Molecule is used on following pages
topic
- Photocatalytic CO2 conversion to CO
- Homogeneous photocatalytic CO2 conversion
- Photocatalytic CO2 conversion to HCOOH
- Photocatalytic CO2 conversion to CH4
publication
- Visible light driven reduction of CO2 catalyzed by an abundant manganese catalyst with zinc porphyrin photosensitizer
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production
- Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction
- Visible-Light Photoredox Catalysis: Selective Reduction of Carbon Dioxide to Carbon Monoxide by a Nickel N-Heterocyclic Carbene–Isoquinoline Complex
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers
- Water-Assisted Highly Efficient Photocatalytic Reduction of CO2 to CO with Noble Metal-Free Bis(terpyridine)iron(II) Complexes and an Organic Photosensitizer
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2
- Merging an organic TADF photosensitizer and a simple terpyridine–Fe(iii) complex for photocatalytic CO2 reduction
- Selective and Efficient Photocatalytic CO2 Reduction to CO Using Visible Light and an Iron-Based Homogeneous Catalyst
- Molecular Catalysis of the Electrochemical and Photochemical Reduction of CO2 with Earth-Abundant Metal Complexes. Selective Production of CO vs HCOOH by Switching of the Metal Center
- Visible-light-driven methane formation from CO2 with a molecular iron catalyst
- Light-Driven Reduction of CO2 to CO in Water with a Cobalt Molecular Catalyst and an Organic Sensitizer
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst
- Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis
- Durable Solar-Powered Systems with Ni-Catalysts for Conversion of CO2 or CO to CH4
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction
investigation
- Visible light driven reduction of CO2 catalyzed by an abundant manganese catalyst with zinc porphyrin photosensitizer/Table 1
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production/Table 1
- Light-Driven Reduction of CO2 to CO in Water with a Cobalt Molecular Catalyst and an Organic Sensitizer/Photocatalytic CO2 Reduction by 1 (2 μM) in CO2-Saturated Aqueous CH3CN Solutions
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers/Optimizations of the conditions
- Molecular Catalysis of the Electrochemical and Photochemical Reduction of CO2 with Earth-Abundant Metal Complexes. Selective Production of CO vs HCOOH by Switching of the Metal Center/Table 1
- Visible-Light Photoredox Catalysis: Selective Reduction of Carbon Dioxide to Carbon Monoxide by a Nickel N-Heterocyclic Carbene–Isoquinoline Complex/Table 1
- Visible-light-driven methane formation from CO2 with a molecular iron catalyst/Table 1
- Visible-light-driven methane formation from CO2 with a molecular iron catalyst/Table 2 CO gas
- Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis/Photocatalytic reduction of CO2: conditions optimization
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst/Photocatalytic reduction of CO2
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst/Photocatalytic reduction of CO
- Water-Assisted Highly Efficient Photocatalytic Reduction of CO2 to CO with Noble Metal-Free Bis(terpyridine)iron(II) Complexes and an Organic Photosensitizer/photocatalytic CO2 conversion
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Effect of proton donor
- Merging an organic TADF photosensitizer and a simple terpyridine–Fe(iii) complex for photocatalytic CO2 reduction/photocatalytic reduction of CO2 to CO
- Selective and Efficient Photocatalytic CO2 Reduction to CO Using Visible Light and an Iron-Based Homogeneous Catalyst/photocatalytic conversion of CO2 to CO
- Durable Solar-Powered Systems with Ni-Catalysts for Conversion of CO2 or CO to CH4/Results for different electron donors and proton donors
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 Conversion with Co catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 conversion with Co catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Table 2 Co catalyst testing
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/testtest2
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results obtained with Co2+ catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/results CO2+ experiments
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/CO2+ results from SI
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results Co2+ experiments taken from SI
other
