Molecule:100507
From ChemWiki
molecule
| Properties | |
|---|---|
| CID | 7618 |
| CAS | 102-71-6 |
| IUPAC-Name | 2-[bis(2-hydroxyethyl)amino]ethanol |
| Abbreviation | TEOA |
| Trivialname | TRIETHANOLAMINE |
| Exact mass | 149.10519334 |
| Molecular formula | C6H15NO3 |
| LogP | -1 |
| Has vendors | true |
| Molecular role | n/a |
| Synonyms | TRIETHANOLAMINE, Trolamine, 2,2',2-Nitrilotriethanol, Sterolamide, Tris(2-hydroxyethyl)amine, Daltogen, Nitrilotriethanol, Triethylolamine, Trihydroxytriethylamine, Thiofaco T-35, Triethanolamin, Sting-Kill, Tri(hydroxyethyl)amine, Tris(beta-hydroxyethyl)amine, Ethanol, 2,2',2-nitrilotris-, Nitrilo-2,2',2-triethanol, Sodium ISA, Alkanolamine 244, Teoa, TEA (amino alcohol), 2,2',2-Nitrilotris(ethanol), Nitrilotris(ethanol), [[Synonym::2-[bis(2-hydroxyethyl)amino]ethanol]], Tris(hydroxyethyl)amine, Triethanolamin-NG, H3tea, Triaethanolamin-NG, 2,2',2-Nitrilotriethanol, N(CH2CH2OH)3, Mobisyl, 2,2',2-Nitrilotrisethanol, Trola, Triethanolamine homopolymer, 2,2',2-Trihydroxytriethylamine, Poly(triethanolamine) ether, Trihydroxyethylamine, Trolamine (NF), [[Synonym::Trolamine [NF]]], UNII-9O3K93S3TK, MFCD00002855, NSC 36718, Mobisy (TN), Triethylamine, 2,2',2-trihydroxy-, Triethanolamine condensate polymer, Ethanol, 2,2',2-nitrilotri-, Ethanol, 2,2',2-nitrilotris-, homopolymer, NCIOpen2_004601, 2,2',2"-Nitrilotriethanol, [[Synonym::2-[bis(2-hydroxyethyl)amino]ethan-1-ol]], 9O3K93S3TK, 2,2',2-Nitrilotris(ethanol), CHEBI:28621, [[Synonym::2,2',2-Nitrilotris[ethanol]]], NSC-36718, NCGC00159411-02, DSSTox_CID_1392, Tri-beta-hydroxy Ethylamine, DSSTox_RID_76134, DSSTox_GSID_21392, Caswell No. 886, Biafine, Tris(2-Hydroxyethyl) Amine, [[Synonym::Trolamine [INN]]], CAS-102-71-6, CCRIS 606, HSDB 893, TRIETHANOL AMINE, EINECS 203-049-8, 2,2,2-Nitrilotriethanol, EPA Pesticide Chemical Code 004208, Ethanolamines, 2,2',2'-Nitrilotriethanol, Cerumenex, Alkano, Mobisy, AI3-01140, Ethanol, 2,2',2'-nitrilotris-, Triethanolamine 85%, Triethanolamine 99%, Mobisyl (Salt/Mix), Triethanolamine, USP, Tris(b-hydroxyethyl)amine, 2,2-Nitrilotriethanol, bmse000379, EC 203-049-8, Nitrilo-2,2-triethanol, SCHEMBL1146, Oprea1_614203, tris-(2-hydroxyethyl)-amine, WLN: Q2N2Q2Q, tris(beta -hydroxyethyl)amine, [[Synonym::2,2-Nitrilotris[ethanol]]], BIDD:ER0261, Ethanol,2',2-nitrilotri-, Tris(.beta.-hydroxyethyl)amine, CHEMBL446061, Ethanol,2',2-nitrilotris-, Triethanolamine, LR, >=99%, 2,2',2'-Nitrilotris-Ethanol, 2,2'2-Nitrilotris-Ethanol, 2,2', 2-Nitrilotriethanol, 2,2',2Quot -Nitrilotriethanol, DTXSID9021392, 2,2',2-Nitrilotri-Ethanol, 2,2',2-Nitrilotris-Ethanol, Nitrilo-2,2',2quot -triethanol, Triethanolamine, p.a., 99.0%, Triethanolamine, AR, >=99.5%, ZINC896409, Triethanolamine 99% Reagent Grade, Triethylamine,2',2-trihydroxy-, ADAL1017515, HY-B1809, NSC36718, Tox21_113166, Tox21_202062, Tox21_300527, Triethanolamine, >=99.0% (GC), 2,2',2-Trihydroxy-Triethylamine, STL264185, Triethanolamine, reagent grade, 98%, AKOS000119997, CS-5859, DB13747, 637-39-8 (unspecified hydrochloride), SMP2_000190, TEA, 0.2M buffer solution, pH 7.0, TEA, 0.2M buffer solution, pH 8.0, NCGC00159411-03, NCGC00159411-04, NCGC00159411-05, NCGC00159411-06, NCGC00254460-01, NCGC00259611-01, 7376-31-0 (unspecified sulfate salt), BP-21029, LS-13235, Triethanolamine, USP, 99.0-107.4%, 7376-31-0 (Unspecified sulphate salt), Triethanolamine, BioUltra, >=99.5% (GC), Triethanolamine, analytical reference material, Triethanolamine, SAJ first grade, >=98.0%, C06771, D00215, Triethanolamine, JIS special grade, >=98.0%, Triethanolamine, puriss. p.a., >=99% (GC), Triethanolamine, Vetec(TM) reagent grade, 97%, Q424314, SR-01000944572, J-525067, SR-01000944572-1, B886EF22-ACA3-4597-9C73-A087E02F54A7, Trolamine, European Pharmacopoeia (EP) Reference Standard, Trolamine, United States Pharmacopeia (USP) Reference Standard, Triethanolamine, puriss., meets analytical specification of NF, >=99% (GC), Trolamine, Pharmaceutical Secondary Standard; Certified Reference Material, Triethanolamine, PharmaGrade, USP, Manufactured under appropriate GMP controls for pharma or biopharmaceutical production. |
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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
- Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3
- Visible-Light Photocatalytic Conversion of Carbon Dioxide by Ni(II) Complexes with N4S2 Coordination: Highly Efficient and Selective Production of Formate
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production
- Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands
- Photocatalytic CO2 Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid
- Pyranopterin Related Dithiolene Molybdenum Complexes as Homogeneous Catalysts for CO2 Photoreduction
- New Photosensitizers Based on Heteroleptic Cu(I) Complexes and CO2 Photocatalytic Reduction with (Ni(II)(cyclam))Cl2
- Photocatalytic CO2 Reduction under Visible-Light Irradiation by Ruthenium CNC Pincer Complexes
- Ir(tpy)(bpy)Cl as a Photocatalyst for CO2 Reduction under Visible-Light Irradiation
- Highly efficient and selective visible-light driven CO2-to-CO conversion by a Co-based cryptate in H2O-CH3CN solution
- Photocatalytic CO2 reduction using a Mn complex as a catalyst
- A Dinuclear Cobalt Cryptate as a Homogeneous Photocatalyst for Highly Selective and Efficient Visible-Light Driven CO2 Reduction to CO in CH3CN-H2O Solution
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction
- A Cu(I) Co(II) cryptate for the visible light-driven reduction of CO2
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes
- Light-Driven Reduction of CO2 to CO in Water with a Cobalt Molecular Catalyst and an Organic Sensitizer
- Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst
- Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light
- Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis
investigation
- Visible-Light Photocatalytic Conversion of Carbon Dioxide by Ni(II) Complexes with N4S2 Coordination: Highly Efficient and Selective Production of Formate/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
- Pyranopterin Related Dithiolene Molybdenum Complexes as Homogeneous Catalysts for CO2 Photoreduction/Table 1
- Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH/Table 1
- Photocatalytic CO2 reduction using a Mn complex as a catalyst/Photocatalytic CO2 reduction: conditions optimization
- Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts/Results for photocatalytic reduction of CO2
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3/Table 1
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3/Table 2
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Control experiments
- Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts/Durability test
- Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis/Photocatalytic reduction of CO2: conditions optimization
- Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction/Table 1
- Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction/Table 2
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst/Photocatalytic reduction of CO
- Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light/Table 1
- Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light/Table 2
- Photocatalytic CO2 Reduction under Visible-Light Irradiation by Ruthenium CNC Pincer Complexes/Conditions optimizations for photocatalytic reduction of CO2
- Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands/Table 1
- Ir(tpy)(bpy)Cl as a Photocatalyst for CO2 Reduction under Visible-Light Irradiation/Photoreduction of CO2
- Photocatalytic CO2 Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid/Control experiments
- A Cu(I) Co(II) cryptate for the visible light-driven reduction of CO2/Photocatalytic reduction of CO2
- New Photosensitizers Based on Heteroleptic Cu(I) Complexes and CO2 Photocatalytic Reduction with (Ni(II)(cyclam))Cl2/Photocatalytic CO2 reduction and control experiments
- Photocatalytic Reduction of CO2 by Highly Efficient Homogeneous FeII Catalyst based on 2,6-Bis(1’,2’,3’-triazolyl-methyl)pyridine. Comparison with Analogues./CO2 reduction experiments testing different catalysts
- Photocatalytic Reduction of CO2 by Highly Efficient Homogeneous FeII Catalyst based on 2,6-Bis(1’,2’,3’-triazolyl-methyl)pyridine. Comparison with Analogues./Optimization of CO2 reduction conditions
- Highly efficient and selective visible-light driven CO2-to-CO conversion by a Co-based cryptate in H2O-CH3CN solution/photocatalytic CO2 conversion under different conditions
- A Dinuclear Cobalt Cryptate as a Homogeneous Photocatalyst for Highly Selective and Efficient Visible-Light Driven CO2 Reduction to CO in CH3CN-H2O Solution/Best result and control experiments
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Solvent effect study between DMA DMF and acetonitrile
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Study on the concentration of catalyst
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Time profile in DMF
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Effect of proton donor
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes/Optimizations of conditions for Co(qpy)(H2O)2(ClO4)2 and Ru(bpy)3Cl2
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes/Optimizations of conditions for Fe(qpy)(H2O)2(ClO4)2 and Ru(bpy)3Cl2
- Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light/Optimization of concentrations
- Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light/CO2 reduction experiments
other
