Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504754394 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754394 |
| Sonrisas canónicas | C1CC2=CC=CC=C2NC1 |
| IUPAC Name | 1,2,3,4-tetrahydroquinoline |
| InChIKey | LBUJPTNKIBCYBY-UHFFFAOYSA-N |
| INCHI | 1S/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-2,4,6,10H,3,5,7H2 |
| Isómeros SMILES | C1CC2=CC=CC=C2NC1 |
| WGK Alemania | 3 |
| PubChem CID | 69460 |
| Peso molecular | 133.19 |
| Beilstein | 116149 |
| Reaxy-Rn | 116149 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Quinolines and derivatives |
| Subclass | Hydroquinolines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Hydroquinolines |
| Alternative Parents | Secondary alkylarylamines Aralkylamines Benzenoids Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Tetrahydroquinoline - Aralkylamine - Secondary aliphatic/aromatic amine - Benzenoid - Azacycle - Secondary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as hydroquinolines. These are derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms. |
| External Descriptors | quinolines |
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Dec 10, 2025 | T107484 | |
| Certificate of Analysis | Dec 10, 2025 | T107484 | |
| Certificate of Analysis | Dec 10, 2025 | T107484 | |
| Certificate of Analysis | Mar 04, 2025 | T107484 | |
| Certificate of Analysis | Jul 08, 2024 | T107484 | |
| Certificate of Analysis | Jul 08, 2024 | T107484 | |
| Certificate of Analysis | Jul 08, 2024 | T107484 | |
| Certificate of Analysis | Jan 07, 2022 | T107484 | |
| Certificate of Analysis | Jan 07, 2022 | T107484 |
| Solubilidad | Miscible with alcohol, ether, carbon disulfide and many organic solvents. Slightly miscible with water. |
|---|---|
| Sensibilidad | Heat & Light & Air sensitive |
| Punto de congelación (°C) | 13 °C |
| Índice de refracción | 1.593-1.595 |
| Punto de inflamación (°F) | 213.8 °F |
| Punto de inflamación (°C) | 100°C |
| Punto de ebullición (°C) | 113-117°C |
| Punto de fusión (°C) | 9-14°C |
| Peso molecular | 133.190 g/mol |
| XLogP3 | 2.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 133.089 Da |
| Monoisotopic Mass | 133.089 Da |
| Topological Polar Surface Area | 12.000 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 111.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Wenbin Huang, Qiang Wei, Haoran Liu, Han Yang, Zhen Xu, Zhengyu Chen, Dongdong Chen, Yasong Zhou. (2023) N-N self-inhibition effect of aromatic N-heterocyclic compounds on NiWS supported γ-Al2O3 hydrotreating catalyst. FUEL, [PMID:] [10.1016/j.fuel.2023.130067] |
| 2. Meili Ding, Pan Ma, Yang Wang, Ying Zhang, Jun Liu, Jianfeng Yao. (2023) Hierarchically porous bimetallic oxide derived from a metal-organic framework for the promotion of catalytic CO2 chemical fixation. Journal of Environmental Chemical Engineering, [PMID:] [10.1016/j.jece.2023.111118] |
| 3. Qiu-Yue Cheng, Ting Wang, Jun Hu, Hong-Yuan Chen, Jing-Juan Xu. (2023) In Situ Probing the Short-Lived Intermediates in Visible-Light Heterogeneous Photocatalysis by Mass Spectrometry. ANALYTICAL CHEMISTRY, [PMID:37665645] [10.1021/acs.analchem.3c03494] |
| 4. Hongmei Yang, Menglu Xu, Lili Zhang, Weiwei Fang, E. Liu, Huaxin Zhang. (2023) Hyper-crosslinked polymer derived porous Co@CN catalyst for selective hydrogenation of quinoline. MICROPOROUS AND MESOPOROUS MATERIALS, [PMID:] [10.1016/j.micromeso.2023.112701] |
| 5. Zhou Zhang, Wengang Liu, Yuanyuan Zhang, Jingwen Bai, Jian Liu. (2020) Bioinspired Atomic Manganese Site Accelerates Oxo-Dehydrogenation of N-Heterocycles over a Conjugated Tri-s-Triazine Framework. ACS Catalysis, [PMID:] [10.1021/acscatal.0c04651] |
| 6. Pengbo Wang, Qian He, Hao Zhang, Qingdi Sun, Yujie Cheng, Tao Gan, Xiaohui He, Hongbing Ji. (2020) N-formylation of amines using phenylsilane and CO2 over ZnO catalyst under mild condition. CATALYSIS COMMUNICATIONS, [PMID:] [10.1016/j.catcom.2020.106195] |
| 7. Lingzhi Wang, Yalei Gao, Yuying Chen, Zhenzhou Tang, Xiao Lin, Meng Bai, Pei Cao, Kai Liu. (2025) Discovery of Novel Pyridin-2-yl Urea Inhibitors Targeting ASK1 Kinase and Its Binding Mode by Absolute Protein–Ligand Binding Free Energy Calculations. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 26 (4): (1527). [PMID:40003993] [10.3390/ijms26041527] |
| 8. Zhefei Zhao, Wenjie Yan, Wenbin Zheng, Lipeng Guo, Ruopeng Yu, Minhao Chen, Huajun Zheng. (2025) Heteroatom Introduction and Electrochemical Reconstruction on Heterostructured Co-Based Electrocatalysts for Hydrogenation of Quinolines. Small, [PMID:40079113] [10.1002/smll.202412626] |
| 9. Zhenye Zhang, Shenghan Zhang, Shijie Wang, Xinliang Guo, Zhilin Wang, Yu Tan, KeXin Liang. (2025) Highly efficient electrochemical hydrogenation and dehydrogenation of quinoline catalyzed by a bifunctional RuNi electrode. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, [PMID:] [10.1016/j.ijhydene.2025.03.054] |
| 10. Zhenye Zhang, Shenghan Zhang, Shijie Wang, Yu Tan, Kexin Liang, Xinliang Guo, Xin Zheng. (2025) Quinoline reversible electrochemical hydrogen storage on phosphide transition metal catalysts. Molecular Catalysis, [PMID:] [10.1016/j.mcat.2025.114964] |