1,2,3,4-Tetrahydroquinoline - ≥97% , CAS No.635-46-1

CAS: 635-46-1 Cat. No.: T107484 Peso molecular: 133.19 Beilstein Registry Number: 116149 Número EC: 211-237-6 PubChem CID: 69460
Disponible para pedir
GRADE & PURITY ≥97%
Synonyms
1,2,3,4-tetrahydro quinoline | 1,2,3,4-Tetrahydroquinoline, purum, >=96.0% (GC) | 3,4-dihydro-2H-quinoline | Q21099119 | A8748 | FT-0606201 | AKOS000119058 | T0113 | 1,3,4-Tetrahydroquinoline | NCGC00188132-01 | UNII-CCR50N1Z9G | F2190-0415 | 1,2,3,4-Hydr
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
10g
T107484-10g
1
9,90US$
25g
T107484-25g
3
10,90US$
100g
T107484-100g
3

17,90US$

26,90US$
Guardar 9,00 US$ (33.46%)
500g
T107484-500g
1

79,90US$

119,90US$
Guardar 40,00 US$ (33.36%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
1, 2, 3, 4-tetrahydro quinoline | 1, 2, 3, 4-Tetrahydroquinoline, purum, >=96.0% (GC) | 3, 4-dihydro-2H-quinoline | Q21099119 | A8748 | FT-0606201 | AKOS000119058 | T0113 | 1, 3, 4-Tetrahydroquinoline | NCGC00188132-01 | UNII-CCR50N1Z9G | F2190-0415 | 1, 2, 3, 4-Hydr
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥97%
Nombres e identificadores
Pubchem Sid504754394
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504754394
Sonrisas canónicasC1CC2=CC=CC=C2NC1
IUPAC Name1,2,3,4-tetrahydroquinoline
InChIKeyLBUJPTNKIBCYBY-UHFFFAOYSA-N
INCHI1S/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

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseQuinolines and derivatives
SubclassHydroquinolines
Intermediate Tree Nodes Not available
Direct ParentHydroquinolines
Alternative Parents Secondary alkylarylamines  Aralkylamines  Benzenoids  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate TypeFechaArticulo
B2219495Certificate of AnalysisDec 10, 2025 T107484
B2219496Certificate of AnalysisDec 10, 2025 T107484
B2219511Certificate of AnalysisDec 10, 2025 T107484
F2101306Certificate of AnalysisMar 04, 2025 T107484
K2420537Certificate of AnalysisJul 08, 2024 T107484
K2420538Certificate of AnalysisJul 08, 2024 T107484
K2420539Certificate of AnalysisJul 08, 2024 T107484
D2409061Certificate of AnalysisJan 07, 2022 T107484
D2502075Certificate of AnalysisJan 07, 2022 T107484
Propiedades químicas y físicas
SolubilidadMiscible with alcohol, ether, carbon disulfide and many organic solvents. Slightly miscible with water.
SensibilidadHeat & Light & Air sensitive
Punto de congelación (°C)13 °C
Índice de refracción1.593-1.595
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 molecular133.190 g/mol
XLogP32.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass133.089 Da
Monoisotopic Mass133.089 Da
Topological Polar Surface Area12.000 Ų
Heavy Atom Count10
Formal Charge0
Complexity111.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
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]
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