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Basic Description
| Synonyms | Z104472800 | DTXCID001899 | RCRA waste no. U191 | .alpha.-Methylpyridine | EINECS 203-643-7 | Picoline, .alpha. | EC 203-643-7 | Picoline | PICOLINE, ALPHA | F0001-0192 | Pyridine, 2-methyl- | 2-Mepy | BCP26524 | DTXSID9021899 | Pyridine-2,3,4,5-d4,6-(met |
|---|---|
| Specifications & Purity | ≥99% |
| Storage Temp | Protected from light,Room temperature |
| Shipped In | Normal |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Pyridines and derivatives
- Subclass Methylpyridines
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Class
Pyridines and derivatives
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Superclass
Organoheterocyclic compounds
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Pyridines and derivatives |
| Subclass | Methylpyridines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Methylpyridines |
| Alternative Parents | Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Methylpyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as methylpyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a methyl group. |
| External Descriptors | methylpyridine |
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Associated Targets(Human)
TBXAS1
Tchem
Thromboxane-A synthase (3355 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Associated Targets(non-human)
Chrna3
Neuronal acetylcholine receptor (756 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Names and Identifiers
| Pubchem Sid | 488180634 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488180634 |
| IUPAC Name | 2-methylpyridine |
| INCHI | InChI=1S/C6H7N/c1-6-4-2-3-5-7-6/h2-5H,1H3 |
| InChIKey | BSKHPKMHTQYZBB-UHFFFAOYSA-N |
| Smiles | CC1=CC=CC=N1 |
| Isomeric SMILES | CC1=CC=CC=N1 |
| WGK Germany | 1 |
| RTECS | TJ4900000 |
| UN Number | 2313 |
| Packing Group | III |
| Molecular Weight | 93.13 |
| Beilstein | 104581 |
| Reaxy-Rn | 104581 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=104581&ln= |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
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.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 D2501403 |
Certificate of Analysis | Apr 29, 2024 | M108694 |
| B2506007 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
| B2514116 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
| C2405104 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
| D2318226 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
| E2304509 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
| D2318255 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
| F2221026 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
| F2221020 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
| F2221031 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
| F2221018 |
Certificate of Analysis | Jun 15, 2022 | M108694 |
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Chemical and Physical Properties
| Solubility | It is miscible with water and soluble in most organic solvents. |
|---|---|
| Sensitivity | Light sensitive. |
| Refractive Index | 1.501 |
| Flash Point(°F) | 29.4℃ |
| Flash Point(°C) | 29.4℃ |
| Boil Point(°C) | 128-129°C |
| Melt Point(°C) | -70°C |
| Molecular Weight | 93.130 g/mol |
| XLogP3 | 1.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 93.0578 Da |
| Monoisotopic Mass | 93.0578 Da |
| Topological Polar Surface Area | 12.900 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 52.100 |
| 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 |
Citations of This Product
| 1. Guo Qiang, Lin Jinyuan, Yang Pengju, Jiang Yong, Zhang Binchuan, Zhu Longxin, Wang Xunqiu. (2023) Isobaric Vapor–Liquid Equilibrium for Binary System of 2-Methylpyridine + 2-Vinylpyridine at (1.9, 4.0 and 5.3) kPa. JOURNAL OF SOLUTION CHEMISTRY, 52 (8): (921-939). |
| 2. Zhengyu Wang, Yufeng Hu, Zhiduo Ding, Hao Zhou, Jianye Zhang, Jingjing Zhan, Minghuo Wu. (2023) Determination of Organic Nitrogen Compounds in Gasoline by Water-Assisted Dispersive Solid-Phase Extraction (DSPE) and High-Performance Liquid Chromatography-High-Resolution Mass Spectrometry (HPLC-HRMS). ANALYTICAL LETTERS, |
| 3. Guangzhi Xu, Zhuoheng Tu, Xingbang Hu, Mian Li, Xiaomin Zhang, Youting Wu. (2023) Protic Brønsted acidic ionic liquids with variable acidity for efficient conversion of xylose and hemicellulose to furfural. FUEL, 339 (127334). |
| 4. Qingmei Chen, Xiujun Peng, Jingwen Xue, Jinjin Li, Chunfeng Pan. (2022) Identification and Quantification of Organic Contaminants and Evaluation of Their Effects on Amine Foaming in the Natural Gas Sweetening Industry. ACS Omega, 7 (50): (46421–46427). |
| 5. Dongyuan Yang, Yanjun Min, Baihui Feng, Xueming Yang, Guorong Wu. (2022) Vibrational-state dependent decay dynamics of 2-pyridone excited to the S1 electronic state. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 24 (37): (22710-22715). |
| 6. Bingbing Luo, Kai Wu, Jiajun Yu, Siyu Wang, Yihan Wang, Chenyang Chu, Huiyan Zhang. (2022) Enhancement of renewable N-heterocycles production via catalytic co-pyrolysis of glycerol and cellulose over HZSM-5 under ammonia atmosphere. JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 167 (105649). |
| 7. Pengfei Li, Dawei Shang, Wenhui Tu, Shaojuan Zeng, Yi Nie, Lu Bai, Haifeng Dong, Xiangping Zhang. (2020) NH3 absorption performance and reversible absorption mechanisms of protic ionic liquids with six-membered N-heterocyclic cations. SEPARATION AND PURIFICATION TECHNOLOGY, 248 (117087). |
| 8. Rongxing Qiu, Xiaoyan Luo, Le Yang, Jiaran Li, Xiaoyan Chen, Cheng Peng, Jinqing Lin. (2020) Regulated Threshold Pressure of Reversibly Sigmoidal NH3 Absorption Isotherm with Ionic Liquids. ACS Sustainable Chemistry & Engineering, 8 (3): (1637–1643). |
| 9. Xin Zhang, Ziguo Yuan, Qian Yao, Ying Zhang, Yao Fu. (2019) Catalytic fast pyrolysis of corn cob in ammonia with Ga/HZSM-5 catalyst for selective production of acetonitrile. BIORESOURCE TECHNOLOGY, 290 (121800). |
| 10. Zhao Shuxue, Hu Chunhui, Guo Lizhong, Li Kuiran, Yu Hao. (2019) Isolation of a 3-hydroxypyridine degrading bacterium, Agrobacterium sp. DW-1, and its proposed degradation pathway. AMB Express, 9 (1): (1-9). |
| 11. Ziguo Yuan, Xin Zhang, Qian Yao, Ying Zhang, Yao Fu. (2019) Production of acetonitrile via catalytic fast pyrolysis of biomass derived polylactic acid under ammonia atmosphere. JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 140 (376). |
| 12. Lujiang Xu, Qian Yao, Ying Zhang, Yao Fu. (2016) Producing pyridines via thermo-catalytic conversion and ammonization of glycerol over nano-sized HZSM-5. RSC Advances, 6 (89): (86034-86042). |
| 13. Muhan Liang, Kangnan Wang, Ruifang Guan, Zhiqiang Liu, Duxia Cao, Qianqian Wu, Yanyan Shan, Yongxiao Xu. (2016) Several hemicyanine dyes as fluorescence chemosensors for cyanide anions. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 160 (34). |
| 14. Duan-Jian Tao, Zhang-Min Li, Zheng Cheng, Na Hu, Xiang-Shu Chen. (2012) Kinetics Study of the Ketalization Reaction of Cyclohexanone with Glycol Using Brønsted Acidic Ionic Liquids as Catalysts. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 51 (50): (16263–16269). |
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