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2,6-Pyridinedimethanol - 97%, high purity , CAS No.1195-59-1
Basic Description
Synonyms
Pyridine-2,6-diyldimethanol | [6-(hydroxymethyl)pyridin-2-yl]methanol | 2,6-Pyridinedimethanol | 2,6-pyridine-dimethanol | EINECS 214-803-0 | pyridine 2,6-dimethanol | AC-6240 | F0001-0321 | Pyridine-2,6-dimethanol | 2,6-Pyridinedimethanol, 98% | A2482 |
Specifications & Purity
≥97%
Shipped In
Normal
Product Description
Ligand used in the synthesis of a variety of metal complexes and catalysts.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Pyridines and derivatives
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pyridines and derivatives
Alternative Parents
Heteroaromatic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Aromatic alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyridines and derivatives. These are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Names and Identifiers
Pubchem Sid
504754594
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504754594
IUPAC Name
[6-(hydroxymethyl)pyridin-2-yl]methanol
INCHI
InChI=1S/C7H9NO2/c9-4-6-2-1-3-7(5-10)8-6/h1-3,9-10H,4-5H2
InChIKey
WWFMINHWJYHXHF-UHFFFAOYSA-N
Smiles
C1=CC(=NC(=C1)CO)CO
Isomeric SMILES
C1=CC(=NC(=C1)CO)CO
WGK Germany
3
Molecular Weight
139.15
Beilstein
116016
Reaxy-Rn
116016
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=116016&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water
Boil Point(°C)
185 °C/15 mmHg
Melt Point(°C)
112-114°C
Molecular Weight
139.150 g/mol
XLogP3
-0.800
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
2
Exact Mass
139.063 Da
Monoisotopic Mass
139.063 Da
Topological Polar Surface Area
53.400 Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
87.600
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.
Qin Yutian, Wang Bowei, Li Jiayi, Wu Xingchun, Chen Ligong.
(2019)
Cobalt imine–pyridine–carbonyl complex functionalized metal–organic frameworks as catalysts for alkene epoxidation.
TRANSITION METAL CHEMISTRY,
44
(7):
(595-602).
2.
Jiwen Hu, Zhangjun Hu, Yang Cui, Xuanjun Zhang, Hong-Wen Gao, Kajsa Uvdal.
(2014)
A rhodamine-based fluorescent probe for Hg2+ and its application for biological visualization.
SENSORS AND ACTUATORS B-CHEMICAL,
203
(452).
3.
Hao Wu, Jinqiu Tao, Junhao Xie, Chengbao Liu, Qianping Ran.
(2024)
Room-temperature fast self-healing graphene polyurethane network with high robustness and ductility through biomimetic interface structures.
Nano Materials Science,
4.
Zhang Zeyu, Peng Dejun, Shang Xueyan, Zhao Xin, Ren Shixue, Pang Jiuyin, Li Shujun.
(2024)
Ultra-tough light-curing ionogels for UV shielding.
Communications Materials,
5
(1):
(1-12).
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