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2,6-Pyridinedimethanol - 97%, high purity , CAS No.1195-59-1

    Grade & Purity:
  • ≥97%
In stock
Item Number
P107906
Grouped product items
SKU Size
Availability
Price Qty
P107906-1g
1g
3
$15.90
P107906-5g
5g
3
$59.90
P107906-10g
10g
2
$91.90
P107906-25g
25g
3
$175.90
P107906-100g
100g
2
$539.90

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

Taxonomy Tree

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

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)

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.

14 results found

Lot Number Certificate Type Date Item
B2528018 Certificate of Analysis Jan 23, 2024 P107906
B24231117 Certificate of Analysis Jan 23, 2024 P107906
B24231118 Certificate of Analysis Jan 23, 2024 P107906
B24231119 Certificate of Analysis Jan 23, 2024 P107906
B24231120 Certificate of Analysis Jan 23, 2024 P107906
B24231121 Certificate of Analysis Jan 23, 2024 P107906
B24231122 Certificate of Analysis Jan 23, 2024 P107906
E2513027 Certificate of Analysis Jan 23, 2024 P107906
A2517122 Certificate of Analysis Jan 23, 2024 P107906
L2201251 Certificate of Analysis Oct 13, 2022 P107906
L2201257 Certificate of Analysis Oct 13, 2022 P107906
L2201245 Certificate of Analysis Oct 13, 2022 P107906
L2201256 Certificate of Analysis Oct 13, 2022 P107906
G1805066 Certificate of Analysis May 10, 2022 P107906

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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,  (1): (1-12). 

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