2,6-Pyridinedimethanol

2,6-Pyridinedimethanol Basic information
Product Name:2,6-Pyridinedimethanol
Synonyms:LABOTEST-BB LT00233124;2,6-Dihydroxymethyl Pyridine;pyridine-2,6-diyldimethanol;2,6-PYRIDINEMETHANOL BIS;2,6-PYRIDINETHANOL;(6-Hydroxymethyl-pyridin-2-yl)-methanol;2,6-Pyridinedimethanol ,98%;2,6-Pyridinedimethan
CAS:1195-59-1
MF:C7H9NO2
MW:139.15
EINECS:214-803-0
Product Categories:Pyridines, Pyrimidines, Purines and Pteredines;Pyridines;Alkohols
Mol File:1195-59-1.mol
2,6-Pyridinedimethanol Structure
2,6-Pyridinedimethanol Chemical Properties
Melting point 112-114 °C (lit.)
Boiling point 185°C 15mm
density 1.1997 (rough estimate)
refractive index 1.4800 (estimate)
Fp 185°C/15mm
storage temp. Inert atmosphere,Room Temperature
pka13.03±0.10(Predicted)
form Crystalline Powder
color Light yellow to beige
Water Solubility Soluble in water.
BRN 116016
InChIKeyWWFMINHWJYHXHF-UHFFFAOYSA-N
CAS DataBase Reference1195-59-1(CAS DataBase Reference)
NIST Chemistry ReferencePyridine, 2,6-dicarbinol(1195-59-1)
Safety Information
Hazard Codes Xi
Risk Statements 37/38-41-36/37/38
Safety Statements 26-39-24/25-36
WGK Germany 3
23
Hazard Note Irritant
HS Code 29333999
MSDS Information
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2,6-Pyridinedimethanol Usage And Synthesis
Chemical Propertieslight yellow to beige crystalline powder
Uses2,6-Pyridinedimethanol can be used as a quantum dot solution for photoelectric device and biomedicine and also a ligand to synthesize a variety of metal complexes and catalysts.
PreparationThe preparation of 2,6-Pyridinedimethanol is as follows:2640g of 2,6-dibromomethylpyridine, 3L of 30% aqueous sodium hydroxide solution, and 10L of ethanol were placed in a 20L reaction flask. Turn on the agitation. The reaction solution was heated to reflux and the reaction was kept for 5h. The TLC to intermediate state reaction is complete. The reaction solution is cooled to room temperature, plus into 20L of ice water, stir for 20min. The aqueous phase was extracted twice with 10L of dichloromethane and the organic phases were combined. The organic phase is concentrated under reduced pressure to dry, a solid of 1232g was obtained, the yield was 88.6%, and the liquid phase was 98%.

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2,2-Bis(hydroxymethyl)propionic acid DIPIPERIDINOMETHANE 2-(Hydroxymethyl)pyridine 4-Methylpyridine CROWN ETHER/DIBENZOPYRIDINO-18-CROWN-6 Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate THIOSTREPTON 4-Piperidinemethanol 2,5-PYRIDINEDICARBOXYLIC ACID 2,6-Pyridinedimethanol 3-Pyridinemethanol 2,6-Lutidine 2,4,6-Collidine (6-[(([(1,2,2-TRICHLOROVINYL)AMINO]CARBONYL)OXY)METHYL]PYRIDIN-2-YL)METHYL N-(1,2,2-TRICHLOROVINYL)CARBAMATE Diethyl 2,6-pyridinedicarboxylate 3-Hydroxy-2,6-pyridinedimethanol,3-HYDROXY-2,6-PYRIDINEDIMETHANOL HYDROCHLORIDE DIBUTYL 2,6-PYRIDINEDICARBOXYLATE, 99 Pyridine-2,4,6-tricarboxylic acid

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