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Sigma-Aldrich

2,6-Pyridinedimethanol

98%

Synonym(s):

2,6-Bis(hydroxymethyl)pyridine

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About This Item

Empirical Formula (Hill Notation):
C7H9NO2
CAS Number:
1195-59-1
Molecular Weight:
139.15
Beilstein:
116016
EC Number:
214-803-0
MDL number:
MFCD00006351
UNSPSC Code:
12352100
PubChem Substance ID:
24849432
NACRES:
NA.22

Assay

98%

form

powder

mp

112-114 °C (lit.)

SMILES string

OCc1cccc(CO)n1

InChI

1S/C7H9NO2/c9-4-6-2-1-3-7(5-10)8-6/h1-3,9-10H,4-5H2

InChI key

WWFMINHWJYHXHF-UHFFFAOYSA-N

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Application

2,6-Pyridinedimethanol can be used as a ligand to synthesize a variety of metal complexes and catalysts. It can also be used as a reactant to prepare Fe(III) complexes [Fe(18)O(6)(OH)(8)(pdm)(10)(pdmH)(4)(H(2)O)(4)](ClO(4))(10) and [Fe(9)O(4)(OH)(2)(O(2)CMe)(10)(pdm)(pdmH)(4)](NO(3)).

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H315,H318,H335

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Catalysis Today, 121, 140-140 (2007)
Taketo Taguchi et al.
Dalton transactions (Cambridge, England : 2003), 39(38), 9131-9139 (2010-09-08)
The syntheses, crystal structures and magnetochemical characterization are reported for two new Fe(III) complexes [Fe(18)O(6)(OH)(8)(pdm)(10)(pdmH)(4)(H(2)O)(4)](ClO(4))(10) (3) and [Fe(9)O(4)(OH)(2)(O(2)CMe)(10)(pdm)(pdmH)(4)](NO(3)) (4). They were synthesized from the use of the potentially O,N,O tridentate chelate, 2,6-pyridinedimethanol (pdmH(2)), in the presence or absence of carboxylate
Large bite bisphosphite, 2,6-C5H3N{CH2OP(?OC10H6)(?-S)(C10H6O?)}2: Synthesis, derivatization, transition metal chemistry and application towards hydrogenation of olefins
Benudhar P, Maravanji SB
Journal of Organometallic Chemistry, 692, 1683-1689 (2007)

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