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2,5-Pyridinedicarboxylic acid

Catalog Number
ACM100265
CAS
100-26-5
Structure
IUPAC Name
Pyridine-2,5-dicarboxylic acid
Synonyms
Pyridine-2,5-dicarboxylic acid;Pyridinedicarboxylic acid;Isocinchomeronic acid
Molecular Weight
167.12
Molecular Formula
C7H5NO4
Canonical SMILES
C1=CC(=NC=C1C(=O)O)C(=O)O
InChI
LVPMIMZXDYBCDF-UHFFFAOYSA-N
InChI Key
InChI=1S/C7H5NO4/c9-6(10)4-1-2-5(7(11)12)8-3-4/h1-3H,(H,9,10)(H,11,12)
Boiling Point
295.67 ºC
Melting Point
242-247 °C
Purity
95%+
Density
1.52g/ml
Solubility
0.01 M
Appearance
Yellow to green powder
Storage
Store under inert gas
Active Content
95%
Physical State
Solid
Typical Applications
Use as dispersing agent.
Use as cleansing agent.
Spec Sheet
Case Study

Synthesis of Rare Earth Metal Organic Framework Materials Based on 2,5-Pyridinedicarboxylic Acid Ligands

Synthesis of Rare Earth Metal Organic Framework Materials Based on 2,5-Pyridinedicarboxylic Acid Ligands Zheng L, et al. Molecular Crystals and Liquid Crystals, 2018, 666(1), 109-118.

2,5-Pyridinedicarboxylic acid can be used to synthesize metal organic framework (MOF) materials. Using 2,5-pyridinedicarboxylic acid (H2Pdc) ligand, Eu salt and gadolinium oxide as raw materials, two MOFs were successfully synthesized using a hydrothermal method, and single crystals were obtained. The following is the synthesis procedure of two MOF materials.
· Synthesis of [Eu (bipy) (CH3COO)·H2O] n (1)
Eu(NO3)3·6H2O(0.113 g, 0.5 mmol), Co(CH3COO)2 (0.125 g, 0.5 mmol), H2Pdc (0.167 g, 1 mmol) were dissolved in distilled water with stirring for 1h at room temperature. Then add the mixture to an autoclave (25 mL) equipped with a Teflon substrate. And then the autoclave was placed in an oven and heated to 140 °C for 72 h. Turn off the oven allowed to cool to room temperature, remove the reactor, yellow needlelike crystals (1) generated, filtered, dried naturally and collected samples. Yield: 60%.
· Synthesis of [Gd (bipy) (CH3COO)] n (2)
The synthesis of [Gd (bipy) (CH3COO)]n (2) is similar to that of 1, except that europium nitrate and cobalt acetate were replaced by gadolinium oxide and zinc acetate. A transparent block crystal is formed, filtered and dried naturally, then collected samples. Yield: 79%.

Synthesis of Samarium(III) Coordination Polymer Based on 2,5-Pyridinedicarboxylic Acid Ligand

Synthesis of Samarium(III) Coordination Polymer Based on 2,5-Pyridinedicarboxylic Acid Ligand Ay B, Doğan N, Yildiz E, et al. Polyhedron, 2015, 88, 176-181.

A Sm(III) coordination polymer was successfully synthesized via hydrothermal reaction from the reaction mixture of Sm(NO3)3·6H2O, 2,5-pyridinedicarboxylic acid (2,5-pydcH2), piperazine and H2O. The metal complex polymer exhibits good thermal stability and photoluminescence emission in the solid state in the phosphorescent region.
Synthesis of the coordination polymer
· A mixture of Sm(NO3)3·6H2O (0.134 g, 0.3 mmol), pyridine 2,5-dicarboxylic acid (0.153 g, 0.9 mmol), piperazine (0.027 g, 0.3 mmol) and H2O (5 mL, 278 mmol) in the mole ratio 1.00:3.00:1.00:927 was sealed in a 23 mL Teflon reactor and kept under autogenous pressure at 160 ºC for 72 hours.
· The mixture was cooled to room temperature at a rate of 20 °C/h, and bright yellow colored crystals were obtained. The heterogeneous solution was separated from the solid phase, the crystals washed with water and dried at room temperature. Yield: 81 % based on Sm. Initial pH; 1.90, final pH; 3.40. The coordination polymer is insoluble in common solvents (ethanol, methanol, acetonitrile etc.) and water.

Custom Q&A

What is molecular formula of 2,5-pyridinedicarboxylic acid?

C7H5NO4

What is deprecated CAS of 2,5-pyridinedicarboxylic acid?

1355602-04-8

What is NSC number of 2,5-pyridinedicarboxylic acid?

177

What is UNII of 2,5-pyridinedicarboxylic acid?

4K1KGR926X

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