Dipicolinic acid
| Names | |
|---|---|
| Preferred IUPAC name
Pyridine-2,6-dicarboxylic acid | |
| Other names
2,6-Pyridinedicarboxylic acid
| |
| Identifiers | |
CAS Number
|
|
3D model (JSmol)
|
|
Beilstein Reference
|
131629 |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.007.178 |
| EC Number |
|
Gmelin Reference
|
50798 |
PubChem CID
|
|
| UNII | |
CompTox Dashboard (EPA)
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|
InChI
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SMILES
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| Properties | |
Chemical formula
|
C7H5NO4 |
| Molar mass | 167.120 g·mol−1 |
| Melting point | 248 to 250 °C (478 to 482 °F; 521 to 523 K) |
| Hazards | |
| GHS labelling:[2] | |
Pictograms
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|
Signal word
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Warning |
Hazard statements
|
H315, H319, H335 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
| |
Dipicolinic acid (pyridine-2,6-dicarboxylic acid or PDC and DPA) is a chemical compound which plays a role in the heat resistance of bacterial endospores. It is also used to prepare dipicolinato ligated lanthanide and transition metal complexes for ion chromatography.[1]
- ^ a b 2,6-Pyridinedicarboxylic acid at Sigma-Aldrich
- ^ "C&L Inventory". echa.europa.eu. Retrieved 13 December 2021.