499-83-2
499-83-2
Chemical Structure
Pyridine-2,6-dicarboxylic acid
Synonym(s): 2,6-Pyridinedicarboxylic acid
- No. CAS: 499-83-2
- Formula:C7H5NO4
- Molecular Weight:167.12
IUPAC Name: pyridine-2,6-dicarboxylic acid
InChIKey: WJJMNDUMQPNECX-UHFFFAOYSA-N
SMILES: O=C(C1=NC(C(O)=O)=CC=C1)O
Biological Activity: Pyridine-2,6-dicarboxylic acid is a dicarboxylic acid containing a pyridine ring with unique chemical properties that make it an important ingredient in a variety of industrial processes. Pyridine-2,6-dicarboxylic acid is commonly used as a ligand for metal ions, a building block in the synthesis of pharmaceuticals and organic compounds, and a precursor in the production of pigments and dyes.
| Referencia número | Nombre del producto | Pureza | Descripciòn | Pricing | |||||||||||||||||||
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Pyridine-2,6-dicarboxylic acid | 99.33% | Pyridine-2,6-dicarboxylic acid is a dicarboxylic acid containing a pyridine ring with unique chemical properties that make it an important ingredient in a variety of industrial processes. Pyridine-2,6-dicarboxylic acid is commonly used as a ligand for metal ions, a building block in the synthesis of pharmaceuticals and organic compounds, and a precursor in the production of pigments and dyes. | ||||||||||||||||||||
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Quinolinic acid (Standard) | 99.96% | Quinolinic acid (Standard) is the analytical standard of Quinolinic acid. This product is intended for research and analytical applications. Quinolinic acid, an endogenous metabolite of tryptophan, is a N-methyl-D-aspartate receptor (NMDA receptor) agonist. Quinolinic acid increases glutamate efflux, induces the generation of ROS, activates nitric oxide synthase, produces excessive NO, leading to calcium ion influx and neuronal apoptosis. | ||||||||||||||||||||
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Quinolinic acid-13C7 | Quinolinic acid-13C7 is the 13C labeled Quinolinic acid (HY-100807). Quinolinic acid, an endogenous metabolite of tryptophan, is a N-methyl-D-aspartate receptor (NMDA receptor) agonist. Quinolinic acid increases glutamate efflux, induces the generation of ROS, activates nitric oxide synthase, produces excessive NO, leading to calcium ion influx and neuronal apoptosis. | |||||||||||||||||||||
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Isophthalic acid | 99.96% | Isophthalic acid is a biomaterial or organic compound that can be used in life science research. | ||||||||||||||||||||
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2,5-Pyridinedicarboxylic acid | 99.65% | 2,5-Pyridinedicarboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2,4-PDCA | 99.82% | 2,4-PDCA (2,4 pyridine dicarboxylic acid) is a broad-spectrum inhibitor of 2OG oxygenase, including JmjC domain-containing family of histone demethylases (JHDMs). 2,4-PDCA is a target chemical in the field of bio-based plastics. | ||||||||||||||||||||
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Pyrazine-2,6-dicarboxylic acid | Pyrazine-2,6-dicarboxylic acid (2,6-Pyrazinedicarboxylic acid) is a metal-organic framework (MOF). | |||||||||||||||||||||
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Pyridazine-3,6-dicarboxylic acid | Pyridazine-3,6-dicarboxylic acid (3,6-Pyridazinedicarboxylic acid) is a metal-organic framework (MOF). | |||||||||||||||||||||
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MNK-IN-5 | MNK-IN-5 is a MNK inhibitor that suppresses MNK activity. | |||||||||||||||||||||
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Quinolinic acid-13C3,15N | Quinolinic acid-13C3, 15N (2,3-Pyridinedicarboxylic Acid-13C3, 15N) is the 13C- and 15N-labeled Quinolinic acid (HY-100807). Quinolinic acid is an endogenous N-methyl-D-aspartate (NMDA) receptor agonist synthesized from L-tryptophan via the kynurenine pathway and thereby has the potential of mediating N-methyl-D-aspartate neuronal damage and dysfunction. | |||||||||||||||||||||
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Phthalic acid-13C | Phthalic acid-13C is the 13C-labeled Phthalic acid. Phthalic acid is the final common metabolite of phthalic acid esters (PAEs). Phthalic acid can be used for the synthesis of synthetic agents, such as isophthalic acid (IPA), and terephthalic acid (TPA). Phthalic acid has applications in the preparation of phthalate ester plasticizers. Phthalic acid exhibits mutagenic effect and causes genetic damage in mammalian germ cells. | |||||||||||||||||||||
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