2,3-pyrazine dicarboxylic acid
2,3-pyrazinedicarboxylic acid
Identification
| Name | 2,3-pyrazine dicarboxylic acid |
| CAS Number | 89-01-0 |
| EINECS | 201-875-3 |
| FDA UNII | QNN35WOF29 |
| Molecular Formula | C6 H4 N2 O4 |
| Molecular Weight | 168.10868000 |
| MDL Number | MFCD00006131 |
| Nikkaji Number | J60.120I |
| Beilstein | 0147982 |
| XlogP3 | -0.70 (est) |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Melting Point | 193.00 °C. @ 760.00 mm Hg |
| Boiling Point | 449.00 to 450.00 °C. @ 760.00 mm Hg (est) |
| Flash Point | 438.00 °F. TCC ( 225.40 °C. ) (est) |
| logP (o/w) | -1.257 (est) |
| Soluble in | alcohol |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | oral-rat LDLo > 500 mg/kg |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | information only not used for fragrances or flavors |
| Recommendation for 2,3-pyrazine dicarboxylic acid usage levels up to | not for fragrance use. |
| Recommendation for 2,3-pyrazine dicarboxylic acid flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
pyrazine 2,3-dicarboxylic acid
pyrazine-2,3-dicarboxylate
pyrazine-2,3-dicarboxylic acid
2,3-
pyrazinedicarboxylic acid
2,3-
pyrazinedicarboxylicacid
PubMed:
Quantum chemical computations, vibrational spectroscopic analysis and antimicrobial studies of 2,3-Pyrazinedicarboxylic acid.
PubMed:
Syntheses, crystal structures and photophysical properties of Ag(I) coordination complexes.
PubMed:
Two new palladium(II) complexes: synthesis, characterization and their interaction with HeLa cells.
PubMed:
Investigation of in situ oxalate formation from 2,3-pyrazinedicarboxylate under hydrothermal conditions using nuclear magnetic resonance spectroscopy.
PubMed:
Photoluminescent lanthanide-organic bilayer networks with 2,3-pyrazinedicarboxylate and oxalate.
PubMed:
Bis(2,4,6-triamino-1,3,5-triazin-1-ium) pyrazine-2,3-dicarboxyl-ate tetra-hydrate: a synchrotron radiation study.
PubMed:
A pillared-layer coordination polymer with a rotatable pillar acting as a molecular gate for guest molecules.
PubMed:
An unprecedented three-dimensional silver(I) cluster built up from pyrazine-2,3-dicarboxylate ligands.
PubMed:
catena-Poly[[diaqua-rubidium(I)](μ(2)-3-carboxy-pyrazine-2-carboxyl-ato)(μ(2)-pyrazine-2,3-dicarboxylic acid)].
PubMed:
Diacridinium trans-diaqua-bis(pyrazine-2,3-dicarboxyl-ato)cobaltate(II) hexa-hydrate.
PubMed:
Poly[μ-aqua-diaqua-(μ(2)-pyrazine-2,3-dicarboxyl-ato)dilithium(I)].
PubMed:
catena-Poly[[aqua-(dipyrido[3,2-a:2',3'-c]phenazine-κN,N)zinc(II)]-μ-pyrazine-2,3-dicarboxyl-ato-κN,O:O].
PubMed:
Structure-activity relationships of cyclic lactam analogues of alpha-melanocyte-stimulating hormone (alpha-MSH) targeting the human melanocortin-3 receptor.
PubMed:
Poly[diaqua(μ(2)-3-carboxypyrazine-2-carboxylato)(μ(2)-pyrazine-2,3-dicarboxylic acid)potassium(I)].
PubMed:
Self-assembly of cuII and niII [2 x 2] grid complexes and a binuclear CuII complex with a new semiflexible substituted pyrazine ligand: multiple anion encapsulation and magnetic properties.
PubMed:
Quinolinate dehydrogenase and 6-hydroxyquinolinate decarboxylase involved in the conversion of quinolinic acid to 6-hydroxypicolinic acid by Alcaligenes sp. strain UK21.
PubMed:
Capillary electrophoretic separation of dicarboxylic acids in atmospheric aerosol particles.
PubMed:
Hydrogen bonding in the inner-salt zwitterion and in two different charged forms of 5,6-bis(2-pyridyl)pyrazine-2,3-dicarboxylic acid.
PubMed:
Design of low molecular weight hematoregulatory agents from the structure-activity relationship of a dimeric pentapeptide.
PubMed:
The effect of pyrazines on the metabolism of tryptophan and nicotinamide adenine dinucleotide in the rat. Evidence of the formation of a potent inhibitor of aminocarboxy-muconate-semialdehyde decarboxylase from pyrazinamide.