2-pyrazine carboxylic acid
2-pyrazinecarboxylic acid
Identification
| Name | 2-pyrazine carboxylic acid |
| IUPAC | pyrazine-2-carboxylic acid |
| CAS Number | 98-97-5 |
| EINECS | 202-718-1 |
| FDA UNII | 2WB23298SP |
| Molecular Formula | C5 H4 N2 O2 |
| Molecular Weight | 124.09928000 |
| MDL Number | MFCD00006130 |
| Nikkaji Number | J11.623H |
| Beilstein | 112305 |
| XlogP3 | 0.10 (est) |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Melting Point | 225.00 °C. @ 760.00 mm Hg |
| Boiling Point | 313.00 to 314.00 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.000217 mmHg @ 25.00 °C. (est) |
| Flash Point | 290.00 °F. TCC ( 143.10 °C. ) (est) |
| logP (o/w) | -0.599 (est) |
| Soluble in | alcohol |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| 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-pyrazine carboxylic acid usage levels up to | not for fragrance use. |
| Recommendation for 2-pyrazine carboxylic acid flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
pyrazine 2-carboxylic acid
pyrazine-2-carboxylic acid
2-
pyrazinecarboxylic acid
2-
pyrazinecarboxylicacid
pyrazinic acid
pyrazinoic acid
2-
pyrazinoic acid
PubMed:
pH and amine-induced various octamolybdate-based metal-organic complexes: assembly, structures and properties.
PubMed:
Investigation of in situ oxalate formation from 2,3-pyrazinedicarboxylate under hydrothermal conditions using nuclear magnetic resonance spectroscopy.
PubMed:
New three-dimensional metal-organic framework with heterometallic [Fe-Ag] building units: synthesis, crystal structure, and functional studies.
PubMed:
Low Temperature Heat Capacities and Standard Molar Enthalpy of Formation of 2-Pyrazinecarboxylic Acid (C5H4N2O2)(s).
PubMed:
Derivatives of pyrazinecarboxylic acid: 1H, 13C and 15N NMR spectroscopic investigations.
PubMed:
LC and LC-MS study on establishment of degradation pathway of glipizide under forced decomposition conditions.
PubMed:
Magnetic properties and molecular structures of binuclear (2-pyrazinecarboxylate)-bridged complexes containing Re(IV) and M(II) (M = Co, Ni).
PubMed:
Versatility in the binding of 2-pyrazinecarboxylate with iron. Synthesis, structure and magnetic properties of iron(II) and iron(III) complexes.
PubMed:
Self-assembly of diorganotin(IV) moieties and 2-pyrazinecarboxylic acid: syntheses, characterizations and crystal structures of monomeric, polymeric or trinuclear macrocyclic compounds.
PubMed:
Cytotoxicity and DNA binding studies of several platinum (II) and palladium (II) complexes of the 2,2'-bipyridine and an anion of 2-pyridinecarboxylic/2-pyrazinecarboxylic acid.
PubMed:
Investigation of UV matrix-assisted laser desorption fourier transform mass spectrometry for peptides.
PubMed:
Biosynthesis of quinoxaline antibiotics: purification and characterization of the quinoxaline-2-carboxylic acid activating enzyme from Streptomyces triostinicus.
PubMed:
Chromophore activating enzyme involved in the biosynthesis of the mikamycin B antibiotic etamycin from Streptomyces griseoviridus.
PubMed:
Eimeria tenella, E. necatrix, E. acervulina, and E. maxima: anticoccidial activity of 1,6-dihydro-6-oxo-2-pyrazinecarboxylic acid 4-oxide.
PubMed:
[Studies on pyrazine derivatives. XIX. Synthesis and tuberculostatic activity of various 3-phenoxy-2-pyrazinecarboxylic acid derivatives].
PubMed:
Anticoccidials. VI. An improved synthesis of 1,6-dihydro-6-oxo-2-pyrazinecarboxylic acid 4-oxide and some related derivatives and determination of anticoccidial activity.
PubMed:
Anticoccidials. VII. Synthesis of 4,5-dihydro-5-oxo-2-pyrazinecarboxylic acid 1-oxides.
PubMed:
[Antitubercular agents. XI. Function derivatives of 5-substituted 2-pyrazinecarboxylic acid].
PubMed:
[Antitubercular agents. X. The action of derivatives of 3-substituted 2 pyrazinecarboxylic acid].
PubMed:
[N-OXIDES OF 2-PYRAZINECARBOXYLIC ACID].