2,3-pyrazine dicarboxylic acid
2,3-pyrazinedicarboxylic acid
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      89-01-0 2,3-Pyrazinedicarboxylic acid 95%
       
  • Synerzine
    • Synerzine, Inc.
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      Product(s):
      623CA Pyrazine 2,3-Dicarboxylic Acid
       
  • TCI AMERICA
    • TCI AMERICA
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      Product(s):
      P0545 2,3-Pyrazinedicarboxylic Acid >98.0%(HPLC)(T)
       
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CAS Number: 89-01-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 201-875-3
FDA UNII: QNN35WOF29
Nikkaji Web: J60.120I
Beilstein Number: 0147982
MDL: MFCD00006131
XlogP3: -0.70 (est)
Molecular Weight: 168.10868000
Formula: C6 H4 N2 O4
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: information only not used for fragrances or flavors
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
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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
 water, 4.329e+005 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
2,3-Pyrazinedicarboxylic acid 95%
EMD Millipore
For experimental / research use only.
2,3-Pyrazinedicarboxylic Acid
Santa Cruz Biotechnology
For experimental / research use only.
2,3-Pyrazine dicarboxylic acid 99%
Sigma-Aldrich: Aldrich
For experimental / research use only.
2,3-Pyrazinedicarboxylic Acid 97%
Synerzine
Pyrazine 2,3-Dicarboxylic Acid
TCI AMERICA
For experimental / research use only.
2,3-Pyrazinedicarboxylic Acid >98.0%(HPLC)(T)
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LDLo  > 500 mg/kg
National Academy of Sciences, National Research Council, Chemical-Biological Coordination Center, Review. Vol. 5, Pg. 7, 1953.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
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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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
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EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 66628
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 pyrazine-2,3-dicarboxylic acid
Chemidplus: 0000089010
RTECS: UQ2500000 for cas# 89-01-0
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References:
 pyrazine-2,3-dicarboxylic acid
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 66628
Pubchem (sid): 135023360
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEMBL: View
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2933.99.9700
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 pyrazine 2,3-dicarboxylic acid
 pyrazine-2,3-dicarboxylate
 pyrazine-2,3-dicarboxylic acid
2,3-pyrazinedicarboxylic acid
2,3-pyrazinedicarboxylicacid
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Articles:
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.
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