2-aminopyrazine
pyrazin-2-ylamine
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
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      5049-61-6 2-aminopyrazine 95%
       
  • Penta International
    • Penta International Corporation
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  • Synerzine
    • Synerzine, Inc.
      Innovation. Customization. Aroma Ingredients.
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      Synerzine expresses what we have grown to embody as an organization - the synergy and connection between raw ingredients, science, technology, and the final product. Our experienced team is passionate about bringing our customers high-quality innovative ingredients that they can trust.
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      410N 2-Aminopyrazine
       
  • TCI AMERICA
    • TCI AMERICA
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      A0989 2-Aminopyrazine >98.0%(GC)(T)
       
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Synonyms   Articles   Notes   Search
CAS Number: 5049-61-6Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 225-748-7
Nikkaji Web: J80.944F
Beilstein Number: 107025
MDL: MFCD00006137
XlogP3: -0.10 (est)
Molecular Weight: 95.10485000
Formula: C4 H5 N3
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: pharmaceuticals / chemical synthisis
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 250.00 to  251.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.246000 mmHg @ 20.00 °C. (est)
Flash Point: 264.00 °F. TCC ( 129.10 °C. ) (est)
logP (o/w): -0.070
Soluble in:
 alcohol
 water, 1.386e+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-aminopyrazine 95%
Penta International
2-AMINOPYRAZINE
Santa Cruz Biotechnology
For experimental / research use only.
2-Aminopyrazine
Sigma-Aldrich: Aldrich
For experimental / research use only.
Aminopyrazine 98%
Synerzine
2-Aminopyrazine
TCI AMERICA
For experimental / research use only.
2-Aminopyrazine >98.0%(GC)(T)
United International
2-Amino Pyrazine
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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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: pharmaceuticals / chemical synthisis
Recommendation for 2-aminopyrazine usage levels up to:
 not for fragrance use.
 
Recommendation for 2-aminopyrazine flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 78747
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 pyrazin-2-amine
Chemidplus: 0005049616
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References:
 pyrazin-2-amine
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 78747
Pubchem (sid): 135034787
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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: 2933.59.9500
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:
2-amino pyrazine
 aminopyrazine
 pyrazin-2-amine
 pyrazin-2-ylamine
2-pyrazinamine
 pyrazine-2-ylamine
 pyrazine, 2-amino-
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Articles:
PubMed: Identification of AKN-032, a novel 2-aminopyrazine tyrosine kinase inhibitor, with significant preclinical activity in acute myeloid leukemia.
PubMed: Poly[bis(mu2-2-aminopyrazine-kappa2N1:N4)(mu2-nitrato-kappa2O:O)(nitrato-kappa2O,O')disilver(I)]: an achiral two-dimensional coordination polymer forming chiral crystals.
PubMed: Synthesis of some new anils: part 1. Reaction of 2-hydroxy-benzaldehyde and 2-hydroxynaphthaldehyde with 2-aminopyridene and 2-aminopyrazine.
PubMed: Mercapturic acid formation from 2-aminopyrazine in rats.
PubMed: Poly[mu-2-aminopyrazine-kappa2N1:N4-mu-cyanido-copper(I)]: a three-dimensional network from laboratory powder diffraction data.
PubMed: [Synthesis of the furan derivatives. XLVII. Synthesis of 5,6-bis(5-nitro-2-furyl)-2-aminopyrazine and its related compound].
PubMed: Multiple hydrogen bonding in excited states of aminopyrazine in methanol solution: time-dependent density functional theory study.
PubMed: Structure-activity-relationship studies around the 2-amino group and pyridine core of antimalarial 3,5-diarylaminopyridines lead to a novel series of pyrazine analogues with oral in vivo activity.
PubMed: In vitro and in vivo activities of 2-aminopyrazines and 2-aminopyridines in experimental models of human African trypanosomiasis.
PubMed: Spin canting and metamagnetism in 2D and 3D cobalt(II) coordination networks with alternating double end-on and double end-to-end azido bridges.
PubMed: Water-induced reversible structural phase transformation with chromotropism in metal supramolecular frameworks containing aminopyrazine and sulfate anions.
PubMed: Chemistry around imidazopyrazine and ibuprofen: discovery of novel fatty acid amide hydrolase (FAAH) inhibitors.
PubMed: New discrete and polymeric supramolecular architectures derived from dinuclear (bis-beta-diketonato)copper(II) metallocycles.
PubMed: Synthesis and spectroscopic characterization of copper(II) tetraazaiminooxime macrocyclic complexes--a tetragonal distortion analysis.
PubMed: Antibacterial cobalt(II) and zinc(II) complexes of pyrazine-derived NNO and NNN donor Schiff-bases.
PubMed: Catechol derivatives of aminopyrazine and cell protection against UVB-induced mortality.
PubMed: Copper(I) cyanide networks: synthesis, luminescence behavior and thermal analysis. Part 1. Diimine ligands.
PubMed: Chemistry of stable iminopropadienones, RN=C=C=C=O.
PubMed: [Studies on pyrazine derivatives. XXVI. Synthesis and tuberculostatic activity of N-pyrazinylthiourea].
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