hypoxanthine
9H-purin-6(1H)-one
 
Notes:
Occurs widely in plant and animal tissue (CCD)
  • BOC Sciences
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      Product(s):
      68-94-0 Hypoxanthine >98%
      Hypoxanthine is a naturally occurring purine derivative.
       
       
  • Glentham Life Sciences
  • TCI AMERICA
    • TCI AMERICA
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      Product(s):
      H0311 Hypoxanthine >98.0%(E)(HPLC)
       
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CAS Number: 68-94-0Picture of molecule3D/inchi
Other(deleted CASRN): 184856-40-4
ECHA EINECS - REACH Pre-Reg: 200-697-3
FDA UNII: 2TN51YD919
Nikkaji Web: J1.934H
Beilstein Number: 0005811
MDL: MFCD00005725
XlogP3: -1.10 (est)
Molecular Weight: 136.11408000
Formula: C5 H4 N4 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
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
Melting Point: 150.00 °C. @ 760.00 mm Hg
Boiling Point: 551.00 °C. @ 760.00 mm Hg (est)
Flash Point: 549.00 °F. TCC ( 287.00 °C. ) (est)
logP (o/w): -0.910 (est)
Soluble in:
 water, 700 mg/L @ 23C (exp)
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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:
Alfa Biotechnology
For experimental / research use only.
Hypoxanthine 98%
BOC Sciences
For experimental / research use only.
Hypoxanthine >98%
Odor: characteristic
Use: Hypoxanthine is a naturally occurring purine derivative.
EMD Millipore
For experimental / research use only.
Hypoxanthine
Glentham Life Sciences
Hypoxanthine
Santa Cruz Biotechnology
For experimental / research use only.
Hypoxanthine ≥99%
Sigma-Aldrich: Sigma
For experimental / research use only.
Hypoxanthine ≥99.0%
TCI AMERICA
For experimental / research use only.
Hypoxanthine >98.0%(E)(HPLC)
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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:
intraperitoneal-mouse LD50  750 mg/kg
National Technical Information Service. Vol. AD691-490,

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for hypoxanthine usage levels up to:
 not for fragrance use.
 
Recommendation for hypoxanthine 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 GENetic TOXicology: Search
EPA Substance Registry Services (TSCA): 68-94-0
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 790
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 3,7-dihydropurin-6-one
Chemidplus: 0000068940
RTECS: UP0791000 for cas# 68-94-0
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References:
 3,7-dihydropurin-6-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 68-94-0
Pubchem (cid): 790
Pubchem (sid): 134971377
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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
CHEBI: View
CHEMBL: View
Golm Metabolome Database: Search
Metabolomics Database: Search
KEGG (GenomeNet): C00262
HMDB (The Human Metabolome Database): HMDB00157
FooDB: FDB003949
YMDB (Yeast Metabolome Database): YMDB00555
Export Tariff Code: 2933.59.9500
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: 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
 beet root
Search Trop  Picture
 celery shoot
Search Trop  Picture
 coffee bean
Search Trop  Picture
 oat plant
Search Trop  Picture
 potato plant
Search Trop  Picture
 rice plant
Search Trop  Picture
 soybean sprout
Search Trop  Picture
 tea plant
Search Trop  Picture
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Synonyms:
1,7-dihydro-6H-purin-6-one
3,7-dihydropurin-6-one
6-hydroxy-1H-purine
6-hydroxypurine
 hypoxanthine enol
 purin-6-ol
9H-purin-6-ol
 purin-6(1H)-one
9H-purin-6(1H)-one
 sarcine
 sarkin
 sarkine
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Articles:
PubMed: The receptor for activated complement factor 5 (C5aR) conveys myocardial ischemic damage by mediating neutrophil transmigration.
PubMed: In vitro evaluation of antioxidants of fruit extract of Momordica charantia L. on fibroblasts and keratinocytes.
PubMed: The Fusarium toxin enniatin B exerts no genotoxic activity, but pronounced cytotoxicity in vitro.
PubMed: Fast simultaneous determination of 14 nucleosides and nucleobases in cultured Cordyceps using ultra-performance liquid chromatography.
PubMed: Choice of endogenous control for gene expression in nonsmall cell lung cancer.
PubMed: Natural and newly synthesized hydroxy-1-aryl-isochromans: a class of potential antioxidants and radical scavengers.
PubMed: Effects of propolis on hypoxanthine-xanthine oxidase-induced toxicity in cultivated human cells and on neutrophil elastase activity.
PubMed: The mutagenic potentiator effect of chlorophyllin by the HGPRT assay.
PubMed: [Production of monoclonal antibodies specific for the ABO blood group and rhesus D antigens].
PubMed: [Role of xanthine oxidase and xanthine dehydrogenase systems in thymocyte apoptosis, induced by papaverine].
PubMed: [Dietary fiber inhibits the incidence of hepatic metastasis with the anti-oxidant activity and portal scavenging functions].
PubMed: Nitric oxide inhibits tissue factor synthesis, expression and activity in human monocytes by prior formation of peroxynitrite.
PubMed: Potential antitumor alpha-methylene-gamma-butyrolactone-bearing nucleic acid base. 3. Synthesis of 5'-methyl-5'-[(6-substituted-9H-purin-9-yl)methyl]-2'-oxo-3'- methylenetetrahydrofurans.
PubMed: Serum hypoxanthine and xanthine concentrations in horses heterozygous for combined immunodeficiency.
PubMed: High-performance liquid chromatographic assay for N2-[5-(hypoxanthin-9-yl)pentyloxycarbonyl]-L-arginine (ST 789) in plasma by cyclization with benzoin and fluorimetric detection.
PubMed: Superoxide radical scavenging activity of phenolic compounds.
PubMed: Effect of a new peptidyl-hypoxanthine derivative on natural killer cells and antitumor activity.
PubMed: Cultivation of a nocardioform acid-fast chemoautotrophic bacterium from armadillo tissues infected with Mycobacterium leprae.
PubMed: Synthetic biological response modifiers; Part 1. Synthesis and immunomodulatory properties of some N2-(omega-(hypoxanthin-9-yl)alkoxycarbonyl)-L-arginines.
PubMed: [Incidence of somatic mutations of the lymphocytes in subjects working in an environment with cancer risk].
PubMed: High-performance liquid chromatographic evaluation of PCF 39, a new immunomodulator agent.
PubMed: [Quantitative evaluation of the mutagenic potential of benzo(a)pyrene by in vitro and in vivo tests].
PubMed: [Creatine kinase of rat lymphocytes and its activity as affected by adenosine, cAMP, AMP and products of their transformation].
PubMed: Ovalbumin is synthesized in mouse cells transformed with the natural chicken ovalbumin gene.
PubMed: [Studies on xanthin, hypoxanthin and calcium urate crystals].
PubMed: [Not available].
PubMed: THE CHEMISTRY OF THE LIVER IN ACUTE YELLOW ATROPHY.
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