auroglaucin
2-[(1E,3E,5E)-1,3,5-heptatrien-1-yl]-3,6-dihydroxy-5-(3-methyl-2-buten-1-yl)benzaldehyde
 
Notes:
None found
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CAS Number: 41451-81-4Picture of molecule3D/inchi
Nikkaji Web: J19.329A
XlogP3-AA: 5.40 (est)
Molecular Weight: 298.38194000
Formula: C19 H22 O3
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
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Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
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PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 477.10 °C. @ 760.00 mm Hg (est)
Flash Point: 494.00 °F. TCC ( 256.50 °C. ) (est)
logP (o/w): 6.210 (est)
Soluble in:
 water, 0.08557 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:
 None found
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Safety Information:
 
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: natural substances and extractives
Recommendation for auroglaucin usage levels up to:
 not for fragrance use.
 
Recommendation for auroglaucin 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 : 6434324
National Institute of Allergy and Infectious Diseases: Data
 2-[(1E,3E,5E)-hepta-1,3,5-trienyl]-3,6-dihydroxy-5-(3-methylbut-2-enyl)benzaldehyde
Chemidplus: 0041451814
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References:
 2-[(1E,3E,5E)-hepta-1,3,5-trienyl]-3,6-dihydroxy-5-(3-methylbut-2-enyl)benzaldehyde
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 6434324
Pubchem (sid): 135001236
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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
HMDB (The Human Metabolome Database): Search
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
 found in nature
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Synonyms:
 auroglaucine
 benzaldehyde, 2-[(1E,3E,5E)-1,3,5-heptatrien-1-yl]-3,6-dihydroxy-5-(3-methyl-2-buten-1-yl)-
2-[(1E,3E,5E)-hepta-1,3,5-trienyl]-3,6-dihydroxy-5-(3-methylbut-2-enyl)benzaldehyde
2-[(1E,3E,5E)-1,3,5-heptatrien-1-yl]-3,6-dihydroxy-5-(3-methyl-2-buten-1-yl)benzaldehyde
2-(1,3,5-heptatrienyl)-3,6-dihydroxy-5-(3-methyl-2-butenyl) benzaldehyde
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Articles:
PubMed: Structure of flavoglaucin and auroglaucin.
PubMed: [Synthetic studies on echinulin and related natural products. IV. Isolation, structure and synthesis of flavoglaucin-auroglaucin type natural products isolated from Aspergillus amstelodami (author's transl)].
PubMed: Inhibitory effects of benzaldehyde derivatives from the marine fungus Eurotium sp. SF-5989 on inflammatory mediators via the induction of heme oxygenase-1 in lipopolysaccharide-stimulated RAW264.7 macrophages.
PubMed: Prenylated indole diketopiperazine alkaloids from a mangrove rhizosphere soil derived fungus Aspergillus effuses H1-1.
PubMed: Benzyl derivatives with in vitro binding affinity for human opioid and cannabinoid receptors from the fungus Eurotium repens.
PubMed: Antioxidants produced by Eurotium herbariorum of filamentous fungi used for the manufacture of karebushi, dried bonito (Katsuobushi).
PubMed: Secondary metabolites from Eurotium species, Aspergillus calidoustus and A. insuetus common in Canadian homes with a review of their chemistry and biological activities.
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