flavoglaucin
benzaldehyde, 2-heptyl-3,6-dihydroxy-5-(3-methyl-2-butenyl)-
 
Notes:
None found
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    • BOC Sciences
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      Product(s):
      523-73-9 Flavoglaucin 98%
      Flavoglaucin is a natural compound isolated from marine fungus Eurotium sp. SF
       
       
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CAS Number: 523-73-9Picture of molecule3D/inchi
Nikkaji Web: J11.709I
XlogP3-AA: 6.70 (est)
Molecular Weight: 304.42976000
Formula: C19 H28 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
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: 433.70 °C. @ 760.00 mm Hg (est)
Flash Point: 446.00 °F. TCC ( 230.20 °C. ) (est)
logP (o/w): 6.860 (est)
Soluble in:
 water, 0.02219 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.
Flavoglaucin 98%
Odor: characteristic
Use: Flavoglaucin is a natural compound isolated from marine fungus Eurotium sp. SF
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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 flavoglaucin usage levels up to:
 not for fragrance use.
 
Recommendation for flavoglaucin flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Chemical Carcinogenesis Research Information System: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 119037
National Institute of Allergy and Infectious Diseases: Data
 2-heptyl-3,6-dihydroxy-5-(3-methylbut-2-enyl)benzaldehyde
Chemidplus: 0000523739
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References:
 2-heptyl-3,6-dihydroxy-5-(3-methylbut-2-enyl)benzaldehyde
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 119037
Pubchem (sid): 135075431
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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:
 benzaldehyde, 2-heptyl-3,6-dihydroxy-5-(3-methyl-2-butenyl)-
6-heptyl-3-(3-methyl-2-butenyl)gentisaldehyde
2-heptyl-3,6-dihydroxy-5-(3-methyl-2-butenyl) benzaldehyde
2-heptyl-3,6-dihydroxy-5-(3-methyl-2-butenyl)benzaldehyde
2-heptyl-3,6-dihydroxy-5-(3-methylbut-2-enyl)benzaldehyde
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Articles:
PubMed: PTP1B inhibitory secondary metabolites from marine-derived fungal strains Penicillium spp. and Eurotium sp.
PubMed: Benzyl derivatives with in vitro binding affinity for human opioid and cannabinoid receptors from the fungus Eurotium repens.
PubMed: Evaluation of flavoglaucin, its derivatives and pyranonigrins produced by molds used in fermented foods for inhibiting tumor promotion.
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.
PubMed: A new radical scavenging anthracene glycoside, asperflavin ribofuranoside, and polyketides from a marine isolate of the fungus microsporum.
PubMed: Effect of weak acid preservatives on growth of bakery product spoilage fungi at different water activities and pH values.
PubMed: Modifying effects of fungal and herb metabolites on azoxymethane-induced intestinal carcinogenesis in rats.
PubMed: Toxicity of flavoglaucin from Aspergillus chevalieri in rabbits.
PubMed: The uncoupling effect of flavoglaucin, a quinol pigment from Aspergillus chevalieri (Mangin), on mitochondrial respiration.
PubMed: Eurotium (Aspergillus) repens metabolites and their biological activity.
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: Structure of flavoglaucin and auroglaucin.
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