decanoyl acetaldehyde
decanoylacetaldehyde
 
Notes:
Isol. from Houttuynia cordata (Yu Xing Cao)
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CAS Number: 56505-80-7Picture of molecule3D/inchi
FDA UNII: NKP6GP1IRH
Nikkaji Web: J2.155.050G
Beilstein Number: 1771322
XlogP3: 3.70 (est)
Molecular Weight: 198.30574000
Formula: C12 H22 O2
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
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Google Scholar: with word "odor"Search
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PubMed: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 277.00 to  278.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.004000 mmHg @ 25.00 °C. (est)
Flash Point: 218.00 °F. TCC ( 103.20 °C. ) (est)
logP (o/w): 3.409 (est)
Soluble in:
 water, 222.7 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:
Aston Chemical
For experimental / research use only.
Dodecanal, 3-oxo-
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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 decanoyl acetaldehyde usage levels up to:
 not for fragrance use.
 
Recommendation for decanoyl acetaldehyde 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 : 122640
National Institute of Allergy and Infectious Diseases: Data
 3-oxododecanal
Chemidplus: 0056505807
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References:
 3-oxododecanal
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 122640
Pubchem (sid): 135078160
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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
KEGG (GenomeNet): C16947
HMDB (The Human Metabolome Database): HMDB34561
FooDB: FDB013073
VCF-Online: VCF Volatile Compounds in Food
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
 houttuynia cordata
Search Trop  Picture
 macadamia integrifolia shell
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Synonyms:
 decanoylacetaldehyde
3-oxododecanal
 dodecanal, 3-oxo-
 houttuynin
 houttuynine
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Articles:
PubMed: A comparative study of sodium houttuyfonate and 2-undecanone for their in vitro and in vivo anti-inflammatory activities and stabilities.
PubMed: Beneficial effects of houttuynin on ventricular remodeling induced by coronary artery ligation in rats.
PubMed: Anti HSV-1 flavonoid derivatives tethered with houttuynin from Houttuynia cordata.
PubMed: Identification of modification sites on human serum albumin and human hemoglobin adducts with houttuynin using liquid chromatography coupled with mass spectrometry.
PubMed: [In vivo studies on metabolic network compatibility of herba houttuyniae injection and sodium neohouttuynin injection in rats].
PubMed: [Effects of a new houttuyfonate derivative on proliferation of NIH3T3 cell and expression of syndecan-4 induced by tumor necrosis factor alpha].
PubMed: Derivatization of beta-dicarbonyl compound with 2,4-dinitrophenylhydrazine to enhance mass spectrometric detection: application in quantitative analysis of houttuynin in human plasma.
PubMed: [Orthogonal experiment using SFE-CO2 in extraction of essential oil from fresh Houttuynia cordata and analysis of essential oil by GC-MS].
PubMed: [Studies on GC fingerprint of volatile oil of Houttuynia cordata].
PubMed: [Studies on antimicrobial and antiviral compounds--synthesis of derivatives of decanoyl acetaldehyde (author's transl)].
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