4-oxononanal
nonanal, 4-oxo-
 
Notes:
Present in used frying oils and water melon aroma. Tentatively identified in roast chicken fat
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CAS Number: 74327-29-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 277-818-1
XlogP3-AA: 1.20 (est)
Molecular Weight: 156.22492000
Formula: C9 H16 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 238.22 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.043000 mmHg @ 25.00 °C. (est)
Flash Point: 189.00 °F. TCC ( 87.00 °C. ) (est)
logP (o/w): 1.582 (est)
Soluble in:
 water, 6438 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 4-oxononanal usage levels up to:
 not for fragrance use.
 
Recommendation for 4-oxononanal 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 : 156288
National Institute of Allergy and Infectious Diseases: Data
 4-oxononanal
Chemidplus: 0074327290
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References:
 4-oxononanal
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 156288
Pubchem (sid): 135112057
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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
HMDB (The Human Metabolome Database): HMDB34716
FooDB: FDB013252
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
 watermelon fruit
Search Trop  Picture
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Synonyms:
4-oxononan-1-al
 nonanal, 4-oxo-
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Articles:
PubMed: Human carbonyl reductase catalyzes reduction of 4-oxonon-2-enal.
PubMed: Localization of isoketal adducts in vivo using a single-chain antibody.
PubMed: Detoxification of 4-hydroxynonenal (HNE) in keratinocytes: characterization of conjugated metabolites by liquid chromatography/electrospray ionization tandem mass spectrometry.
PubMed: Rapid cross-linking of proteins by 4-ketoaldehydes and 4-hydroxy-2-alkenals does not arise from the lysine-derived monoalkylpyrroles.
PubMed: The lipid peroxidation product 4-hydroxynonenal inhibits neurite outgrowth, disrupts neuronal microtubules, and modifies cellular tubulin.
PubMed: Immunochemical evidence supporting 2-pentylpyrrole formation on proteins exposed to 4-hydroxy-2-nonenal.
PubMed: Pyrrole formation from 4-hydroxynonenal and primary amines.
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