1-heptacosanol
heptacosyl alcohol
 
Notes:
None found
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CAS Number: 2004-39-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 217-906-9
FDA UNII: VO02AJN4KP
Nikkaji Web: J128.783D
MDL: MFCD00057822
XlogP3: 13.30 (est)
Molecular Weight: 396.74252000
Formula: C27 H56 O
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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PubMed: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 420.20 °C. @ 760.00 mm Hg (est)
Flash Point: 279.00 °F. TCC ( 137.40 °C. ) (est)
logP (o/w): 13.100 (est)
Soluble in:
 water, 4.485e-007 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:
ExtraSynthese
For experimental / research use only.
1-Heptacosanol
Santa Cruz Biotechnology
For experimental / research use only.
1-Heptacosanol
Sigma-Aldrich: Sigma
For experimental / research use only.
1-Heptacosanol ≥98%
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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:
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 1-heptacosanol usage levels up to:
 not for fragrance use.
 
Recommendation for 1-heptacosanol 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 : 74822
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 heptacosan-1-ol
Chemidplus: 0002004399
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References:
 heptacosan-1-ol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 2004-39-9
Pubchem (cid): 74822
Pubchem (sid): 135033258
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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): Search
FooDB: FDB004328
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
 brussel sprout flower
Search Trop  Picture
 elder black elder flower
Search Trop  Picture
 grape root
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Synonyms:
1-heptacosanol (8CI)(9CI)
 heptacosyl alcohol
 heptacosan-1-ol
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Articles:
PubMed: Application and recovery of ionic liquids in the preparative separation of four flavonoids from Rhodiola rosea by on-line three-dimensional liquid chromatography.
PubMed: Microwave-assisted extraction of herbacetin diglucoside from flax (Linum usitatissimum L.) seed cakes and its quantification using an RP-HPLC-UV system.
PubMed: Herbacetin, a constituent of ephedrae herba, suppresses the HGF-induced motility of human breast cancer MDA-MB-231 cells by inhibiting c-Met and Akt phosphorylation.
PubMed: Separation of four flavonoids from Rhodiola rosea by on-line combination of sample preparation and counter-current chromatography.
PubMed: LC-NMR, NMR, and LC-MS identification and LC-DAD quantification of flavonoids and ellagic acid derivatives in Drosera peltata.
PubMed: Characterization of phenolic constituents from ephedra herb extract.
PubMed: Herbacetin induces apoptosis in HepG2 cells: Involvements of ROS and PI3K/Akt pathway.
PubMed: The antioxidant and anti-inflammatory effects of phenolic compounds isolated from the root of Rhodiola sachalinensis A. BOR.
PubMed: [Studies on the chemical constituents of Rhodiola rosea].
PubMed: The chain length of lignan macromolecule from flaxseed hulls is determined by the incorporation of coumaric acid glucosides and ferulic acid glucosides.
PubMed: Calpain inhibitory flavonoids isolated from Orostachys japonicus.
PubMed: Microbial metabolism of biologically active secondary metabolites from Nerium oleander L.
PubMed: Flavonol glucuronides and C-glucosidic ellagitannins from Melaleuca squarrosa.
PubMed: seco-Cycloartane triterpenes from Gardenia aubryi.
PubMed: The flavonoid herbacetin diglucoside as a constituent of the lignan macromolecule from flaxseed hulls.
PubMed: [Studies on the chemical constituents of Rhodiola dumulosa (II)].
PubMed: [Studies on the chemical constituents from Rhodiola dumulosa (I)].
PubMed: Electrospray mass spectrometric decomposition of some glucuronic acid-containing flavonoid diglycosides.
PubMed: New erythroxane-type diterpenoids from Fagonia boveana (Hadidi) Hadidi & Graf.
PubMed: Antioxidative phenolic compounds from the roots of Rhodiola sachalinensis A. Bor.
PubMed: [Studies on the chemical constituents of Rhodiola fastigita].
PubMed: Flavan-3-ols and flavonoids from Potentilla anserina.
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