EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

octacosanoic acid
montanic acid

Supplier Sponsors

Name:octacosanoic acid
CAS Number: 506-48-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:208-041-8
FDA UNII: 4BKL1A0KJY
Nikkaji Web:J11.820F
Beilstein Number:1801616
MDL:MFCD00002812
XlogP3:12.90 (est)
Molecular Weight:424.75272000
Formula:C28 H56 O2
NMR Predictor:Predict (works with chrome, Edge 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
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 5.603e-008 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Octacosanoic acid >98.0%(T)
Santa Cruz Biotechnology
For experimental / research use only.
Octacosanoic Acid ≥98%
Sigma-Aldrich: Aldrich
For experimental / research use only.
Octacosanoic Acid synthetic, ≥98%
sds
TCI AMERICA
For experimental / research use only.
Octacosanoic Acid >98.0%(T)
sds
 
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
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for octacosanoic acid usage levels up to:
 not for fragrance use.
 
Recommendation for octacosanoic acid flavor usage levels up to:
 not for flavor use.
 
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 :10470
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:nwg
octacosanoic acid
Chemidplus:0000506489
 
References:
 octacosanoic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):10470
Pubchem (cas):506-48-9
 
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
Golm Metabolome Database:Search
HMDB (The Human Metabolome Database):HMDB02348
FooDB:FDB007128
Export Tariff Code:2915.90.1800
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 marango stem
Search Trop Picture
 potato leaf
Search Trop Picture
 
Synonyms:
 montanic acid
 octacosoic acid
 

Articles:

PubMed:Sugarcane cells as origin of acid beverage floc in cane sugar.
PubMed:Comparison of three methods for the methylation of aliphatic and aromatic compounds.
PubMed:Chemical profiling of the major components in natural waxes to elucidate their role in liquid oil structuring.
PubMed:A new triterpenoid bearing octacosanoate from the stems and roots of Clerodendrum philippinum var. simplex (Verbenaceae).
PubMed:[Chemical constituents from the aerial part of Echinacea purpurea].
PubMed:Inhibition of saturated very-long-chain fatty acid biosynthesis by mefluidide and perfluidone, selective inhibitors of 3-ketoacyl-CoA synthases.
PubMed:[Studies on the chemical constituents of the petroleum ether portion of Nervilia fordii].
PubMed:Trace quantification of 1-octacosanol and 1-triacontanol and their main metabolites in plasma by liquid-liquid extraction coupled with gas chromatography-mass spectrometry.
PubMed:Chemical constituents from the fruits of Hippophae rhamnoides.
PubMed:[Studies on chemical constituents from roots of Angelica polymorpha].
PubMed:Chemical constituents from aerial part of Curcuma wenyujin.
PubMed:[Studies on chemical constituents from roots of Craibiodendron henryi].
PubMed:[Studies on the chemical constituents from Inula cappa (II)].
PubMed:The influence of the long chain fatty acid on the antagonistic activities of Rhizobium sin-1 lipid A.
PubMed:Partial phase behavior and micellar properties of tetrabutylammonium salts of fatty acids: unusual solubility in water and formation of unexpectedly small micelles.
PubMed:Lack of protective effect of D-003, a mixture of high-molecular-weight primary acids from sugar cane wax, on liver damage induced by galactosamine in rats.
PubMed:Effect of D-003 on intimal thickening and circulating endothelial cells in rabbit cuffed carotid artery.
PubMed:In vitro and in vivo study of octacosanol metabolism.
PubMed:Effect of D-003 on a subconvulsive dose of kainic Acid in rats.
PubMed:[Studies on chemical constituents from Eucommia ulmoides Oliv].
PubMed:Sinorhizobium meliloti strain 1021 produces a low-molecular-mass capsular polysaccharide that is a homopolymer of 3-deoxy-D-manno-oct-2-ulosonic acid harboring a phospholipid anchor.
PubMed:D-003 and warfarin interaction on the bleeding time and venous thrombosis experimentally induced in rats.
PubMed:Effect of D-003, a mixture of high molecular weight primary acids from sugar cane wax, on paracetamol-induced liver damage in rats.
PubMed:Synthesis and biological evaluation of Rhizobium sin-1 lipid A derivatives.
PubMed:[Studies on chemical constituents of two plants from Costus].
PubMed:Synergistic effect of D-003 and aspirin on experimental thrombosis models.
PubMed:Effect of D-003, a mixture of high molecular weight primary acids from sugar cane wax, on CL4C-induced liver acute injury in rats.
PubMed:[Studies on chemical constituents from Buddleja lindleyana Fert].
PubMed:Lack of developmental toxicity of D-003: a mixture of long-chain fatty acids in rats.
PubMed:D-003, a potential antithrombotic compound isolated from sugar cane wax with effects on arachidonic acid metabolites.
PubMed:Preliminary evaluation of the cytotoxic and genotoxic potential of D-003: Mixture of very long chain fatty acids.
PubMed:Inhibition of rat lipoprotein lipid peroxidation by the oral administration of D003, a mixture of very long-chain saturated fatty acids.
PubMed:Cellular fatty acid composition from Sarcobium lyticum (Legionella lytica comb. nov.)--an intracellular bacterial pathogen of amoebae.
PubMed:Inhibition of cholesterol biosynthesis in cultured fibroblasts by D003, a mixture of very long chain saturated fatty acids.
PubMed:Antiplatelet and antithrombotic effect of D-003.
PubMed:Chemical characterization of lipopolysaccharides from Legionella feeleii, Legionella hackeliae and Legionella jordanis.
PubMed:Lipopolysaccharides of Legionella erythra and Legionella oakridgensis.
PubMed:[The endotoxins of gram-negative bacteria: their structure and biological role].
PubMed:Chemical composition of lipopolysaccharides from Legionella bozemanii and Legionella longbeachae.
PubMed:Isolation and characterization of eceriferum (cer) mutants induced by T-DNA insertions in Arabidopsis thaliana.
PubMed:Long-chain alpha-hydroxy-(omega-1)-oxo fatty acids and alpha-hydroxy-1,omega-dioic fatty acids are cell wall constituents of Legionella (L. jordanis, L. maceachernii and L. micdadei).
PubMed:Identification of 27-oxo-octacosanoic acid and heptacosane-1,27-dioic acid in Legionella pneumophila.
PubMed:[Chemical constituents of the roots of Ostericum grosseserratum (Maxim.) Kitag].
PubMed:Distribution and phylogenetic significance of 27-hydroxy-octacosanoic acid in lipopolysaccharides from bacteria belonging to the alpha-2 subgroup of Proteobacteria.
PubMed:[The structure of trijuganone C from Salvia trijuga].
PubMed:[Chemical constituents of Adenophora stricta Miq].
PubMed:Structure and Biosynthesis of Cuticular Lipids: Hydroxylation of Palmitic Acid and Decarboxylation of C(28), C(30), and C(32) Acids in Vicia faba Flowers.
 
Notes:
Octacosanoic acid is a very-long-chain fatty acid found in human brain and visceral organs (PMID: 2474624) Octacosanoic acid is a higher aliphatic primary acids purified from sugar-cane (Saccharum officinarum L.) wax that has been shown to inhibit platelet aggregation induced ex vivo by addition of agonists to platelet-rich plasma (PRP) of rats, guinea pigs, and healthy human volunteers. (PMID: 5099499) Octacosanoic acid is formed from octacosanol via beta-oxidation. (PMID: 15847942) [HMDB]
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