octacosanoic acid
montanic acid
Identification
| Name | octacosanoic acid |
| IUPAC | octacosanoic acid |
| CAS Number | 506-48-9 |
| EINECS | 208-041-8 |
| FDA UNII | 4BKL1A0KJY |
| Molecular Formula | C28 H56 O2 |
| Molecular Weight | 424.75272000 |
| MDL Number | MFCD00002812 |
| Nikkaji Number | J11.820F |
| Beilstein | 1801616 |
| XlogP3 | 12.90 (est) |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 5.603e-008 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| 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. |
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Potential Uses
Natural Occurrence
Synonyms
montanic acid
octacosoic acid
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.