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Octanoic acid
Octanoic acid
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Octanoic acid
Price: $30 / 20mg
CAS No.: 124-07-2
Catalog No.: CFN70050
Molecular Formula: C8H16O2
Molecular Weight: 144.2 g/mol
Purity: >=98%
Type of Compound: Miscellaneous
Physical Desc.: Oil
Source: The fruits of Morinda citrifolia
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / $7.0 / In-stock
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Octanoic acid is toxic for many insect species.
In vitro:
Plant Growth Regulation, 1996, 19(3):197-201.
The effect of ethylene, octanoic acid and a plant-derived smoke extract on the germination of light-sensitive lettuce seeds.[Reference: WebLink]
The effects of an aqueous plant-derived smoke extract, Octanoic acid and ethylene on germination of light-sensitive Grand Rapids lettuce seeds were investigated.
METHODS AND RESULTS:
The smoke extract brought about a concentration dependent increase in germination and a complete inhibition of germination at high concentrations. Octanoic acid could not induce germination. Ethylene at concentrations over 5 L L–1 increased lettuce seed germination, but not to the same degree as smoke. Aqueous smoke in combination with ethylene showed a synergistic effect on germination at suboptimal smoke concentrations. At high smoke concentrations the effect of ethylene was almost completely inhibited. Octanoic acid in combination with ethylene brought about a higher level of germination than with ethylene alone, but only at the highest concentration of Octanoic acid tested (1 mM). Standardized hexane and dichloromethane-partitioned smoke extracts and Octanoic acid were subjected to TLC separation. The R f -fractions in the smoke lanes showing activity in the lettuce seed bioassay did not correspond to the R f -value of Octanoic acid. As aqueous smoke can withstand autoclaving and can be separated by TLC and HPLC without loosing activity it is unlikely that the activity of aqueous smoke is linked to ethylene.
CONCLUSIONS:
It thus appears that the active compound in smoke is neither Octanoic acid nor ethylene.
Pesticide Biochemistry and Physiology, 1999, 65(2):90-101.
The Relation between Structures and Toxicity of Oxygenated Aliphatic Compounds Homologous to the Insecticide Octanoic Acid and the Chemotaxis of Two Species of Drosophila.[Reference: WebLink]
Octanoic acid is the main toxic compound for Drosophila melanogaster of the fruit of Morinda citrifolia, the host plant of Drosophila sechellia. It is known that Octanoic acid is toxic for many insect species.
METHODS AND RESULTS:
The possible relation between structure and toxic activity was compared in both species. Among fatty acids with 4 to 10 carbons, a stronger toxicity of the 8-carbon chain length was observed for D. melanogaster flies. Aldehydes and ethylic esters are much less toxic than the corresponding acids. Alcohols with similar chain lengths are also highly toxic but with similar LD50 values for both species. The structure-activity studies together with species differences suggest two different toxicity mechanisms. One of these is linked to the role of Octanoic acid, for which the D. melanogaster strain Indifferent, mutant for its atypical nonrepulsion by nonanol, shows resistance comparable to that of D. sechellia.
CONCLUSIONS:
Two other behaviors were shown to be modulated by Octanoic acid and in a species-different way: oviposition and chemotaxis. The oviposition of fertilized D. melanogaster females is inhibited, while that of D. sechellia is stimulated and in a quantitatively similar way. Hexanoic acid induces a similar, strong, stimulating effect on the egg laying of D. sechellia but only weak inhibition in D. melanogaster. Both acids also attract D. sechellia and repel D. melanogaster females. Behavioral data are discussed together with genetic information.
Octanoic acid Description
Source: The fruits of Morinda citrifolia
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

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After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 6.9348 mL 34.6741 mL 69.3481 mL 138.6963 mL 173.3703 mL
5 mM 1.387 mL 6.9348 mL 13.8696 mL 27.7393 mL 34.6741 mL
10 mM 0.6935 mL 3.4674 mL 6.9348 mL 13.8696 mL 17.337 mL
50 mM 0.1387 mL 0.6935 mL 1.387 mL 2.7739 mL 3.4674 mL
100 mM 0.0693 mL 0.3467 mL 0.6935 mL 1.387 mL 1.7337 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
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