Caprylic acid
| Names | |
|---|---|
| Preferred IUPAC name
Octanoic acid | |
| Other names
1-Heptanecarboxylic acid
Octylic acid Octoic acid C8:0 (lipid numbers) | |
| Identifiers | |
CAS Number
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3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.004.253 |
| EC Number |
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| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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InChI
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SMILES
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| Properties | |
Chemical formula
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C8H16O2 |
| Molar mass | 144.214 g/mol |
| Appearance | Oily colorless liquid |
| Odor | Faint, fruity-acid; irritating |
| Density | 0.910 g/cm3[1] |
| Melting point | 16.7 °C (62.1 °F; 289.8 K)[3] |
| Boiling point | 239.7 °C (463.5 °F; 512.8 K)[1] |
Solubility in water
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0.068 g/100 mL[1] |
| Solubility | Soluble in alcohol, chloroform, ether, CS2, petroleum ether, acetonitrile |
| log P | 3.05 |
| Vapor pressure | 0.25 Pa |
| Acidity (pKa) |
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Magnetic susceptibility (χ)
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−101.60·10−6 cm3/mol |
Refractive index (nD)
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1.4285 |
| Thermochemistry | |
Heat capacity (C)
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297.9 J/K·mol |
Std enthalpy of
formation (ΔfH⦵298) |
−636 kJ/mol |
| Hazards | |
| GHS labelling: | |
Pictograms
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[4] |
Signal word
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Danger |
Hazard statements
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H314 |
Precautionary statements
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P264, P280, P301+P330+P331, P303+P361+P353, P304+P340+P310, P305+P351+P338+P310, P363, P405, P501 |
| NFPA 704 (fire diamond) | |
| Flash point | 130 °C (266 °F; 403 K) |
Autoignition
temperature |
440 °C (824 °F; 713 K) |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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10.08 g/kg (orally in rats)[1] |
| Related compounds | |
Related compounds
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Heptanoic acid, nonanoic acid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Caprylic acid (from Latin capra 'goat'), also known under the systematic name octanoic acid or C8 Acid, is a saturated fatty acid, medium-chain fatty acid (MCFA). It has the structural formula H3C−(CH2)6−COOH, and is a colorless oily liquid that is minimally soluble in water with a slightly unpleasant rancid-like smell and taste.[1] Salts and esters of octanoic acid are known as octanoates or caprylates. The name of the related acyl group is octanoyl, capryloyl, or caprylyl.[5] It is a common industrial chemical, which is produced by oxidation of the C8 aldehyde.[6] Its compounds are found naturally in the milk of various mammals and as a minor constituent of coconut oil and palm kernel oil.[3]
Two other acids are named after goats via the Latin word capra: caproic acid (C6) and capric acid (C10). Together, these three fatty acids comprise 15% of the fatty acids in goat milk fat.
- ^ a b c d e Budavari, Susan, ed. (1996). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (12th ed.). Merck. ISBN 0911910123.
- ^ Lide, D.R. (Ed.) (1990). CRC Handbook of Chemistry and Physics (70th Edn.). Boca Raton (FL):CRC Press.
- ^ a b Beare-Rogers, J.; Dieffenbacher, A.; Holm, J.V. (2001). "Lexicon of lipid nutrition (IUPAC Technical Report)". Pure and Applied Chemistry. 73 (4): 685–744. doi:10.1351/pac200173040685. S2CID 84492006.
- ^ Sigma-Aldrich Co., Octanoic acid. Retrieved on 2022-08-11.
- ^ "CHEBI:25650 - octanoyl group". Chemical Entities of Biological Interest (ChEBI). 23 November 2010. Retrieved 4 July 2024.
- ^ Riemenschneider, Wilhelm (2002). "Carboxylic Acids, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a05_235. ISBN 978-3-527-30673-2.