Chemistry:Myristic acid
From HandWiki
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| Names | |
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| Preferred IUPAC name
Tetradecanoic acid | |
| Other names
C14:0 (Lipid numbers)
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C14H28O2 | |
| Molar mass | 228.376 g·mol−1 |
| Appearance | colorless or white solid |
| Density | 1.03 g/cm3 (−3 °C)[2] 0.99 g/cm3 (24 °C)[3] 0.8622 g/cm3 (54 °C)[4] |
| Melting point | 54.4 °C (129.9 °F; 327.5 K)[9] |
| Boiling point | 326.2 °C (619.2 °F; 599.3 K) at 760 mmHg 250 °C (482 °F; 523 K) at 100 mmHg[4] 218.3 °C (424.9 °F; 491.4 K) at 32 mmHg[3] |
| 13 mg/L (0 °C) 20 mg/L (20 °C) 24 mg/L (30 °C) 33 mg/L (60 °C)[5] | |
| Solubility | Soluble in alcohol, acetates, C6H6, haloalkanes, phenyls, nitros[5] |
| Solubility in acetone | 2.75 g/100 g (0 °C) 15.9 g/100 g (20 °C) 42.5 g/100 g (30 °C) 149 g/100 g (40 °C)[5] |
| Solubility in benzene | 6.95 g/100 g (10 °C) 29.2 g/100 g (20 °C) 87.4 g/100 g (30 °C) 1.29 kg/100 g (50 °C)[5] |
| Solubility in methanol | 2.8 g/100 g (0 °C) 17.3 g/100 g (20 °C) 75 g/100 g (30 °C) 2.67 kg/100 g (50 °C)[5] |
| Solubility in ethyl acetate | 3.4 g/100 g (0 °C) 15.3 g/100 g (20 °C) 44.7 g/100 g (30 °C) 1.35 kg/100 g (40 °C)[5] |
| Solubility in toluene | 0.6 g/100 g (−10 °C) 3.2 g/100 g (0 °C) 30.4 g/100 g (20 °C) 1.35 kg/100 g (50 °C)[5] |
| log P | 6.1[4] |
| Vapor pressure | 0.01 kPa (118 °C) 0.27 kPa (160 °C)[6] 1 kPa (186 °C)[4] |
| -176·10−6 cm3/mol | |
| Thermal conductivity | 0.159 W/m·K (70 °C) 0.151 W/m·K (100 °C) 0.138 W/m·K (160 °C)[7] |
Refractive index (nD)
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1.4723 (70 °C)[4] |
| Viscosity | 7.2161 cP (60 °C) 3.2173 cP (100 °C) 0.8525 cP (200 °C) 0.3164 cP (300 °C)[8] |
| Structure | |
| Monoclinic (−3 °C)[2] | |
| P21/c[2] | |
a = 31.559 Å, b = 4.9652 Å, c = 9.426 Å[2] α = 90°, β = 94.432°, γ = 90°
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| Thermochemistry | |
Heat capacity (C)
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432.01 J/mol·K[4][6] |
Std enthalpy of
formation (ΔfH⦵298) |
−833.5 kJ/mol[4][6] |
Std enthalpy of
combustion (ΔcH⦵298) |
8675.9 kJ/mol[6] |
| Hazards | |
| GHS pictograms |  [10]
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| GHS Signal word | Warning |
| H315[10] | |
| NFPA 704 (fire diamond) | |
| Flash point | > 110 °C (230 °F; 383 K)[11] |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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>10 g/kg (rats, oral)[11] |
| Related compounds | |
Related esters of myristic acid
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Isopropyl myristate Phorbol myristate acetate Myristylbenzylmorphine Dimyristoylphosphatidylethanolamine |
Related compounds
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Tridecanoic acid, Pentadecanoic acid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Myristic acid (IUPAC name: tetradecanoic acid) is a common saturated fatty acid with the molecular formula CH
3(CH
2)
12COOH. Its salts and esters are commonly referred to as myristates or tetradecanoates. The name of the acyl group derived from myristic acid is myristoyl or tetradecanoyl. The acid is named after the binomial name for nutmeg (Myristica fragrans), from which it was first isolated in 1841 by Lyon Playfair.[12]
Occurrence
Nutmeg butter has 75% trimyristin, the triglyceride of myristic acid and a source from which it can be synthesised.[13] Besides nutmeg, myristic acid is found in palm kernel oil, coconut oil, butterfat, 8–14% of bovine milk, and 8.6% of breast milk as well as being a minor component of many other animal fats.[9] It is found in spermaceti, the crystallized fraction of oil from the sperm whale. It is also found in the rhizomes of the Iris, including Orris root.[14][15]
Chemical behaviour
Myristic acid acts as a lipid anchor in biomembranes.[16]
Reduction of myristic acid yields myristyl aldehyde and myristyl alcohol.
Health effects
Myristic acid consumption raises low-density lipoprotein (LDL) cholesterol.[17][18]
See also
References
- ↑ Merck Index, 11th Edition, 6246
- ↑ 2.0 2.1 2.2 2.3 Bond, Andrew D. (2003). "On the crystal structures and melting point alternation of the n-alkyl carboxylic acids". Royal Society of Chemistry. http://www.rsc.org/suppdata/nj/b3/b307208h/b307208h.pdf.
- ↑ 3.0 3.1 Chuah, T.G.; Rozanna, D.; Salmiah, A.; Thomas, Choong S.Y.; Sa’ari, M. (2006). "Fatty Acids used as Phase Change Materials (PCMs) for Thermal Energy Storage in Building Material Applications". University Putra Malaysia. http://dspace.unimap.edu.my/bitstream/handle/123456789/14118/008_010_012_014-015_fatty%20a.pdf.
- ↑ 4.0 4.1 4.2 4.3 4.4 4.5 4.6 Lide, David R., ed (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. ISBN 978-1-4200-9084-0.
- ↑ 5.0 5.1 5.2 5.3 5.4 5.5 5.6 Seidell, Atherton; Linke, William F. (1940). Solubilities of Inorganic and Organic Compounds (3rd ed.). New York: D. Van Nostrand Company. pp. 762–763. http://babel.hathitrust.org/cgi/pt?id=mdp.39015082385801;view=1up;seq=770.
- ↑ 6.0 6.1 6.2 6.3 Tetradecanoic acid in Linstrom, Peter J.; Mallard, William G. (eds.); NIST Chemistry WebBook, NIST Standard Reference Database Number 69, National Institute of Standards and Technology, Gaithersburg (MD), http://webbook.nist.gov
- ↑ Vargaftik, Natan B. (1993). Handbook of Thermal Conductivity of Liquids and Gases (illustrated ed.). CRC Press. p. 305. ISBN 978-0-8493-9345-7. https://books.google.com/books?id=DFo1sZBwdNgC&pg=PA305.
- ↑ Yaws, Carl L. (2009). Transport Properties of Chemicals and Hydrocarbons. New York: William Andrew Inc.. p. 177. ISBN 978-0-8155-2039-9. https://books.google.com/books?id=NbvExWe30YsC&pg=PA177.
- ↑ 9.0 9.1 Beare-Rogers, J.L.; 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.
- ↑ 10.0 10.1 Sigma-Aldrich Co., Myristic acid.
- ↑ 11.0 11.1 11.2 "Myristic Acid". AroKor Holdings Inc.. http://www.chemicalland21.com/industrialchem/organic/MYRISTIC%20ACID.htm.
- ↑ Playfair, Lyon (2009). "XX. On a new fat acid in the butter of nutmegs". Philosophical Magazine. Series 3 18 (115): 102–113. doi:10.1080/14786444108650255. ISSN 1941-5966. https://zenodo.org/record/1431027.
- ↑ Beal, G. D. (1926). "Myristic Acid". Organic Syntheses 6: 66. doi:10.15227/orgsyn.006.0066. http://www.orgsyn.org/demo.aspx?prep=CV1P0379.
- ↑ Council of Europe, August 2007 Natural Sources of Flavourings, Volume 2, p. 103, at Google Books
- ↑ John Charles Sawer Odorographia a natural history of raw materials and drugs used in the perfume industry intended to serve growers, manufacturers and consumers, p. 108, at Google Books
- ↑ Cox, David L. Nelson, Michael M. (2005). Lehninger principles of biochemistry (4th ed.). New York: W.H. Freeman. ISBN 978-0716743392. https://archive.org/details/lehningerprincip00lehn_0.
- ↑ Mensink, Ronald P. (2016). "Effects of saturated fatty acids on serum lipids and lipoproteins: a systematic review and regression analysis". World Health Organization. https://apps.who.int/iris/bitstream/handle/10665/246104/9789241565349-eng.pdf.
- ↑ "Effects of oils and solid fats on blood lipids: a systematic review and network meta-analysis". J Lipid Res 59 (9): 1771–1782. 2018. doi:10.1194/jlr.P085522. PMID 30006369.
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