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Capric acid

From Wikipedia, the free encyclopedia
(Redirected from Sodium decanoate)
Not to be confused with Caproic acid or Caprylic acid.
Decanoic acid
Skeletal formula of decanoic acid
Ball-and-stick model of decanoic acid
Names
Preferred IUPAC name
Decanoic acid
Other names
Caprinic acid; Caprynic acid; Decoic acid; Decylic acid;
1-Nonanecarboxylic acid;
C10:0 (Lipid numbers)
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.005.798 Edit this at Wikidata
EC Number
  • 206-376-4
KEGG
RTECS number
  • HD9100000
UNII
  • InChI=1S/C10H20O2/c1-2-3-4-5-6-7-8-9-10(11)12/h2-9H2,1H3,(H,11,12) checkY
    Key: GHVNFZFCNZKVNT-UHFFFAOYSA-N checkY
  • InChI=1/C10H20O2/c1-2-3-4-5-6-7-8-9-10(11)12/h2-9H2,1H3,(H,11,12)
    Key: GHVNFZFCNZKVNT-UHFFFAOYAC
  • O=C(O)CCCCCCCCC
Properties
C10H20O2
Molar mass 172.268 g·mol−1
Appearance White crystals
Odor Strong rancid and unpleasant[1]
Density 0.893 g/cm3 (25 °C)[2]
0.8884 g/cm3 (35.05 °C)
0.8773 g/cm3 (50.17 °C)[3]
Melting point 31.6 °C (88.9 °F; 304.8 K)[6]
Boiling point 268.7 °C (515.7 °F; 541.8 K)[4]
0.015 g/100 mL (20 °C)[4]
Solubility Soluble in alcohol, ether, CHCl3, C6H6, CS2, acetone[1]
log P 4.09[4]
Vapor pressure 4.88·10−5 kPa (25 °C)[1]
0.1 kPa (108 °C)[4]
2.03 kPa (160 °C)[5][2]
Acidity (pKa) 4.9[1]
Thermal conductivity 0.372 W/m·K (solid)
0.141 W/m·K (liquid)[3]
1.4288 (40 °C)[1]
Viscosity 4.327 cP (50 °C)[4]
2.88 cP (70 °C)[3]
Structure
Monoclinic (−3.15 °C)[7]
P21/c[7]
a = 23.1 Å, b = 4.973 Å, c = 9.716 Å[7]
α = 90°, β = 91.28°, γ = 90°
Thermochemistry
475.59 J/mol·K[5]
−713.7 kJ/mol[4]
6079.3 kJ/mol[5]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Medium toxicity
Ingestion hazards
 May be toxic
Inhalation hazards
 May cause irritation
Skin hazards
 May be toxic on contact
GHS labelling:
GHS07: Exclamation mark[2]
Warning
H315, H319, H335[2]
P261, P305+P351+P338[2]
NFPA 704 (fire diamond)
[8]
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
1
0
Flash point 110 °C (230 °F; 383 K)[2]
Lethal dose or concentration (LD, LC):
10 g/kg (rats, oral)[8]
Safety data sheet (SDS) External MSDS
Related compounds
Related fatty acids
 Nonanoic acid, Undecanoic acid
Related compounds
 Decanol
Decanal
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Capric acid, also known as decanoic acid or decylic acid, is a saturated fatty acid, medium-chain fatty acid (MCFA), and carboxylic acid. Its formula is CH3(CH2)8COOH. Salts and esters of decanoic acid are called caprates or decanoates. The term capric acid is derived from the Latin "caper / capra" (goat) because the sweaty, unpleasant smell of the compound is reminiscent of goats.[9]

Occurrence

[edit]

Capric acid occurs naturally in coconut oil (about 10%) and palm kernel oil (about 4%), otherwise it is uncommon in typical seed oils.[10] It is found in the milk of various mammals and to a lesser extent in other animal fats.[6]

Two other acids are named after goats: caproic acid (a C6:0 fatty acid) and caprylic acid (a C8:0 fatty acid). Along with capric acid, these total 15% in goat milk fat.[11]

Production

[edit]

Capric acid can be prepared from oxidation of the primary alcohol decanol by using chromium trioxide (CrO3) oxidant under acidic conditions.[12]

Neutralization of capric acid or saponification of its triglyceride esters with sodium hydroxide yields sodium caprate, CH3(CH2)8CO−2Na+. This salt is a component of some types of soap.

Uses

[edit]

Capric acid is used in the manufacture of esters for artificial fruit flavors and perfumes. It is also used as an intermediate in chemical syntheses. It is used in organic synthesis and industrially in the manufacture of perfumes, lubricants, greases, rubber, dyes, plastics, food additives and pharmaceuticals.[8]

Pharmaceuticals

[edit]

Caprate ester prodrugs of various pharmaceuticals are available. Since capric acid is a fatty acid, forming a salt or ester with a drug will increase its lipophilicity and its affinity for adipose tissue. Since distribution of a drug from fatty tissue is usually slow, one may develop a long-acting injectable form of a drug (called a depot injection) by using its caprate form. Some examples of drugs available as a caprate ester include nandrolone (as nandrolone decanoate),[13] fluphenazine (as fluphenazine decanoate),[14] bromperidol (as bromperidol decanoate),[15] and haloperidol (as haloperidol decanoate).[15]

Effects

[edit]

Capric acid acts as a non-competitive AMPA receptor antagonist at therapeutically relevant concentrations, in a voltage- and subunit-dependent manner, and this is sufficient to explain its antiseizure effects.[16] This direct inhibition of excitatory neurotransmission by capric acid in the brain contributes to the anticonvulsant effect of the MCT ketogenic diet.[16] Decanoic acid and the AMPA receptor antagonist drug perampanel act at separate sites on the AMPA receptor, and so it is possible that they have a cooperative effect at the AMPA receptor, suggesting that perampanel and the ketogenic diet could be synergistic.[16]

Capric acid may be responsible for the mitochondrial proliferation associated with the ketogenic diet, and that this may occur via PPARγ receptor agonism and its target genes involved in mitochondrial biogenesis.[17][18] Complex I activity of the electron transport chain is substantially elevated by decanoic acid treatment.[17]

It should however be noted that orally ingested medium chain fatty acids would be very rapidly degraded by first-pass metabolism by being taken up in the liver via the portal vein, and are quickly metabolized via coenzyme A intermediates through β-oxidation and the citric acid cycle to produce carbon dioxide, acetate and ketone bodies.[19] Whether the ketones, β-hydroxybutyrate and acetone have direct antiseizure activity is unclear.[16][20][21][22]

See also

[edit]

References

[edit]
  1. ^ a b c d e CID 2969 from PubChem
  2. ^ a b c d e f Sigma-Aldrich Co., Decanoic acid. Retrieved on 2014-06-15.
  3. ^ a b c Mezaki, Reiji; Mochizuki, Masafumi; Ogawa, Kohei (2000). Engineering Data on Mixing (1st ed.). Elsevier Science B.V. p. 278. ISBN 978-0-444-82802-6.
  4. ^ a b c d e f 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. ^ a b c n-Decanoic 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) (retrieved 2014-06-15)
  6. ^ a b Beare-Rogers, J. L.; Dieffenbacher, A.; Holm, J.V. (1 January 2001). "Lexicon of lipid nutrition (IUPAC Technical Report)". Pure and Applied Chemistry. 73 (4): 685–744. doi:10.1351/pac200173040685. S2CID 84492006.
  7. ^ a b c D. Bond, Andrew (2004). "On the crystal structures and melting point alternation of the n -alkyl carboxylic acids". New Journal of Chemistry. 28 (1): 104–114. doi:10.1039/B307208H.
  8. ^ a b c "CAPRIC ACID". chemicalland21.com. AroKor Holdings. Archived from the original on 2018-10-19. Retrieved 2014-06-15.
  9. ^ "capri-, capr- +". Archived from the original on 2017-12-23. Retrieved 2012-09-28.
  10. ^ David J. Anneken, Sabine Both, Ralf Christoph, Georg Fieg, Udo Steinberner, Alfred Westfechtel "Fatty Acids" in Ullmann's Encyclopedia of Industrial Chemistry, 2006, Wiley-VCH, Weinheim. doi:10.1002/14356007.a10_245.pub2
  11. ^ Hilditch, T. P.; Jasperson, H. (1944). "The component acids of milk fats of the goat, ewe and mare". Biochemical Journal. 38 (5): 443–447. doi:10.1042/bj0380443. PMC 1258125. PMID 16747831.
  12. ^ McMurry, John (2008). Organic Chemistry (7th ed.). Thompson - Brooks/Cole. p. 624.
  13. ^ "ROLON 250mg/ml Solution for Injection - Summary of Product Characteristics (SmPC) - (emc)". www.medicines.org.uk. Archived from the original on 2020-09-22. Retrieved 2020-10-09.
  14. ^ "fluphenazine decanoate". The American Society of Health-System Pharmacists. Archived from the original on 8 December 2015. Retrieved 1 December 2015.
  15. ^ a b J. Elks, ed. (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 182–. ISBN 978-1-4757-2085-3. OCLC 1058412474.
  16. ^ a b c d Chang, Pishan; Augustin, Katrin; Boddum, Kim; Williams, Sophie; Sun, Min; Terschak, John A.; Hardege, Jörg D.; Chen, Philip E.; Walker, Matthew C.; Williams, Robin S. B. (February 2016). "Seizure control by decanoic acid through direct AMPA receptor inhibition". Brain. 139 (2): 431–443. doi:10.1093/brain/awv325. PMC 4805082. PMID 26608744.
  17. ^ a b Hughes, Sean David; Kanabus, Marta; Anderson, Glenn; Hargreaves, Iain P.; Rutherford, Tricia; Donnell, Maura O’; Cross, J. Helen; Rahman, Shamima; Eaton, Simon; Heales, Simon J. R. (May 2014). "The ketogenic diet component decanoic acid increases mitochondrial citrate synthase and complex I activity in neuronal cells". Journal of Neurochemistry. 129 (3): 426–433. doi:10.1111/jnc.12646. PMID 24383952. S2CID 206089968.
  18. ^ Malapaka, Raghu R. V.; Khoo, SokKean; Zhang, Jifeng; Choi, Jang H.; Zhou, X. Edward; Xu, Yong; Gong, Yinhan; Li, Jun; Yong, Eu-Leong; Chalmers, Michael J.; Chang, Lin; Resau, James H.; Griffin, Patrick R.; Chen, Y. Eugene; Xu, H. Eric (2 January 2012). "Identification and Mechanism of 10-Carbon Fatty Acid as Modulating Ligand of Peroxisome Proliferator-activated Receptors". Journal of Biological Chemistry. 287 (1): 183–195. doi:10.1074/jbc.M111.294785. PMC 3249069. PMID 22039047.
  19. ^ Chang, Pishan; Terbach, Nicole; Plant, Nick; Chen, Philip E.; Walker, Matthew C.; Williams, Robin S.B. (June 2013). "Seizure control by ketogenic diet-associated medium chain fatty acids". Neuropharmacology. 69: 105–114. doi:10.1016/j.neuropharm.2012.11.004. PMC 3625124. PMID 23177536.
  20. ^ Viggiano, Andrea; Pilla, Raffaele; Arnold, Patrick; Monda, Marcellino; D׳Agostino, Dominic; Coppola, Giangennaro (August 2015). "Anticonvulsant properties of an oral ketone ester in a pentylenetetrazole-model of seizure". Brain Research. 1618: 50–54. doi:10.1016/j.brainres.2015.05.023. PMID 26026798.
  21. ^ Rho, Jong M.; Anderson, Gail D.; Donevan, Sean D.; White, H. Steve (22 April 2002). "Acetoacetate, Acetone, and Dibenzylamine (a Contaminant in l-(+)-β-Hydroxybutyrate) Exhibit Direct Anticonvulsant Actions in Vivo". Epilepsia. 43 (4): 358–361. doi:10.1046/j.1528-1157.2002.47901.x. PMID 11952765. S2CID 31196417.
  22. ^ Ma, Weiyuan; Berg, Jim; Yellen, Gary (4 April 2007). "Ketogenic Diet Metabolites Reduce Firing in Central Neurons by Opening KATP Channels". The Journal of Neuroscience. 27 (14): 3618–3625. doi:10.1523/JNEUROSCI.0132-07.2007. PMC 6672398. PMID 17409226.
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