Nonadecylic acid

Nonadecylic acid
Names
	IUPAC name Nonadecanoic acid
Identifiers
CAS Number	646-30-0 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	1786261
ChEBI	CHEBI:39246 ;
ChEMBL	ChEMBL1169674 ;
ChemSpider	12071 ;
ECHA InfoCard	100.010.431
EC Number	211-472-4;
PubChem CID	12591;
UNII	H6M3VYC62P ;
CompTox Dashboard (EPA)	DTXSID3060954 ;
	InChI InChI=1S/C19H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21/h2-18H2,1H3,(H,20,21) Key: ISYWECDDZWTKFF-UHFFFAOYSA-N ;
	SMILES O=C(O)CCCCCCCCCCCCCCCCCC;
Properties
Chemical formula	CH3(CH2)17COOH
Molar mass	298.50382 g/mol
Appearance	White flakes or powder
Melting point	68 to 70 °C (154 to 158 °F; 341 to 343 K)
Boiling point	236 °C (457 °F; 509 K) (10 mmHg) ; 297 °C (100 mmHg)
Solubility in water	Insoluble
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Nonadecylic acid, or nonadecanoic acid, is a 19-carbon saturated fatty acid with the chemical formula CH₃(CH₂)₁₇COOH. It forms salts called nonadecylates. Nonadecylic acid can be found in fats and vegetable oils, although it is rare.^{[citation needed]}

It is also present in the world of insects as the major constituent of the substance secreted by soldiers of the termite Rhinotermes marginalis for defence purposes.^[2]

Nonadecanoic acid has found applications in the field of metal lubrication.^[3]

The compound can be prepared by permanganate oxidation of 1-eicosene.^[4]

References

^ "Nonadecanoic acid". pubchem.ncbi.nlm.nih.gov.
^ Blum MS, Jones TH, Howard DF, Overal W (1982). "Biochemistry of termite defenses: Coptotermes, Rhinotermes and Cornitermes species". Comparative Biochemistry and Physiology Part B: Comparative Biochemistry. 71 (4): 731–733. doi:10.1016/0305-0491(82)90489-8.
^ Smith, Hilton A.; McGill, Robert M. (1957). "The Adsorption of n-Nonadecanoic Acid on Mechanically Activated Metal Surfaces". The Journal of Physical Chemistry. 61 (8): 1025–1036. doi:10.1021/j150554a001.
^ Lee, Donald G.; Lamb, Shannon E.; Chang, Victor S. (1981). "Carboxylic Acids from the Oxidation of Terminal Alkenes by Permanganate: Nonadecanoic Acid". Organic Syntheses. 60: 11. doi:10.15227/orgsyn.060.0011.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

[1] "Nonadecanoic acid". pubchem.ncbi.nlm.nih.gov.

[Blum-2] Blum MS, Jones TH, Howard DF, Overal W (1982). "Biochemistry of termite defenses: Coptotermes, Rhinotermes and Cornitermes species". Comparative Biochemistry and Physiology Part B: Comparative Biochemistry. 71 (4): 731–733. doi:10.1016/0305-0491(82)90489-8.

[Smith-3] Smith, Hilton A.; McGill, Robert M. (1957). "The Adsorption of n-Nonadecanoic Acid on Mechanically Activated Metal Surfaces". The Journal of Physical Chemistry. 61 (8): 1025–1036. doi:10.1021/j150554a001.

[OS-4] Lee, Donald G.; Lamb, Shannon E.; Chang, Victor S. (1981). "Carboxylic Acids from the Oxidation of Terminal Alkenes by Permanganate: Nonadecanoic Acid". Organic Syntheses. 60: 11. doi:10.15227/orgsyn.060.0011.

[1]

[2]

[3]

[4]

Nonadecylic acid

See also

References