Chemistry:Undecylic acid
From HandWiki
Names | |
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IUPAC name
Undecanoic acid
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Other names
Hendecanoic acid
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
EC Number |
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KEGG | |
PubChem CID
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UNII | |
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Properties | |
C11H22O2 | |
Molar mass | 186.29 g/mol |
Appearance | Colourless crystals |
Density | 0.89 g/cm3 |
Melting point | 28.6 °C (83.5 °F; 301.8 K) |
Boiling point | 284 °C (543 °F; 557 K) |
Viscosity | mPa·s |
Structure | |
D | |
Hazards | |
Main hazards | Corrosive |
GHS pictograms | |
GHS Signal word | Warning |
H315, H319, H335 | |
P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501 | |
NFPA 704 (fire diamond) | |
Flash point | 113 °C (235 °F; 386 K) |
Related compounds | |
Related fatty acids
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Decanoic acid, Lauric acid |
Related compounds
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Undecanol |
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 | |
Undecylic acid (systematically named undecanoic acid) is a carboxylic acid with chemical formula CH
3(CH
2)
9COOH. It is often used as an antifungal agent, to treat ringworm and athlete's foot, for example.[1] Like decanoic acid, it has a distinctive, unpleasant odor.
See also
References
- ↑ Voicu, Raluca; Boukherroub, Rabah; Bartzoka, Vasiliki; Ward, Tim; Wojtyk, James T. C.; Wayner, Danial D. M. (2004-12-21). "Formation, characterization, and chemistry of undecanoic acid-terminated silicon surfaces: patterning and immobilization of DNA". Langmuir: The ACS Journal of Surfaces and Colloids 20 (26): 11713–11720. doi:10.1021/la047886v. ISSN 0743-7463. PMID 15595802. https://pubmed.ncbi.nlm.nih.gov/15595802/.
External links
Original source: https://en.wikipedia.org/wiki/Undecylic acid.
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