Chemistry:Thapsic acid
From HandWiki
| Names | |
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| Preferred IUPAC name
Hexadecanedioic acid | |
| Other names
1,14-Tetradecanedicarboxylic acid
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
| EC Number |
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| KEGG | |
| MeSH | C012346 |
PubChem CID
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| UNII | |
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| Properties | |
| C16H30O4 | |
| Molar mass | 286.412 g·mol−1 |
| Density | 1.209 g/cm3 |
| Melting point | 120 to 126 °C (248 to 259 °F; 393 to 399 K) |
| Boiling point | 457.5 °C (855.5 °F; 730.6 K) at 760 mmHg |
| 0.0057 g/L | |
| Hazards | |
| GHS pictograms | |
| GHS Signal word | Warning |
| H335, H319, H315 | |
| P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |

Thapsic acid (hexadecanedioic acid) is a naturally occurring dicarboxylic acid with the formula C16H30O4.[1] The name is derived from Thapsia, the Latin name for a Mediterranean perennial whose roots contain thapsic acid. It has a role as a human metabolite.[2] It is the conjugate acid of hexadecanedioate.
References
- ↑ Loewus, F. (6 December 2012) (in en). The Structure, Biosynthesis, and Degradation of Wood. Springer Science & Business Media. p. 189. ISBN 978-1-4615-8873-3. https://www.google.ru/books/edition/The_Structure_Biosynthesis_and_Degradati/d0P0BwAAQBAJ?hl=en&gbpv=1&dq=%22Isanolic+acid+%22&pg=PA189&printsec=frontcover. Retrieved 5 April 2025.
- ↑ Pettersen, JE; Aas, M (Nov 1974). "Subcellular localization of hexadecanedioic acid activation in human liver". J Lipid Res 15 (6): 551–556. PMID 4372285.
