Hopane
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| Names | |
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| IUPAC name
Hopane[2]
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| Systematic IUPAC name
(3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-3-(propan-2-yl)icosahydro-1H-cyclopenta[a]chrysene | |
| Other names
A'-Neogammacerane
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3D model (JSmol)
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PubChem CID
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| Properties | |
| C30H52 | |
| Molar mass | 412.746 g·mol−1 |
| Density | 0.952 g/ml |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Template:Chembox Footer/trackingTemplate:Short description
Hopane is a natural chemical compound classified as a triterpene. It forms the central core of a variety of other chemical compounds which are collectively known as hopanoids. The first compound of the hopane family to be isolated and characterised was hydroxyhopanone, found in dammar resin.[3] The name derives from Hopea, a tree genus from which dammar is obtained.[4]
See also
References
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- ^ Page Module:Citation/CS1/styles.css has no content."Hopane". IUPAC Recommendations 1999, Revised Section F: Natural Products and Related Compounds. 1999. Archived from the original on 2011-06-09. Retrieved 2021-03-30.
- ^ Page Module:Citation/CS1/styles.css has no content.International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 1536. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
- ^ Page Module:Citation/CS1/styles.css has no content.Mills J.S.; Werner A.E.A. (1955). "The Chemistry of Dammar Resin". Journal of the Chemical Society: 3132–40. doi:10.1039/jr9550003132.
- ^ Page Module:Citation/CS1/styles.css has no content.Pauzi Zakaria, Mohamad; Suratman, Suhaimi; Sayzwani Sukri, Nor; Vaezzadeh, Vahab; Wei Bong, Chu (2017). "APPLICATION OF PENTACYCLIC TRITERPANES AS A BIOMARKER IN IDENTIFYING THE SOURCE OF OIL POLLUTION IN THE EAST COAST OF PENINSULAR MALAYSIA". Perintis. 7 (2): 95–110.
