1-Dotriacontanol
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| Identifiers
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CAS Number
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3D model (JSmol)
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| ChemSpider
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| UNII
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InChI=1S/C32H66O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-32-33/h33H,2-32H2,1H3 YKey: QOEHNLSDMADWEF-UHFFFAOYSA-N YInChI=1/C32H66O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-32-33/h33H,2-32H2,1H3 Key: QOEHNLSDMADWEF-UHFFFAOYAH
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OCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
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| Properties
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Chemical formula
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C32H66O
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| Molar mass
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466.879 g·mol−1
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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1-Dotriacontanol is a fatty alcohol with 32 carbon atoms. It has been found in Prosopis glandulosa and Euphorbia granulata.[1]
References
Alcohols |
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| By consumption | Alcohols found in alcoholic drinks | |
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| Medical alcohol | |
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| Toxic alcohols | |
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Primary alcohols (1°) | | Methanol |
- 4-Methylcyclohexanemethanol
- Aminomethanol
- Cyclohexylmethanol
- Methoxymethanol
- Methylazoxymethanol
- Trifluoromethanol
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| Ethanol | |
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| Butanol | |
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Straight-chain saturated C1 — C9 | |
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Straight-chain saturated C10 — C19 | |
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Straight-chain saturated C20 — C29 | |
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Straight-chain saturated C30 — C39 |
- 1-Triacontanol (melissyl / myricyl)
- 1-Hentriacontanol
- 1-Dotriacontanol (lacceryl)
- 1-Tritriacontanol
- 1-Tetratriacontanol (geddyl)
- 1-Pentatriacontanol
- 1-Hexatriacontanol
- 1-Heptatriacontanol
- 1-Octatriacontanol
- 1-Nonatriacontanol
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Straight-chain saturated C40 — C49 |
- 1-Tetracontanol
- 1-Hentetracontanol
- 1-Dotetracontanol
- 1-Tritetracontanol
- 1-Tetratetracontanol
- 1-Pentatetracontanol
- 1-Hexatetracontanol
- 1-Heptatetracontanol
- 1-Octatetracontanol
- 1-Nonatetracontanol
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Secondary alcohols (2°) | |
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Tertiary alcohols (3°) | |
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| Hydric alcohols | |
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| Amyl alcohols | |
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| Aromatic alcohols | |
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Saturated fatty alcohols | |
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Branched and unsaturated fatty alcohols | |
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| Sugar alcohols | | C1 — C7 | |
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Deoxy sugar alcohols | |
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Cyclic sugar alcohols | |
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| Glycylglycitols | |
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| Terpene alcohols | Monoterpene alcohols | |
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Sesquiterpene alcohols | |
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Diterpene alcohols | |
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| Dialcohols | |
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| Trialcohols | |
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| Sterols | |
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| Fluoroalcohols | |
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| Preparations |
- Substitution of haloalkane
- Carbonyl reduction
- Ether cleavage
- Hydrolysis of epoxide
- Hydration of alkene
- Ziegler process
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| Reactions |
- Deprotonation
- Protonation
- Alcohol oxidation
- Nucleophilic substitution
- Fischer–Speier esterification
- Williamson ether synthesis
- Elimination reaction
- Nucleophilic substitution of carbonyl group
- Friedel-Crafts alkylation
- Nucleophilic conjugate addition
- Transesterification
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Category
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