1-Nonanol - Wikipedia
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Names | |
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Preferred IUPAC name Nonan-1-ol | |
Other names 1-NonanolPelargonic alcoholNonyl alcoholn-Nonyl alcohol | |
Identifiers | |
CAS Number |
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3D model (JSmol) |
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ChEBI |
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ChEMBL |
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ChemSpider |
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DrugBank |
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ECHA InfoCard | 100.005.076 |
KEGG |
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PubChem CID |
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UNII |
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CompTox Dashboard (EPA) |
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InChI
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SMILES
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Properties | |
Chemical formula | C9H20O |
Molar mass | 144.258 g·mol−1 |
Appearance | Colorless liquid |
Density | 0.83 g/cm3[1] |
Melting point | −6 °C (21 °F; 267 K)[1] |
Boiling point | 214 °C (417 °F; 487 K)[1] |
Solubility in water | 0.13 g/L[1] |
Hazards | |
NFPA 704 (fire diamond) | 1 2 0 |
Flash point | 96 °C (205 °F; 369 K) |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose) | 3560 mg/kg (oral, rat)[2]4680 mg/kg (dermal, rabbit)[2] |
Related compounds | |
Related alcohols | 2-Nonanol |
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 |
1-Nonanol/ˈnoʊnənɒl/ is a straight chain fatty alcohol with nine carbon atoms and the molecular formula CH3(CH2)8OH. It is a colorless oily liquid with a citrus odor similar to citronella oil.
Nonanol occurs naturally in orange oil. The primary use of nonanol is in the manufacture of artificial lemon oil. Various esters of nonanol, such as nonyl acetate, are used in perfumery and flavors.
Nonanols
[edit]More common than 1-nonanol are its many isomers, including isononyl alcohol, which are typically produced by hydroformylation of octenes. Isomeric octenes are produced by dimerization of butenes. These alcohol mixtures are used as solvents in paints and as precursors to plasticizers.[3]
Toxicity
[edit]The LD50 (oral, rats) is about 2.98 g/kg.[3]
References
[edit]- ^ a b c d Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
- ^ a b Opdyke, DL (1973). "Monographs on fragrance raw materials". Food and Cosmetics Toxicology. 11 (1): 95–115. doi:10.1016/0015-6264(73)90065-5. PMID 4716134.
- ^ a b Falbe, Jürgen; Bahrmann, Helmut; Lipps, Wolfgang; Mayer, Dieter; Frey, Guido D. (2013). "Alcohols, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a01_279.pub2. ISBN 978-3-527-30385-4.
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Amyl alcohols |
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Saturatedfatty alcohols |
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Sugar alcohols |
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Terpene alcohols |
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Trialcohols |
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Sterols |
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Fluoroalcohols |
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Preparations |
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Reactions |
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- Fatty alcohols
- Primary alcohols
- Nonanols
- Chemical articles with multiple compound IDs
- Multiple chemicals in an infobox that need indexing
- ECHA InfoCard ID from Wikidata
- Articles containing unverified chemical infoboxes
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