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Product Name: |
Citronellol |
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Synonyms: |
2,6-Dimethyl-2-coten-8-ol;3,7-dimethyl-6-octanol;3,7-dimethyl-6-octen-1-o;3,7-dimethyl-6-octen-1-ol (citronellol);3,7-Dimethyl-6-octen-l-ol;Cephrol;Elenol;Rodinol |
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CAS: |
106-22-9 |
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MF: |
C10H20O |
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MW: |
156.27 |
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EINECS: |
203-375-0 |
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Product Categories: |
Flavors and Fragrances;Acyclic;Alcohols;Alkenes;Building Blocks;C9 to C10;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Acyclic Monoterpenes;Biochemistry;Terpenes;Alphabetical Listings;C-D |
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Mol File: |
106-22-9.mol |
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Melting point |
77-83 °C(lit.) |
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alpha |
-0.3～+0.3°(D/20℃)(neat) |
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Boiling point |
225 °C(lit.) |
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density |
0.857 g/mL at 25 °C(lit.) |
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vapor density |
5.4 (vs air) |
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vapor pressure |
~0.02 mm Hg ( 25 °C) |
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FEMA |
2309 | DL-CITRONELLOL |
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refractive index |
n20/D 1.456(lit.) |
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Fp |
209 °F |
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storage temp. |
2-8°C |
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pka |
15.13±0.10(Predicted) |
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form |
Liquid |
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color |
Clear almost colorless |
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Water Solubility |
SLIGHTLY SOLUBLE |
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JECFA Number |
1219 |
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Merck |
14,2330 |
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BRN |
1721507 |
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Stability: |
Stable. Incompatible with oxidizing agents. |
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InChIKey |
QMVPMAAFGQKVCJ-UHFFFAOYSA-N |
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CAS DataBase Reference |
106-22-9(CAS DataBase Reference) |
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NIST Chemistry Reference |
6-Octen-1-ol, 3,7-dimethyl-(106-22-9) |
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EPA Substance Registry System |
Citronellol (106-22-9) |
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Hazard Codes |
Xi,N |
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Risk Statements |
36/37/38-51/53-43-36/38 |
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Safety Statements |
26-36-24/25-61-37-24 |
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RIDADR |
UN 3082 9 / PGIII |
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WGK Germany |
1 |
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RTECS |
RH3400000 |
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Hazard Note |
Irritant |
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TSCA |
Yes |
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HazardClass |
9 |
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HS Code |
29052220 |
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Description |
Citronellol is a kind of natural occurring acyclic monoterpenoid which can be found in citronella oils such as Cymbopogon nardus ((+)-citronellol) and rose oils and Pelargonium geraniums ((-)-citronellol). In addition to be extracted from natural oils, it can also be manufactured by the hydrogenation of geraniol or nerol. It is mainly used in perfumes and insects repellents as well as being used as a mite attractant. It should be noted that it is an excellent mosquito repellent at short distances. Combination with beta-cyclodextrin can make it has an average duration time of 1.5 hour against the mosquitoes. It can also be used for the manufacture of rose oxide. One of its most common applications is for adding floral and citrus notes to perfumes, soaps and cosmetics. |
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Chemical Properties |
colourless liquid with a characteristic, rose-like, smell |
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Chemical Properties |
Citronellol has a characteristic rose-like odor. Because odor plays such an important part in selecting this material, there may be special grades of citronellol that do not meet the Essential Oil Association specification. These limits have been broadened enough to include best qualities of commercial citronellol and chemically pure citronellol. l-Citronellol has a sweet, peach-like flavor; d-citronellol has a bitter taste. |
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Occurrence |
l-Citronellol has been found in the plants of the Rosaceae family; d- and dl-citronellol have been identified in Verbenaceae, Labiatae, Rutaceae, Geraniaceae and others; citronellol has been reported in about 70 essential oils and in the oil of Rosa bourbonia; the Bulgarian rose oil has been reported to contain more than 50% l-citronellol, whereas East African geranium contains more than 80% of the d-isomer; the natural product is always optically active. Reported found in guava fruit, orange, bilberry, blackcurrant, nutmeg, ginger, corn mint oil (Mentha arvensis L. var. piperascens), mustard, pennyroyal oil (Mentha pulegium L.), hop oil, tea, coriander seed, cardamom, beer, rum, and apple juice. |
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Uses |
Perfumery, flavoring agent. |
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Uses |
citronellol is a constituent of plant essential oils. Found abundantly in eucalyptus oil. It is used for masking odor or providing a fragrance component to a cosmetic product. |
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Definition |
ChEBI: A monoterpenoid that is oct-6-ene substituted by a hydroxy group at position 1 and methyl groups at positions 3 and 7. |
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Aroma threshold values |
Detection at 11 ppb to 2.2 ppm; l-form, 40 ppb |
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Taste threshold values |
Taste characteristics at 20 ppm: floral, rose, sweet and green with fruity citrus nuances. |
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Safety Profile |
Poison by intravenous route. Moderately toxic by ingestion, skin contact, and intramuscular routes. A severe skin irritant. A combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALCOHOLS. |
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Chemical Synthesis |
It is generally accepted to distinguish rhodinol as the product isolated from geranium consisting of a mixture of l-citronellol and geraniol, whereas the name l-citronellol should be used to indicate the corresponding synthetic product with the highest level of purity; dl-citronellol can be prepared by catalytic hydrogenation of geraniol or by oxidation of allo-cyrnene; l-citronellol is prepared from (+) d-pinene via (+) cis-pinene to (+) 2,6-dimethyl-2,7-octadiene and, finally, isolating l-citronellol by hydrolysis of the aluminum-organo compound. |
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Purification Methods |
Purify them bydistillation through a cannon packed (Ni) column and the main cut collected at 84o/14mm and redistilled. Also purify via the benzoate. [IR: Eschenazi J Org Chem 26 3072 1961, Naves Bull Soc Chim Fr 505 1951, Beilstein 1 IV 2188.] |
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References |
https://eic.rsc.org/magnificent-molecules/citronellol/2000020.article |
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Preparation Products |
Geraniol-->Citronellal-->CITRONELLIC ACID-->Rose Oil-->3,7-DIMETHYL-7-OCTEN-1-OL-->Citronellyl acetate-->CITRONELLYL ISOBUTYRATE-->3,7-DIMETHYL-1-OCTANOL |
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Raw materials |
Etanol-->Hydrogen-->tert-Butanol-->Ferrous sulfate heptahydrate-->Citral-->Geraniol-->Citronellal-->NEROL-->ALPHA-PINENE-->Diisobutylaluminium hydride-->Eucalyptus oil-->Citronella oil-->Triisobutylaluminium-->Platinum balck-->Dihydromyrcene-->Citronellol –dextro |
