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| | (R)-(+)-BETA-CITRONELLOL Basic information |
| Product Name: | (R)-(+)-BETA-CITRONELLOL | | Synonyms: | (R)-(+)-BETA-CITRONELLOL;(R)-(+)-3,7-dimethyl-oct-6-en-1-ol;3,7-dimethyl-,(R)-6-Octen-1-ol;7-dimethyl-(theta)-6-octen-1-o;(+)-B-CITRONELLOL;(r)-(+)-β-citronellol;6-Octen-1-ol, 3,7-dimethyl- (R)-;R-(+)-B-CITRONELLOL | | CAS: | 1117-61-9 | | MF: | C10H20O | | MW: | 156.27 | | EINECS: | 214-250-5 | | Product Categories: | | | Mol File: | 1117-61-9.mol |  |
| | (R)-(+)-BETA-CITRONELLOL Chemical Properties |
| Melting point | -4.05°C (estimate) | | Boiling point | 112-113 °C12 mm Hg(lit.) | | density | 0.857 g/mL at 25 °C(lit.) | | vapor pressure | ~0.02 mm Hg ( 25 °C) | | refractive index | n20/D 1.456(lit.) | | Fp | 213 °F | | storage temp. | 2-8°C | | solubility | Chloroform (Sparingly, Sonicated), Ethyl Acetate, Methanol (Slightly) | | form | Oil | | pka | 15.13±0.10(Predicted) | | color | Colourless | | Odor | at 100.00 %. citronella oil rose leaf oily petal | | Odor Type | floral | | optical activity | [α]19/D +5.3°, neat | | BRN | 1721506 | | LogP | 3.239 (est) | | CAS DataBase Reference | 1117-61-9(CAS DataBase Reference) | | EPA Substance Registry System | 6-Octen-1-ol, 3,7-dimethyl-, (3R)- (1117-61-9) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | RIDADR | 3082 | | WGK Germany | 3 |
| | (R)-(+)-BETA-CITRONELLOL Usage And Synthesis |
| Description | (+)-β-Citronellol is a monoterpene that has been found in Cannabis. It inhibits degranulation of cultured mast cells by 21.3% when used at a concentration of 0.5 mM. Unlike (R)-citronellal, it does not reduce the perceived bitterness of caffeine when used at a concentration of 5.9 nM. Formulations containing (+)-β-citronellol have been used as fragrance ingredients in various cosmetics, toiletries, and cleaning products. | | Uses | (R)-(+)-β-Citronellol can undergo:
- Oxidation to form (R)-(+)-citronellal, an antifungal agent and (R)-(+)-citronellic acid.
- Intermolecular olefin aziridination with 2,2,2-trichloroethoxysulfonamide to form citronellol aziridine for ring-opening reactions.
- Series of reactions to form α2δ-ligands for treating generalized anxiety disorder and insomnia.
| | Definition | ChEBI: A citronellol that is oct-6-ene substituted by a hydroxy group at position 1 and methyl groups at positions 3 and 7 (the 3R-enantiomer). |
| | (R)-(+)-BETA-CITRONELLOL Preparation Products And Raw materials |
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