|
| Jasmone Basic information |
Product Name: | Jasmone | Synonyms: | CIS-3-METHYL-2-(2-PENTENYL)-2-CYCLOPENTEN-1-ONE;FEMA 3196;JASMONE;JASMONE, CIS-;3-METHYL-2-(CIS-2-PENTENYL)-2-CYCLOPENTEN-1-ONE;3-METHYL-2-(2-PENTENYL)-2-CYCLOPENTEN-1-ONE;(z)-2-cyclopenten-1-on;2-Cyclopenten-1-one,3-methyl-2-(2-pentenyl)-,(Z)- | CAS: | 488-10-8 | MF: | C11H16O | MW: | 164.24 | EINECS: | 207-668-4 | Product Categories: | ketone Flavor | Mol File: | 488-10-8.mol | |
| Jasmone Chemical Properties |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-37/39 | WGK Germany | 2 | RTECS | GY7301000 | TSCA | Yes | HS Code | 29142990 | Hazardous Substances Data | 488-10-8(Hazardous Substances Data) | Toxicity | rabbit,LD50,skin,> 5gm/kg (5000mg/kg),Food and Cosmetics Toxicology. Vol. 17, Pg. 845, 1979. |
| Jasmone Usage And Synthesis |
Description | This has a jasmine odor. | Chemical Properties | Colorless viscous liquid | Chemical Properties | Jasmone has a floral, fruity, jasmine odor. cis-Jasmone is widely used in the creation of high quality florals like jasmine
and tuberose. Also used in the reconstitution of synthetic essential oils. | Occurrence | The cis-form is reportedly occurring naturally; it is found in the essential oils of jasmine (3%), jonquil, and
Pittosporum glabratum, in neroli oil, in peppermint (Mentha piperita), and in bergamot, apricot, raspberry, cinnamon, corn mint and
spearmint oils, beer, tea, soybean and heated beans. | Uses | Perfumery. | Definition | A ketone found in jasmine oil and other flower oils. | Taste threshold values | Taste characteristics at 25 ppm: woody, bitter, tea, with a citrus and floral nuance. | Synthesis Reference(s) | The Journal of Organic Chemistry, 39, p. 2317, 1974 DOI: 10.1021/jo00929a053 Synthetic Communications, 5, p. 1, 1975 DOI: 10.1080/00397917508063507 | Flammability and Explosibility | Notclassified | Synthesis | A review and classification on the synthesis of jasmone is available. |
| Jasmone Preparation Products And Raw materials |
|