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| | 2-N-HEPTYLCYCLOPENTANONE Basic information |
| Product Name: | 2-N-HEPTYLCYCLOPENTANONE | | Synonyms: | NSC 78468;2-N-HEPTYLCYCLOPENTANONE;2-HEPTYLCYCLOPENTANONE;2-HEPTYLCYCLOPENTAN-1-ONE;HEPTONE;FLEURAMONE;2-heptyl-cyclopentanon;2-Heptyl-1-cyclopentanone | | CAS: | 137-03-1 | | MF: | C12H22O | | MW: | 182.3 | | EINECS: | 205-273-1 | | Product Categories: | | | Mol File: | 137-03-1.mol |  |
| | 2-N-HEPTYLCYCLOPENTANONE Chemical Properties |
| Boiling point | 264 °C | | density | 0.89 | | vapor pressure | 2.4Pa at 24℃ | | refractive index | 1.4526 (589.3 nm 20℃) | | storage temp. | Inert atmosphere,Room Temperature | | solubility | Practically insoluble in water, soluble in alcohol and oils. | | form | clear liquid | | color | Colorless to Almost colorless | | Odor | at 100.00 %. fresh fruity peach isojasmone oily tropical | | Odor Type | fruity | | Water Solubility | 31mg/L at 24℃ | | Cosmetics Ingredients Functions | FRAGRANCE
PERFUMING | | InChI | InChI=1S/C12H22O/c1-2-3-4-5-6-8-11-9-7-10-12(11)13/h11H,2-10H2,1H3 | | InChIKey | PJXHBTZLHITWFX-UHFFFAOYSA-N | | SMILES | C1(=O)CCCC1CCCCCCC | | LogP | 3.8 at 25℃ | | CAS DataBase Reference | 137-03-1(CAS DataBase Reference) | | EPA Substance Registry System | Cyclopentanone, 2-heptyl- (137-03-1) |
| Risk Statements | 36/37/38 | | Safety Statements | 26-37 | | RTECS | GY4950000 | | TSCA | TSCA listed | | HS Code | 2914.29.5000 | | toxicity | The acute oral LD50 value in rats was reported as > 5 g/kg (Shelanski, 1973). The acute dermal LD50 value in rabbits was reported as 5 g/kg (Shelanski, 1973). |
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ALFA
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| | 2-N-HEPTYLCYCLOPENTANONE Usage And Synthesis |
| Chemical Properties | 2-N-HEPTYLCYCLOPENTANONE is a colorless, viscous
liquid with a fruity, slightly herbaceous, jasmine odor; it has not yet been found in
nature.
2-Heptylcyclopentanone is used in, for example, jasmine, honeysuckle, and
lavender compositions. | | Occurrence | Has apparently not been reported to occur in nature. | | Uses | 2-Heptylcyclopentanone is used in perfume compositions for Jasmin, Honeysuckle, Reseda, Chypre, and many other fruity floral types. It blends exceptionally well with macrocyclic musks and Undecanolide and related materials. It also lends freshness and power to Lavender and other non-floral fragrance types. | | Preparation | By catalytic reduction of heptylidene cyclopentanone (Arctander, 1969). | | Flammability and Explosibility | Non flammable | | Trade name | Fleuramone (IFF), Projasmon P (Symrise） |
| | 2-N-HEPTYLCYCLOPENTANONE Preparation Products And Raw materials |
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