Description

Jasmone (CAS 488-10-8) is a naturally occurring organic compound belonging to the class of cyclopentenones, with the molecular formula C₁₁H₁₆O. This high-purity compound is widely recognized for its role as a key fragrance ingredient, imparting a delicate floral and jasmine-like aroma, making it indispensable in perfumery and flavor industries. Available in stabilized and analytical standard grades, our Jasmone is rigorously tested for quality, ensuring consistency in research and industrial applications. Its cis-configuration ((Z)-Jasmone) enhances its olfactory properties, making it a preferred choice for high-end formulations. Suitable for GC/MS, HPLC, and other analytical techniques, this product is ideal for researchers and manufacturers requiring premium-grade materials.

Properties

• CAS Number: 488-10-8
• Complexity: 233
• IUPAC Name: 3-methyl-2-[(Z)-pent-2-enyl]cyclopent-2-en-1-one
• InChI: InChI=1S/C11H16O/c1-3-4-5-6-10-9(2)7-8-11(10)12/h4-5H,3,6-8H2,1-2H3/b5-4-
• InChI Key: XMLSXPIVAXONDL-PLNGDYQASA-N
• Exact Mass: 164.120115130
• Molecular Formula: C11H16O
• Molecular Weight: 164.24
• SMILES: CC/C=CCC1=C(CCC1=O)C
• Topological: 17.1
• Monoisotopic Mass: 164.120115130
• Physical Description: Liquid
• Color/Form: Oil
• Odor: Odor of jasmine
• Taste: Woody, bitter, tea, with a citrus and floral nuance at 25 ppm
• Boiling Point: 285 °C
• Flash Point: 107 °C – closed cup
• Solubility: Slightly soluble in water
• Density: 0.9437 g/cu cm at 22 °C
• Stability/Shelf Life: Stable under recommended storage conditions.
• Refractive Index: Oil, odor of jasmine, boiling pt: 142 °C at 23 mm Hg, refraction index: 1.4974 at 20 °C, uv max: 234 nm /trans-Jasmone/
• Synonyms: cis-Jasmone, JASMONE, 488-10-8, (Z)-Jasmone, FEMA No. 3196, cis-3-Methyl-2-(2-pentenyl)-2-cyclopenten-1-one, UNII-RC4W0G9YUK, 3-Methyl-2-pent-2-enylcyclopent-2-enone, RC4W0G9YUK, EINECS 207-668-4, BRN 1907713, DTXSID4047092, 3-Methyl-2-(2-pentenyl)-2-cyclopenten-1-one, (Z)-, JASMONE [FHFI], JASMONE [MI], 3-Methyl-2-(2-pentenyl)-2-cyclopenten-1-one, DTXCID2027092, 3-methyl-2-(pent-2Z-enyl)cyclopent-2-enone, 3-Methyl-2-n-penten-2′-ylcyclopenten-2-one, HSDB 8273, 4-07-00-00337 (Beilstein Handbook Reference), 3-Methyl-2-(2-cis-pentenyl)-2-cyclopenten-1-one, 2-Cyclopenten-1-one, 3-methyl-2-(2Z)-2-penten-1-yl-, (z)-3-methyl-2-(2-pentenyl)-2-cyclopenten-1-one, 3-Methyl-2-[(2Z)-2-pentenyl]-2-cyclopenten-1-one, METHYL-2-(2-PENTENYL)-2-CYCLOPENTEN-1-ONE, (Z)-, 3-, 3-Methyl-2-((2Z)-2-pentenyl)-2-cyclopenten-1-one, 3-Methyl-2-(2Z)-2-penten-1-yl-2-cyclopenten-1-one, 2-Cyclopenten-1-one, 3-methyl-2-((2Z)-2-penten-1-yl)-, xmlsxpivaxondl-plngdyqasa-n, cis-Jasmon, (Z)-3-Methyl-2-(pent-2-en-1-yl)cyclopent-2-enone, cis-?Jasmone, 2-Cyclopenten-1-one, 3-methyl-2-(2-pentenyl)-, (Z)-, 3-methyl-2-[(Z)-pent-2-enyl]cyclopent-2-en-1-one, 3-Methyl-2-(cis-2-penten-1-yl)-2-cyclopenten-1-one, MFCD00001402, CHEBI:6084, 3-Methyl-2-(cis-2-pentenyl)-2-cyclopenten-1-one, 3-methyl-2-[(2Z)-pent-2-en-1-yl]cyclopent-2-en-1-one, 2-Cyclopenten-1-one, 3-methyl-2-(2Z)-2-pentenyl- (9CI), (Z)-3-Methyl-2-(2-pentenyl)-2-cyclopentenone, 2-Cyclopenten-1-one, 3-methyl-2-(2-pentenyl)-, (Z)- (8CI), 2-Cyclopenten-1-one, 3-methyl-2-(2Z)-2- pentenyl-, Jasmone (6CI), Jasmone, 90%, cis-3-methyl-2-pent-2-enyl-cyclopent-2-enone, cis-Jasmone, stabilized, cis-?Jasmone (Standard), Jasmone, analytical standard, SCHEMBL20385, CHEMBL2251602, SCHEMBL19327677, HY-N7058R, AAA48810, BCP18948, CMC_7381, HY-N7058, Tox21_301825, AC7789, LMFA02020009, MSK014169, s4960, AKOS024318891, CCG-266315, CS-W017899, GS-3251, NCGC00256139-01, CAS-488-10-8, DA-62347, J0003, NS00012777, ST50407058, C08490, EN300-7400412, Q418077, 2-((2Z)pent-2-enyl)-3-methylcyclopent-2-en-1-one, 3-methyl-2-[(Z)-pent-2-enyl]-cyclopent-2-en-1-one, 2-cyclopenten-1-one, 3-methyl-2-[(2Z)-2-pentenyl]-, 3-Methyl-2-[(2Z)-2-pentenyl]-2-cyclopenten-1-one #

Jasmone is primarily used as a fragrance component in perfumes, cosmetics, and personal care products due to its floral and jasmine-like scent. In agriculture, it serves as a semiochemical, influencing insect behavior and plant defense mechanisms. Researchers also utilize Jasmone in studies related to plant signaling pathways and stress responses.

Safety and Hazards

GHS Hazard Statements

• H315: Causes skin irritation [Warning Skin corrosion/irritation]
• H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335: May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Skin Irrit. 2 (13.4%)
• Eye Irrit. 2 (13.4%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.