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| | METHYL JASMONATE Basic information |
| Product Name: | METHYL JASMONATE | | Synonyms: | (1R)-3-Oxo-2α-[(Z)-2-pentenyl]-1α-cyclopentaneacetic acid methyl ester;(1R)-3-Oxo-2α-[(Z)-2-pentenyl]cyclopentane-1α-acetic acid methyl ester;(1R,2S)-2-[(Z)-2-Pentenyl]-3-oxocyclopentane-1-acetic acid methyl ester;Methyl 3R,7S-jasmonate;(1R)-3-Oxo-2β-[(Z)-2-pentenyl]cyclopentaneacetic acid methyl ester;Methyl cis-jasmonate;Methyl 2-(3-oxo-2-((Z)-pent-2-enyl)-cyclopentyl)-acetate;(3R,7R)-Methyl jasmonate | | CAS: | 1211-29-6 | | MF: | C13H20O3 | | MW: | 224.3 | | EINECS: | 214-918-6 | | Product Categories: | Aromatic Esters;Elisa Kit-plant ELISA Kit | | Mol File: | 1211-29-6.mol |  |
| | METHYL JASMONATE Chemical Properties |
| | METHYL JASMONATE Usage And Synthesis |
| Description | Methyl jasmonate has a powerful, floral-herbaceous, sweet, persistent odor. Can be isolated from jasmine oil; or it may be prepared synthetically (probably in the trans-form) from muconic
acid via the methyl-3-oxo-cyclopenthyl acetate. | | Chemical Properties | Methyl jasmonate has a powerful, floral–herbaceous, sweet, persistent odor. | | Chemical Properties | METHYL JASMONATE is a volatile component of jasmine flower absolute. It is
a colorless to pale yellow liquid, bp0.125 kPa 116–118 °C, d20
20 1.022–1.028, n20
D
1.473–1.477, possessing an odor reminiscent of the floral heart of jasmine.
Synthesis of the title compound is accomplished by reaction of (2Z)-2-buten-1-yl
bromide with Li in the presence of copper-(I) iodide, and the product is treated
with a mixture of 2-methylene- and 4-methylene-3-oxocyclopentylacetic acid
methyl ester. The aforementioned ester mixture is obtained by reaction of methyl
3-oxocyclopentylacetate with formaldehyde.
An alternative route uses a palladium-catalyzed decarboxylation of the readily
available substituted allyl 2-oxocyclopentanecarboxylates, which leads to the
corresponding cyclopentenones. Addition of dimethylmalonate, with subsequent
saponification/decarboxylation and, if necessary, (Z)-selective hydrogenation,
yields methyl jasmonate:
Methyl jasmonate exists in an equilibrium mixture in which the trans-isomer
dominates. But of all possible four enantiomeric isomers, chiefly the minor (+)-cis-isomer is responsible for the typical sensory properties of methyl jasmonate.
Therefore, several approaches to obtain this material selectively have been developed
either by directed syntheses or by enrichment using
special isomerization distillation techniques.
Methyl jasmonate is used in fine fragrances where it provides rich, soft effects in jasmine and muguet compositions. | | Occurrence | Reportedly identified in jasmine oil (Jasminum grandiflorum L.) and in Tunisian rosemary. Also found in
lemon peel oil, peppermint oil and green and fermented tea | | Uses | (-)-Jasmonic Acid Methyl Ester can be used in biological study where it can exert concn.-dependent effect on SE1 and upregulated SE1 expression in both young and mature leaves of Gynostemma pentaphyllum, with greater upregulation in young leaves than in mature leaves. | | Uses | Methyl ester in perfumes. | | Definition | ChEBI: A jasmonate ester that is the methyl ester of jasmonic acid. | | Aroma threshold values | Detection: 5.7 ppm | | Taste threshold values | Taste characteristics at 15 ppm: floral, fruity, green, waxy, seedy and melon-like | | Trade name | Jasmoneige® (Nippon Zeon), Splendione® (Firmenich) | | Synthesis | Can be isolated from jasmine oil; synthetically it can be prepared (probably in the trans-form) from muconic acid via the
methyl-3-oxo-cyclopentyl acetate |
| | METHYL JASMONATE Preparation Products And Raw materials |
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