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METHYL JASMONATE

METHYL JASMONATE Structure
CAS No.
1211-29-6
Chemical Name:
METHYL JASMONATE
Synonyms
Methyl cis-jasmonate;JASMONIC ACID METHYL ESTER;(1R)-3-Oxo-2α-[(Z)-2-pentenyl]-1α-cyclopentaneacetic acid methyl ester;Cmc_7389;Cmc_13964;FEMA 3410;JASMONEIGE;,2beta(z)]]-;METHYL JASMONATE;(-)-methyljasmonate
CBNumber:
CB4100148
Molecular Formula:
C13H20O3
Molecular Weight:
224.3
MOL File:
1211-29-6.mol
MSDS File:
SDS
Modify Date:
2024/8/13 17:19:14

METHYL JASMONATE Properties

alpha D -76.5° (c = 3.4 in CH3OH)
Boiling point 110 °C0.2 mm Hg(lit.)
Density 1.03 g/mL at 25 °C(lit.)
FEMA 3410 | METHYL JASMONATE
refractive index n20/D 1.474(lit.)
Flash point >230 °F
storage temp. Sealed in dry,Room Temperature
solubility Almost insoluble in water, soluble in alcohol and oils.
form oily liquid
Specific Gravity 1.02
color Colorless
Odor at 100.00 %. floral fresh petal magnolia oily waxy
Odor Type floral
JECFA Number 1400
LogP 2.12
CAS DataBase Reference 1211-29-6(CAS DataBase Reference)
EPA Substance Registry System Cyclopentaneacetic acid, 3-oxo-2-(2Z)-2-pentenyl-, methyl ester, (1R,2R)- (1211-29-6)

SAFETY

Risk and Safety Statements

WGK Germany  3

METHYL JASMONATE Chemical Properties,Uses,Production

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 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

Methyl ester in perfumes.

Definition

ChEBI: A jasmonate ester that is the methyl ester of jasmonic acid.

Trade name

Jasmoneige® (Nippon Zeon), Splendione® (Firmenich)

METHYL JASMONATE Preparation Products And Raw materials

Raw materials

Preparation Products

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(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 2-(3-oxo-2-((Z)-pent-2-enyl)-cyclopentyl)-acetate (3R,7R)-Methyl jasmonate Cmc_13964 Cmc_7389 Cyclopentaneacetic acid, 3-oxo-2-(2-pentenyl)-, methyl ester, (Z)-trans- (8ci) (1R,2R)-3-Oxo-2-(2Z)-2-penten-1-ylcyclopentaneacetic acid methyl ester methyl [1R-[1alpha,2beta(Z)]]-3-oxo-2-(pent-2-enyl)cyclopentaneacetate TRANS-3-OCTEN-2-ONE 98+% (-)-JASMONIC ACID METHYL ESTER 98% (HPLC) (±)-JASMONIC ACID METHYL ESTER 95% (HPLC) methyljasmonate,(E)-methyljasmonate Cyclopentaneacetic acid, 3-oxo-2-(2Z)-2-pentenyl-, methyl ester, (1R,2R)- 2-(2-PENTENYL)-3-METHOXYCARBONYLMETHYLCYCLOPENTANONE 3-OXO-2-(2-PENTENYL)CYCLOPENTANEACETIC ACID METHYL ESTER METHYL 3-OXO-2-(2-PENTENYL)CYCLOPENTANEACETATE METHYL (+/-)-JASMINATE METHYL (+/-)-JASMONATE METHYL JASMONATE FEMA 3410 ,2beta(z)]]- 3-oxo-2-(2-pentenyl)-,methylester,[1R-[1.alpha.,2.beta.(Z)]]-Cyclopentaneaceticacid Cyclopentaneacetic acid, 3-oxo-2-(2-pentenyl)-, methyl ester, [1R-[1alpha,2beta(Z)]]- Cyclopentaneacetic acid, 3-oxo-trans-2-(cis-2-pentenyl), methyl ester Cyclopentaneaceticacid,3-oxo-2-(2-pentenyl)-,methylester,[1R-[1.alpha.,2.beta.(Z)]]- cyclopentaneaceticacid,3-oxo-2-(2-pentenyl)-,methylester,[1theta-[1alpha Cyclopentaneaceticacid,3-oxo-trans-2-(cis-2-pentenyl),methylester Methyl (3-oxo-2-[(2E)-2-pentenyl]cyclopentyl)acetate methyl(1r-(1a,2b(z))) methyl(1r-(1a,2b(z)))-3- methyl(1r-(1a,2b(z)))-3-oxo-2-(pent-2-enyl)cyclopentaneacetate Methyl 2-((1R,2R)-3-oxo-2-((Z)-pent-2-en-1-yl)cyclopentyl)acetate (Z)-methyl epi-jasmonate Anabasine Methyl (2-pent-2-enyl-3-oxo-1-cyclopentyl)acetate Jasmonic Acid Impurity 6 ((-)-Jasmonic Acid Methyl Ester) (-)-methyljasmonate METHYL JASMONATE USP/EP/BP JASMONEIGE Methyl Jasmonate CAS No.?1211-29-6?with Best Price Methyl [1R-[1?,2?(Z)]]-3-oxo-2-(pent-2-enyl)cyclopentaneacetate (1R)-3-Oxo-2α-[(Z)-2-pentenyl]-1α-cyclopentaneacetic acid methyl ester Methyl cis-jasmonate JASMONIC ACID METHYL ESTER 2-Nitro-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene 102121-55-1 METHYL JASMONATE,Methyl dihydrojasmonate 1211-29-6 39924-52-3 Organic Building Blocks Esters Plant Growth Trgulators (Others) Plant Growth Regulators C12 to C63 Carbonyl Compounds Building Blocks Aromatic Esters