1211-29-6

1211-29-6 - Names and Identifiers

Name	Methyl jasmonate
Synonyms	Methyl jasmonate Methyl Jasmonate methyl (Z)-jasmonate trans-Methyl jasmonate rac-trans JasMonic Acid Methyl Ester methyl [3-oxo-2-(pent-2-en-1-yl)cyclopentyl]acetate 1-cyclopentyl-1-methoxy-3-methyl-hex-3-ene-1,4-dione methyl {(1S,2S)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetate methyl {(1R,2R)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetate methyl {(1R,2R)-3-oxo-2-[(2E)-pent-2-en-1-yl]cyclopentyl}acetate methyl [1alpha,2beta(Z)]-(±)-3-oxo-2-(pent-2-enyl)cyclopentaneacetate (1R,2R)-rel-3-Oxo-2-(2Z)-2-penten-1-ylcyclopentaneacetic Acid Methyl Ester (1R,2R)-rel-3-Oxo-2-(2Z)-2-penten-1-ylcyclopentaneacetic Acid-13C2 Methyl Ester
CAS	1211-29-6 20073-13-6
EINECS	243-497-1
InChI	InChI=1S/C13H20O3/c1-3-4-5-6-11-10(7-8-12(11)14)9-13(15)16-2/h4-5,10-11H,3,6-9H2,1-2H3

1211-29-6 - Physico-chemical Properties

Molecular Formula	C13H20O3
Molar Mass	224.3
Density	1,02 g/cm3
Boling Point	175 °C(Press: 0.08 Torr)
Flash Point	156°C
Solubility	Chloroform, Methanol
Appearance	Oil
Color	Colourless
Storage Condition	Refrigerator

1211-29-6 - Risk and Safety

Safety Description

S23 - Do not breathe vapour.
S24/25 - Avoid contact with skin and eyes.

1211-29-6 - Introduction

Methyl jasmonate, also known as Methyl benzoylpropionate, is an organic compound. The following is an introduction to the nature, use, formulation and safety information of Methyl jasmonate:

Nature:
Methyl jasmonate is a colorless to pale yellow liquid with a floral odor. It has a low melting and boiling point and can be dissolved in organic solvents such as alcohols and ethers. Its molecular formula is C11H12O3.

Use:
Methyl jasmonate has important applications in the flavor industry. It has the characteristics of similar jasmine fragrance, and is often used as a fragrance ingredient in perfumes, soaps, hair care products, etc. In addition, jasmonates can also be used in the fields of cosmetics, detergents and food flavoring agents.

Preparation Method:
The preparation methods of Methyl jasmonate mainly include synthesis and extraction. The synthesis is usually obtained by chemical reactions, such as the condensation of aromatic aldehydes with acetone ketones. The extraction method takes advantage of the presence of Methyl jasmonate in natural plants and obtains it through extraction and separation and purification.

Safety Information:
Methyl jasmonate is generally safe for the human body under normal use, but try to avoid long-term exposure and excessive contact. In case of skin contact, wash immediately with soap and water. Avoid inhaling vapors, use them in a well-ventilated area and keep them away from sources of fire. When storing and handling, please follow the relevant safety procedures.

Last Update：2024-04-09 01:59:53