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Factory Provide Bulk Myrcene Price for Export

Payment Type:
T/T,Paypal,Money Gram,Western Union
Incoterm:
CIF,EXW,FCA
Min. Order:
1
Transportation:
Ocean,Land,Air
Port:
Shanghai,Guangzhou,Hongkong
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Overview
Product Attributes

Model No.HQ-1930

Raw MaterialOil

Supply Ability & Additional Information

Packaging1kg,5kg,25kg,180kg for bulk packing ,10ml ,20ml ,50ml ,100ml for samll samples

TransportationOcean,Land,Air

PortShanghai,Guangzhou,Hongkong

Payment TypeT/T,Paypal,Money Gram,Western Union

IncotermCIF,EXW,FCA

Packaging & Delivery
Package Type:
1kg,5kg,25kg,180kg for bulk packing ,10ml ,20ml ,50ml ,100ml for samll samples
Product Description

 

 

Myrcene, or β-myrcene, is an olefinic natural organic hydrocarbon. It is more precisely classified as a monoterpene. Monoterpenes are dimers of isoprenoid precursors, and myrcene is a significant component of the essential oil of several plants, including bayylang-ylangwild thymeparsleycardamom, and hops. It is produced mainly semi-synthetically from myrcia, from which it gets its name. It is a key intermediate in the production of several fragrances. α-Myrcene is the name for the structural isomer 2-methyl-6-methylene-1,7-octadiene, which is not found in nature and is little used.

Production

Myrcene is produced by the pyrolysis (400 °C) of β-pinene, which is obtained from turpentine. It is rarely obtained directly from plants.

Terpenes arise naturally from dehydration of terpenol geraniol. Plants biosynthesize myrcene via geranyl pyrophosphate (GPP). The mevalonate pathway gives the precursors dimethylallyl pyrophosphate (Fig. 1a) and isopentenyl pyrophosphate (Fig.1b). These two precursors combine to produce GPP (Fig. 1c), which then isomerizes into linalyl pyrophosphate (Fig. 1d). The rearrangement and release of the pyrophosphate (OPP), and the double bond formation creates the product myrcene (Fig. 1e).

Use in fragrance and Flavor industries

Myrcene is an important intermediate used in the perfumery industry. It has a pleasant odor but is rarely used directly. It is also unstable in air, tending to polymerize. Samples are stabilized by the addition of alkylphenols or tocopherol. It is thus more highly valued as an intermediate for the preparation of flavor and fragrance chemicals such as mentholcitralcitronellol,citronellalgeraniolnerol, and linalool. Myrcene is converted to myrcenol, another fragrance found in lavender, via hydroamination of the 1,3-diene by diethylamine followed by hydrolysis and Pd-catalyzed removal of the amine.


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