Myrcene

Base Information

  • PRODUCT:Myrcene
  • CAS.:123-35-3
  • MF:C10H16
  • Molecular Weight:136.237
  • Purity:99%

Product Details

CAS: 123-35-3

MF: C10H16

Appearance: clear to pale yellow liquid

Reliable factory customized supply Myrcene 123-35-3

  • Molecular Formula:C10H16
  • Molecular Weight:136.237
  • Appearance/Colour:clear to pale yellow liquid 
  • Vapor Pressure:~7 mm Hg ( 20 °C) 
  • Melting Point:<-10 °C 
  • Refractive Index:1.4690 
  • Boiling Point:167 °C at 760 mmHg 
  • Flash Point:44.4 °C 
  • PSA:0.00000 
  • Density:0.769 g/cm3 
  • LogP:3.47500 

Myrcene(Cas 123-35-3) Usage

Preparation

From linalool

Definition

ChEBI: A monoterpene that is octa-1,6-diene bearing methylene and methyl substituents at positions 3 and 7 respectively.

Aroma threshold values

Aroma characteristics at 10%: terpy, herbaceous, woody with a rosy celery and carrot nuance

Taste threshold values

Taste characteristics at 5 to 100 ppm: woody, vegetative, citrus fruity with a tropical mango and slight, leafy, minty nuance

Synthesis Reference(s)

Journal of the American Chemical Society, 97, p. 3252, 1975 DOI: 10.1021/ja00844a073The Journal of Organic Chemistry, 47, p. 4161, 1982 DOI: 10.1021/jo00142a031Tetrahedron Letters, 25, p. 5193, 1984 DOI: 10.1016/S0040-4039(01)81561-6

General Description

A yellow oily liquid with a pleasant odor. Flash point below 200°F. Insoluble in water and less dense than water.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

The unsaturated aliphatic hydrocarbons, such as MYRCENE, are generally much more reactive than the alkanes. Strong oxidizers may react vigorously with them. Reducing agents can react exothermically to release gaseous hydrogen. In the presence of various catalysts (such as acids) or initiators, compounds in this class can undergo very exothermic addition polymerization reactions. Many of these compounds undergo autoxidation upon exposure to the air to form explosive peroxides. Violent explosions have occurred at low temperatures in ammonia synthesis gas units. These explosions have been traced to the addition products of dienes and oxides of nitrogen, produced from the interaction of nitrogen oxide and oxygen [Bretherick, 1995].

Health Hazard

May be harmful by inhalation, ingestion or skin absorption.

Fire Hazard

Special Hazards of Combustion Products: Vapor may travel considerable distance to a source of ignition and flashback.

Safety Profile

Low toxicity by ingestion and skin contact. Experimental reproductive effects. A moderate skin and eye irritant. A flammable liquid. When heated to decomposition it emits acrid smoke and irritating fumes.

InChI:InChI=1/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H3

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123-35-3 Relevant articles

-

Walker,Hawkins

, p. 4209 (1952)

-

Acid-catalyzed hydrolysis of alcohols and their β-D-glucopyranosides

Skouroumounis, George K.,Sefton, Mark A.

, p. 2033 - 2039 (2000)

The hydrolysis, in model wine at pH 3, o...

Palladium-Catalyzed Reactions of Allylic Electrophiles with Organometallic Reagents. A Regioselective 1,4-Elimination and a Regio- and Stereoselective Reduction of Allylic Derivatives

Matsushita, Hajime,Negishi, Ei-ichi

, p. 4161 - 4165 (1982)

-

-

Yasuda,A. et al.

, p. 1752 - 1756 (1979)

-

Molybdenum- and tungsten-catalyzed allylation of aromatic compounds with allylic esters and alcohols

Shimizu, Isao,Sakamoto, Toshiaki,Kawaragi, Saeko,Maruyama, Yooichiro,Yamamoto, Akio

, p. 137 - 138 (1997)

A novel method to substitute aromatic co...

-

Haley et al.

, p. 264 (1969)

-

Preparation of 1-Alkenes by the Palladium-Catalyzed Hydrogenolysis of Terminal Allylic Carbonates and Acetates with Formic Acid-Triethylamine

Tsuji, Jiro,Minami, Ichiro,Shimizu, Isao

, p. 623 - 627 (1986)

A useful method for the preparation of 1...

Selective Synthesis of 1,3-Dienic Terpenes in a β-Form through Regioselective 1,4-Elimination of Allylic Ethers

Otera, Junzo,Niibo, Yoshihisa,Okuda, Kazuhiro

, p. 1829 - 1832 (1986)

γ-Methyl-substituted allylic ethers prov...

Thermal behaviour of selected C10H16 monoterpenes

Stolle, Achim,Brauns, Claudia,Nuechter, Matthias,Ondruschka, Bernd,Bonrath, Werner,Findeisen, Matthias

, p. 3317 - 3325 (2006)

The presented work investigates the ther...

Flash vacuum thermolysis of terpenic compounds in the pinane series

Lemee,Ratier,Duboudin,Delmond

, p. 1313 - 1318 (1995)

The flash pyrolysis of various derivativ...

-

Tanaka,S. et al.

, p. 3252 - 3254 (1975)

-

-

Liu,R.S.H.,Hammond,G.S.

, p. 1892 - 1893 (1964)

-

-

Hunt,Hawkins

, p. 5618 (1950)

-

Novel route to a fruitful mixture of terpene fragrances in particular phellandrene starting from natural feedstock geraniol using weak acidic boron based catalyst

Eisenacher, Matthias,Beschnitt, Stefan,H?lderich, Wolfgang

, p. 214 - 217 (2012)

Myrcene, ocimene and in particular phell...

Thermal behavior of pinan-2-ol and linalool

Leiner, Janne,Stolle, Achim,Ondruschka, Bernd,Netscher, Thomas,Bonrath, Werner

, p. 8358 - 8375 (2013)

Linalool is an important intermediate fo...

Comparative thermolysis of β-and α-pinenes in supercritical ethanol: The reaction characterization and enantiomeric ratios of products

Chibiryaev,Yermakova,Kozhevnikov,Sal'nikova,Anikeev

, p. 1234 - 1238 (2007)

The thermolysis of β-pinene and the co-t...

Preparation method of myrcene

-

Paragraph 0031-0032; 0041-0042; 0045-0046, (2021/11/19)

The method uses geraniol and/or nerol an...

Method and Means for Releasing a Terpene Mixture to a Cannabis Flower During Storage

-

, (2021/09/17)

A method and means for releasing a terpe...

A donor-acceptor complex enables the synthesis of: E -olefins from alcohols, amines and carboxylic acids

Chen, Kun-Quan,Shen, Jie,Wang, Zhi-Xiang,Chen, Xiang-Yu

, p. 6684 - 6690 (2021/05/31)

Olefins are prevalent substrates and fun...

Method for synthesizing high-purity 13C2-myrcene from 13C2-geraniol

-

Paragraph 0045; 0048, (2020/08/06)

The invention relates to a method for sy...

123-35-3 Process route

styrene
100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6

styrene

3-methyl-butan-2-one
563-80-4

3-methyl-butan-2-one

7-methyl-3-methene-1,6-octadiene
123-35-3

7-methyl-3-methene-1,6-octadiene

β-thujene

β-thujene

Conditions
Conditions Yield
at 610 ℃;
 
3,7-dimethyl-oct-6-enal
106-23-0,26489-02-1

3,7-dimethyl-oct-6-enal

7-methyl-3-methene-1,6-octadiene
123-35-3

7-methyl-3-methene-1,6-octadiene

1-methyl-4-isopropyl-1,3-cyclohexadiene
99-86-5

1-methyl-4-isopropyl-1,3-cyclohexadiene

3,8-p-Menthadien
586-67-4

3,8-p-Menthadien

3-p-menthene
500-00-5

3-p-menthene

(+/-)-menthone
491-07-6,1074-95-9,1196-31-2,3391-87-5,10458-14-7,14073-97-3,18309-28-9,36977-92-1,117773-78-1,89-80-5,17627-49-5,7786-64-3

(+/-)-menthone

Conditions
Conditions Yield
With aluminum oxide; carbon dioxide; In hexane; at 190 ℃; Supercritical conditions;
21.4%
6.6%
8.2%
6.9%
6.3%

123-35-3 Upstream products

  • 126-91-0
    126-91-0

    linalool

  • 115-95-7
    115-95-7

    linalool acetate

  • 13066-51-8
    13066-51-8

    γ-geraniol

  • 18172-67-3
    18172-67-3

    beta-pinene

123-35-3 Downstream products

  • 107821-52-3
    107821-52-3

    4-(4-methyl-pent-3-enyl)-cyclohex-4-ene-1,2-dicarboxylic acid

  • 29811-04-9
    29811-04-9

    4-(4-methyl-3-pentenyl)-4-cyclohexene-1,2-dicarboxylic acid anhydride

  • 29811-04-9
    29811-04-9

    (+/-)-4-(4-methyl-pent-3-enyl)-cyclohex-4-ene-1r,2c-dicarboxylic acid-anhydride

  • 29414-55-9
    29414-55-9

    6,7-epoxymyrcene

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