ChemicalBook > CAS DataBase List > Myrcene

Myrcene

Product Name
Myrcene
CAS No.
123-35-3
Chemical Name
Myrcene
Synonyms
β-myrcene;BETA-MYRCENE;OIL;b-Myrcene;7-METHYL-3-METHYLENE-1,6-OCTADIENE;7-methyl-3-methyleneocta-1,6-diene;Geraniolene;Myrcene CAS;MYRCENE;FEMA 2762
CBNumber
CB0135735
Molecular Formula
C10H16
Formula Weight
136.23
MOL File
123-35-3.mol
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Myrcene Property

Melting point:
<-10 °C
Boiling point:
167 °C (lit.)
Density 
0.791 g/mL at 25 °C (lit.)
vapor density 
4.7 (vs air)
vapor pressure 
~7 mm Hg ( 20 °C)
refractive index 
n20/D 1.469(lit.)
FEMA 
2762 | MYRCENE
Flash point:
103 °F
storage temp. 
2-8°C
solubility 
water: soluble0.00109g/L at 20°C
form 
Viscous Liquid
color 
Clear light yellow
PH
7 (H2O, 20℃)(saturated aqueous solution)
Odor
at 5.00 % in dipropylene glycol. peppery terpene spicy balsam plastic
Odor Type
spicy
Water Solubility 
practically insoluble
Merck 
14,6331
JECFA Number
1327
BRN 
1719990
Dielectric constant
2.0(Ambient)
Stability:
Unstable - may be inhibited by the addition of ca. 400 ppm tenox GT-1 or 1000 ppm BHT. Flammable. Incompatible with strong oxidizing agents, radical initiators.
LogP
4.82 at 30℃
CAS DataBase Reference
123-35-3(CAS DataBase Reference)
NIST Chemistry Reference
Beta-myrcene(123-35-3)
IARC
2B (Vol. 119) 2019
EPA Substance Registry System
Myrcene (123-35-3)
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Safety

Hazard Codes 
Xi,Xn
Risk Statements 
10-36/37/38-R36/37/38-R10-65-38
Safety Statements 
16-26-36-37/39-S37/39-S26-S16-62
RIDADR 
UN 2319 3/PG 3
WGK Germany 
2
RTECS 
RG5365000
10-23
HazardClass 
3.2
PackingGroup 
III
HS Code 
29012990
Hazardous Substances Data
123-35-3(Hazardous Substances Data)
Toxicity
Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg (Moreno, 1972).
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H226Flammable liquid and vapour

H315Causes skin irritation

H319Causes serious eye irritation

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P273Avoid release to the environment.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W276212
Product name
Myrcene
Purity
sum of isomers, ≥90%, natural, FG
Packaging
100G
Price
$83.4
Updated
2024/03/01
Sigma-Aldrich
Product number
W276212
Product name
Myrcene
Purity
sum of isomers, ≥90%, natural, FG
Packaging
SAMPLE-K
Price
$169
Updated
2024/03/01
Sigma-Aldrich
Product number
W276212
Product name
Myrcene
Purity
sum of isomers, ≥90%, natural, FG
Packaging
1KG
Price
$596
Updated
2024/03/01
Sigma-Aldrich
Product number
W276200
Product name
Myrcene
Purity
stabilized, FCC, FG
Packaging
1kg
Price
$142
Updated
2024/03/01
Sigma-Aldrich
Product number
W276200
Product name
Myrcene
Purity
stabilized, FCC, FG
Packaging
8kg
Price
$947
Updated
2024/03/01
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Myrcene Chemical Properties,Usage,Production

Description

Myrcene has a pleasant odor. Prepared from linalool.

Description

β-Myrcene is a terpene that has been found in Cannabis and has antioxidative properties. It reduces thiobarbituric acid reactive substance (TBARS) and increases glutathione (GSH), catalase, GSH peroxidase, and CuZn superoxide dismutase levels in a rat model of persistent environmental pollutant-induced oxidative stress when administered at a dose of 200 mg/kg per day.

Chemical Properties

Myrcene has a pleasant, sweet, balsamic, plastic odor.

Chemical Properties

colourless viscous liquid

Occurrence

Reported found in Mircia acris D.C.; in the distillates from leaves of Rhus cotinus and Barosma venustum (52 and 43%, respectively); in lemongrass, cypress, artemisia; in the fruits of Phellodendron amurense (92%) and Phellodendron japonicum; in the oils of Picea balsamea, Tsuga canadenis, Abies balsamea, clary sage and others. Also reported in over 200 foods and beverages including citrus peel oils and juices, apricot, sweet and sour cherry, berries, guava, pineapple, carrot, celery, potato, bell pepper, black currants, anise, anise seed, cardamom, cinnamon, cassia, clove, capsicum varities, ginger, mentha oils, mace, parsley, thyme, cheeses, cream, pork, hop oil, beer, white wine, rum, cocoa, coffee, tea, mango, tamarind, coriander, gin, sweet bay, prickly pear, calamus, dill, lovage, caraway, buckwheat, corn, basil, fennel, kiwifruit, rosemary, myrtle berry, turmeric, lemon balm, sage, pimento, angelica oil, Roman and German chamomile oil, eucalyptus and mastic gum oil

Uses

Found in oil of bay, verbena, hop, etc. Used as an intermediate in the manufacturing of perfume chemicals.

Uses

Myrcene is the suitable synthetic standard used in the identification of E-myrcenol (2-methyl-6-methylene-E-2,7-octadien-1-01) as a major hindgut constituent in Eurasian bark beetle Ips duplicatus by GC-MS.

Definition

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

Preparation

From linalool

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/ja00844a073
The Journal of Organic Chemistry, 47, p. 4161, 1982 DOI: 10.1021/jo00142a031
Tetrahedron 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.

Biochem/physiol Actions

Odor at 1%

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.

Synthesis

Myrcene occurs naturally in many organisms, but its extraction is uneconomic; it is produced industrially by pyrolysis of b-pinene. The fragmentation of linalool and linalyl acetate and the catalytic dimerization of isoprene have been described as laboratory synthesis methods of myrcene.

Myrcene Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Myrcene manufacturers

Hebei Dangtong Import and export Co LTD
Product
Myrcene 123-35-3
Price
US $10.00-1.00/kg
Min. Order
10kg
Purity
99%
Supply Ability
600tons
Release date
2023-09-14
Shanghai Affida new material science and technology center
Product
Myrcene 123-35-3
Price
US $0.00/KG
Min. Order
1KG
Purity
99
Supply Ability
20tons
Release date
2024-04-15
airuikechemical co., ltd.
Product
Myrcene 123-35-3
Price
US $0.00-0.00/Kg
Min. Order
1Kg
Purity
99.9%
Supply Ability
20tons
Release date
2024-04-03

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