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
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)
- Water Solubility
- practically insoluble
- Merck
- 14,6331
- JECFA Number
- 1327
- BRN
- 1719990
- 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)
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
- F
- 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).
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.
N-Bromosuccinimide Price
- Product number
- W276212
- Product name
- Myrcene
- Purity
- sum of isomers, ≥90%, natural, FG
- Packaging
- 100G
- Price
- $83.4
- Updated
- 2023/01/07
- Product number
- W276212
- Product name
- Myrcene
- Purity
- sum of isomers, ≥90%, natural, FG
- Packaging
- SAMPLE-K
- Price
- $169
- Updated
- 2023/01/07
- Product number
- W276212
- Product name
- Myrcene
- Purity
- sum of isomers, ≥90%, natural, FG
- Packaging
- 1KG
- Price
- $596
- Updated
- 2023/01/07
- Product number
- W276200
- Product name
- Myrcene
- Purity
- stabilized, FCC, FG
- Packaging
- 1kg
- Price
- $142
- Updated
- 2023/01/07
- Product number
- W276200
- Product name
- Myrcene
- Purity
- stabilized, FCC, FG
- Packaging
- 8kg
- Price
- $673
- Updated
- 2023/01/07
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.
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/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.
Myrcene Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from Myrcene manufacturers
- Product
- Myrcene 123-35-3
- Price
- US $5.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 500MT/month
- Release date
- 2021-12-29
- Product
- Myrcene 123-35-3
- Price
- US $10.50/KG
- Min. Order
- 1KG
- Purity
- 80%
- Supply Ability
- 10 ton
- Release date
- 2021-06-30
- Product
- Myrcene 123-35-3
- Price
- US $10.00/PCS
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 100 mt
- Release date
- 2021-04-23