Dipentene

Origin
Indonesia
CAS Number
138-86-3
HS Code
-

Basic Info

IUPAC Name
1-methyl-4-(prop-1-en-2-yl)cyclohexene
Molecular Formula
C10H16
Molecular Weight (g/mol)
136.2300
Synonyms & Trade Names
Dipentene; Limonene racemate; dl-Limonene; Technical limonene
Purity / Assay (%)
90% min
Grade / Quality Level
Technical Grade
Physical Form
Liquid
Concentration
Pure substance
Appearance / Color
Clear to slightly colored liquid
Odor
Citrus-like
Melting Point (°C)
-97.0000
Boiling Point (°C)
178
Density (g/cm³)
0.8400
Solubility in Water
Insoluble
Signal Word
Warning
UN Number
2052
GHS Hazard Class
Flammable; Skin sensitizer; Aquatic hazard
H-Statements
H226|H315|H317|H410
P-Statements
P210|P261|P272|P273|P280
REACH Status
Registered
Drug Precursor Status
Non-precursor
Storage Class (GHS)
3
Storage Conditions
Cool, dry; away from ignition

Categories

Technical Document

Brief Overview
Dipentene (also called D-Limonene), is a terpene liquid found in various volatile oils such as cardamon, mace, nutmeg , turpentine oil. Dipentene is mainly composed of Limonene, beta-Phellandrene, Myrcene and other terpenes.
Manufacturing Process
In nature, limonene is formed from the molecule geranyl pyrophosphate, via cyclization of a neryl carbocation or its equivalent. In the final step, the C=C double bond is formed through the loss of a proton from the carbocation.
Commercially, d-limonene is obtained from citrus fruits through the process of steam distillation and centrifugal separation. Commonly, orange oil is extracted as a by-product of orange juice production by centrifugation. The orange oil obtained composes greater than 90% of d-limonene. Further separation takes place via steam distillation, where steam is passed through the orange oil to distill limonene. Limonene is relatively stable and can be distilled without decomposition, but at elevated temperatures, it cracks to form isoprene. The limonene extracted is commonly D-limonene, but at 300°C it racemizes to dipentene.