Dipentene

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
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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.