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Home > Products >  (+)-DipenteneCAS NO.:5989-27-5

(+)-DipenteneCAS NO.:5989-27-5 CAS NO.5989-27-5

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Keywords

  • (+)-Dipentene
  • (+)-1,8-p-menthadiene,(R)-(+)-limonene
  • (+)-4-isopropenyl-1-methylcyclohexene

Quick Details

  • ProName: (+)-DipenteneCAS NO.:5989-27-5
  • CasNo: 5989-27-5
  • Molecular Formula: C10H16
  • Appearance: white powder
  • Application: Pharmaceutical intermediates
  • DeliveryTime: In stock
  • PackAge: bag
  • Port: China main port
  • ProductionCapacity: 10000 Gram/Day
  • Purity: 0.99
  • Storage: Room temperature
  • Transportation: By Sea/Air/DHL
  • LimitNum: 1 Gram
  • Heavy metal: N/A
  • Grade: Industrial Grade
  • top grade: 1-10

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Details

(+)-Dipentene Chemical Properties
Melting point  -75--73°C
alpha  112o (10% IN ETHANOL)
Boiling point  176-177 °C(lit.)
density  0.842 g/mL at 20 °C(lit.)
vapor density  4.7 (vs air)
vapor pressure  1 mm Hg ( 20 °C)
FEMA  2633 | D-LIMONENE
refractive index  n20/D 1.473(lit.)
Fp  119 °F
storage temp.  2-8°C
solubility  water: insoluble
form  neat
Specific Gravity 0.842 (20/4℃)
explosive limit 0.7-6.1%(V)
optical activity [α]20/D +120°, neat
Water Solubility  Miscible with alcohol,chloroform,ether and carbondisulfide.Immiscible with water.
Merck  14,5493
JECFA Number 1326
BRN  2204754
Stability: Stable. Flammable. Incompatible with strong oxidizing agents.
CAS DataBase Reference 5989-27-5(CAS DataBase Reference)
IARC 3 (Vol. 56, 73) 1999
EPA Substance Registry System D-Limonene (5989-27-5)
 
Safety Information
Hazard Codes  Xi,N,Xn
Risk Statements  10-38-43-50/53-65
Safety Statements  24-37-60-61
RIDADR  UN 2052 3/PG 3
WGK Germany  2
RTECS  GW6360000
8-10-23
Autoignition Temperature 255 °C
TSCA  Yes
HS Code  2902 19 00
HazardClass  3
PackingGroup  III
Toxicity LD50 orally in Rabbit: > 2000 mg/kg LD50 dermal Rabbit > 2000 mg/kg
MSDS Information
 
 
(+)-Dipentene Usage And Synthesis
Description d-Limonene has a pleasant, lemon-like odors free from campho raceous and turpentine-like. d-Limonene may be obtained by steam distillation of citrus peels and pulp resulting from the pro duction of juice and cold-pressed oils, or from deterpenation of citrus oils; it is sometimes redistilled.
The most important and widespread terpene; it is known in the el and I- optically active forms and in the optically inactive dl-form (known as dipentene); it has been reported found in more than 300 essential oils in amounts ranging from 90 - 95% (lemon, orange, mandarin) to as low as 1% (palmarosa);1 the most widespread form is the d-limonene, followed by the racemic form, and then ι- limonene.
Chemical Properties d-, l- or dl-Limonene has a pleasant, lemon-like odor free from camphoraceous and turpentine-like notes. Limonene is the most important and widespread terpene; it is known in the d- and l- optically active forms and in the optically inactive dl-form (known as dipentene).
Chemical Properties colourless liquid
Occurrence It has been reported found in more than 300 essential oils in amounts ranging from 90 to 95% (lemon, orange, mandarin) to as low as 1% (palmarosa); the most widespread form is the d-limonene, followed by the racemic form and then l-limo nene. Also reported found in ginger, nutmeg, pepper, mace, hop oil, coriander seed, calamus, dill herb, caraway seed and rosemary.
Preparation d-Limonene may be obtained by steam distillation of citrus peels and pulp resulting from the production of juice and cold pressed oils, or from deterpenation of citrus oils; it is sometimes redistilled.
Definition ChEBI: An optically active form of limonene having (4R)-configuration.
Aroma threshold values Detection: 4 to 229 ppb
Taste threshold values Taste characteristics at 30 ppm: sweet, orange, citrus and terpy.
General Description Clear colorless mobile liquid with a pleasant lemon-like odor.
Air & Water Reactions Highly flammable. Insoluble in water.
Reactivity Profile (+)-Dipentene is sensitive to exposure to light. Atmospheric oxidation can occur. (+)-Dipentene is incompatible with strong oxidizing agents. (+)-Dipentene reacts violently with (iodine pentafluoride + tetrafluoroethylene). With dry hydrogen chloride or hydrogen bromide, (+)-Dipentene forms monohalides. With aqueous hydrogen chloride or hydrogen bromide, (+)-Dipentene forms the dihalide.
Fire Hazard (+)-Dipentene is combustible.
Agricultural Uses Insecticide, Animal and insect repellant, Slimicide: Used as an insecticide, insect repellent, and animal repellent. Not listed for use in EU countries. Registered for use in the U.S., Canada and other countries. There are 49 global suppliers.
Trade name BUGAWAY®[C]; BUGCHASER®[C]; CARVENE®; DOO-NOT®; HOLIDAY FIRE ANT KILLER®
Contact allergens d-Limonene is contained in Citrus species such as citrus, orange, mandarin, and bergamot. d-limonene, used as a solvent, may be found in cleansing or in degreasing agents. Its sensitizing potential increases with prolonged air contact, which induces oxidation and leads to oxidation products. The presence of d-limonene has to be mentioned by name in cosmetics of the EU.

 

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