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ChemicalBook--->CAS DataBase List--->13466-78-9

13466-78-9

13466-78-9 Structure

13466-78-9 Structure
IdentificationBack Directory
[Name]

3-CARENE
[CAS]

13466-78-9
[Synonyms]

carene
3-Karen
3-CARENE
D-CARENE
3-CARVENE
Car-3-ene
FEMA 3821
Isodiprene
S-3-Carene
DELTA-CARENE
3-Carene 90%
DELTA-3-CARENE
CAREN-(3), ROH
3-delta-carene
CARENE, DELTA-3
DELTA-car-3-ene
3-CARENE WITH GC
3-CARENE (DELTA)
delta(Sup3)-Carene
CARENE, Delta-3-(SG)
3-Karen (jfr terpener)
3-Carene,90%,stabilized
delta-3-CARENE, NATURAL
3-Carene, stabilized, 90%
3,7,7-trimethyl-3-norcaren
4,7,7-Trimethyl-3-norcarene
3,7,7-Trimethyl-3-norcarene
3-Carene, stabilized, 90% 1LT
3-Norcarene, 3,7,7-trimethyl-
3-Carene, stabilized, 90% 25ML
3,7,7-trimethyl-bicyclo(4.1.0)hept-3-en
3,7,7-trimethyl-bicyclo[4.1.0]hept-3-en
3,7,7-TRIMETHYLBICYCLO[4.1.0]HEPT-3-ENE
3,7,7-TRIMETHYLBICYCLO[4.1.0]-3-HEPTENE
bicyclo[4.1.0]hept-3-ene,3,7,7-trimethyl-
Bicyclo[4.1.0]hept-3-ene, 3,7,7-trimethyl-
δ-3-carene,3,7,7-trimethylbicyclohept-3-ene
δ3-Carene, 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene
3,7,7-Trimethylbicyclo(4.1.0)hept-3-ene for synthesis
3-Carene,δ3-Carene, 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene
[EINECS(EC#)]

236-719-3
[Molecular Formula]

C10H16
[MDL Number]

MFCD00001315
[MOL File]

13466-78-9.mol
[Molecular Weight]

136.23
Chemical PropertiesBack Directory
[Definition]

A terpene hydrocarbon with both a 6-member and 3-member ring.
[Appearance]

liquid
[Melting point ]

25°C
[Boiling point ]

168-169 °C705 mm Hg(lit.)
[density ]

0.857 g/mL at 25 °C(lit.)
[FEMA ]

3821 | DELTA-3-CARENE
[refractive index ]

n20/D 1.474(lit.)
[Fp ]

115 °F
[storage temp. ]

Flammables area
[solubility ]

Chloroform: Soluble; Methanol: Soluble
[form ]

Liquid
[color ]

Clear colorless to slightly yellow
[Odor]

at 100.00 %. citrus terpenic herbal pine solvent resinous phenolic cypress medicinal woody
[Stability:]

Stable. Flammable. Incompatible with strong oxidizing agents.
[Odor Type]

citrus
[optical activity]

[α]20/D +15°, neat
[JECFA Number]

1342
[Merck ]

1836
[Contact allergens]

Hydroperoxides of D-3-carene are allergens contained in turpentine. Occupational exposure occurs in painters, varnishers, or ceramic decoration. The percentage of D-3-carene is higher in Indonesian than in Portuguese turpentine.
[LogP]

4.38
[Uses]

Solvent, intermediate.
[EPA Substance Registry System]

3-Carene (13466-78-9)
Hazard InformationBack Directory
[Chemical Properties]

liquid
[General Description]

Colorless liquid with a sweet, turpentine-like odor. Floats on water.
[Reactivity Profile]

3-CARENE may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to release hydrogen gas. In the presence of various catalysts (such as acids) or initiators, may undergo exothermic addition polymerization reactions. Will attack some forms of plastics [USCG, 1999].
[Health Hazard]

Inhalation causes headache, confusion, respiratory distress. Ingestion irritates entire digestive system and may injure kidneys; if liquid enters lungs, it causes severe pneumonitis. Contact with eyes or skin causes irritation.
[Description]

(±)-3-Carene is a bicyclic monoterpene found in a variety of plants, including Cannabis. It decreases phagocytosis by rat alveolar macrophages when used at a concentration of 0.5 μM and decreases their viability at a concentration of 5 μM. (±)-3-Carene increases the expression and activity of alkaline phosphatase in mouse osteoblastic MC3T3-E1 subclone 4 cells, indicating induction of osteoblastic differentiation. It also induces calcium formation and increases the expression of osteopontin and type I collagen, which are related to osteoblast mineralization. (±)-3-Carene induces bronchoconstriction in isolated guinea pig lungs when exposed at an air concentration of 3,000 mg/m3.
[Description]

Hydroperoxides of Δ-3-carene are allergens contained in turpentine. Occupational exposure occurs in painters, varnishers, or in ceramic decoration. The percentage of Δ-3-Carene is higher in Indonesian turpentine than in Portugese.
[Occurrence]

Reported present in basil oil, bell pepper, bilberry, black currant berry juice and buds, fennel oil, grapefruit juice, kumquat peel oil, lemon peel oil, lime peel oil (cold pressed and distilled), lovage seed, mandarin peel oil, orange juice, orange peel oil, orange (bitter) peel oil, tangerine peel oil and other natural products.
[Preparation]

Extracted from the pine tree oil.
[Synthesis Reference(s)]

Tetrahedron Letters, 25, p. 5255, 1984 DOI: 10.1016/S0040-4039(01)81577-X
Safety DataBack Directory
[Hazard Codes ]

Xi,N,Xn
[Risk Statements ]

10-43-50/53-65-38-52/53
[Safety Statements ]

16-26-36/37-60-61-62-37-24
[RIDADR ]

UN 2319 3/PG 3
[WGK Germany ]

2
[RTECS ]

FH8400000
[HazardClass ]

3.2
[PackingGroup ]

III
[HS Code ]

29021990
Raw materials And Preparation ProductsBack Directory
[Preparation Products]

METHYL(2R,3S)-2,2-DIMETHYL-3-(2-OXOPROPYL)-CYCLOPROPANEACETATE-->2,6,6-TRIMETHYL-2,4-CYCLOHEPTADIEN-1-ONE
Spectrum DetailBack Directory
[Spectrum Detail]

3-CARENE(13466-78-9)1HNMR
3-CARENE(13466-78-9)IR
3-CARENE(13466-78-9)Raman
3-CARENE(13466-78-9)FT-IR
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