β-Caryophyllene 87-44-5

(-)-Caryophyllene

Bicyclo[7.2.0]undec-4-ene,4,11,11-trimethyl-8-methylene-,(1R,4E,9S)-;Bicyclo[7.2.0]undec-4-ene,4,11,11-trimethyl-8-methylene-,(E)-(1R,9S)-(-)-;Bicyclo[7.2.0]undec-4-ene,4,11,11-trimethyl-8-methylene-,[1R-(1R*,4E,9S*)]-;(1R,4E,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene;trans-Caryophyllene;Caryophyllene;l-Caryophyllene;β-Caryophyllene;β-Caryophyllen;(-)-β-Caryophyllene;β-Caryophyllene,(-);(-)-Caryophyllene;(-)-trans-Caryophyllene;(-)-E-Caryophyllene;(E)-Caryophyllene;(-)-(E)-Caryophyllene;NSC 11906;Caryophyllene B;trans-β-Caryophyllene;Caryophylline;1407-53-0;8007-38-3;1233519-47-5

87-44-5

C15H24

InChIKey=NPNUFJAVOOONJE-FLFDDASRSA-N

204.35

204.35

201-746-1

DTXSID8024739

2902199090

Alcohols, Phenols, Phenol Alcohols

0 Ų

4.72520

Beta-caryophyllene is a pale yellow oily liquid with an odor midway between odor of cloves and turpentine. (NTP, 1992)

0.9052 g/cm³ @ Temp: 17 °C

<25 °C

129.5 °C

205 °F

1.495

less than 1 mg/mL at 70° F (NTP, 1992)

2-8°C

Celiac-rat LD:> 48 mg/kg

In case of high temperature, open flame, strong oxidant is flammable; thermal decomposition is spicy and stimulates smoke

D -8 to -9° (chloroform)

2.00e-10 cm3/molecule*sec

Insoluble in water.

Hydrocarbons, Aliphatic Unsaturated

The unsaturated aliphatic hydrocarbons, such as BETA-CARYOPHYLLENE, 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.