Beta-pinene

Beta-pinene Structure
Beta-pinene structure
Common Name Beta-pinene
CAS Number 18172-67-3 Molecular Weight 136.234
Density 0.9±0.1 g/cm3 Boiling Point 166.0±0.0 °C at 760 mmHg
Molecular Formula C10H16 Melting Point -61ºC
MSDS Chinese USA Flash Point 34.9±5.8 °C
Symbol GHS02 GHS07 GHS08
GHS02, GHS07, GHS08
Signal Word Danger

Antioxidant activity and cytotoxicity on tumour cells of the essential oil from Cedronella canariensis var. canariensis (L.) Webb & Berthel. (Lamiaceae).

Nat. Prod. Res. , 1-9, (2015)

Cedronella canariensis is a lemon-scented species of the family Lamiaceae endemic to the Canary Islands where it is used in the traditional medicine to prepare infusions or inhalations for anti-catarrhal, tonic, diuretic, hypoglycaemiant, hypotensive, anti-in...

Eucalyptol is an attractant of the Redbay ambrosia beetle, Xyleborus glabratus.

J. Chem. Ecol. 40(4) , 355-62, (2014)

The redbay ambrosia beetle, Xyleborus glabratus, is an invasive wood-boring beetle that has become established in the southeastern United States. The beetle transmits the causal pathogen of lethal laurel wilt to susceptible host trees, which include redbay, a...

Evidence for the existence of organosulfates from beta-pinene ozonolysis in ambient secondary organic aerosol.

Environ. Sci. Technol. 41(19) , 6678-83, (2007)

The formation of organosulfates from the gas-phase ozonolysis of beta-pinene in the presence of neutral or acidic sulfate particles was investigated in a series of indoor aerosol chamber experiments. The organosulfates were analyzed using high-performance liq...

Chemical composition, antimicrobial, insecticidal, phytotoxic and antioxidant activities of Mediterranean Pinus brutia and Pinus pinea resin essential oils.

Chin. J. Nat. Med. 12(12) , 901-10, (2014)

Essential oils of the resins of Pinus brutia and Pinus pinea were evaluated for their biological potential. Essential oils were characterized using GC-MS and GC/FID. in vitro antimicrobial, phytotoxic, antioxidant, and insecticidal activities were carried out...

Aldrichimica Acta 13 , 13, (1980)

Tetrahedron Lett. 30 , 6653, (1989)

Modelling the formation and composition of secondary organic aerosol from α-and β-pinene ozonolysis using MCM v3. Jenkin M E.

Atmos. Chem. Phys. 4(7) , 1741-57, (2004)

Reversible in situ acid formation for ß-pinene hydrolysis using CO 2 expanded liquid and hot water. Chamblee TS, et al.

Green Chem. 6(8) , 382-6, (2004)

Hydroboration of Terpenes. II. The Hydroboration of α-and β-Pinene-The Absolute Configuration of the Dialkylborane from the Hydroboration of α-Pinene. Zweifel G and Brown HC.

J. Am. Chem. Soc. 86(3) , 393-397, (1964)

Reactions of ozone with α-pinene and β-pinene in air: Yields of gaseous and particulate products. Hatakeyama S, et al.

J. Geophys. Res. Atmos. 94(D10) , 13013-13024, (1989)