Pinane

Pinane Structure
Pinane structure
Common Name Pinane
CAS Number 4795-86-2 Molecular Weight 138.250
Density 0.8±0.1 g/cm3 Boiling Point 157.0±7.0 °C at 760 mmHg
Molecular Formula C10H18 Melting Point -53ºC
MSDS USA Flash Point 36.0±11.7 °C
Symbol GHS02
GHS02
Signal Word Warning

Metabolic profiling of GuanXin II prescription based on metabolic fingerprinting and chemical analysis.

J. Pharm. Biomed. Anal. 54(4) , 789-98, (2011)

A sensitive LC/MS method was established to investigate the in vivo metabolism of GuanXin II prescription, a five-component Chinese herbal medicine formulation. Rat plasma, bile, urine, and feces were collected and analyzed following oral administration of th...

Chemistry around pinene and pinane: a facile synthesis of cyclobutanes and oxatricyclo-derivative of pinane from cis- and trans-pinanols.

Chem. Biodivers. 5(6) , 910-9, (2008)

Alpha-pinene and beta-pinene are abundantly represented in nature; they are obtained from renewable sources and are irreplaceable synthons for commercial-scale production of other terpenes. In a well-known process practiced by Millennium Specialty Chemicals (...

Acute toxicities to larval rainbow trout of representative compounds detected in Great Lakes fish.

Bull. Environ. Contam. Toxicol. 46(2) , 173-8, (1991)

Role of thromboxane and angiotensin in cyclosporine-induced renal vasoconstriction in the dog.

J. Heart Lung Transplant. 12(5) , 851-5, (1993)

Cyclosporine is associated with renal insufficiency characterized by a reduction in glomerular filtration rate that may result from renal vasoconstriction. Injection of cyclosporine in the isolated renal artery perfused at a constant flow induces a potent dos...

Selective boron-containing thrombin inhibitors--X-ray analysis reveals surprising binding mode.

Bioorg. Med. Chem. 8(9) , 2291-303, (2000)

Based on the structural comparison of the S1 pocket in different trypsin-like serine proteases, a series of Boc-D-trimethylsilylalanine-proline-boro-X pinanediol derivatives, with boro-X being different amino boronic acids, have been synthesized as inhibitors...

Terpenoids biotransformation in mammals III: Biotransformation of alpha-pinene, beta-pinene, pinane, 3-carene, carane, myrcene, and p-cymene in rabbits.

J. Pharm. Sci. 70(4) , 406-15, (1981)

The biotransformation of (+)-, (-)-, and (+-)-alpha-pinenes, (-)-beta-pinene (nopinene), (-)-cis-pinane, (+)-3-carene, (-)-cis-carane, myrcene, and p-cymene in rabbits was investigated. The major metabolites were as follows: (-)-trans-verbenol from (+)-, (-)-...

Monoterpene-based chiral β-amino acid derivatives prepared from natural sources: syntheses and applications.

Amino Acids 41(3) , 597-608, (2011)

Natural monoterpenes have proved to be good starting materials for the synthesis of β-amino acid derivatives. In the past decade, a number of well-known synthetic procedures have been applied for the preparation of monoterpene-based β-amino acid derivatives, ...

Synthesis of mesoporous silica with embedded nickel nanoparticles for catalyst applications.

J. Nanosci. Nanotechnol. 2(1) , 89-94, (2002)

Here we describe a new route for the synthesis of nanometric Ni particles embedded in a mesoporous silica material with excellent potential for catalytic applications. Mesoporous silica with a surface area in the range of 202-280 m2/g, with narrow pore size d...

Thermal isomerization of (+)-cis- and (-)-trans-pinane leading to (-)-beta-citronellene and (+)-isocitronellene.

Chemistry 14(22) , 6805-14, (2008)

Catalyzed and uncatalyzed rearrangement reactions of terpenoids play a major role in laboratory and industrial-scale synthesis of fine chemicals. Herein, we present our results on the thermally induced isomerization of pinane (1). Investigation of the thermal...

Sublethal effects of phenanthrene, nicotine, and pinane on Daphnia pulex.

Bull. Environ. Contam. Toxicol. 42(5) , 778-84, (1989)