What is Pristane used for?

It is used as a lubricant, a transformer oil, an immunologic adjuvant, and an anti-corrosion agent, biological marker, plasmocytomas inducer and in production of monoclonal antibodies. Biosynthetically, pristane is derived from phytol and is used as a biomarker in petroleum studies.

What is Pristane used for?

It is used as a lubricant, a transformer oil, an immunologic adjuvant, and an anti-corrosion agent, biological marker, plasmocytomas inducer and in production of monoclonal antibodies. Biosynthetically, pristane is derived from phytol and is used as a biomarker in petroleum studies.

Is Pristane an acyclic alkane?

Pristane is a norterpene that is an acyclic saturated hydrocarbon derived from phytane by loss of its C-16 terminal methyl group. It has a role as a biomarker and an immunological adjuvant. It is a norterpene and a long-chain alkane.

What is the condensed structural formula for Pristane?

Identification of PRISTANE Chemical Compound

Chemical Formula C19H40
IUPAC Name 2,6,10,14-tetramethylpentadecane
SMILES String CC(C)CCCC(C)CCCC(C)CCCC(C)C
InChI InChI=1S/C19H40/c1-16(2)10-7-12-18(5)14-9-15-19(6)13-8-11-17(3)4/h16-19H,7-15H2,1-6H3
InChIKey XOJVVFBFDXDTEG-UHFFFAOYSA-N

What is the boiling point of Nonadecane?

626°F (330°C)Nonadecane / Boiling point

What is Pristane and Phytane?

Pristane and phytane are common constituents in petroleum and have been used as proxies for depositional redox conditions, as well as for correlating oil and its source rock (i.e. elucidating where oil formed).

What is Pristane induced lupus?

Tetramethylpentadecane (TMPD, or commonly known as pristane)-induced lupus is a murine model of systemic lupus erythematosus (SLE). Renal disease and autoantibody production strictly depend on signaling through the interferon (IFN)-I receptor.

What is the molar mass of Pristane?

268.51 g/molPristane / Molar mass

Is Nonadecane polar?

Nonadecane is a hydrocarbon lipid molecule that is very hydrophobic, practically insoluble in water, and relatively neutral….Structure for FDB012627 (Nonadecane)

Property Value Source
Polar Surface Area 0 Ų ChemAxon
Rotatable Bond Count 16 ChemAxon
Refractivity 89.22 m³·mol⁻¹ ChemAxon

What is Phytane number?

IUPAC name. 2,6,10,14-Tetramethylhexadecane. Identifiers. CAS Number. 638-36-8.

How do you induce lupus in mice?

Pristane can induce systemic lupus with characteristic organ involvement and autoantibodies in various mouse strains. The intraperitoneal injection of pristane stimulates the formation of lupus-associated autoantibodies against multiple nuclear antigens.

What is condensed formula in chemistry?

The condensed formula of a molecule is the formula where the symbols of atoms are listed in order as they appear in the molecule’s structure with bond dashes omitted or limited. While vertical bonds are always omitted, sometimes horizontal bonds are included to indicate polyatomic groups.

What is pentadecane used for?

IDENTIFICATION AND USE: Pentadecane is a colorless liquid. It is used in organic synthesis and as solvent. It is also used for the production of both ionic and nonionic detergents. HUMAN EXPOSURE AND TOXICITY: Pentadecane may be harmful by inhalation, ingestion, or skin absorption during industrial use.

What is NPN-pentadecane?

N-pentadecane is a colorless liquid. (NTP, 1992) National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.

What is the color of N-pentadecane?

N-pentadecane is a colorless liquid. (NTP, 1992) National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina. Colorless liquid Lewis, R.J. Sr.; Hawley’s Condensed Chemical Dictionary 15th Edition.

How is pentadecane made from n-paraffins?

Pentadecane is produced by isolation of n-paraffins (C9-C17) from kerosene and gas oil fractions of crude oil by selective adsorption and fractional distillation. Bingham, E.; Cohrssen, B.; Powell, C.H.; Patty’s Toxicology Volumes 1-9 5th ed. John Wiley & Sons.