Pristane - ≥95% , CAS No.1921-70-6

CAS: 1921-70-6 Cat. No.: P106824 Formule: C₁₉H₄₀ Poids moléculaire: 268.52 Beilstein Registry Number: 1720538 Numéro CE: 217-650-8

GRADE & PURITY ≥95%

Synonyms

2,6,10,14-Tetramethylpentadecane

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Vue d’ensemble

A hydrocarbon oil adjuvant

Specifications

Synonymes

2,6,10,14-Tetramethylpentadecane

Spécifications et pureté

≥95%

Mécanismes biochimiques et physiologiques

Pristane is a hydrocarbon oil adjuvant widely used to induce tumorgenesis in mice and arthritis and lupus nephritis in rats.

Conditions de stockage de stockage

Store at 2-8°C,Argon charged

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥95%

Noms et identifiants

Pubchem Sid

508813225

Sourires canoniques

CC(C)CCCC(C)CCCC(C)CCCC(C)C

IUPAC Name

2,6,10,14-tetramethylpentadecane

InChIKey

XOJVVFBFDXDTEG-UHFFFAOYSA-N

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

Isomères SMILES

CC(C)CCCC(C)CCCC(C)CCCC(C)C

WGK Allemagne

3

RTECS

RZ1880000

Poids moléculaire

268.52

Beilstein

1720538

Reaxy-Rn

1720538

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1720538&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Prenol lipids
      • Subclass Diterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Prenol lipids
• Subclass: Diterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Acyclic diterpenoids
• Alternative Parents: Branched alkanes
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acyclic diterpenoid - Branched alkane - Acyclic alkane - Saturated hydrocarbon - Alkane - Hydrocarbon - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle.
• External Descriptors: long-chain alkane - norterpene

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriétés chimiques et physiques

• Solubilité: Soluble in hexane (10%[v/v]), ether, petroleum ether, benzene, chloroform, and carbon tetrachloride. Insoluble in water.
• Sensibilité: Moisture sensitive;Air sensitive
• Indice de réfraction: 1.4369-1.4389
• Point d'éclair (°F): >230.0 °F
• Point d'éclair (°C): >110°C
• Point d'ébullition (°C): 296°C
• Point de fusion (°C): -99°C
• Poids moléculaire: 268.500 g/mol
• XLogP3: 9.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 12
• Exact Mass: 268.313 Da
• Monoisotopic Mass: 268.313 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 160.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1