Squalane - ≥98%, used for 角鲨烷已被用于：作为溶剂合成二苯甲酰甲基三乙铵铕（目前已知最亮的摩擦发光材料）；作为润滑剂用于吸附在氧化铁表面的脂肪酸表面活性剂膜。 various applications , CAS No.111-01-3

CAS: 111-01-3 Cat. No.: S141335 Peso molecular: 422.81 Beilstein Registry Number: 776019 Número EC: 203-825-6 PubChem CID: 8089

GRADE & PURITY ≥98%

Synonyms

H0096 | SQUALANE [II] | Squalane, European Pharmacopoeia (EP) Reference Standard | squalane-d62 | H12051 | s5407 | SQUALANE [MART.] | EPA Pesticide Chemical Code 045503 | EINECS 203-825-6 | UNII-GW89575KF9 | Squalane, analytical standard | CAS-111-01-3 |

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

H0096 | SQUALANE [II] | Squalane, European Pharmacopoeia (EP) Reference Standard | squalane-d62 | H12051 | s5407 | SQUALANE [MART.] | EPA Pesticide Chemical Code 045503 | EINECS 203-825-6 | UNII-GW89575KF9 | Squalane, analytical standard | CAS-111-01-3 |

Especificaciones y pureza

≥98%

Aplicación

角鲨烷已被用于：作为溶剂合成二苯甲酰甲基三乙铵铕（目前已知最亮的摩擦发光材料）；作为润滑剂用于吸附在氧化铁表面的脂肪酸表面活性剂膜。

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504751572
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751572
• Sonrisas canónicas: CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C
• IUPAC Name: 2,6,10,15,19,23-hexamethyltetracosane
• InChIKey: PRAKJMSDJKAYCZ-UHFFFAOYSA-N
• INCHI: 1S/C30H62/c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4/h25-30H,9-24H2,1-8H3
• Isómeros SMILES: CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C
• WGK Alemania: 3
• RTECS: XB6070000
• PubChem CID: 8089
• Peso molecular: 422.81
• Beilstein: 776019
• Reaxy-Rn: 776019

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Prenol lipids
      • Subclass Triterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Prenol lipids
• Subclass: Triterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Triterpenoids
• Alternative Parents: Branched alkanes
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Triterpenoid - Branched alkane - Acyclic alkane - Saturated hydrocarbon - Alkane - Hydrocarbon - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.
• External Descriptors: Not available

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Not miscible or difficult to mix in water. Chloroform, Hexanes (Slightly). Soluble in ether, chloroform, benzene, slightly soluble in ethanol, acetone, methanol, insoluble in water
• Índice de refracción: 1.45-1.452
• Punto de inflamación (°F): 424.4 °F
• Punto de inflamación (°C): 218 °C
• Punto de ebullición (°C): 350 °C
• Punto de fusión (°C): -38 °C
• Peso molecular: 422.800 g/mol
• XLogP3: 14.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 21
• Exact Mass: 422.485 Da
• Monoisotopic Mass: 422.485 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 30
• Formal Charge: 0
• Complexity: 308.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 4
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

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