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 Fórmula: C₃₀H₆₂ Peso molecular: 422.81 Beilstein Registry Number: 776019 Número CE: 203-825-6

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 |

Especificações e pureza

≥98%

Aplicação

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。

Condições de armazenamento de armazenamento

Store at 2-8°C

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Pureza

≥98%

Nomes e identificadores

Pubchem Sid

504751572

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504751572

Sorrisos canónicos

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

SMILES isoméricas

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

WGK Alemanha

3

RTECS

XB6070000

CAS alternativo

111-01-4

Peso molecular

422.81

Beilstein

776019

Reaxy-Rn

776019

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: 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
• Descrição: 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 ação

Propriedades químicas e físicas

• Solubilidade: 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 refração: 1.45-1.452
• Ponto de inflamação (°F): 424.4 °F
• Ponto de inflamação (°C): 218 °C
• Ponto de ebulição (°C): 350 °C
• Ponto de fusão (°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