1459-09-2

Basic information

• Product Name: HEXADECYLBENZENE
• Synonyms: Cetylbenzene 1-Phenylhexadecane;benzene,hexadecyl-;Hexadecane, 1(or 16)-phenyl-;Hexadecane, 1-phenyl-;hexadecane,1(or16)-phenyl-;hexadecyl-benzen;Phenyl hexadecane;N-HEXADECYLBENZENE
• CAS NO: 1459-09-2
• Molecular Formula: C₂₂H₃₈
• Molecular Weight: 302.54
• EINECS: 215-949-8
• Mol File: 1459-09-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: 27 °C(lit.)
• Boiling Point: 172 °C1 mm Hg(lit.)
• Flash Point: 25 °C
• Appearance: /
• Density: 0.855 g/mL at 20 °C(lit.)
• Vapor Pressure: 8.59E-06mmHg at 25°C
• Refractive Index: n20/D 1.481
• CAS DataBase Reference: HEXADECYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: HEXADECYLBENZENE(1459-09-2)
• EPA Substance Registry System: HEXADECYLBENZENE(1459-09-2)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 1459-09-2(Hazardous Substances Data)

Usage

Chemical Properties

white to light yellow low melting solid

InChI:InChI=1/C22H38/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-22-20-17-15-18-21-22/h15,17-18,20-21H,2-14,16,19H2,1H3

Upstream product

• 108-86-1 bromobenzene 
• 544-77-4 1-iodohexadecane 
• 591-50-4 iodobenzene 
• 6697-12-7 hexadecanophenone 
• 629-73-2 1-Hexadecene 
• 71-43-2 benzene 
• 124-13-0 Octanal 
• 13633-25-5 1-Bromo-4-phenylbutane 
• 2030-84-4 n-Dodec-4-en 
• 64283-87-0 4-phenyl-1-iodobutane 
• 112-67-4 n-hexadecanoyl chloride 
• 38775-38-1 1-hexadecanesulfonyl chloride 
• 112-82-3 hexadecanyl bromide 

Downstream Products

• 6812-38-0 hexadecylcyclohexane 
• 16722-32-0 4-Hexadecyl-benzolsulfonsaeure 
• 103167-95-9 1-(4-hexadecyl-phenyl)-ethanone 
• 79098-13-8 4-hexadecylaniline 
• 1306630-59-0 C₆₄H₈₅N₅O₆ 
• 1223591-64-7 C₂₈H₄₂N₂O 
• 1191951-83-3 4-hexadecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide 
• 50671-25-5 p-hexadecylbenzenesulfonyl chloride 
• 105374-48-9 2-Dimethylaminoaethyl-<4-hexadecyl-benzhydryl>-aether 
• 23812-34-2 4-hexadecylbenzoic acid 
• 54337-95-0 Hexadecylbenzyltrimethylammonium chloride 

Relevant articles and documents

Visible-Light-Induced Nickel-Catalyzed Cross-Coupling with Alkylzirconocenes from Unactivated Alkenes

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Iron-catalyzed desulfinylative C-C cross-coupling reactions of sulfonyl chlorides with grignard reagents

(Chemical Equation Presented) A friendly couple: Conditions have been uncovered that allow the desulfinylative C-C cross-coupling reaction of inexpensive sulfonyl chlorides and Grignard reagents (see scheme, acac = acetylacetonate, NMP = N-methylpyrrolidone). The reactions rely on environmentally friendly iron catalysts and do not require expensive and/or toxic ligands.

Environmentally Friendly Catalysis using Supported Reagents: Evolution of a Highly Active Form of Immobilised Aluminium Chloride

An entirely heterogeneous form of aluminium chloride that is highly active in the liquid-phase alkylation of aromatics using alkenes and chloroalkanes is prepared by treating porous support materials with AlCl3 in solution.