2131-18-2

Basic information

• Product Name: 1-PHENYLPENTADECANE
• Synonyms: 1-phenyl-pentadecan;benzene,pentadecyl-;Pentadecane, 1-phenyl-;pentadecane,1-phenyl-;pentadecyl-benzen;1-PHENYLPENTADECANE;N-PENTADECYLBENZENE;PENTADECYLBENZENE
• CAS NO: 2131-18-2
• Molecular Formula: C₂₁H₃₆
• Molecular Weight: 288.51
• EINECS: 218-352-0
• Mol File: 2131-18-2.mol

Chemical Properties

• Melting Point: 22 °C(lit.)
• Boiling Point: 373 °C(lit.)
• Flash Point: 12 °C
• Appearance: /
• Density: 0.855 g/mL at 20 °C(lit.)
• Vapor Pressure: 2.01E-05mmHg at 25°C
• Refractive Index: n20/D 1.482
• CAS DataBase Reference: 1-PHENYLPENTADECANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-PHENYLPENTADECANE(2131-18-2)
• EPA Substance Registry System: 1-PHENYLPENTADECANE(2131-18-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 2131-18-2(Hazardous Substances Data)

Usage

Uses

Used in Perfume and Cosmetic Industry:
1-Phenylpentadecane is used as a fragrance enhancer for its ability to provide a long-lasting scent. It is incorporated into perfumes, cosmetics, and other personal care products to improve their olfactory appeal and longevity.
Used in Specialty Chemicals Production:
1-Phenylpentadecane is utilized in the production of specialty chemicals due to its unique chemical structure and properties. Its presence in these products can contribute to their performance and functionality.
Used in Lubricants and Coatings Industry:
This chemical is also used in the formulation of lubricants and coatings, where its long-chain alkane structure and phenyl group attachment can offer specific benefits in terms of performance and durability.
However, there is limited information available on the specific properties and potential health effects of 1-Phenylpentadecane, indicating a need for further research to fully understand its safety and broader applications.

InChI:InChI=1/C21H36/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-18-21-19-16-14-17-20-21/h14,16-17,19-20H,2-13,15,18H2,1H3

Upstream product

• 15071-57-5 Methyl 3-n-pentadecylphenyl ether 
• 930118-25-5 3-pentadecyl-1-(1-phenyl-tetrazolyloxy)benzene 

Downstream Products

• 76964-45-9 Pentadecylbenzolsulfonsaeure 
• 68777-63-9 4'-pentadecylacetophenone 
• 94859-75-3 4-n-pentadecylbenzoyl chloride 
• 62443-08-7 4-n-pentadecylbenzoic acid 
• 222631-68-7 oxo-(4-pentadecyl-phenyl)-acetic acid ethyl ester 
• 127570-82-5 1-(4-Pentadecyl-phenyl)-heptan-1-one 

Relevant articles and documents

Nickel-Catalyzed Reductive Cleavage of Carbon-Oxygen Bonds in Anisole Derivatives Using Diisopropylaminoborane

The catalytic removal of a methoxy group on an aromatic ring allows this group to be used as a traceless activating and directing group for aromatic functionalization reactions. Although several catalytic methods for the reductive cleavage of anisole derivatives have been reported, all are applicable only to π-extended aryl ethers, such as naphthyl and biphenyl ethers, while monocyclic aryl ethers cannot be reduced. Herein, we report a nickel-catalyzed reductive cleavage reaction of C-O bonds in aryl ethers using diisopropylaminoborane as the reducing agent. Unlike previously reported methods, this reducing reagent allows effective C-O bond reduction in a much wider range of aryl ether substrates, including monocyclic and heterocyclic ethers bearing various functional groups.

Bisphenol compound and process for preparation thereof

The present invention provides a novel bisphenol compound of formula (I). wherein R1 and R2 are the same or different and are independently either hydrogen or methyl at each occurrence. The present invention also provides a process for preparation of these bisphenol compounds starting from Cashew Nut Shell Liquid (CNSL); —a renewable resource material. The bisphenols prepared in the present invention can be utilized as difunctional monomers for the preparation of various polymers such as epoxy resins, polyesters, polyethersulfones, polyetherketones, polyetherimides, polyarylates, polycarbonates, etc.