14289-73-7

Basic information

• Product Name: (3-propoxypropyl)benzene
• Synonyms: (3-propoxypropyl)benzene;3-Phenylpropylpropyl ether;Einecs 238-213-8
• CAS NO: 14289-73-7
• Molecular Formula: C₁₂H₁₈O
• Molecular Weight: 178.27072
• EINECS: 238-213-8
• Mol File: 14289-73-7.mol

Chemical Properties

• Boiling Point: 250.9 °C at 760 mmHg
• Flash Point: 108.5 °C
• Appearance: /
• Density: 0.915 g/cm³
• Vapor Pressure: 0.0335mmHg at 25°C
• Refractive Index: 1.488
• CAS DataBase Reference: (3-propoxypropyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (3-propoxypropyl)benzene(14289-73-7)
• EPA Substance Registry System: (3-propoxypropyl)benzene(14289-73-7)

Safety Data

• Hazardous Substances Data: 14289-73-7(Hazardous Substances Data)

Usage

Uses

Used in Fragrance Industry:
(3-Propoxypropyl)benzene is used as a fragrance ingredient for its fresh and sweet scent, commonly found in perfumes and personal care products.
Used in Personal Care Products:
(3-Propoxypropyl)benzene is used as a solvent and scent enhancer in personal care products to provide a pleasant and long-lasting fragrance.
It is important to handle (3-propoxypropyl)benzene with care, as it can cause irritation to the skin, eyes, and respiratory system. Despite this, its versatility and widespread use in the fragrance and personal care industries make it a valuable chemical compound.

InChI:InChI=1/C12H18O/c1-2-10-13-11-6-9-12-7-4-3-5-8-12/h3-5,7-8H,2,6,9-11H2,1H3

Upstream product

• 123-38-6 propionaldehyde 
• 69404-95-1 tert-butyldimethyl(3-phenylpropoxy)silane 
• 71-23-8 propan-1-ol 
• 637-59-2 1-Bromo-3-phenylpropane 
• 6819-41-6 sodium n-propoxide 

Downstream Products

• 1294006-07-7 3-(4-fluorophenyl)propyl propyl ether 
• 130601-72-8 4-propyloxypropylphenol 

Relevant articles and documents

An efficient and convenient method for the direct conversion of alkyl silyl ethers into the corresponding alkyl ethers catalyzed by iron(III) chloride

Various alcohol silyl ethers were readily and efficiently transformed into the corresponding alkyl ethers in high yields by the use of aldehydes combined with triethylsilane in the presence of a catalytic amount of iron(III) chloride. Georg Thieme Verlag Stuttgart.

Synthesis and Physical Properties of Alkoxymethylene Substituted Phenyl Cyclohexanecarboxylates

The homologous series of 4-alkoxymethylene-substituted-phenyl 4'-alkylcyclohexanecarboxylates are prepared.And their transition temperatures, bulk viscosities and birefringences have been measured comparing with the series of 4-alkoxy-substituted-phenyl 4'-alkylcyclohexanecarboxylates.The differences between the alkoxymethylene-substituted series and alkoxy-substituted series are discussed.Alkoxymethylene groups contribute to lowering the transition temperatures, and also reducing the bulk viscosities and optical anisotropy compared to the alkoxy groups as terminal groups of mesogens.This is apparently due to the higher flexibility of the alkoxymethylene groups, which affected the packing of molecules.