5519-35-7

Upstream product

• 92186-10-2 methyl 4-n-dodecylbenzoate 
• 693-67-4 bromoundecane 
• 123-01-3 1-dodecylbenzene 
• 6313-88-8 4-dodecylacetophenone 
• 99-94-5 p-Toluic acid 
• 21021-55-6 4-dodecylbenzoic acid 
• 104-37-0 4-dodecylbenzyl chloride 

Downstream Products

• 189139-40-0 1,3-bis(4-dodecylphenyl)-propan-2-one 
• 133633-73-5 (4-Dodecyl-2-iodo-phenyl)-acetic acid 
• 7073-31-6 p-(n-dodecyl)benzyl nitrile 
• 133633-72-4 p-(n-dodecyl)phenylacetic acid 
• 104-37-0 4-dodecylbenzyl chloride 
• 5519-26-6 N--Phe-Ala- 
• 5519-21-1 N-(p-Decyloxy-benzyloxy-carbonyl)-Ala-p-dodecylbenzylester 
• 56636-86-3 1-tert-Butoxymethyl-4-dodecyl-benzene 

Relevant academic research and scientific papers

Method for synthesizing long-chain alkyl benzyl alcohol through basic hydrolysis of long-chain alkyl benzyl halides

The invention discloses a method for synthesizing long-chain alkyl benzyl alcohol through basic hydrolysis of long-chain alkyl benzyl halides, relates to a method for synthesizing long-chain alkyl benzyl alcohol through phase transfer catalysis of hydroth

Photodegradative surfactants: p-dodecylbenzyltrimethylammonium bromide as a photodegradative emulsifier for microemulsion polymerization

A photodegradative surfactant, p-dodecylbenzyltrimethylammonium bromide, was used as an emulsifier for micro-emulsion polymerization of methyl methacrylate in water. The resulting polymer latex was coagulated during UV irradiation. The analysis of the centrifuged solid after irradiation indicated almost perfection of both recovery of the polymer and removal of surface-active species from it. Copyright

Photodegradative surfactants: Photolysis of p-dodecylbenzyltrimethylammonium bromide in aqueous solution

Upon UV irradiation, a benzyl-containing cationic surfactant, p-dodecylbenzyltrimethylammonium bromide, has been converted to a nonsurfactant, which can be separated from the aqueous solution by coprecipitation with CaSO4.

Sebosuppressive preparations containing benzyl alcohol derivatives

Sebosuppressive cosmetic preparations containing benzyl alcohol derivatives which are substituted on the benzene ring by alkyl, aryl, alkyloxymethyl radicals or by a fused aromatic ring, and methods for their use.

Reactions in Microemulsion Media. Nucleophilic Substitution Reactions of Benzyl and p-Alkylbenzyl Chlorides

A kinetic and synthetic study of nucleophilic displacement reaction of bromide ion with benzyl chloride (1a) and its p-ethyl-substituted (1b) and p-n-dodecyl-substituted (1c) analogues has been performed in microemulsions prepared from combinations of a 1.23:1 (w/w) mixture (S) of cetyltrimethylammonium bromide (CTABr) and 1-butanol, a 1:5 (w/w) KBr-H2O solution (W), and hexane (O).The rates of reaction decreased differentially with increasing hexane content at a constant ratio of S:W to indicate that the interphase was the microemulsion reactive site.For microemulsion with respect to aqueous micellar and aqueous ethanol reaction media, solubilization of substrate was higher, initial reaction rates were comparable or slightly less, and overall conversions were greater.