5519-35-7

Basic information

• Product Name: Benzenemethanol, 4-dodecyl-
• CAS NO: 5519-35-7
• Molecular Formula: C19H32O
• Molecular Weight: 276.462
• Mol File: 5519-35-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 4-dodecyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 4-dodecyl-(5519-35-7)
• EPA Substance Registry System: Benzenemethanol, 4-dodecyl-(5519-35-7)

Safety Data

• Hazardous Substances Data: 5519-35-7(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 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 
• 189139-40-0 1,3-bis(4-dodecylphenyl)-propan-2-one 
• 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 articles and documents

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: 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.