28488-47-3

Basic information

• Product Name: Benzoic acid,5-hexyl-2-hydroxy-
• Synonyms: Salicylicacid, 5-hexyl- (7CI,8CI);5-Hexyl-2-hydroxybenzoic acid;5-Hexylsalicylic acid
• CAS NO: 28488-47-3
• Molecular Formula: C₁₃H₁₈O₃
• Molecular Weight: 222.28
• Mol File: 28488-47-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 368.702 °C at 760 mmHg
• Flash Point: 190.967 °C
• Density: 1.116 g/cm³
• CAS DataBase Reference: Benzoic acid,5-hexyl-2-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid,5-hexyl-2-hydroxy-(28488-47-3)
• EPA Substance Registry System: Benzoic acid,5-hexyl-2-hydroxy-(28488-47-3)

Safety Data

• Hazardous Substances Data: 28488-47-3(Hazardous Substances Data)

Upstream product

• 78417-95-5 methyl 5-n-hexanoylsalicylate 
• 7487-94-7 mercury (II) chloride 
• 111-25-1 1-bromo-hexane 
• 89-55-4 5-bromosalicyclic acid 
• 119-36-8 methyl salicylate 
• 142-61-0 Hexanoyl chloride 
• 78418-00-5 5-n-hexanoylsalicylic acid 
• 21017-36-7 5-n-hexyl-salicylic acid methyl ester 
• 40523-63-5 2-hexanoyloxy-benzoic acid methyl ester 

Downstream Products

• 78417-64-8 4'-bromo-5-n-hexylsalicylanilide 
• 78417-83-1 5-Hexyl-2-hydroxy-N-(4-methyl-3-nitro-phenyl)-benzamide 
• 78417-81-9 5-n-hexyl-4'nitrosalicylanilide 
• 78417-82-0 5-Hexyl-2-hydroxy-N-(3-nitro-phenyl)-benzamide 
• 78417-78-4 N-Benzothiazol-2-yl-5-hexyl-2-hydroxy-benzamide 
• 78417-80-8 N-(3,4-Dichloro-benzyl)-5-hexyl-2-hydroxy-benzamide 
• 80617-09-0 5-Hexyl-2-hydroxy-N-(4-trifluoromethyl-phenyl)-benzamide 
• 78417-79-5 N-(4-Chloro-benzyl)-5-hexyl-2-hydroxy-benzamide 

Relevant articles and documents

Synthetic method of alkyl salicylic acid

A synthetic method of alkyl salicylic acid comprises the following steps: brominated alkanes used as a raw material reacts with lithium metal in a solvent, namely ether to obtain lithium alkyl; the lithium alkyl reacts with cuprous iodide in ether to generate lithium dialkylcuprate; and the lithium dialkylcuprate and bromosalicylic acid are mixed and coupling is carried out to obtain alkyl salicylic acid.

Potential salicylamide antiplaque agents: In vitro antibacterial activity against Actinomyces viscosus

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