4462-09-3

Basic information

• Product Name: Piperidine, 1-(3-methylbutyl)-
• Synonyms: Piperidine, 1-(3-methylbutyl)-;N-Isopentyl-piperidin;1-(CH3)2CHCH2CH2C5H10N;N-isopentylpiperidine;1-Isopentyl-piperidin;1-(3-methyl-butyl)-piperidine;1-isopentyl-piperidine
• CAS NO: 4462-09-3
• Molecular Formula: C10H21N
• Molecular Weight: 155.283
• Mol File: 4462-09-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 76-79 °C(Press: 20 Torr)
• Density: 0.8249 g/cm3(Temp: 420 °C)
• CAS DataBase Reference: Piperidine, 1-(3-methylbutyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Piperidine, 1-(3-methylbutyl)-(4462-09-3)
• EPA Substance Registry System: Piperidine, 1-(3-methylbutyl)-(4462-09-3)

Safety Data

• Hazardous Substances Data: 4462-09-3(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 541-28-6 isopentyl iodide 
• 110-86-1 pyridine 
• 123-51-3 i-Amyl alcohol 
• 107-82-4 i-pentyl bromide 
• 36794-55-5 N-(3-methyl-2-buten-1-yl)-piperidine 
• 503-60-6 3,3-dimethyl-allyl chloride 
• 543-87-3 isopentyl nitrate 
• 77664-41-6 1-(2-Methyl-1-trichloromethyl-propyl)-piperidine 
• 100-99-2 triisobutylaluminum 
• 90524-38-2 1-(tert-Butyl-dimethyl-silanyloxymethyl)-piperidine 
• 107-85-7 1-amino-3-methylbutane 
• 111-24-0 1,5-dibromo-pentane 

Downstream Products

• 54868-48-3 (E)-5-isopropyl-8-methylnona-6,8-dien-2-one 

Relevant articles and documents

Synthesis and properties of pentane amino derivatives

Synthesis of pentane amino derivatives by the reaction of the corresponding amines with 1-bromopentanes of n-and iso-structure by environmentally safe methods in water medium was carried out. The structure of the compounds obtained was confirmed by elemental analysis, IR, 1H and 13C NMR spectroscopy. The products synthesized were tested as reagents for the suppression of growth of the sulfate-reducing bacteria and as the anticorrosive substances. It was found that they are effective bactericides for the sulfate-reducing bacteria and exhibit high anticorrosive properties. Pleiades Publishing, Ltd., 2010.

Reduction of 2,2,2-trichloroethylamines with lithium aluminum hydride

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