Home Amines 123-82-0
123-82-0,MFCD00008101
Catalog No.:AA000JV1

123-82-0 | 2-Aminoheptane

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Purity
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Price(USD)
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1g
95%
in stock  
$18.00   $13.00
- +
5g
95%
in stock  
$34.00   $24.00
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25g
95%
in stock  
$99.00   $69.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA000JV1
Chemical Name:
2-Aminoheptane
CAS Number:
123-82-0
Molecular Formula:
C7H17N
Molecular Weight:
115.2166
MDL Number:
MFCD00008101
SMILES:
CCCCCC(N)C
Properties
Properties
 
BP:
142.0°C  
Form:
Liquid  
MP:
-19°C (estimate)  
Refractive Index:
n20/D 1.418(lit.)  
Stability:
Air Sensitive  
Storage:
2-8℃;Inert atmosphere;  

Computed Properties
 
Complexity:
43.7  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
1  
XLogP3:
2.4  

Literature

Title: Controlling cell growth on titanium by surface functionalization of heptylamine using a novel combined plasma polymerization mode.

Journal: Journal of biomedical materials research. Part A 20110501

Title: Detection in urine of 4-methyl-2-hexaneamine, a doping agent.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20091101

Title: The amine-containing cutaneous irritant heptylamine inhibits the volume-regulated anion channel and mobilizes intracellular calcium in normal human epidermal keratinocytes.

Journal: Molecular pharmacology 20070601

Title: Determination of tuaminoheptane in doping control urine samples.

Journal: European journal of mass spectrometry (Chichester, England) 20070101

Title: Zaremba I, et, al. Differentiation of isomeric heptylamines by in-source collision-induced dissociation of [M + H + ions. Rapid Commun Mass Spectrom. 2019 May 15;33(9):848-856.

Title: Yun H, et, al. Use of enrichment culture for directed evolution of the Vibrio fluvialis JS17 omega-transaminase, which is resistant to product inhibition by aliphatic ketones. Appl Environ Microbiol. 2005 Aug;71(8):4220-4.

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SDS
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