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N-octylpyridin-4-amine

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Products Intro: Product Name:N-octylpyridin-4-amine
CAS:64690-19-3
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Products Intro: Product Name:4-(Octylamino)pyridine
CAS:64690-19-3
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CAS:64690-19-3
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CAS:64690-19-3
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N-octylpyridin-4-amine manufacturers

  • N-octylpyridin-4-amine
  • N-octylpyridin-4-amine pictures
  • $1.00 / 1kg
  • 2026-05-13
  • CAS:64690-19-3
  • Min. Order: 0.10000000kg
  • Purity: 99%
  • Supply Ability: 200KG
N-octylpyridin-4-amine Basic information
Product Name:N-octylpyridin-4-amine
Synonyms:N-octylpyridin-4-amine;4-(OCTYLAMINO)PYRIDINE;N-Octyl-4-pyridinamine;N-Octylpyridine-4-amine;N-oCLylpyridin-4-aMine;4-(Octylamino)pyridine/N-Octyl-4-pyridinamine;4-Pyridinamine, N-octyl-;N-octylpyridin-4-amine ISO 9001:2015 REACH
CAS:64690-19-3
MF:C13H22N2
MW:206.33
EINECS:265-019-0
Product Categories:Amines;Aromatics;Heterocycles;Heterocycle-Pyridine series
Mol File:64690-19-3.mol
N-octylpyridin-4-amine Structure
N-octylpyridin-4-amine Chemical Properties
Melting point 70-73 °C(Solv: hexane (110-54-3))
Boiling point 327.3±15.0 °C(Predicted)
density 0.947±0.06 g/cm3(Predicted)
vapor pressure 0.004Pa at 25℃
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka8.32±0.26(Predicted)
color Light Brown to Dark Brown
InChIInChI=1S/C13H22N2/c1-2-3-4-5-6-7-10-15-13-8-11-14-12-9-13/h8-9,11-12H,2-7,10H2,1H3,(H,14,15)
InChIKeyRHDWCSIBVZKRRU-UHFFFAOYSA-N
SMILESC1=NC=CC(NCCCCCCCC)=C1
LogP2.28 at 22.5℃ and pH7
Surface tension58mN/m at 1g/L and 20℃
Safety Information
MSDS Information
N-octylpyridin-4-amine Usage And Synthesis
Chemical PropertiesWhite crystals, melting point 65-66℃.
UsesN-Octylpyridin-4-amine is used in the synthesis of antimicrobial agent Octenidine (O239150), as chelating agent.
Synthesis
Octylamine

111-86-4

4-Chloropyridinium chloride

7379-35-3

N-octylpyridin-4-amine

64690-19-3

Add n-octylamine (100 mg), 4-chloropyridine hydrochloride (30 kg) and sodium fluoride (10 kg) to a 200 L reactor and raise the temperature to 130 °C. The reaction was stirred at this temperature for 2 hours. Upon completion of the reaction, the unreacted n-octylamine was recovered by distillation under reduced pressure. Subsequently, the pH of the reaction mixture was adjusted with hot aqueous sodium carbonate to about 7. Ethyl acetate (120 kg) was added for extraction and the aqueous layer was separated. The organic layer was cooled, filtered and dried to afford the target product 4-(octylamino)pyridine (32.3 kg) in 99.3% purity and 78.5% yield.

References[1] Journal of the American Chemical Society, 2008, vol. 130, # 20, p. 6586 - 6596
[2] Patent: CN107501173, 2017, A. Location in patent: Paragraph 0018
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