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64690-19-3

64690-19-3 Structure

64690-19-3 Structure
IdentificationBack Directory
[Name]

N-octylpyridin-4-amine
[CAS]

64690-19-3
[Synonyms]

N-octylpyridin-4-amine
4-(OCTYLAMINO)PYRIDINE
N-Octyl-4-pyridinamine
N-oCLylpyridin-4-aMine
N-Octylpyridine-4-amine
4-Pyridinamine, N-octyl-
N-octylpyridin-4-amine ISO 9001:2015 REACH
4-(Octylamino)pyridine/N-Octyl-4-pyridinamine
[EINECS(EC#)]

265-019-0
[Molecular Formula]

C13H22N2
[MDL Number]

MFCD09743883
[MOL File]

64690-19-3.mol
[Molecular Weight]

206.33
Chemical PropertiesBack Directory
[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
[pka]

8.32±0.26(Predicted)
[color ]

Light Brown to Dark Brown
[InChI]

InChI=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)
[InChIKey]

RHDWCSIBVZKRRU-UHFFFAOYSA-N
[SMILES]

C1=NC=CC(NCCCCCCCC)=C1
[LogP]

2.28 at 22.5℃ and pH7
[Surface tension]

58mN/m at 1g/L and 20℃
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H332-H335-H302
[Precautionary statements ]

P261-P271-P304+P340-P312-P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Raw materials And Preparation ProductsBack Directory
[Raw materials]

OCTYLAMINE HYDROCHLORIDE-->4-chloropyridine-->2-IODOOCTANE-->4-Aminopyridine-->4-Iodopyridine-->Octylamine-->4-Bromopyridine hydrochloride-->Octanal-->4-Chloropyridinium chloride
Hazard InformationBack Directory
[Uses]

N-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
Spectrum DetailBack Directory
[Spectrum Detail]

N-octylpyridin-4-amine(64690-19-3)1HNMR
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