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496138

Sigma-Aldrich

N-Methylpentylamine

98%

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About This Item

Linear Formula:
CH3(CH2)4NHCH3
CAS Number:
25419-06-1
Molecular Weight:
101.19
EC Number:
246-966-9
MDL number:
MFCD00041354
UNSPSC Code:
12352100
PubChem Substance ID:
24872691

assay

98%

refractive index

n20/D 1.41 (lit.)

bp

116-118 °C (lit.)

density

0.738 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCCCCNC

InChI

1S/C6H15N/c1-3-4-5-6-7-2/h7H,3-6H2,1-2H3

InChI key

UOIWOHLIGKIYFE-UHFFFAOYSA-N

Application

N-Methylpentylamine can be used as an organic structure-directing agent in the preparation of microporous silicoaluminophosphate (SAPO) molecular sieves.[1]
It can also be used as a reactant to synthesize:
  • N


  • ′-tert-butyl-N-methyl-N-pentylsulfamide by reacting with triethylammonium N-tert-butylsulfamate in the presence of triphenylphosphine oxide and trifluoromethanesulfonic anhydride.[2]
  • 1-methyl-3-(methylpentylamino)-4-(phenylseleno) 1H-pyrrole-2,5-dione (aminoarylselenated maleimide) by Cu-catalyzed four-component coupling reaction with methyl maleimide, Se powder and iodobenzene.[3]

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Flam. Liq. 2 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

55.0 °F - closed cup

flash_point_c

12.77 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
10802EO
11414ES

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Xue Gao et al.
Organic letters, 21(3), 745-748 (2019-01-15)
The first example of copper-catalyzed four-component coupling reaction of aryl iodides, Se powder, secondary amines, and maleimides is developed. This reaction provides an efficient and concise route to access aminoarylselenated maleimides via double C-Se bonds and C-N bond formation. The
A novel approach for facilitating the targeted synthesis of silicoaluminophosphates
Yan Nana, et al.
Journal of Material Chemistry A, 6(47), 24186-24193 (2018)
Interactions of alkylamines with the silicon (001) surface.
Cao X and Hamers RJ.
J. Vac. Sci. Technol. B, 20(4), 1614-1619 (2002)
Efficient synthesis of unsymmetrical sulfamides from sulfamic acid salts by activation with triphenylphosphine ditriflate
Shehata MF, et al.
Tetrahedron, 75(24), 3186-3194 (2019)
Oliver Wahl et al.
Journal of pharmaceutical and biomedical analysis, 114, 254-264 (2015-06-21)
The modern bisphosphonate drug ibandronate sodium, a challenging candidate for impurity profiling, was analyzed using high performance liquid chromatography (HPLC) combined with corona charged aerosol detection (CAD). Separation was achieved on a mixed mode column combining hydrophobic C18 and strong

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