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496138

Sigma-Aldrich

N-Methylpentylamine

98%

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About This Item

Linear Formula:
CH3(CH2)4NHCH3
CAS Number:
Molecular Weight:
101.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

98%

refractive index

n20/D 1.41 (lit.)

bp

116-118 °C (lit.)

density

0.738 g/mL at 25 °C (lit.)

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.
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.
  • 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.

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

55.0 °F - closed cup

Flash Point(C)

12.77 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A novel approach for facilitating the targeted synthesis of silicoaluminophosphates
Yan Nana, et al.
Journal of Material Chemistry A, 6(47), 24186-24193 (2018)
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
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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