Skip to Content
Merck
All Photos(1)

Documents

171409

Sigma-Aldrich

Amylamine

99%

Synonym(s):

Pentylamine, 1-Aminopentane, n-Amylamine

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)4NH2
CAS Number:
Molecular Weight:
87.16
Beilstein:
505953
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

3.01 (vs air)

Assay

99%

form

liquid

expl. lim.

22 %

refractive index

n20/D 1.411 (lit.)

bp

104 °C (lit.)

mp

−50 °C (lit.)

density

0.752 g/mL at 25 °C (lit.)

SMILES string

CCCCCN

InChI

1S/C5H13N/c1-2-3-4-5-6/h2-6H2,1H3

InChI key

DPBLXKKOBLCELK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Amylamine can be used in the imidization of 2,6-dibromonaphthalene and 2,3,6,7-tetrabromonaphthalene bisanhydride, which are used to synthesize polybromo naphthalenetetracarboxylic acid diimides (NDIs).
It can be also be used to synthesize:
  • N


  • -pentyl side chains of a cyclic heptapeptoid which forms the core of verticilide
  • N-pentyl sulfamides from sulfamate salts.

Amylamine is a general reagent used in functionalizing the target molecules with pentyl chain. It has also been used as a cosurfactant to increase the phase stability of the bilayer systems.

Caution

May darken in storage.

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

44.6 °F

Flash Point(C)

7 °C

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Substituted heterocyclic naphthalene diimides with unexpected acidity. Synthesis, properties, and reactivity
Doria F, et al.
The Journal of Organic Chemistry, 74(22), 8616-8625 (2009)
Efficient Synthesis of 5H-Cyclopenta [c] quinoline Derivatives via Palladium-Catalyzed Domino Reactions of o-Alkynylhalobenzene with Amine.
Luo Y, et al.
Organic Letters, 13(5), 1150-1153 (2011)
Investigations on the 4-quinolone-3-carboxylic acid motif. 7. Synthesis and pharmacological evaluation of 4-quinolone-3-carboxamides and 4-hydroxy-2-quinolone-3-carboxamides as high affinity cannabinoid receptor 2 (CB2R) ligands with improved aqueous solubility.
Mugnaini C, et al.
Journal of Medicinal Chemistry, 59(3), 1052-1067 (2016)
Microwave-mediated synthesis of a cyclic heptapeptoid through consecutive Ugi reactions
Barreto AS and Andrade CZ
Tetrahedron, 74(48), 6861-6865 (2018)
Synthesis of nanosized silver platelets in octylamine-water bilayer systems.
Yener D O, et al.
Langmuir, 18(22), 8692-8699 (2002)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service