Skip to Content
MilliporeSigma
All Photos(1)

Documents

171409

Sigma-Aldrich

Amylamine

99%

Synonym(s):

Pentylamine, 1-Aminopentane, n-Amylamine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3(CH2)4NH2
CAS Number:
110-58-7
Molecular Weight:
87.16
Beilstein/REAXYS Number:
505953
EC Number:
203-780-2
MDL number:
MFCD00008236
UNSPSC Code:
12352100
PubChem Substance ID:
24850059
NACRES:
NA.22

vapor density

3.01 (vs air)

Quality Level

100

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

Related Categories

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.

signalword

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

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

44.6 °F

flash_point_c

7 °C

ppe

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

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

Slide 1 of 2

1 of 2

Isopentylamine 99%

Sigma-Aldrich

126810

Isopentylamine

≥99%

Sigma-Aldrich

W313009

Butylamine

Synthesis of nanosized silver platelets in octylamine-water bilayer systems.
Yener D O, et al.
Langmuir, 18(22), 8692-8699 (2002)
Microwave-mediated synthesis of a cyclic heptapeptoid through consecutive Ugi reactions
Barreto AS and Andrade CZ
Tetrahedron, 74(48), 6861-6865 (2018)
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)
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)
Tetrathiafulvalene in a perylene-3, 4: 9, 10-bis (dicarboximide)-based dyad: a new reversible fluorescence-redox dependent molecular system.
Leroy-Lhez S, et al.
The Journal of Organic Chemistry, 70(16), 6313-6320 (2005)
View All Related Papers

Protocols

GC Analysis of Primary Amines on Carbowax® Amine

Separation of Propylamine; Butylamine; Pentylamine; Hexylamine; Heptylamine; Octylamine; Nonylamine; Decylamine

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