171409
Amylamine
99%
Synonym(s):
Pentylamine, 1-Aminopentane, n-Amylamine
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
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.)
functional group
amine
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:
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 Statements
Precautionary Statements
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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.
Journal of Medicinal Chemistry, 59(3), 1052-1067 (2016)
Synthesis of nanosized silver platelets in octylamine-water bilayer systems.
Langmuir, 18(22), 8692-8699 (2002)
Microwave-mediated synthesis of a cyclic heptapeptoid through consecutive Ugi reactions
Tetrahedron, 74(48), 6861-6865 (2018)
Substituted heterocyclic naphthalene diimides with unexpected acidity. Synthesis, properties, and reactivity
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.
Organic Letters, 13(5), 1150-1153 (2011)
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