171409
Amylamine
99%
Synonyme(s) :
Pentylamine, 1-Aminopentane, n-Amylamine
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A propos de cet article
Formule linéaire :
CH3(CH2)4NH2
Numéro CAS:
Poids moléculaire :
87.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-780-2
Beilstein/REAXYS Number:
505953
MDL number:
Assay:
99%
Form:
liquid
Service technique
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Laissez-nous vous aidervapor density
3.01 (vs air)
Quality Level
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
Application
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.
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.
Disclaimer
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
Classe de stockage
3 - Flammable liquids
wgk
WGK 1
flash_point_f
44.6 °F
flash_point_c
7 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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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)
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)