171409
Amylamine
99%
Synonym(s):
Pentylamine, 1-Aminopentane, n-Amylamine
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About This Item
Linear Formula:
CH3(CH2)4NH2
CAS Number:
Molecular Weight:
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
vapor 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 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.
Disclaimer
May darken in storage.
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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
WGK 1
flash_point_f
44.6 °F
flash_point_c
7 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 171409-50ML | 04061838750907 |
| 171409-250ML | 04061837506413 |
| 171409-25ML | 04061838750891 |