123048
5-Amino-1-pentanol
≥92.0% (GC)
Synonym(s):
5-Aminopentanol
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About This Item
Linear Formula:
NH2(CH2)5OH
CAS Number:
Molecular Weight:
103.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-718-2
Beilstein/REAXYS Number:
1732302
MDL number:
Assay:
≥92.0% (GC)
Form:
solid
InChI key
LQGKDMHENBFVRC-UHFFFAOYSA-N
InChI
1S/C5H13NO/c6-4-2-1-3-5-7/h7H,1-6H2
SMILES string
NCCCCCO
assay
≥92.0% (GC)
form
solid
refractive index
n20/D 1.4615 (lit.)
bp
120-122 °C/16 mmHg (lit.)
mp
33-35 °C (lit.)
density
0.949 g/mL at 25 °C (lit.)
functional group
amine, hydroxyl
Quality Level
Related Categories
General description
5-Amino-1-pentanol undergoes facile intramolecular cyclocondensation with piperidine and methyl or ethyl piperidine in the presence of methanol or ethanol over zeolite catalyst.
Application
5-Amino-1-pentanol has been used in the synthesis of S-glycosyl amino-acid building blocks. It has been used as starting reagent in the synthesis of aminofunctionalized 4-chloro-2,2′:6′,2′′-terpyridine.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 2
flash_point_f
150.8 °F - closed cup
flash_point_c
66 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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4'-Functionalized 2, 2′ : 6′, 2′′-terpyridines as building blocks for supramolecular chemistry and nanoscience.
Schubert US,et al.
Tetrahedron, 42(28), 4705-4707 (2001)
Thomas Ziegler et al.
Nature protocols, 1(4), 1987-1994 (2007-05-10)
Complex glycosylation patterns on cell surfaces are involved in many fundamental biological processes like specific cell-cell interactions and signal transduction. Furthermore, the glycon part of glycopeptides and glycosylated proteins play a crucial role in numerous ligand-receptor interactions of biological significance.
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Zeolite catalysed intramolecular cyclization of 5-amino-1-pentanol to piperidine bases.
Reddy BN, et al.
Applied Catalysis A: General, 119(1), 23-32 (1994)
Ahmed A Eltoukhy et al.
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