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123048

Sigma-Aldrich

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:
2508-29-4
Molecular Weight:
103.16
Beilstein/REAXYS Number:
1732302
EC Number:
219-718-2
MDL number:
MFCD00008237
UNSPSC Code:
12352100
PubChem Substance ID:
24847516
NACRES:
NA.22

Quality Level

200

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

SMILES string

NCCCCCO

InChI

1S/C5H13NO/c6-4-2-1-3-5-7/h7H,1-6H2

InChI key

LQGKDMHENBFVRC-UHFFFAOYSA-N

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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.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCK0641
BCCH1982
BCCH9368
BCCG1968
BCCF6478

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Sigma-Aldrich

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3-Amino-1-propanol

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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.
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