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About This Item
Linear Formula:
NH2(CH2)5OH
CAS Number:
Molecular Weight:
103.16
Beilstein/REAXYS Number:
1732302
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
concentration
50% in H2O
bp
122 °C/16 mmHg (lit.)
density
0.99 g/mL at 20 °C
SMILES string
NCCCCCO
InChI
1S/C5H13NO/c6-4-2-1-3-5-7/h7H,1-6H2
InChI key
LQGKDMHENBFVRC-UHFFFAOYSA-N
General description
5-Aminopentan-1-ol is a colorless to faint yellow liquid.
Application
5-amino-1-pentanol is used in the preparation of fibres from random copolypeptides consisting of N-hydroxyalkyl L-glutamine and gamma-methyl L-glutamate with different monomer ratios[1]. 5-amino-1-pentanol (5-Aminopentan-1-ol) was also used in the preparation of 5-phthalimidopentanal[2] and tetracyclic core of the natural compound (+/-)-dibromoagelaspongin[3].
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1A
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Sylvain Picon et al.
Organic letters, 11(12), 2523-2526 (2009-05-19)
A six-step synthesis of the tetracyclic core of the natural compound (+/-)-dibromoagelaspongin, isolated from Agelas sp. Sponge, was achieved from the commercially available 5-aminopentan-1-ol, 2-trichloroacetylpyrrole, and 2-aminopyrimidine. Following a biomimetic inspired approach, successive oxidative reactions including the final DMDO biomimetic
Miller D, et al.
Journal of the Chemical Society. Perkin Transactions 1, 1, 131-142 (1998)
T Hayashi et al.
Biomaterials, 11(6), 409-413 (1990-08-01)
Fibres from random copolypeptides consisting of N-hydroxyalkyl L-glutamine and gamma-methyl L-glutamate with different monomer ratios were prepared by aminoalcoholysis of a poly(gamma-methyl L-glutamate) fibre with 2-amino-1-ethanol or 5-amino-1-pentanol, both with 1,8-octamethylenediamine as cross-linking agent. The initial tensile properties as well
Ahmed A Eltoukhy et al.
ACS nano, 8(8), 7905-7913 (2014-07-11)
Despite intensive research effort, the rational design of improved nanoparticulate drug carriers remains challenging, in part due to a limited understanding of the determinants of nanoparticle entry and transport in target cells. Recent studies have shown that Niemann-Pick C1 (NPC1)
Yohei Ishibashi et al.
Biochemical and biophysical research communications, 452(4), 873-880 (2014-08-27)
Galactosylglycerolipids (GGLs) and chlorophyll are characteristic components of chloroplast in photosynthetic organisms. Although chlorophyll is anchored to the thylakoid membrane by phytol (tetramethylhexadecenol), this isoprenoid alcohol has never been found as a constituent of GGLs. We here described a novel
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