11318
5-Amino-1-pentanol solution
50% in H2O
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About This Item
Formule linéaire :
NH2(CH2)5OH
Numéro CAS:
Poids moléculaire :
103.16
Numéro Beilstein :
1732302
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Produits recommandés
Concentration
50% in H2O
Point d'ébullition
122 °C/16 mmHg (lit.)
Densité
0.99 g/mL at 20 °C
Chaîne SMILES
NCCCCCO
InChI
1S/C5H13NO/c6-4-2-1-3-5-7/h7H,1-6H2
Clé InChI
LQGKDMHENBFVRC-UHFFFAOYSA-N
Description générale
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. 5-amino-1-pentanol (5-Aminopentan-1-ol) was also used in the preparation of 5-phthalimidopentanal and tetracyclic core of the natural compound (+/-)-dibromoagelaspongin.
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 4 Oral - Skin Corr. 1A
Code de la classe de stockage
8B - Non-combustible corrosive hazardous materials
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
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
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
Miller D, et al.
Journal of the Chemical Society. Perkin Transactions 1, 1, 131-142 (1998)
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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