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Merck
CN

11318

5-氨基-1-戊醇 溶液

50% in H2O

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关于此项目

线性分子式:
NH2(CH2)5OH
化学文摘社编号:
分子量:
103.16
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
1732302
MDL number:
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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. 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.


pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1A

存储类别

8B - Non-combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)