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Merck
CN

178330

4-Amino-1-butanol

98%

Synonym(s):

4-Hydroxybutylamine

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About This Item

Linear Formula:
H2N(CH2)4OH
CAS Number:
13325-10-5
Molecular Weight:
89.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24850731
EC Number:
236-364-4
Beilstein/REAXYS Number:
1731411
MDL number:
MFCD00008230

Key Documents

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Product Name

4-Amino-1-butanol, 98%

InChI key

BLFRQYKZFKYQLO-UHFFFAOYSA-N

InChI

1S/C4H11NO/c5-3-1-2-4-6/h6H,1-5H2

SMILES string

NCCCCO

assay

98%

form

liquid

refractive index

n20/D ~1.462 (lit.)

bp

206 °C (lit.)

mp

16-18 °C (lit.)

density

0.967 g/mL at 25 °C (lit.)

functional group

amine
hydroxyl

Quality Level

200

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Application

4-Amino-1-butanol was used in the synthesis of cyclic amines.
4-Amino-1-butanol was used:
  • As a linker in the synthesis of highly branched poly(β-amino esters)(HPAEs) for gene delivery.
  • As a side chain to modulate antimicrobial and hemolytic activities of copolymers.
  • In the total synthesis of (+)-fawcettimine,(+)-fawcettidine, and (−)-lycojapodine A.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

219.2 °F - closed cup

flash_point_c

104 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB5643
STBL2230
BCBQ8586V
STBK4078
STBK2726

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Synthesis of cyclic amines and their alkyl derivatives from amino alcohols over supported copper catalysts.
Applied Catalysis, 53(1), 107-115 (1989)
Collective synthesis of lycopodium alkaloids and tautomer locking strategy for the total synthesis of (−)-lycojapodine A.
Li H, et al.
The Journal of Organic Chemistry, 78(3), 800-821 (2012)
Pieter Vader et al.
Pharmaceutical research, 29(2), 352-361 (2011-08-13)
Use of RNA interference as novel therapeutic strategy is hampered by inefficient delivery of its mediator, siRNA, to target cells. Cationic polymers have been thoroughly investigated for this purpose but often display unfavorable characteristics for systemic administration, such as interactions
Total Syntheses of Lycopodium Alkaloids (+)?Fawcettimine,(+)?Fawcettidine, and (−)?8?Deoxyserratinine.
Li H, et al.
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 124(2), 506-510 (2012)
Cationic spacer arm design strategy for control of antimicrobial activity and conformation of amphiphilic methacrylate random copolymers.
Palermo E F, et al.
Biomacromolecules, 13(5), 1632-1641 (2012)
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