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178330

Sigma-Aldrich

4-Amino-1-butanol

98%

Synonym(s):

4-Hydroxybutylamine

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1 G
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About This Item

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

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Quality Level

200

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

SMILES string

NCCCCO

InChI

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

InChI key

BLFRQYKZFKYQLO-UHFFFAOYSA-N

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Application

4-Amino-1-butanol was used in the synthesis of cyclic amines[1].
4-Amino-1-butanol was used:
  • As a linker in the synthesis of highly branched poly(β-amino esters)(HPAEs) for gene delivery.[2]
  • As a side chain to modulate antimicrobial and hemolytic activities of copolymers.[3]
  • In the total synthesis of (+)-fawcettimine,(+)-fawcettidine,[4] and (−)-lycojapodine A.[5]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

219.2 °F - closed cup

Flash Point(C)

104 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBL2230
BCBQ8586V
STBK4078
STBK2726
STBJ9491

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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)
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)
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)
Synthesis of cyclic amines and their alkyl derivatives from amino alcohols over supported copper catalysts.
Applied Catalysis, 53(1), 107-115 (1989)
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