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178330

Sigma-Aldrich

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
Beilstein:
1731411
EC Number:
236-364-4
MDL number:
MFCD00008230
UNSPSC Code:
12352100
PubChem Substance ID:
24850731
NACRES:
NA.22

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.)

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.
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

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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)
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