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19170

Sigma-Aldrich

3-Buten-1-ol

purum, ≥98.0% (GC)

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Synonym(s):
Allylcarbinol
Linear Formula:
CH2=CHCH2CH2OH
CAS Number:
627-27-0
Molecular Weight:
72.11
Beilstein/REAXYS Number:
1633504
EC Number:
210-991-3
MDL number:
MFCD00002959
UNSPSC Code:
12352100
PubChem Substance ID:
329751827
NACRES:
NA.22

grade

purum

Quality Level

100

assay

≥98.0% (GC)

refractive index

n20/D 1.421 (lit.)
n20/D 1.422

bp

112-114 °C (lit.)

density

0.838 g/mL at 25 °C (lit.)

SMILES string

OCCC=C

InChI

1S/C4H8O/c1-2-3-4-5/h2,5H,1,3-4H2

InChI key

ZSPTYLOMNJNZNG-UHFFFAOYSA-N

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Application

3-Buten-1-ol was used as a starting reagent in asymmetric total synthesis of natural seimatopolide B. It was also used in the synthesis of catalytic bimetallic nanoparticles.

replaced by

Product No.
Description
Pricing

496839

3-Buten-1-ol, 96%

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

ppe

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

Certificates of Analysis (COA)

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Chada Raji Reddy et al.
Organic & biomolecular chemistry, 11(20), 3355-3364 (2013-04-09)
The asymmetric total synthesis of natural seimatopolide B along with its enantiomer is described starting from readily available 5-hexen-1-ol and 3-buten-1-ol. The key steps involved are Jacobson hydrolytic kinetic resolution, proline-catalyzed α-hydroxylation, Yamaguchi esterification and ring-closing metathesis. This asymmetric total
Alternating copolymers of functional alkenes with carbon monoxide.
Kacker S, et al.
Macromolecules, 29(18), 5852-5858 (1996)
Biologically programmed synthesis of bimetallic nanostructures.
Slocik JM and Naik RR.
Advanced Materials, 18(15), 1988-1992 (2006)

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