Skip to Content
Merck
CN

Key Documents

View All Documentation

19170

3-Buten-1-ol

purum, ≥98.0% (GC)

Synonym(s):

Allylcarbinol

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
CH2=CHCH2CH2OH
CAS Number:
627-27-0
Molecular Weight:
72.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329751827
EC Number:
210-991-3
Beilstein/REAXYS Number:
1633504
MDL number:
MFCD00002959
Assay:
≥98.0% (GC)
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

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.)

functional group

allyl, hydroxyl

SMILES string

OCCC=C

InChI

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

InChI key

ZSPTYLOMNJNZNG-UHFFFAOYSA-N

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.

Still not finding the right product?

Explore all of our products under 3-Buten-1-ol

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

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

91.4 °F - closed cup

flash_point_c

33 °C - closed cup

ppe

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

Regulatory Information

危险化学品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBP1862V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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

Global Trade Item Number

SKUGTIN
19170-5ML04061837331299
19170-25ML04061838760265