Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

306894

Sigma-Aldrich

3-Hexyne

99%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C2H5C≡CC2H5
CAS Number:
Molecular Weight:
82.14
Beilstein/REAXYS Number:
1731158
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

186 mmHg ( 37.7 °C)

assay

99%

form

liquid

refractive index

n20/D 1.411 (lit.)

bp

81-82 °C (lit.)

density

0.723 g/mL at 25 °C (lit.)

SMILES string

CCC#CCC

InChI

1S/C6H10/c1-3-5-6-4-2/h3-4H2,1-2H3

InChI key

DQQNMIPXXNPGCV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

3-Hexyne was used in the synthesis of fused hetero-hydropyridyl ligands bonded to the {Ru(p-cymene)} organometallic moiety by reacting with ruthenacycles. It was also used in the preparation of [4+2] cycloaddition product by reacting with borole.

signalword

Danger

Hazard Classifications

Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

6.8 °F - closed cup

flash_point_c

-14 °C - closed cup

ppe

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


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

Luciano Cuesta et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(47), 15178-15189 (2012-09-29)
Novel cycloruthenated complexes 2 a-c, 4 a-c, and 6 a, b based on heteroaromatic cores have been synthesized by reaction of a series of heterocycle-based imines with [{RuCl(η(6)-p-cymene)}(2)(μ-Cl)(2)] and Cu(OAc)(2). This approach has proved efficient for the cyclometalation of thiophene, benzothiophene, furan, benzofuran, pyrrole
Fang Ge et al.
Journal of the American Chemical Society, 136(1), 68-71 (2013-12-21)
Bis(trimethylsilylethynyl)diphenylaminoborane was reacted with the strong Lewis acid B(C6F5)3 at ambient temperature to give the borole 9 admixed with a small amount of its thermal follow-up product 12. Compound 9 was subsequently stabilized by adduct formation with pyridine (10). Treatment
He Nan et al.
Journal of chromatography. A, 1523, 316-320 (2017-06-26)
Silver ion or argentation chromatography utilizes stationary phases containing silver ions for the separation of unsaturated compounds. In this study, a mixed-ligand silver-based ionic liquid (IL) was evaluated for the first time as a gas chromatographic (GC) stationary phase for
Davide Albani et al.
Nature communications, 9(1), 2634-2634 (2018-07-08)
Ensemble control has been intensively pursued for decades to identify sustainable alternatives to the Lindlar catalyst (PdPb/CaCO3) applied for the partial hydrogenation of alkynes in industrial organic synthesis. Although the geometric and electronic requirements are known, a literature survey illustrates

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service