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About This Item
Linear Formula:
CH3C≡CCH3
CAS Number:
Molecular Weight:
54.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-962-2
Beilstein/REAXYS Number:
1361340
MDL number:
Assay:
99%
Form:
liquid
vapor pressure
11.47 psi ( 20 °C)
assay
99%
form
liquid
refractive index
n20/D 1.393 (lit.)
bp
27 °C (lit.)
mp
−32 °C (lit.)
density
0.691 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
CC#CC
InChI
1S/C4H6/c1-3-4-2/h1-2H3
InChI key
XNMQEEKYCVKGBD-UHFFFAOYSA-N
General description
The ion-molecule reaction of the aromatic distonic N-methyl-pyridinium-4-yl radical cation with 2-butyne has been investigated using ion trap mass spectrometry.
Application
2-Butyne has been used in preparation of THF-free metallacyclobutene complexes.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-13.0 °F - closed cup
flash_point_c
-25 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Regulatory Information
危险化学品
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Living polymerization of 2-butyne using a well-characterized tantalum catalyst.
Wallace KC, et al.
Organometallics, 8(3), 644-654 (1989)
C J Kees-Jan Weststrate et al.
Nature communications, 11(1), 750-750 (2020-02-08)
Facile C-C bond formation is essential to the formation of long hydrocarbon chains in Fischer-Tropsch synthesis. Various chain growth mechanisms have been proposed previously, but spectroscopic identification of surface intermediates involved in C-C bond formation is scarce. We here show
Oleg G Salnikov et al.
Chemical science, 8(3), 2426-2430 (2017-04-30)
Mechanistic insight into the semihydrogenation of 1-butyne and 2-butyne on Cu nanoparticles supported on partially dehydroxylated silica (Cu/SiO
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 254339-5G | 04061825998671 |
| 254339-25G | 04061833431726 |

