SDSDownload

1-Hexyne / 100 ML

Purity: 97 %
Synonym: Butylacetylene
Molecular Formula: CH3(CH2)3C‰¡CH
Molecular Weight: 82.14
SKU: MND-51118
CAS Number: 693-02-7
MDL number: MFCD00009504
EC Number: 211-736-9
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 100 ML  
105.70 EUR



Safety Information


Hazard Statements

H225
H304
H315
H319
H335

Precautionary Statements

P210
P280
P301 + P310
P303 + P361 + P353
P264
P501
P305 + P351 + P338
P331
P261
P271
P233
P240
P241
P242
P405
P302 + P352
P403 + P235
P362 + P364
P243
P403 + P233
P370 + P378
P304 + P340
P321
P264 + P265
P319
P332 + P317
P337 + P317
P301 + P316

Pictograms



Properties

Signal WordDanger
Flash Point (C)-20 °C - closed cup
Flash Point (F)-4.0 °F - closed cup
Vapor Pressure253 mmHg ( 37.7 °C)
Density0.715 g/mL at 25 °C (lit.)
Boiling Point71-72 °C (lit.)
Melting Point−132 °C (lit.)

 Product Description

1-Hexyne is an alkyne hydrocarbon with a triple bond between the first and second carbon atoms in its six-carbon chain. It is commonly used as a building block in organic synthesis.

 

Application:

1-Hexyne is utilized in organic synthesis for the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its reactive alkyne group.

 

 

Articles:

- Transhydrogenation of pentane and 1-hexyne over CrOx/Al2O3 and potassium-doped CrOx/Al2O3 catalysts

Publication Date: 19 June 2019

Mustapha D. Garba & S. David Jackson

https://doi.org/10.1007/s13203-019-0231-3

 

- Evidence of metallocycle formation by decomposition of 1-hexyne on Ru(0001): a RAIRS study

Publication Date: Available online 6 January 2002

Ana R Garcia, Ricardo Brito de Barros, Laura M Ilharco

https://doi.org/10.1016/S0039-6028(01)01929-X

 

- Mesostructured silicas as supports for palladium-catalyzed hydrogenation of phenyl acetylene and 1-phenyl-1-hexyne to alkenes

Publication Date: Available online 28 December 2005

Norman Marín-Astorga, Gina Pecchi, Thomas J. Pinnavaia, Gabriela Alvez-Manoli, Patricio Reyes

https://doi.org/10.1016/j.molcata.2005.11.031