1-octyne

from Wikipedia, the free encyclopedia
Structural formula
Structural formula of 1-octyne
General
Surname 1-octyne
other names
  • Oct-1-in
  • Hexylethine
Molecular formula C 8 H 14
Brief description

colorless liquid with a characteristic odor

External identifiers / databases
CAS number 629-05-0
EC number 211-069-3
ECHA InfoCard 100.010.064
PubChem 12370
Wikidata Q161668
properties
Molar mass 110.20 g mol −1
Physical state

liquid

density

0.7461 g cm −3 (20 ° C)

Melting point

−79.3 ° C

boiling point

126.3 ° C

Vapor pressure

18 hPa (25 ° C)

solubility

practically insoluble in water (0.024 g l −1 at 25 ° C)

Refractive index

1.4159 (20 ° C)

safety instructions
GHS labeling of hazardous substances
02 - Highly / extremely flammable 08 - Dangerous to health

danger

H and P phrases H: 225-304
P: 210-301 + 310-331
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C

1-Octyne is a chemical compound from the alkynes group . It has the basic structure of octane with a CC triple bond at the 1-position.

Extraction and presentation

1-Octyne can be obtained from 1-Octene in a two-step reaction . It is also possible to produce it by reacting lithium acetylide with 1-hexyl bromide .

properties

1-Octyne is a colorless liquid with a characteristic odor that is practically insoluble in water.

use

1-Octyne can be used to make alkylboranes .

safety instructions

The vapors of 1-octyne can form an explosive mixture with air ( flash point 16 ° C, ignition temperature 225 ° C).

Individual evidence

  1. a b c d e f g h Entry on 1-octyne in the GESTIS substance database of the IFA , accessed on October 14, 2012(JavaScript required) .
  2. a b c d David R. Lide (Ed.): CRC Handbook of Chemistry and Physics . 90th edition. (Internet version: 2010), CRC Press / Taylor and Francis, Boca Raton, FL, Physical Constants of Organic Compounds, pp. 3-406.
  3. L. Brandsma, HD Verkruijsse: Synthesis of acetylenes, allenes and cumulenes: methods and techniques . 2003, ISBN 978-0-12-125751-4 ( page 99 in the Google book search).

Web links