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1,6-HEPTADIYNE

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1,6-HEPTADIYNE Basic information

Product Name:
1,6-HEPTADIYNE
Synonyms:
  • 1,6-HEPTADIYNE, 97%1,6-HEPTADIYNE, 97%1,6-HEPTADIYNE, 97%1,6-HEPTADIYNE, 97%
  • 1,6-HEPTADIYNE 98%
  • 1,6-Heptadiyne, 97+%
  • 1,6-Heptadiyne (6CI, 8CI, 9CI)
  • Heptane-1,6-diyne
  • 1,6-Heptadiyne,98%
  • 1,6-HEPTADIYNE
  • 1,6-Heptadiyne>
CAS:
2396-63-6
MF:
C7H8
MW:
92.14
EINECS:
219-253-5
Product Categories:
  • Industrial/Fine Chemicals
  • Acetylenes
  • Acetylenic Hydrocarbons
  • Alkynes
  • Organic Building Blocks
  • Terminal
Mol File:
2396-63-6.mol
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1,6-HEPTADIYNE Chemical Properties

Melting point:
-85 °C
Boiling point:
111.5 °C (lit.)
Density 
0.805 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.441(lit.)
Flash point:
49 °F
storage temp. 
2-8°C
form 
Liquid
Specific Gravity
0.805
color 
Clear yellow
Water Solubility 
Insoluble in water.
BRN 
1731756
CAS DataBase Reference
2396-63-6(CAS DataBase Reference)
EPA Substance Registry System
1,6-Heptadiyne (2396-63-6)
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Safety Information

Hazard Codes 
F
Risk Statements 
11
Safety Statements 
16-29-33
RIDADR 
UN 3295 3/PG 2
WGK Germany 
2
RTECS 
MI5600000
TSCA 
Yes
HazardClass 
3
PackingGroup 
II
HS Code 
29012990
Toxicity
dog,LD50,oral,3830mg/kg (3830mg/kg),GASTROINTESTINAL: NAUSEA OR VOMITINGLIVER: "HEPATITIS, FIBROUS (CIRRHOSIS, POST-NECROTIC SCARRING)"BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY),Federation Proceedings, Federation of American Societies for Experimental Biology. Vol. 19, Pg. 389, 1960.

MSDS

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1,6-HEPTADIYNE Usage And Synthesis

Chemical Properties

clear yellow liquid

Uses

1,6-Heptadiyne may be used in the preparation of free-standing polymer films of poly(1,6-heptadiyne). Polymerization of 1,6-heptadiyne using an insoluble Zeigler-Natta catalyst affords soluble polymer having six-membered ring containing polyene. Ruthenium(II)-catalyzed reaction of a substituted 1,6-heptadiyne with norbornene affords a tandem [2+ 2+ 2]/[4+2] cycloaddition product and a [2+ 2+2] cycloadduct.

General Description

Polymerization of 1,6-heptadiyne using an insoluble Zeigler-Natta catalyst affords soluble polymer having six-membered ring containing polyene. Ruthenium(II)-catalyzed reaction of a substituted 1,6-heptadiyne with norbornene affords a tandem [2+ 2+ 2]/[4+2] cycloaddition product and a [2+ 2+2] cycloadduct. Cyclocopolymerization of 1,6-heptadiyne with dipropargyl ether under nitrogen atmosphere using KSCN, KBr and KI as initiators in N,N-dimethyl formamide has been studied.

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