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1,5-Diiodopentane

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1,5-Diiodopentane Basic information

Product Name:
1,5-Diiodopentane
Synonyms:
  • 1,5-diiodo-pentan
  • Pentane,1,5-diiodo-
  • PENTAMETHYLENE DIIODIDE
  • 1,5-Diiodepentane
  • 1 5-DIIODOPENTANE 99% (GC)
  • 1,5-Diiodopentane,97%
  • 1,5-DIIODOPENTANE
  • 1,5-DIIODOPENTANE1,5-DIIODOPENTANE1,5-DIIODOPENTANE1,5-DIIODOPENTANE
CAS:
628-77-3
MF:
C5H10I2
MW:
323.94
EINECS:
211-054-1
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Alkyl
  • Halogenated Hydrocarbons
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Iodine Compounds
  • Organic Building Blocks
Mol File:
628-77-3.mol
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1,5-Diiodopentane Chemical Properties

Melting point:
9°C
Boiling point:
101-102 °C/3 mmHg (lit.)
Density 
2.177 g/mL at 25 °C (lit.)
refractive index 
1.5992-1.6012
Flash point:
>110°C
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
clear liquid
color 
Light yellow to Yellow to Orange
Water Solubility 
insoluble
Sensitive 
Light Sensitive
BRN 
1697281
CAS DataBase Reference
628-77-3(CAS DataBase Reference)
NIST Chemistry Reference
Pentane, 1,5-diiodo-(628-77-3)
EPA Substance Registry System
Pentane, 1,5-diiodo- (628-77-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
RIDADR 
2810
WGK Germany 
3
RTECS 
SA0425000
TSCA 
Yes
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29033990
Toxicity
mmo-sat 10 mmol/plate MUREAV 141,11,84

MSDS

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1,5-Diiodopentane Usage And Synthesis

Chemical Properties

clear light yellow to orange liquid

Uses

1,5-Diiodopentane is used as a crosslinking reagent. It is used in the preparation of (iodoalkylaminocarbene)tungsten complexes. It is also used as alkylation to form unsubstituted cyclohexane. It is involved in the preparation of poly(1-vinyl imidazole-co-elthylene glycol methyl ether acrylate electrolytes and used for quasi-solid state dye-sensitized solar cells.

General Description

Electrochemical reduction of 1,5-diiodopentane at carbon electrodes in DMF containing tetramethylammonium perchlorate has been studied by cyclic voltammetry and controlled-potential electrolysis.

Safety Profile

Mutation data reported. When heated to decomposition it emits toxic vapors of Ií.

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