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2-Iodopropane

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2-Iodopropane Basic information

Product Name:
2-Iodopropane
Synonyms:
  • 2-iodo-propan
  • 2-Jodpropan
  • 2-IODOPROPANE
  • 2-Iodopropane 98+ %
  • 2-Iodopropane,stab. with copper
  • 2-IODOPROPANE, STAB. WITH SILVER WOOL
  • 2-IODOPROPANE (ISOPROPYL IODIDE )
  • 2-Iodopropane, stabilized, 98+%
CAS:
75-30-9
MF:
C3H7I
MW:
169.99
EINECS:
200-859-3
Product Categories:
  • Pyridines ,Halogenated Heterocycles
  • Organics
  • Iodine Compounds
Mol File:
75-30-9.mol
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2-Iodopropane Chemical Properties

Melting point:
-90 °C
Boiling point:
90 °C
Density 
1.703 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.498(lit.)
Flash point:
108 °F
storage temp. 
Store below +30°C.
solubility 
1.4g/l
form 
Liquid
color 
Clear colorless to light yellow
Water Solubility 
Soluble in water(1.4g/L).
Sensitive 
Light Sensitive
Merck 
14,5214
BRN 
1098244
Exposure limits
ACGIH: TWA 0.2 mg/m3; TWA 1 mg/m3
OSHA: TWA 0.1 mg/m3; TWA 1 mg/m3
NIOSH: IDLH 100 mg/m3; TWA 1 mg/m3; TWA 0.1 mg/m3
Dielectric constant
8.1899999999999995
Stability:
Stable, but may discolour on exposure to light. Air sensitive. Incompatible with strong bases, strong oxidizing agents.
InChIKey
FMKOJHQHASLBPH-UHFFFAOYSA-N
LogP
2.890
CAS DataBase Reference
75-30-9(CAS DataBase Reference)
NIST Chemistry Reference
Propane, 2-iodo-(75-30-9)
EPA Substance Registry System
Propane, 2-iodo- (75-30-9)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
10-22-36/37/38
Safety Statements 
36/37-37/39-26-16
RIDADR 
UN 2392 3/PG 3
WGK Germany 
3
RTECS 
TZ4200000
8
TSCA 
Yes
HazardClass 
3
PackingGroup 
III
HS Code 
29033990

MSDS

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2-Iodopropane Usage And Synthesis

Chemical Properties

Colorless liquid that discolors in air and light; miscible with chloroform, ether, alcohol and benzene; slightly soluble in water.

Uses

2-Iodopropane is used to prepare butyric and isobutyric acid, as a solvent, also used in medicine and organic synthesis.

Uses

Organic synthesis, pharmaceuticals. 2-Iodopropane (Isopropyl iodide) was used to prepare butyric and isobutyric acid.

Purification Methods

Treat the iodide with bromine, followed by extraction of free halogen with aqueous Na2S2O3 or NaHSO3, washing with water, drying (MgSO4 or CaCl2) and distilling. (The treatment with bromine is optional.) Other purification methods include passage through activated alumina, or shaking with copper powder or mercury to remove iodine, drying with P2O5 and distilling. Washing with conc H2SO4 or conc HCl (to remove any alcohol), water, aqueous Na2SO3, water and aqueous Na2CO3 has also been used. Treatment with silica gel causes some liberation of iodine. Distillations should be carried out at slightly reduced pressure. Purified isopropyl iodide is stored in the dark in the presence of a little mercury. [Beilstein 1 IV 223.]

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