1-Iodopropane

1-Iodopropane Basic information
Product Name:1-Iodopropane
Synonyms:1-iodo-propan;n-C3H7I;n-Propyliodid;Propane,1-iodo-;Propyljodid;N-PROPYL IODIDE;PROPYL IODIDE;1-IODOPROPANE1-IODOPROPANE1-IODOPROPANE1-IODOPROPANE
CAS:107-08-4
MF:C3H7I
MW:169.99
EINECS:203-460-2
Product Categories:Iodine Compounds;Organics;Pharmaceutical Intermediates
Mol File:107-08-4.mol
1-Iodopropane Structure
1-Iodopropane Chemical Properties
Melting point -101 °C
Boiling point 101-102 °C(lit.)
density 1.743 g/mL at 25 °C(lit.)
vapor pressure 43 mm Hg ( 25 °C)
refractive index n20/D 1.504(lit.)
Fp 112 °F
storage temp. Store below +30°C.
solubility 1.1g/l
form Liquid
color Clear colorless to yellow
Water Solubility Fully miscible in water.
Sensitive Light Sensitive
Merck 14,7862
BRN 505937
Henry's Law Constant(x 10-3 atm?m3/mol): 9.09 at 25 °C (Hine and Mookerjee, 1975)
Stability:Stable, but may discolour on exposure to light. Incompatible with strong oxidizing agents, strong bases. Flammable.
CAS DataBase Reference107-08-4(CAS DataBase Reference)
NIST Chemistry ReferencePropane, 1-iodo-(107-08-4)
EPA Substance Registry SystemPropane, 1-iodo- (107-08-4)
Safety Information
Hazard Codes Xn,Xi,N
Risk Statements 10-20-36/37/38-52/53-2017/10/20
Safety Statements 16-26-36/37-61
RIDADR UN 2392 3/PG 3
WGK Germany 3
RTECS TZ4100000
8
Hazard Note Irritant
TSCA Yes
HazardClass 3
PackingGroup III
HS Code 29033080
ToxicityLD50 (inhalation) for rats 73,000 mg/m3/30-min (quoted, RTECS, 1985).
MSDS Information
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1-Iodopropane Usage And Synthesis
Chemical Propertiescolourless liquid
Physical propertiesClear, colorless liquid with a characteristic sharp, penetrating odor. On exposure to light, 1- iodopropane may become pale yellow.
Uses1-Iodopropane is used in wide range of medicals industrial applications as well as in human and animal nutrition products, pharmaceutical intermediates, polarizing films for Liquid Crystal Display (LCD) chemicals. Iodine derivatives are also used as organic building blocks, analytical reagents etc. It is also used as a solvent and intermediate of organic synthesis.
Synthesis Reference(s)Tetrahedron Letters, 8, p. 4131, 1967 DOI: 10.1016/S0040-4039(01)89706-9
Environmental fateBiological. A strain of Acinetobacter sp. isolated from activated sludge degraded 1-iodopropane to 1-propanol and iodide ions (Janssen et al., 1987).
Chemical/Physical. Slowly hydrolyzes in water forming 1-propanol and hydroiodic acid.
Purification MethodsIt should be distilled first under reduced pressure to avoid decomposition. Dry the iodide with MgSO4 or silica gel and fractionally distil it. Store it under nitrogen with mercury in a brown bottle. Prior to distillation, free iodine can be removed by shaking with copper powder or by washing with aqueous Na2S2O3 and drying. Alternatively, the n-propyl iodide can be treated with bromine, then washed with aqueous Na2S2O3, dried and distilled. See also n-butyl iodide. [Beilstein 1 IV 222.]
1-Iodododecane 1,3-Propane sultone Propane 2-Methyl-1-iodopropane 1-IODODECANE 1-IODOHEXADECANE Trimethylolpropane 1,1,1,2,3,3,3-Heptafluoropropane 1-Iodobutane Iodopropane 1,10-DIIODODECANE 1-Bromopropane 2-Iodobutane Epichlorohydrin 1-IODOUNDECANE 1-Iodopropane N,N-Dimethylacetamide Propylene oxide

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