Iodine chloride(Iodine monochloride),Also known as iodine monochloride.The molecular formula isICl,The molecular weight is162.30. Reddish brown liquid or black crystal,There are two variants of crystallization.Non hygroscopic,However, it can form iodine pentoxide when exposed to air.Insoluble in water\Soluble in ethanol\Ether\Carbon disulfide and acetic acid.It can be used for iodine value determination,Organic synthesis,And can be used as a strongOxidizing agent.
Names and Identifiers
Iodine monochloride
Iodine monochloride solution
Iodomonochloride
Iodine monochloride, 1M solution in dichloromethane
Iodine Monochloride, 1M solution in dichloroMethane, AcroSeal
Chlorineiodide
Chlorine iodide (ClI)
Chlorine monoiodide
Iodine chloride
Iodine(I) chloride
Iodochlorine
Iodoniumchloride
Wijs' chloride
Iodinemonochloride
EINECS 232-236-7
iodine monochioride
EC 232-236-7
iodonium chloride
Iodine monochloride solution (Wijs' chloride)
Protochlorure D'iode
QZRGKCOWNLSUDK-UHFFFAOYSA-N
NS00082340
iodomonochloride
Chloroiodide
MFCD00011354
Iodine monochloride [UN1792] [Corrosive]
FT-0627251
Iodo monochloride
AMY39425
Iodine monochloride, ACS reagent, 1.10+/-0.1 I/Cl ratio basis
UNII-0SMG5NLU45
iodochloride
0SMG5NLU45
iodine(I) chloride
HSDB 601
Iodine monochloride, 99.998% trace metals basis
IODINE MONOCHLORIDE [MI]
Iodine monochloride, reagent grade, >=95%
Protochlorure d'iode [French]
L-methioninetert.butylesterhydrochloride
Q414607
ICL
AKOS015853771
Iodine monochloride, approx. 0.22N soln. in glacial acetic acid
2.
195. Electrolytic dissociation processes. Part I. The dipole moment of iodine monochloride in solution
Fred Fairbrother
J. Chem. Soc. 1936 847
3.
The absorption spectra of solutions of iodide bromide, cyanogen iodine, and cyanogen bromide
A. E. Gillam
Trans. Faraday Soc. 1933 29 1132
4.
203. The electrical conductivity of iodine monochloride and iodine trichloride
N. N. Greenwood,H. J. Emeléus
J. Chem. Soc. 1950 987
5.
The kinetics of ionic polymerisations. Part IV. The action of iodine chloride and iodine bromide on n-butyl vinyl ether
D. D. Eley,J. Saunders
J. Chem. Soc. 1954 1668
6.
318. The kinetics of chlorine, iodine chloride, and bromine chloride addition to olefinic compounds
E. P. White,P. W. Robertson
J. Chem. Soc. 1939 1509