34-0015
Wijs (iodine monochloride) solution | Chloroiodide | 7790-99-0 solution
Synonym(s):
Iodine monochloride solution, Chloroiodide solution, Wijs solution
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About This Item
Linear Formula:
ICl
CAS Number:
Molecular Weight:
162.36
PubChem Substance ID:
UNSPSC Code:
12352307
Beilstein/REAXYS Number:
3587194
MDL number:
Grade:
SAJ special grade
Form:
liquid
SMILES string
ClI
InChI
1S/ClI/c1-2
InChI key
QZRGKCOWNLSUDK-UHFFFAOYSA-N
grade
SAJ special grade
form
liquid
availability
available only in Japan
storage temp.
15-25°C
Related Categories
Application
for the iodine value determination
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
102.2 °F
flash_point_c
39 °C
Regulatory Information
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L C Knight et al.
Thrombosis and haemostasis, 46(3), 593-596 (1981-10-01)
The properties of human fibrinogen labeled with 125-Iodine using Iodogen (1, 3, 4, 6-tetrachloro-3 alpha, 6 alpha-diphenylglycoluril) as an oxidizing agent were compared with those of an iodine monochloride labeled counterpart. It was found that thrombin clottability, binding to staphylococci
Iodine monochloride (IC1) iodination techniques.
M A Contreras et al.
Methods in enzymology, 92, 277-292 (1983-01-01)
C P Coyne et al.
American journal of veterinary research, 46(12), 2578-2581 (1985-12-01)
Two methods were analyzed for the rapid extraction of equine fibrinogen from fresh plasma, using ammonium sulfate-sodium phosphate buffer. Fibrinogen from each of these 2 methods was then radiolabeled with 125I (half-life = 60.2 days, gamma = 35 keV), using
Cell surface labeling by iodine monochloride.
E J Victoria et al.
The International journal of biochemistry, 13(9), 1011-1017 (1981-01-01)
Suman Lata et al.
Analytical biochemistry, 313(1), 155-159 (2003-02-11)
A single-step procedure was developed for the incorporation of iodoazide into oleic acid, triolein, and phosphatidylcholine. Iodoazide was generated using [125I]iodomonochloride and sodium azide that was found to add stereospecifically in a variety of olefins. Photoreactive and radiolabeled triacylglycerol and
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