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34-0015

Sigma-Aldrich

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
Beilstein:
3587194
MDL number:
UNSPSC Code:
12352307
PubChem Substance ID:

form

liquid

availability

available only in Japan

storage temp.

15-25°C

SMILES string

ClI

InChI

1S/ClI/c1-2

InChI key

QZRGKCOWNLSUDK-UHFFFAOYSA-N

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Related Categories

Suitability

for the iodine value determination

Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

WGK

WGK 2

Flash Point(F)

102.2 °F

Flash Point(C)

39 °C

Regulatory Information

新产品

Certificates of Analysis (COA)

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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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