Skip to Content
Merck
CN

481556

Iodine monochloride

99.998% trace metals basis

Synonym(s):

Chloroiodide

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
ICl
CAS Number:
Molecular Weight:
162.36
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
EC Number:
232-236-7
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Iodine monochloride, 99.998% trace metals basis

InChI key

QZRGKCOWNLSUDK-UHFFFAOYSA-N

InChI

1S/ClI/c1-2

SMILES string

ClI

assay

99.998% trace metals basis

impurities

<25 ppm total metallic impurities

bp

97.4 °C (lit.)

density

3.24 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

Looking for similar products? Visit Product Comparison Guide

Features and Benefits

Meets A.C.S. reagent specifications.

pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Polymethylbenzene complexes of iodine and iodine monochloride.
Andrews LJ and Keefer RM.
Journal of the American Chemical Society, 74(18), 4500-4503 (1952)
Ultrasonic-assisted synthesis of flavones by oxidative cyclization of 2'-hydroxychalcones using iodine monochloride.
Lahyani A and Trabelsi M.
Ultrasonics Sonochemistry, 31, 626-630 (2016)
Ahmed Khalil et al.
Nucleosides, nucleotides & nucleic acids, 33(12), 786-799 (2014-11-06)
The reaction of thymidine, 3-mono-, and 3,3',5'-trialkylsubstitued thymidine analogues with iodine monochloride (ICl) was investigated. Treatment with ICl resulted in rapid deglycosylation, anomerization, and isomerization of thymidine and 3-substituted thymidine analogues under various reaction conditions leading to the formation of
Cation radicals as intermediates in aromatic halogenation with iodine monochloride: solvent and salt effects on the competition between chlorination and iodination.
Hubig SM, et al.
The Journal of Organic Chemistry, 59(21), 6233-6244 (1994)
F Ibrahim et al.
Journal of pharmaceutical and biomedical analysis, 9(2), 101-107 (1991-01-01)
Two simple and sensitive spectrophotometric methods are described for the assay of three MAO inhibitors: isocarboxazid, tranylcypromine sulphate and iproniazid phosphate. The first method is based on the formation of a highly coloured stable radical anion between the drug as

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service