Cookies disclaimer

I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.

A16158 Iodine monobromide, 98%

CAS Number
7789-33-5
Synonyms
Bromoiodine

Stock No. Size Price ($) Quantity Availability
A16158-14 25g 33.60
A16158-22 100g 92.10
A16158-30 250g 207.00
Add to Cart Bulk/Specialty Print Quote View Item

Iodine monobromide, 98%

MDL
MFCD00011353
EINECS
232-159-9

Chemical Properties

Formula
IBr
Formula Weight
206.81
Melting point
50° subl.
Boiling Point
116° dec.
Flash Point
None
Density
4.416
Storage & Sensitivity
Keep Cold. Moisture Sensitive. Light Sensitive. Store under Nitrogen.
Solubility
Soluble in water, alcohol, ether, carbon disulfide and glacial acetic acid.

Applications

Iodine monobromide is used as an electrophile employed in a new synthetic approach to polyketide structural units. It is also used in iodometry and serves as a source of I+. It is a powerful iodinating agent used in organic synthesis as well as involved in the synthesis of radioiodinated fatty acids for heart imaging.

Notes

Air, light and moisture sensitive. Store in cool place. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with alcohols, phosphorus, sodium and sodiumoxides and potassium.

Literature References

Selective brominating agent, considered to be intermediate in electrophilic power between bromine and iodine: J. Chem. Soc., 1509 (1939); J. Am. Chem. Soc., 60, 256 (1938); Chem. Commun., 849 (1968).

Also found to give higher diastereoselectivity than iodine in the cyclization of certain homoallylic carbonates: Tetrahedron Lett., 33, 6439 (1992).

Reagent for mild, selective deprotection of TBDMS ethers in carbohydrates and nucleosides: Synlett, 311 (1999).

Khalil, A.; Ishita, K.; Ali, T.; Tiwari, R.; Riachy, R.; Toppino, A.; Tjarks, W. Iodine Monochloride Facilitated Deglycosylation, Anomerization, and Isomerization of 3-Substituted Thymidine Analogues. Nucleosides Nucleotides Nucleic Acids 2014, 33 (12), 786-799.

Janas, D.; Herman, A. P.; Boncel, S.; Koziol, K. K. Iodine monochloride as a powerful enhancer of electrical conductivity of carbon nanotube wires. Carbon 2014, 73, 225-233.

GHS Hazard and Precautionary Statements

Hazard Statements: H314-H335

Causes severe skin burns and eye damage. May cause respiratory irritation.

Precautionary Statements: P260-P264b-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P501c

Do not breathe dust/fume/gas/mist/vapours/spray. Wash face, hands and any exposed skin thoroughly after handling Use only outdoors or in a well-ventilated area. Wear protective gloves/protective clothing/eye protection/face protection. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER or doctor/physician. Wash contaminated clothing before reuse. Dispose of contents/ container to an approved waste disposal plant

Other References

Merck
14,5016
Beilstein
3902973
Hazard Class
8
Packing Group
II
Harmonized Tariff Code
2812.90
TSCA
Yes

Recommended

Recently Viewed

Chemicals

Life Science

Metals & Materials

Catalysts

Analytical & Labware