4,4'-DIIODOBIPHENYL

PRODUCT IDENTIFICATION

CAS NO. 3001-15-8

4,4'-DIIODBIPHENYL

EINECS NO. 221-080-5
FORMULA C12H8I2
MOL WT. 406.00

H.S. CODE

 

TOXICITY

 
SYNONYMS 4,4'-Diiodobifenil (Spanish); 4,4'-Diiodobiphényl (French);
SMILES

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE yellow crystals
MELTING POINT 201 - 204 C
BOILING POINT  
SPECIFIC GRAVITY  
SOLUBILITY IN WATER  
pH  
VAPOR DENSITY

 

AUTOIGNITION

 

NFPA RATINGS  

REFRACTIVE INDEX

 
FLASH POINT

 

STABILITY

Stable under ordinary conditions

APPLICATIONS

Iodine is a nonmetallic halogen element in Group 17 of periodic table; atomic number 53; atomic mass 126.9; melting point ca 114 C; boiling point ca 184 C; specific gravity 4.93 g/cm3; Oxidation states: 7,5,1,-1; [Kr] 4d10 5s2 5p5. Iodine is a nearly black poisonous, corrosive solid at room temperature and readily sublimes to a deep violet vapour, the colour of which is responsible for its name from Greek. It is insoluble in water, soluble in common solvents. Iodine is required in small amounts in human body for the function of the thyroid gland. Iodine forms many important compounds of iodine such as iodine(V)oxide, potassium iodide, iodine trichloride and iodoform of an Iodine containing organic compound. Iodine is used as a component in germicides and disinfectants with surfactants to carry iodine. Potassium iodide is used as a heat stabilizer and a catalyst in synthetic fiber manufacturing. Organic iodides and Iodine metal salts are used in formulating antiseptics and x-ray contrast media compounds in pharmaceuticals. Potassium iodate and other forms like calcium iodate and ethylene diamine dihydroiodide are used in animal feeds to prevent deficiency of iodine. Iodine and its organic compounds are useful in dye industry for   the high bright colors as well as pharmaceutical industry. An example of organic Iodine, iodoform has weak bactericidal qualities and is used to treat minor skin diseases.

SALES SPECIFICATION

APPEARANCE

yellow crystals

PURITY

99.0% min

WATER

0.15% max

TRANSPORTATION
PACKING
25kgs in drum
HAZARD CLASS  
UN NO.  
OTHER INFORMATION
Hazard Symbols: XN, Risk Phrases: 20/21/22, Safety Phrases: 36

GENERAL DESCRIPTION OF BIPHENYL

Biphenyl (also called Diphenyl, but exactly one of two compounds. The other is o-phenylphenol, used to prevent the growth of moulds ) is an aromatic hydrocarbon; molecule structure is composed of two six-sided carbon rings connected at one carbon site on each ring. Pure biphenyl is a toxic colourless crystalline solid with a pleasant odour; melting point 70 C, boiling point 255 C, which gives plates or monoclinic prismatic crystals; it is insoluble in water but soluble in ordinary organic solvents. It is directly used in the preservation of citrus fruits  as a fungistat in transportation containers. It is a raw material for polychlorinated diphenyls (PCB) in which chlorine replaces hydrogen in biphenyls. There are 209 chlorinated isomers of biphenyl theoretically. But PCBs are referred to the biphenyl compounds with one to ten chlorine substitutions. PCBs are used heat-transfer agents and as electric insulators that block the flow of electric current across in electrical equipments. They are known as environmental pollution materials which are accumulated in animal tissues and cause toxic effects including carcinogenesis. Biphenyl is used as an intermediate for the production of a wide range of organic compounds (e.g. emulsifiers, optical brighteners, crop protection products, plastics), as a heat transfer medium alone or with diphenyl ether in heating fluids, as a dyestuff carrier for textiles and copying paper and as a solvent in pharmaceutical production. Aminodiphenyls are used as rubber antioxidants and intermediates for the synthesis of organic compounds ( azo dyes and pharmaceuticals). Biphenyl derivatives are used as an intermediate for the synthesis of organic compounds including pharmaceuticals, antifungal agents, optical brightening agents and dyes. Biphenyl compounds also used in luminescence chemistry, spectrophotometric analysis, molecular chemistry, and as a stating material for organometallic-complexes.