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4,4'-OXYBIS(PHENYL ISOCYANATE)

Basic information Safety Supplier Related

4,4'-OXYBIS(PHENYL ISOCYANATE) Basic information

Product Name:
4,4'-OXYBIS(PHENYL ISOCYANATE)
Synonyms:
  • OXYBIS(4-PHENYL ISOCYANATE)
  • 1,1’-oxybis[4-isocyanato-benzen
  • 4,4'-OXYBIS(PHENYL ISOCYANATE)
  • 4,4'-Diisocyanato[1,1'-oxybisbenzene]
  • 4,4'-Oxybis(isocyanatobenzene)
  • Oxybis(1,4-phenylene)bisisocyanate
  • Oxybis(1,4-phenylene)diisocyanate
  • Oxybis(4-phenyl isocyanate),99%
CAS:
4128-73-8
MF:
C14H8N2O3
MW:
252.22
Product Categories:
  • Isocyanates
  • Nitrogen Compounds
  • Organic Building Blocks
Mol File:
4128-73-8.mol
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4,4'-OXYBIS(PHENYL ISOCYANATE) Chemical Properties

Melting point:
64-68 °C(lit.)
Boiling point:
196 °C5 mm Hg(lit.)
Density 
1.2700 (rough estimate)
refractive index 
1.5910 (estimate)
solubility 
Acetonitrile (Soluble)
form 
Solid
color 
White to Off-White
Stability:
Moisture Sensitive
CAS DataBase Reference
4128-73-8
EPA Substance Registry System
4,4'-Diisocyanatodiphenyl ether (4128-73-8)
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Safety Information

Hazard Codes 
Xn,T+
Risk Statements 
20/21/22-36/37/38-42/43-26-25-21
Safety Statements 
23-26-36/37/39-45-36/37-28-22
RIDADR 
UN 2206 6.1/PG 3
WGK Germany 
3

MSDS

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4,4'-OXYBIS(PHENYL ISOCYANATE) Usage And Synthesis

Chemical Properties

WHITE CRYSTALLINE SOLID

Uses

4,4'-Bis(isocyanatophenyl)oxide is a reagent used in the synthesis of lipid-conjugated Smac analogs with antitumor activity against human breast cancer cell lines.Environmental toxin on US EPA Toxic Release Inventory list (TRI) list.

Reactivity Profile

Isocyanates and thioisocyanates are incompatible with many classes of compounds, reacting exothermically to release toxic gases. Reactions with amines, aldehydes, alcohols, alkali metals, ketones, mercaptans, strong oxidizers, hydrides, phenols, and peroxides can cause vigorous releases of heat. Acids and bases initiate polymerization reactions in these materials. Some isocyanates react with water to form amines and liberate carbon dioxide. Polyurethanes are formed by the condensation reaction of diisocyanates with, for example, ethyl glycol.

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