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1,3-PHENYLENE DIISOCYANATE

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1,3-PHENYLENE DIISOCYANATE Basic information

Product Name:
1,3-PHENYLENE DIISOCYANATE
Synonyms:
  • isocyanicacid,m-phenyleneester
  • m-Phenylene isocyanate
  • m-phenyleneisocyanate
  • Nacconate 400
  • nacconate400
  • Isocyanic acid, m-phenylene ester
  • M-PHENYLENE DIISOCYANATE
  • BENZENE 1,3-DIISOCYANATE
CAS:
123-61-5
MF:
C8H4N2O2
MW:
160.13
EINECS:
204-637-7
Product Categories:
  • Isocyanate Monomers
  • Monomers
  • Polymer Science
Mol File:
123-61-5.mol
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1,3-PHENYLENE DIISOCYANATE Chemical Properties

Melting point:
49-51 °C(lit.)
Boiling point:
121 °C25 mm Hg(lit.)
Density 
1.3848 (rough estimate)
refractive index 
1.4900 (estimate)
Flash point:
>230 °F
storage temp. 
2-8°C
form 
powder to lump
color 
Crystals
Water Solubility 
Soluble in hot benzene. Hydrolyzes in water.
Sensitive 
Moisture Sensitive
BRN 
776957
CAS DataBase Reference
123-61-5(CAS DataBase Reference)
EPA Substance Registry System
1,3-Phenylene diisocyanate (123-61-5)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38-42
Safety Statements 
22-26-36/37
RIDADR 
UN 2810 6.1/PG 3
WGK Germany 
3
RTECS 
NR0150000
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29291000
Toxicity
LD50 ivn-mus: 5600 mg/kg CSLNX* NX#07804

MSDS

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1,3-PHENYLENE DIISOCYANATE Usage And Synthesis

Chemical Properties

White to off-white fused solid

Uses

1,??3-??Phenylene Diisocyanate is a reagent used in the synthesis of polyurethane materials and other thermoplastics.Environmental toxin on US EPA Toxic Release Inventory list (TRI) list.

Reactivity Profile

Isocyanates and thioisocyanates, such as 1,3-PHENYLENE DIISOCYANATE, 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. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence, [Wischmeyer(1969)].

Safety Profile

A sensitizer at very low concentrations. Deadly poison by intravenous route. When heated to decomposition it emits toxic fumes of NOx and CN-. See also ESTERS.

1,3-PHENYLENE DIISOCYANATESupplier

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