| | Hexamethylene Diisocyanate Basic information |
| | Hexamethylene Diisocyanate Chemical Properties |
| Melting point | -55°C | | Boiling point | 82-85 °C/0.1 mmHg | | density | 1.047 g/mL at 20 °C (lit.)
1.047 g/mL at 20 °C | | vapor pressure | 0.05 mm Hg ( 25 °C) | | refractive index | n20/D 1.453 | | Fp | 248 °F | | storage temp. | Store below +30°C. | | form | Liquid | | color | Clear colorless to slightly yellow | | Specific Gravity | 1.05 | | explosive limit | 0.9-9.5%(V) | | Water Solubility | Reacts | | Sensitive | Moisture Sensitive | | BRN | 956709 | | Exposure limits | TLV-TWA 0.0343 mg/m3 (0.005 ppm)
(ACGIH). | | Stability: | Stable. Moisture sensitive. Combustible. Incompatible with strong oxidizing agents, strong bases, amines, acids. May react explosively with alcohols in the presence of base without a diluting solvent. Heating above 200 C may cause polymerization. | | InChIKey | RRAMGCGOFNQTLD-UHFFFAOYSA-N | | LogP | 3.2 at 20℃ | | CAS DataBase Reference | 822-06-0(CAS DataBase Reference) | | NIST Chemistry Reference | 1,6-Hexamethylene diisocyanate(822-06-0) | | EPA Substance Registry System | Hexamethylene-1,6-diisocyanate (822-06-0) |
| | Hexamethylene Diisocyanate Usage And Synthesis |
| Description | This diisocyanate compound is used in the manufacture
of various polyurethane products: elastic and rigid
foams, paints, lacquers, adhesives, bin ding agents,
synthetic rubbers, and elastomeric fibers.
| | Chemical Properties | Hexamethylene diisocyanate is a colorless
liquid. Sharp, irritating odor. | | Chemical Properties | Hexamethylene diisocyanate is a liquid with a volatility of the same order as
that of tolylene diisocyanate. It is respiratory irritant and also has powerful
effects on the skin and eyes. | | Uses | 1,6-Hexamethylenediisocyanate is a chemical intermediate used in the production of urethane products. | | Uses | Cross-linking agent (hardener) in the
production of polyurethane materials such as
car paints, dental materials, and contact lenses | | Uses | Hexamethylene diisocyanate (HDI) is one of the most common aliphatic disocyanates, It is a monomer used in the production of polyurethane foams and exceptionally high-quality coatings, and is found in some industrial paints and spray painting operations. It is a compound which reacts readily with water and alcohols (Von Burg 1993). It has a vapor pressure of 0.05 mm Hg at room temperature, but can be present in aerosol form allowing a potentially higher exposure to individuals. The HDI-BT trimer is often present for similar industrial uses. It would be expected to have a lower vapor pressure; however, the aerosol form can also be present, allowing potentially higher exposure of HDI-BT to individuals. Hexamethylene diisocyanate reacts slowly with water to form carbon dioxide (HSDB 1996). The base-catalyzed reaction of Hexamethylene diisocyanate with alcohols should be carried out in inert solvents; the reaction may occur with explosive violence in the absence of solvents (NFPA 1994). | | Definition | ChEBI: A diisocyanate compound with the two isocyanates linked by a hexane-1,6-diyl group. | | Preparation | Hexamethylene diisocyanate (HDI) is prepared by the phosgenation of hexamethylenediamine (section lO.2.2(b)):
H2N-(CH2)6-NH2--COCl2-->OCN-(CH2)6-NCO
Hexamethylene diisocyanate is a liquid with a volatility of the same order as that of tolylene diisocyanate. It is respiratory irritant and also has powerful effects on the skin and eyes. Hexamethylene diisocyanate was one of the first diisocyanates utilized for making polyurethanes, being used to prepare fibres and moulding compounds. These applications are no longer of importance but hexamethylene diisocyanate now finds use mainly in coatings which are more light stable than those based on aromatic isocyanates. | | Application | Hexamethylene diisocyanate is an aliphatic diisocyanate monomer typically used to produce oligomers and prepolymers that when combined with a polyol produce light-stable polyurethane.
Highly reactive 1,6-hexamethylene diisocyanate (HMDI) was used to synthesize lactic acid polymers from oligomers by the addition of 2,2′-bis(2-oxazoline) (BOX) as chain extenders. Self-healing ability was rendered to polyurethane elastomer by synthesizing alkoxyamine-based diol and reacting it with tri-functional homopolymer of HMDI and polyethylene glycol (PEG). Plastic optical fiber (POF) was prepared by the bulk homopolymerization of HMDI catalyzed by Tin(II)-2 ethylhexanoate (SnOct). | | General Description | A colorless crystalline solid. Toxic by ingestion and is strongly irritating to skin and eyes. 1,6-Diisocyanatohexane is used to make nylon. | | Air & Water Reactions | Contact with moisture or temperatures over 399°F may cause polymerization. Soluble in water. | | Reactivity Profile | 1,6-Diisocyanatohexane reacts with water. Base-catalyzed reactions of 1,6-Diisocyanatohexane with alcohols may be explosively violent in the absence of diluting solvents. 1,6-Diisocyanatohexane is incompatible with strong bases, amines, acids and strong oxidizers. 1,6-Diisocyanatohexane is also incompatible with metal compounds and surface active materials. . | | Hazard | Combustible. | | Health Hazard | HDI is moderately toxic by inhalation. Inhumans the acute toxic symptoms could bewheezing, dyspnea, sweating, coughing, dif-ficulty in breathing, and insomnia. In addition, this compound can produce irritationof the skin, eyes, nose, and respiratory tract.Chronic exposure may cause obstruction ofairways and asthma.
The lethal concentration for rats frominhalation of this compound for 4 hourswas 60 mg/m3. The oral toxicity of thiscompound was found to be low in testanimals. The toxicity order was much higherwhen given intravenously.
LD50 value, oral (mice): 350 mg/kg
LD50 value, intravenous (mice): 5.6 mg/kg
There is no report of any carcinogenic orteratogenic study for this compound.
| | Fire Hazard | Combustible material: may burn but does not ignite readily. Substance will react with water (some violently) releasing flammable, toxic or corrosive gases and runoff. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapors may travel to source of ignition and flash back. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated or if contaminated with water. | | Flammability and Explosibility | Notclassified | | Contact allergens | This diisocyanate compound is used in the manufac ture of various polyurethane products: elastic and
rigid foams, paints, lacquers, adhesives, binding
agents, synthetics rubbers, and elastomer fibers. | | Safety Profile | Poison by inhalation
and intravenous routes. Moderately toxic by
ingestion and skin contact. Potentially
explosive reaction with alcohols + base.
When heated to decomposition it emits
toxic fumes of NOx. See also CYANATES. | | Potential Exposure | Used to make other chemicals, coat ings, and polyurethane. It is also used as a hardener in
automobile and airplane paints. | | Environmental Fate | HDI is not readily soluble (low mg l-1 range) in water.
However, upon contact with water, reactivity is rapid with
a half-life of 0.23 h at 23 ℃. This nonhomogeneous reaction is
expected to produce principally polyureas. In the occupational
environment, an aerosol can be formed by nebulization;
however, with a vapor pressure of 0.007 hPa, HDI is expected
to exist in the ambient atmosphere in its vapor state. As a vapor,
HDI is expected to degrade in the atmosphere by reaction with
hydroxyl radicals (half-life approximately 2 days). In direct
contact with water, its rapid hydrolysis reduces the likelihood
for HDI to bioaccumulate in the aquatic compartment or
transfer to groundwater. Therefore, the rapid hydrolysis in an
aquatic environment and relatively rapid degradation in
atmosphere limits the ability of this substance to be bioaccumulative
or persistent. | | Shipping | UN2281 Hexamethylene diisocyanate, Hazard
Class: 6.1; Labels: 6.1-Poisonous materials. | | Toxicity evaluation | Toxicity predominantly results from direct interaction of HDI
with tissues or macromolecules at the portal of entry. HDI
reacts with biologic macromolecules containing nucleophilic
–NH, –SH, –OH, or –COOH groups, and these interactions
are thought to account for acute irritation to skin and mucus
membranes, sensory irritation, and dermal sensitization. Less
clear is the etiology of HDI-induced occupational asthma. A
number of mechanisms, including immunologic, neurologic,
and pharmacologic, have been postulated without a clear
resolution. Overall, these mechanisms account for the principal
effects associated with HDI that lead to toxicity at the
portal of entry with no evidence of primary systemic organ
toxicity. | | Incompatibilities | May form explosive mixture with air.
Isocyanates are highly flammable and reactive with many
compounds, even with themselves. Incompatible with oxi dizers (chlorates, nitrates, peroxides, permanganates, per chlorates, chlorine, bromine, fluorine, etc.); contact may
cause fires or explosions. Reaction with moist air, water or
alcohols may form amines and insoluble polyureas and
react exothermically, releasing toxic, corrosive or flamma ble gases, including carbon dioxide; and, at the same time,
may generate a violent release of heat increasing the con centration of fumes in the air. Incompatible with amines,
aldehydes, alkali metals, ammonia, carboxylic acids, capro lactum, alkaline materials, glycols, ketones, mercaptans,
hydrides, organotin catalysts, phenols, strong acids, strong
bases, strong reducing agents such as hydrides, urethanes,
ureas. Elevated temperatures or contact with acids, bases,
tertiary amines, and acyl-chlorides may cause explosive
polymerization. Attacks some plastics, rubber and coatings.
Contact with metals may evolve flammable hydrogen gas.
May accumulate static electrical charges, and may cause
ignition of its vapors. Temperatures above 200℃ can cause
polymerization. Attacks copper. | | Waste Disposal | Disposal is by chemical incineration of HDIsolution in a combustible solvent. |
| | Hexamethylene Diisocyanate Preparation Products And Raw materials |
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