 | |
 | |
| Names | |
|---|---|
| Preferred IUPAC name 1,6-Diisocyanatohexane | |
| Other names HDI 1,6-hexane diisocyanate | |
| Identifiers | |
| |
3D model (JSmol) | |
| ChEBI | |
| ChemSpider |
|
| ECHA InfoCard | 100.011.350 |
| UNII |
|
| |
| |
| Properties | |
| C8H12N2O2 | |
| Molar mass | 168.2 g/mol |
| Appearance | Colourless liquid |
| Odor | sharp, pungent[1] |
| Density | 1.047 g/cm3, liquid |
| Melting point | −67 °C (−89 °F; 206 K) |
| Boiling point | 255 °C (491 °F; 528 K) |
| Vapor pressure | 0.05 mmHg (25 °C)[1] |
| Viscosity | 3cP at 25 °C |
| Hazards | |
| Flash point | 130–140 °C (266–284 °F; 403–413 K) (Cleveland open cup) |
| NIOSH (US health exposure limits): | |
PEL (Permissible) | none[1] |
REL (Recommended) | TWA 0.005 ppm (0.035 mg/m3) C 0.020 ppm (0.140 mg/m3) [10-minute][1] |
IDLH (Immediate danger) | N.D.[1] |
| Related compounds | |
Relatedisocyanates | Isophorone diisocyanate |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Hexamethylene diisocyanate (HDI) is theorganic compound with the formula (CH2)6(NCO)2. It is classified as an diisocyanate. It is a colorless liquid.[2] It has sometimes been called HMDI[3] but this not usually done to avoid confusion withHydrogenated MDI.
Compared to other commercial diisocyanates, HDI is produced in relatively small quantities, accounting for (withisophorone diisocyanate) only 3.4% of the global diisocyanate market in the year 2000.[4] It is produced byphosgenation ofhexamethylene diamine.
Aliphatic diisocyanates are used in specialty applications, such as enamel coatings which are resistant to abrasion and degradation by ultraviolet light. These properties are particularly desirable in, for instance, the exterior paint applied to aircraft and vessels. HDI is also sold oligomerized as the trimer orbiuret which are used in automotive refinish coatings.[5][6] Although more viscous in these forms, it reduces the volatility and toxicity. At least 3 companies sell material in this form commercially. It is also used as an activator in process of in situ polymerization of caprolactam i.e. cast nylon process. HDI is also usedbisoxazolidine synthesis as the hydroxyl group on the molecule allows for further reaction with hexamethylene diisocyanate.[7][8]
HDI is considered toxic, and its pulmonary toxicity has been studied as well as its oligomers.[9][10][11][12]
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