52650

Hexamethylene diisocyanate

purum, ≥98.0% (GC)

• Synonyme(s) : 1,6-Diisocyanatohexane
• Formule linéaire : OCN(CH₂)₆NCO
• Numéro CAS: 822-06-0
• Poids moléculaire : 168.19
• Numéro Beilstein : 956709
• Numéro CE : 212-485-8
• Numéro MDL: MFCD00002047
• Code UNSPSC : 12162002
• ID de substance PubChem : 329757867
• Nomenclature NACRES : NA.23

Propriétés

• Qualité: purum
• Niveau de qualité: 200
• Pureté: ≥98.0% (GC)
• Indice de réfraction: n20/D 1.453
• Point d'ébullition: 82-85 °C/0.1 mmHg
• Densité: 1.047 g/mL at 20 °C (lit.)
• Chaîne SMILES: O=C=NCCCCCCN=C=O
• InChI: 1S/C8H12N2O2/c11-7-9-5-3-1-2-4-6-10-8-12/h1-6H2
• Clé InChI: RRAMGCGOFNQTLD-UHFFFAOYSA-N

Description

Description générale

Hexamethylene diisocyanate (HDI) is an aliphatic diisocyanate monomer belonging to the class of isocyanates. It is primarily used in the production of polyurethanes. The isocyanate functional groups in hexamethylene diisocyanate react readily with polyols to form polyurethane polymers. Polyurethanes derived from HDI are commonly used in various products, including coatings, adhesives, sealants, elastomers, foams, thin-film transistors, flexible or rigid plastics, biomedical applications, electronics and aerospace industries. It is also used to produce oligomers and prepolymers that when combined with a polyol produce light-stable polyurethane.

Application

Hexamethylene diisocyanate (HDI) is used as:

• A crosslinker to crosslink the polyurethane chains in the triblock copolymer gate dielectric, which is then deposited on the substrate to fabricate low-voltage organic thin-film transistors.
• A precursor in the preparation of electroactive shape memory polyurethane/graphene nanocomposites. These materials are usually used as actuators, sensors, artificial muscles, smart devices, and microswitches.
• A crosslinker in conjunction with Pluronic F127, a nonionic surfactant, to synthesize a poly(lactic acid) (PLA)-based hydrogel for biomedical applications.

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).

Informations sur la sécurité

• Pictogrammes: GHS06,GHS08,GHS05
• Mention d'avertissement: Danger
• Mentions de danger: H302,H314,H317,H330,H334,H335
• Conseils de prudence: P260 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Classification des risques: Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1C - Skin Sens. 1 - STOT SE 3
• Organes cibles: Respiratory system
• Code de la classe de stockage: 6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
• Classe de danger pour l'eau (WGK): WGK 1
• Point d'éclair (°F): 266.0 °F - Pensky-Martens closed cup
• Point d'éclair (°C): 130 °C - Pensky-Martens closed cup
• Équipement de protection individuelle: Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter