Determine the necessary mass, volume, or concentration for preparing a solution.
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In 316 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.
4,4′-Methylenebis(phenyl isocyanate) (MDI) is an aromatic diisocyanates class of monomer that is widely used in the production of polyurethane plastics, foam insulation, coatings, adhesives, and sealants. It is highly reactive due to the presence of two isocyanate functional groups. MDI is known for its excellent strength, durability, and resistance to chemical and environmental damage, which makes it useful in resin composition, lithographic printing plates, coating films, optical films, image display devices, semiconductor devices, and polyurethane foam production.
Application:
4,4′-Methylenebis(phenyl isocyanate) can be used as a starting material to synthesize:
Polyurethane cationomers, that are applicable in medical implants.
A prepolymer for preparing self-healable polyurethane elastomers.
It can also be used as a cross-linking agent to synthesize PEBA (polyether-block-amide) copolymer with improved mechanical properties, which are mainly used in soles, medical tubes, aerospace parts, and chemical separation. Additionally, MDI is also used as a crosslinker to covalently modify graphene oxide (GO) and enhance the corrosion resistance of polystyrene coatings. The resultant polystyrene/GO-MDI composite coatings showed superior corrosion resistance to unmodified polystyrene coatings. This approach can potentially be used to improve the durability of materials in various industrial and biomedical applications.
Umfassendes Dokument zu Gefahren, Handhabung, Lagerung und Einhaltung regulatorischer Vorschriften.
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Spezifikationsblatt ansehen →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Klasse | Benzene and substituted derivatives |
| Subclass | Diphenylmethanes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Diphenylmethanes |
| Alternative Parents | Isocyanates Propargyl-type 1,3-dipolar organic compounds Organopnictogen compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Diphenylmethane - Isocyanate - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic homomonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups. |
| External Descriptors | diisocyanate |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
| Certificate of Analysis | Oct 09, 2026 | M106783 | |
| Certificate of Analysis | Sep 16, 2026 | M106783 | |
| Certificate of Analysis | Sep 16, 2026 | M106783 | |
| Certificate of Analysis | Sep 16, 2026 | M106783 | |
| Certificate of Analysis | Sep 16, 2026 | M106783 | |
| Certificate of Analysis | Aug 13, 2026 | M106783 | |
| Certificate of Analysis | Aug 13, 2026 | M106783 | |
| Certificate of Analysis | Aug 13, 2026 | M106783 | |
| Certificate of Analysis | Aug 13, 2026 | M106783 | |
| Certificate of Analysis | Jun 29, 2026 | M106783 | |
| Certificate of Analysis | Jun 29, 2026 | M106783 | |
| Certificate of Analysis | Jun 29, 2026 | M106783 | |
| Certificate of Analysis | Jun 29, 2026 | M106783 | |
| Certificate of Analysis | Apr 25, 2026 | M106783 | |
| Certificate of Analysis | Apr 25, 2026 | M106783 | |
| Certificate of Analysis | Apr 25, 2026 | M106783 | |
| Certificate of Analysis | Apr 25, 2026 | M106783 | |
| Certificate of Analysis | Jan 23, 2026 | M106783 | |
| Certificate of Analysis | Jan 23, 2026 | M106783 | |
| Certificate of Analysis | Jan 23, 2026 | M106783 | |
| Certificate of Analysis | Jan 23, 2026 | M106783 | |
| Certificate of Analysis | Sep 11, 2025 | M106783 | |
| Certificate of Analysis | Sep 11, 2025 | M106783 | |
| Certificate of Analysis | Sep 11, 2025 | M106783 | |
| Certificate of Analysis | Sep 11, 2025 | M106783 | |
| Certificate of Analysis | Feb 19, 2025 | M106783 | |
| Certificate of Analysis | Feb 19, 2025 | M106783 | |
| Certificate of Analysis | Feb 19, 2025 | M106783 | |
| Certificate of Analysis | Feb 19, 2025 | M106783 | |
| Certificate of Analysis | Jul 05, 2024 | M106783 | |
| Certificate of Analysis | Jul 05, 2024 | M106783 | |
| Certificate of Analysis | Jul 05, 2024 | M106783 | |
| Certificate of Analysis | Jul 05, 2024 | M106783 | |
| Certificate of Analysis | Jul 05, 2024 | M106783 | |
| Certificate of Analysis | Apr 29, 2024 | M106783 | |
| Certificate of Analysis | Apr 29, 2024 | M106783 | |
| Certificate of Analysis | Apr 29, 2024 | M106783 | |
| Certificate of Analysis | Feb 29, 2024 | M106783 | |
| Certificate of Analysis | Feb 29, 2024 | M106783 | |
| Certificate of Analysis | Feb 29, 2024 | M106783 | |
| Certificate of Analysis | Aug 07, 2023 | M106783 | |
| Certificate of Analysis | Aug 07, 2023 | M106783 | |
| Certificate of Analysis | Aug 07, 2023 | M106783 | |
| Certificate of Analysis | Aug 07, 2023 | M106783 | |
| Certificate of Analysis | Apr 10, 2023 | M106783 | |
| Certificate of Analysis | Apr 10, 2023 | M106783 | |
| Certificate of Analysis | Apr 10, 2023 | M106783 | |
| Certificate of Analysis | Apr 10, 2023 | M106783 | |
| Certificate of Analysis | Apr 10, 2023 | M106783 | |
| Certificate of Analysis | Aug 25, 2022 | M106783 | |
| Certificate of Analysis | Aug 25, 2022 | M106783 | |
| Certificate of Analysis | Aug 25, 2022 | M106783 | |
| Certificate of Analysis | Aug 25, 2022 | M106783 | |
| Certificate of Analysis | Aug 25, 2022 | M106783 | |
| Certificate of Analysis | May 24, 2021 | M106783 | |
| Certificate of Analysis | May 24, 2021 | M106783 |
| Löslichkeit | Insoluble in water. Soluble in acetone, benzene and kerosene. |
|---|---|
| Empfindlichkeit | Heat & Moisture sensitive. |
| Flammpunkt (°C) | 113℃ |
| Siedepunkt (°C) | 200°C/5mmHg |
| Schmelzpunkt (°C) | 42-45°C |
| Molekulargewicht | 250.250 g/mol |
| XLogP3 | 5.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 250.074 Da |
| Monoisotopic Mass | 250.074 Da |
| Topological Polar Surface Area | 58.900 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 332.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |