Polymers & Resins Available — Bulk Only

Trimethylhexamethylene Diisocyanate (2,2,4-/2,4,4- isomer mixture)

CAS 32052-51-0 · Formula C11H18N2O2 · MW 210.27 g/mol

A branched aliphatic diisocyanate crosslinker for non-yellowing polyurethane coatings, elastomers, and adhesives requiring light stability and flexibility.

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CAS Number
32052-51-0
Formula
C11H18N2O2
Molecular Weight
210.27 g/mol
Material Family
Polymers & Resins
At a Glance
Material Family
Polymers & Resins
Primary Role
Crosslinking / Curing · Synthesis Intermediate
Applications & Use Cases
  • Liquid aliphatic diisocyanate used to build light-stable polyurethane prepolymers and coatings
  • Crosslinks hydroxyl resins in weatherable 2K-PU coatings, elastomers and adhesives
  • Provides low color and good UV stability versus aromatic diisocyanates
Safety & Handling
Full SDS available on request

A grade-specific Safety Data Sheet (SDS) — with the complete hazard classification, handling precautions, and transport information — is supplied with every shipment and available on request. Confirm all safety and regulatory details against the SDS for your specific grade.

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Chemical Identity
CAS Number
32052-51-0
Molecular Formula
C11H18N2O2
Molecular Weight
210.27 g/mol
IUPAC Name
1,6-diisocyanato-2,2,4-trimethylhexane
PubChem CID
InChI Key
ATOUXIOKEJWULN-UHFFFAOYSA-N
XLogP
4.5
Full Description

Trimethylhexamethylene diisocyanate (TMDI) is a branched aliphatic diisocyanate (2,2,4-/2,4,4-isomer mixture) used as a light-stable building block and crosslinker for high-performance, flexible, non-yellowing polyurethanes. Identity: CAS 32052-51-0.

What it is

TMDI (CAS 32052-51-0) is a liquid branched aliphatic diisocyanate. The methyl branches give low viscosity, liquid handling and flexibility, and it is fully aliphatic (light-stable).

How it works

Its two NCO groups react with polyols/amines to build polyurethane/polyurea; being aliphatic and branched it gives non-yellowing, flexible, low-viscosity systems and is also a building block for specialty polyisocyanates.

Applications

TMDI is used in light-stable polyurethane coatings, elastomers and adhesives and as a building block. It derives from TMD.

Forms, grades and handling

TMDI is supplied as a clear liquid in drums and bulk. Properties are typical reference values; the Certificate of Analysis (CoA) for the lot you buy governs. Isocyanates are moisture-sensitive and require respiratory/skin precautions; handle per the current Safety Data Sheet (SDS). Each lot ships with CoA, TDS and SDS.

Bulk supply and RFQ

RawSource sources Trimethylhexamethylene Diisocyanate direct from producers in bulk, with CoA, TDS and SDS per lot. Tell us your binder system, cure schedule and the performance you need, and we will quote the right grade. See the polyurethane catalysts guide for the catalysts that drive these reactions.

Typical Properties

Typical reference values, not a specification; the Certificate of Analysis (CoA) for the lot governs.

Property Typical Value
Chemical / class Aliphatic diisocyanate (TMDI)
Function Light-stable PU building block
CAS Number 32052-51-0
Molecular Formula C11H18N2O2
Molecular Weight 210.27 g/mol
Handling Refer to the current SDS

Regulatory & registration requirements

  • TSCA (US): Not found on the public (non-confidential) TSCA Inventory
  • REACH (EU):
  • EC number: 915-277-1

Source: EPA TSCA Inventory (July 2025 release) · ECHA CHEM — retrieved 2026-07-12

Frequently Asked Questions

What is trimethylhexamethylene diisocyanate (TMDI) used for?

TMDI (CAS 32052-51-0) is a branched aliphatic diisocyanate used as a light-stable, flexible, low-viscosity building block and crosslinker for high-performance polyurethane coatings, elastomers and adhesives.

How is bulk TMDI supplied and quoted?

RawSource supplies TMDI in bulk with CoA, TDS and SDS per lot. Pricing is quote-based on grade and volume; submit an RFQ with your binder system and cure schedule.

What is the REACH and TSCA regulatory status of Trimethylhexamethylene Diisocyanate (2,2,4-/2,4,4- isomer mixture)?

Trimethylhexamethylene Diisocyanate (2,2,4-/2,4,4- isomer mixture) (CAS 32052-51-0) is recorded as REACH-registered in ECHA's public CHEM database (EC 915-277-1); it was not found on EPA's public (non-confidential) TSCA Inventory file.

Disclaimer. Information on this page — including properties, identifiers, hazard, transport (DOT/UN) and tariff (HS) classifications, and applications — is provided for general reference and is compiled from authoritative public sources (e.g. PubChem/ECHA, 49 CFR 172.101, the Harmonized Tariff Schedule). Values are typical and are not a guaranteed specification; the Certificate of Analysis (CoA) for the lot purchased governs. Products are sold for industrial and professional use only. Nothing here is a medical, health, or efficacy claim or advice. Always consult the current Safety Data Sheet (SDS) before handling, storage, transport or disposal, and confirm regulatory status, classification and suitability for your application and jurisdiction. Hazard, transport and tariff classifications must be verified for your specific shipment. RawSource makes no warranty, express or implied, and assumes no liability for use of this information. Trademarks. Third-party trademarks and brand names are the property of their respective owners; any reference is nominative — used only to identify a comparable product — and does not imply affiliation with, sponsorship by, or endorsement by the trademark owner.