Amines & Amides Available — Bulk Only

4,4′-Bis(diethylamino)benzophenone

CAS 90-93-7 · Formula C21H28N2O · MW 324.5 g/mol

An electron-rich aminoketone photosensitizer that amplifies primary photoinitiators and extends visible-light response in UV-cured coatings, inks.

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CAS Number
90-93-7
Formula
C21H28N2O
Molecular Weight
324.5 g/mol
Material Family
Amines & Amides
At a Glance
Material Family
Amines & Amides
Primary Role
Crosslinking / Curing · Synthesis Intermediate
Applications & Use Cases
  • Aminobenzophenone sensitizer/co-initiator that extends Type II cure to longer wavelengths in UV coatings (Coatings & Construction)
  • Photosensitizer for UV/UV-LED inks, often paired with thioxanthones (Industrial Manufacturing)
  • Sensitizes cure of pigmented UV-curable plastics and adhesives (Plastics & Polymers)
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
90-93-7
Molecular Formula
C21H28N2O
Molecular Weight
324.5 g/mol
IUPAC Name
bismethanone
PubChem CID
InChI Key
VYHBFRJRBHMIQZ-UHFFFAOYSA-N
XLogP
5.3
Full Description

4,4′-Bis(diethylamino)benzophenone is an aminoketone photosensitizer and co-synergist — an electron-rich benzophenone that boosts other photoinitiators (especially thioxanthones and benzophenones) and extends response toward visible light. It is used as a sensitizer/co-initiator, not as a standalone surface initiator. Identity: CAS 90-93-7.

What it is

4,4′-Bis(diethylamino)benzophenone (CAS 90-93-7, the diethyl analogue of Michler’s ketone) is a yellow solid. Its two diethylamino groups make it a strong electron donor, so it works as a photosensitizer/co-initiator that amplifies a primary initiator.

How it cures

Rather than curing alone, it acts as a sensitizer/donor: it absorbs and transfers energy/electrons to a primary Type II initiator (e.g. a thioxanthone or benzophenone), extending spectral response and accelerating cure, including toward the visible. It is dosed at low levels as part of an initiator package.

Applications

Used as a sensitizer/co-initiator in UV/visible coatings and inks, paired with a thioxanthone (ITX) or benzophenone and an amine synergist (EDB) to broaden and speed cure.

Forms, grades and handling

It is supplied as a yellow crystalline solid. Photoinitiators are light-sensitive — store cool, dry and dark, away from light and ignition sources. Handle per the current Safety Data Sheet (SDS); each lot ships with a Certificate of Analysis (CoA) and Technical Data Sheet (TDS).

Bulk supply and RFQ

RawSource sources 4,4′-Bis direct from producers in bulk, with CoA, TDS and SDS per lot. Tell us your lamp (mercury or LED wavelength), system (clear or pigmented) and cure target, and we will quote the right grade. Compare the full range and selection logic in the photoinitiators guide.

Typical Properties

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

Property Typical Value
Chemical / type Photosensitizer (aminoketone co-initiator)
Photoinitiator type Photosensitizer / amine co-synergist
Absorption Visible / long-UV
Function Sensitizer/donor; dosed at low levels in a package
CAS Number 90-93-7
Molecular Formula C21H28N2O
Molecular Weight 324.5 g/mol
Handling Light-sensitive; refer to the current SDS

Regulatory & registration requirements

  • TSCA (US):
  • REACH (EU):
  • EC number: 202-025-4

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

Frequently Asked Questions

What is 4,4′-bis(diethylamino)benzophenone used for?

4,4′-Bis(diethylamino)benzophenone (CAS 90-93-7) is a photosensitizer/co-synergist used at low levels to boost Type II photoinitiators (thioxanthones, benzophenones) and extend spectral response toward visible light; it is not used as a standalone surface initiator.

Is it a photoinitiator or a sensitizer?

It functions mainly as a photosensitizer/co-initiator — an electron donor that amplifies a primary initiator — rather than cleaving on its own.

How is bulk 4,4′-bis(diethylamino)benzophenone supplied and quoted?

RawSource supplies 4,4′-bis(diethylamino)benzophenone in bulk with CoA, TDS and SDS per lot. Pricing is quote-based on grade and volume; submit an RFQ with your target quantity.

What is the REACH and TSCA regulatory status of 4,4'-Bis(diethylamino)benzophenone?

4,4'-Bis(diethylamino)benzophenone (CAS 90-93-7) is subject to U.S. TSCA Inventory requirements; supplying it into the EU requires valid REACH registration ((EC) No 1907/2006). RawSource cannot verify a third-party supplier's registrations — buyers should require documented TSCA and REACH compliance for their jurisdiction and volume (EC 202-025-4).

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.