Specialty Additives Available — Bulk Only

4-Benzoylbiphenyl (PBZ)

PBZ
CAS 2128-93-0 · Formula C19H14O · MW 258.3 g/mol

A crystalline benzophenone-type photoinitiator with extended conjugation for red-shifted UV absorption, used in surface-cure coatings with amine synergists.

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CAS Number
2128-93-0
Formula
C19H14O
Molecular Weight
258.3 g/mol
Material Family
Specialty Additives
At a Glance
Material Family
Specialty Additives
Record Type
UVCB
Primary Role
Crosslinking / Curing
Functional Roles
Applications & Use Cases
  • Type II benzophenone-class photoinitiator with red-shifted absorption for high-throughput surface cure of UV coatings (Coatings & Construction)
  • Used with amine synergists in UV/UV-LED inks (Industrial Manufacturing)
  • Cures UV-curable plastics and adhesives (Plastics & Polymers)
Physical Properties
Appearance
White to pale-yellow crystalline solid
Molecular Weight
258.3 g/mol
Melting Point
101-103 °C
Log P XLogP
4.9
Water Solubility
Practically insoluble in water
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
2128-93-0
Molecular Formula
C19H14O
Molecular Weight
258.3 g/mol
IUPAC Name
phenyl-(4-phenylphenyl)methanone
PubChem CID
InChI Key
LYXOWKPVTCPORE-UHFFFAOYSA-N
XLogP
4.9
Synonyms & Trade Names
4-Phenylbenzophenone p-Phenylbenzophenone 4-Benzoyldiphenyl p-Benzoylbiphenyl [1,1'-Biphenyl]-4-yl(phenyl)methanone Phenyl 4-biphenylyl ketone Trigonal 12
Full Description

4-Benzoylbiphenyl is a red-shifted Type II benzophenone-type photoinitiator. The extra biphenyl ring extends conjugation, shifting absorption to longer UV than benzophenone — useful where deeper or slightly longer-wavelength surface cure is needed (with an amine synergist). Identity: CAS 2128-93-0.

What it is

4-Benzoylbiphenyl (CAS 2128-93-0) is a benzophenone analogue carrying a biphenyl group, a crystalline solid. The extended aromatic system red-shifts and strengthens its UV absorption relative to benzophenone.

How it cures

A Type II initiator that abstracts a hydrogen from an amine co-initiator under UV. Its longer-wavelength absorption helps it initiate where benzophenone is weak, and it is often used as a benzophenone upgrade in surface-cure packages with an amine synergist such as EDB or EHA.

Applications

Used in UV coatings and inks for surface cure where a stronger, longer-UV benzophenone is wanted, alongside a Type I initiator (TPO/184) for through cure. Compare benzophenone.

Forms, grades and handling

4-Benzoylbiphenyl is supplied as a 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-Benzoylbiphenyl 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 Photoinitiator (Type II, benzophenone derivative)
Photoinitiator type Type II (H-abstraction)
Absorption Red-shifted UV (extended conjugation)
CAS Number 2128-93-0
Molecular Formula C19H14O
Molecular Weight 258.3 g/mol
Handling Light-sensitive; refer to the current SDS

Regulatory & registration requirements

  • TSCA (US):
  • REACH (EU):
  • EC number: 218-345-2

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

Frequently Asked Questions

What is 4-benzoylbiphenyl used for?

4-Benzoylbiphenyl (PBZ, CAS 2128-93-0) is a Type II photoinitiator for UV surface cure with absorption red-shifted versus benzophenone; it is used with an amine synergist, usually with a Type I initiator for through cure.

How is bulk 4-benzoylbiphenyl supplied and quoted?

RawSource supplies 4-benzoylbiphenyl 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-Benzoylbiphenyl (PBZ)?

4-Benzoylbiphenyl (PBZ) (CAS 2128-93-0) 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 218-345-2).

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.