Specialty Additives Available — Bulk Only

4-Chlorobenzophenone (CBZ)

CAS 134-85-0 · Formula C13H9ClO · MW 216.66 g/mol

A chloro-substituted benzophenone photoinitiator that accelerates UV surface cure of clear coatings and inks when paired with amine co-initiators.

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CAS Number
134-85-0
Formula
C13H9ClO
Molecular Weight
216.66 g/mol
Material Family
Specialty Additives
At a Glance
Material Family
Specialty Additives
Primary Role
Crosslinking / Curing · Synthesis Intermediate
Applications & Use Cases
  • Type II chlorinated-benzophenone photoinitiator with shifted absorption for surface cure of UV coatings (Coatings & Construction)
  • Used with amine synergists in UV inks and varnishes (Industrial Manufacturing)
  • Cures 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
134-85-0
Molecular Formula
C13H9ClO
Molecular Weight
216.66 g/mol
IUPAC Name
(4-chlorophenyl)-phenylmethanone
PubChem CID
InChI Key
UGVRJVHOJNYEHR-UHFFFAOYSA-N
XLogP
4.1
Full Description

4-Chlorobenzophenone is a Type II benzophenone-derivative photoinitiator. The chlorine substituent raises reactivity over plain benzophenone, giving faster surface cure of clear UV systems — but, like all Type II initiators, it works with an amine synergist. Identity: CAS 134-85-0.

What it is

4-Chlorobenzophenone (CAS 134-85-0) is a chloro-substituted diaryl ketone, a crystalline solid. It is one of several substituted benzophenones used to tune reactivity, solubility and volatility in UV-curable surface-cure packages.

How it cures

As a Type II initiator it does not cleave; on UV excitation it abstracts a hydrogen from an amine co-initiator to form the curing radicals. The chlorine substituent increases its activity relative to benzophenone, so it is chosen where a faster, more reactive benzophenone is wanted. Always paired with an amine synergist such as EDB or EHA.

Applications

Used for surface cure of UV coatings, overprint varnishes and inks where higher reactivity than benzophenone is needed, typically alongside a Type I initiator such as TPO for through cure. Compare 4-methylbenzophenone and benzophenone.

Forms, grades and handling

4-Chlorobenzophenone 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-Chlorobenzophenone 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 UV (mercury-lamp range)
CAS Number 134-85-0
Molecular Formula C13H9ClO
Molecular Weight 216.66 g/mol
Handling Light-sensitive; refer to the current SDS

Regulatory & registration requirements

  • TSCA (US):
  • REACH (EU):
  • EC number: 205-160-7

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

Frequently Asked Questions

What is 4-chlorobenzophenone used for?

4-Chlorobenzophenone (CAS 134-85-0) is a Type II photoinitiator for surface cure of UV coatings and inks; the chlorine substituent makes it more reactive than benzophenone. It is used with an amine synergist and usually with a Type I initiator for through cure.

Does 4-chlorobenzophenone need an amine?

Yes — as a Type II initiator it cures by hydrogen abstraction and requires an amine synergist (such as EDB or EHA) to generate radicals.

How is bulk 4-chlorobenzophenone supplied and quoted?

RawSource supplies 4-chlorobenzophenone 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-Chlorobenzophenone (CBZ)?

4-Chlorobenzophenone (CBZ) (CAS 134-85-0) 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 205-160-7).

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.