Specialty Additives Available — Bulk Only

4-Benzoyl-4′-methyldiphenyl sulfide (BMS)

CAS 83846-85-9 · Formula C20H16OS · MW 304.4 g/mol

A pale solid benzophenone photoinitiator with thioether substitution for red-shifted UV absorption.

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CAS Number
83846-85-9
Formula
C20H16OS
Molecular Weight
304.4 g/mol
Material Family
Specialty Additives
At a Glance
Material Family
Specialty Additives
Primary Role
Crosslinking / Curing
Functional Roles
Applications & Use Cases
  • Type II thioether-benzophenone photoinitiator with extended absorption, used with amine synergists in UV coatings (Coatings & Construction)
  • Improves cure speed and surface cure of UV/UV-LED inks and varnishes (Industrial Manufacturing)
  • Sensitizes cure of 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
83846-85-9
Molecular Formula
C20H16OS
Molecular Weight
304.4 g/mol
IUPAC Name
-phenylmethanone
PubChem CID
InChI Key
DBHQYYNDKZDVTN-UHFFFAOYSA-N
XLogP
5.9
Full Description

4-Benzoyl-4′-methyldiphenyl sulfide (BMS) is a thioether-substituted Type II benzophenone photoinitiator. The sulfur group red-shifts absorption to longer UV, giving efficient surface cure and self-sensitizing behavior — used with an amine synergist. Identity: CAS 83846-85-9.

What it is

4-Benzoyl-4′-methyldiphenyl sulfide (CAS 83846-85-9) is a benzophenone bearing a methyl-phenyl thioether, a pale solid. The thioether extends absorption into longer UV, similar in spirit to thioxanthones.

How it cures

A Type II initiator that abstracts hydrogen from an amine co-initiator under UV. Its red-shifted absorption makes it more efficient than plain benzophenone in many systems and a useful sensitizer; pair with an amine synergist such as EDB or EHA.

Applications

Used for surface cure of UV coatings and inks, including slightly pigmented systems, where a longer-UV benzophenone is wanted, alongside a Type I initiator for through cure. Compare the thioxanthone ITX and DETX.

Forms, grades and handling

BMS is supplied as a pale 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-Benzoyl-4′-methyldiphenyl Sulfide 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, thioether benzophenone)
Photoinitiator type Type II (H-abstraction)
Absorption Red-shifted UV (thioether)
CAS Number 83846-85-9
Molecular Formula C20H16OS
Molecular Weight 304.4 g/mol
Handling Light-sensitive; refer to the current SDS

Regulatory & registration requirements

  • TSCA (US):
  • REACH (EU):
  • EC number: 281-064-9

TSCA Inventory flag PMN: a commenced PMN (premanufacture notice) substance (EPA flag legend).

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

Frequently Asked Questions

What is 4-benzoyl-4′-methyldiphenyl sulfide used for?

BMS (CAS 83846-85-9) is a Type II benzophenone-type photoinitiator with thioether-red-shifted absorption, used for efficient UV surface cure with an amine synergist, often in slightly pigmented systems.

How is bulk BMS supplied and quoted?

RawSource supplies BMS 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-Benzoyl-4'-methyldiphenyl sulfide (BMS)?

4-Benzoyl-4'-methyldiphenyl sulfide (BMS) (CAS 83846-85-9) 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 281-064-9).

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.